[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"balance\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:balance":28},{"pageToken":4,"total":5,"offset":6,"count":7,"results":8},null,50,0,25,[9,52,95,124,148,173,204,233,261,283,306,337,363,388,410,440,458,484,515,538,573,601,629,653,673],{"id":10,"slug":11,"hasResults":12,"nctId":13,"briefTitle":14,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":12,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":31,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":40,"lastUpdatePostDateStruct":41,"startDateStruct":44,"completionDateStruct":46,"leadSponsor":48,"locationsCount":51},"100652708","effects-of-otago-exercise-versus-multisensory-integration-training-on-balance-and-gait-in-elderly-with-diabetes-100652708",false,"NCT07776535","Effects Of Otago Exercise Versus Multisensory Integration Training On Balance And Gait In Elderly With Diabetes","Balance - DM","Inclusion Criteria:\n\n1. Ninety elderly Patients of both genders.\n2. Their age will range from 65 to 75th.\n3. They will be diagnosed with type 2 diabetes for 5 years or more.\n4. Patients with mild \\& moderate neuropathy will be included. (Based on the Toronto scale: -mild (6-8); moderate (9-11)\n5. Berg balance between (21 to \\\u003C50) patients with mild \\&moderate risk of fall .\n6. Time up \\& go dual task: patient takes longer than 10 sec.\n7. HBA1C for these patients was ≥ 6.5% .\n8. BMI will range from (18: 29,9 kg\u002Fm2).\n9. Able to walk independently, with or without assistive devices.\n\nExclusion Criteria:\n\n1. Any musculoskeletal disorder affecting the lower limb (fracture of the lower limb, tumors, any infection, ligament injuries, foot injuries).\n2. Any other neurological disorder influences gait such as (stroke, Parkinson's disease, cerebellar dysfunction, ataxia, vestibular disorders)\n3. Any other cardiovascular disease (arrhythmia, cardiac pacemakers).\n4. Unstable proliferative retinopathy and visual impairments without correction.\n5. Non-diabetic neuropathy (inflammatory, autoimmune disease, infections, tumors, vitamin B12 deficiency, hypothyroidism, alcoholism, injury or pressure on the nerve).\n6. The use of medications significantly impacting postural control (e.g., sedatives).\n7. Vestibular system and Cognitive disorders.\n8. Uncontrolled hypertension.\n9. Common peroneal nerve injury.\n10. Orthostatic hypotension.","ALL","65 Years","75 Years",{"count":21,"type":22},90,"ESTIMATED","INTERVENTIONAL",[25],"NA","The goal of this clinical trial is to compare the effect of the Otago exercise and Multisensory integration training on balance and gait in the elderly with type 2 diabetes mellitus.\n\nThe main question it aims to answer is:\n\n• Is there a significant difference between the effect of Otago exercise and Multisensory integration training on balance and gait in the elderly with type 2 diabetes mellitus? Researchers will compare Otago exercise to Multisensory integration training to know which one has the greatest benefit on balance \\&gait in the elderly with type2 diabetes.\n\nParticipants will be divided into 3 groups; each group takes a certain training program for 8 weeks:\n\n* First group: Otago exercise group plus conventional treatment for neuropathy.\n* Second group: Multisensory integration training group plus conventional treatment for neuropathy.\n* Third group: control group takes only conventional treatment for neuropathy.",[28,29,30],"Balance","Gait","Diabetes Mellitus",[32,33,34,35,36,37,38],"otago exercise","multisensory integration","balance disorder","gait proplem","diabetes","elderly","older adults","NOT_YET_RECRUITING","2026-08-17",{"date":42,"type":43},"2026-08-20","ACTUAL",{"date":45,"type":22},"2026-10",{"date":47,"type":22},"2027-11",{"name":49,"class":50},"Cairo University","OTHER",1,{"id":53,"slug":54,"hasResults":12,"nctId":55,"briefTitle":56,"officialTitle":56,"acronym":4,"eligibilityCriteria":57,"healthyVolunteers":58,"sex":17,"minAge":59,"maxAge":60,"enrollmentInfo":61,"targetDuration":4,"studyType":23,"phases":63,"briefSummary":64,"conditions":65,"keywords":69,"overallStatus":87,"whyStopped":4,"lastUpdateSubmitDate":40,"lastUpdatePostDateStruct":88,"startDateStruct":89,"completionDateStruct":91,"leadSponsor":93,"locationsCount":51},"100652548","sensor-ankle-brace-for-special-operations-rehabilitation---phase-2-100652548","NCT07776223","Sensor Ankle Brace for Special Operations Rehabilitation - Phase 2","Inclusion Criteria:\n\n* Healthy adults: ages 18 - 40 years\n* considered \"healthy to exercise\" as determined by the physical activity readiness questionnaire (PAR-Q)\n* Classified as \"moderate\" or \"high\" activity level as defined by the scoring criteria of the International Physical Activity Questionnaire - Short Form (IPAQ)\n* Comfortably fit into combat boots provided by the laboratory (Men's sizes 8, 9, 10, 11, 12 and Women's sizes 6, 7, 8, 9, 10 will be purchased, and so participants with foot lengths of 22.54-29.27.8 cm are expected to fit in the boots provided).\n\nExclusion Criteria:\n\n* Smoking tobacco on a regular basis\n* Previous lower back or lower limb surgery (including the joints of the pelvis and lower limbs)\n* Musculoskeletal injury sustained within the 12-weeks prior to enrollment . A musculoskeletal injury is defined as musculoskeletal pain causing a reduction or stoppage of normal physical activity for at least 3 days within a 7-day period, and have not returned to their normal physical activity and exercise without pain for at least the last 6-weeks.\n* Pregnant (women only)\n* Current or history of an unresolved musculoskeletal, neurological, cardiovascular, pulmonary\u002Frespiratory, metabolic, renal condition, disease, or problem.\n* Torn anterior or posterior cruciate ligament (ACL or PCL).\n* Any other disease or problems that may affect movement or the ability to exercise even at a low intensity.\n* Identification of Functional Ankle Instability (IDFAI) score of \\\u003C11.\n* unable to comfortably perform the drop landing condition.\n* Feet are too large or too small to fit comfortably in the combat boots provided.",true,"18 Years","40 Years",{"count":62,"type":22},40,[25],"The primary purpose of this study overall is to validate a modified version of a commercially available ankle brace. Inertial measurement unit sensors will be incorporated into an existing ankle brace (\"sXAB\") by TayCo Brace, Inc. In two consecutive studies, gait metrics data collected from the sensor enabled ankle brace will be compared to data collected by the gold-standard equipment that is used in research and clinical settings to determine whether the sXAB performs adequately in terms of measurement or technical feasibility prior to further clinical evaluation. In the Phase 2 protocol, the sXAB will be validated on healthy subjects wearing combat boots performing walking, running, jumping, and stair climbing activities. These movements were selected because they simulate key movements performed during operational activities. All participants experience both conditions: with an ankle brace and without an ankle brace. Comparisons are made within-subject between brace and no-brace conditions. It is hypothesized that the sensor-enabled ankle brace will measure gait metrics with a high degree of accuracy (within 5%) when compared against the gold-standard lab equipment (i.e., motion capture and research-grade inertial measurement units).",[29,28,66,67,68],"Biomechanical Data","Postural Control","Locomotion",[70,71,72,73,74,75,76,77,78,79,80,81,82,83,84,85,86],"adult","gait","gait analysis","humans","ankle brace","motion capture","sensor validation","wearable electronic devices","wearable sensors","inertial measurement unit","IMU","locomotion","running","walking","landing","stair ascent","stair descent","RECRUITING",{"date":42,"type":43},{"date":90,"type":43},"2026-05-05",{"date":92,"type":22},"2026-09-01",{"name":94,"class":50},"Indiana University",{"id":96,"slug":97,"hasResults":12,"nctId":98,"briefTitle":99,"officialTitle":100,"acronym":101,"eligibilityCriteria":102,"healthyVolunteers":12,"sex":17,"minAge":59,"maxAge":103,"enrollmentInfo":104,"targetDuration":4,"studyType":23,"phases":106,"briefSummary":107,"conditions":108,"keywords":114,"overallStatus":87,"whyStopped":4,"lastUpdateSubmitDate":116,"lastUpdatePostDateStruct":117,"startDateStruct":119,"completionDateStruct":121,"leadSponsor":122,"locationsCount":51},"100648655","dynamic-neuromuscular-stability-exercises-with-and-without-rhythmic-auditory-stimulation-in-lateral-ankle-sprain-100648655","NCT07726810","Dynamic Neuromuscular Stability Exercises With and Without Rhythmic Auditory Stimulation in Lateral Ankle Sprain","Effect of Dynamic Neuromuscular Stability Exercises With and Without Rhythmic Auditory Stimulation on Balance, Proprioception, and Performance Among Badminton Players With Lateral Ankle Sprain","DNS","Inclusion Criteria:\n\n* Age 18-30 years\n* Both male and female genders\n* Diagnosed with Grade I or II lateral ankle sprain (subacute to chronic phase)\n* Within 2-8 weeks post-injury\n\nExclusion Criteria:\n\n* History of ankle surgery\n* Vestibular, neurological, or hearing disorders\n* Acute pain prevents participation\n* Current involvement in other rehab programs\n* Any fracture or other injury\n* Any systemic illness\n* Any inflammatory disease (Rheumatoid arthritis, gout)","30 Years",{"count":105,"type":22},44,[25],"To examine the effects of Dynamic Neuromuscular Stability exercises with and without Rhythmic Auditory Stimulation on balance, proprioception, and functional performance in badminton players with lateral ankle sprain.",[109,110,111,112,28,113],"Ankle Sprain","Lateral Ankle Sprain","Lateral Ankle Instability","Dynamic Neuromuscular Stabilization (DNS)","Proprioception",[115],"Rhythmic Auditory Stimulation","2026-08-10",{"date":118,"type":43},"2026-08-12",{"date":120,"type":43},"2026-07-14",{"date":92,"type":22},{"name":123,"class":50},"Riphah International University",{"id":125,"slug":126,"hasResults":12,"nctId":127,"briefTitle":128,"officialTitle":129,"acronym":37,"eligibilityCriteria":130,"healthyVolunteers":58,"sex":17,"minAge":18,"maxAge":131,"enrollmentInfo":132,"targetDuration":4,"studyType":134,"phases":4,"briefSummary":135,"conditions":136,"keywords":4,"overallStatus":87,"whyStopped":4,"lastUpdateSubmitDate":140,"lastUpdatePostDateStruct":141,"startDateStruct":142,"completionDateStruct":144,"leadSponsor":146,"locationsCount":51},"100606782","figure-of-eight-backward-walk-test-in-elderly-100606782","NCT07180030","Figure-of-eight Backward Walk Test in Elderly","Determination of Reliability, Validity, and Minimal Detectable Change (MDC) of the Figure-of-eight Backward Walking Test in Elderly Adults","Inclusion Criteria:\n\n* Healthy elderly individuals over 65 years of age.\n* Elderly individuals who have fluent in Turkish and able to communicate.\n* Elderly individuals who have no cognitive impairment.\n\nExclusion Criteria:\n\n* Elderly individuals who have any neurological problems (Parkinson's, hemiplegia, etc.)\n* Elderly individuals who have any orthopedic problems (fractures, etc., in the last year)\n* Elderly individuals who have a body mass index (BMI) ≥ 40 kg\u002Fm2\n* Elderly individuals who havevision problems\n* Elderly individuals who have had any lower extremity surgery in the last year\n* Elderly individuals who use any mobility aids\n* Elderly individuals who refuse to participate in the study.","85 Years",{"count":133,"type":22},87,"OBSERVATIONAL","Mobility is a fundamental element of healthy aging. Balance is a necessary function during mobility for all movements throughout life in elderly individuals. Falls due to balance disorders in elderly individuals cause a decrease in the quality of life. Studies in the literature indicate that 13% of individuals aged 65-69 experience falls, and this rate rises to 46% in individuals over 85. Lower extremity muscle volume and strength gradually decrease with aging. This decreased muscle strength directly impacts individuals' activities of daily living.Normal walking speed for elderly individuals is related to balance and overall health performance. However, walking assessments generally focus on walking activities in a forward direction and in a straight line. However, in daily life, we may need to sit on a chair, walk backward to navigate a narrow space, or change direction suddenly due to obstacles or environmental cues. Walking backward requires more complex motor control, and these gait training programs are known to be effective in improving balance and walking skills.Clinically, balance assessments in the elderly persons are commonly measured by using the TUG, 10-meter walk test, functional reach test, 4-square step test, and Berg balance scale. The methods used to assess balance are still not fully standardized. The best test for assessing dynamic balance and fall risk is still up for debate, especially when it comes to elderly individuals who live freely in the community. Further research is needed to determine whether lateral walking tests can identify those at high risk of falling in elderly adults. The purpose of this study was to determine the reliability, validity, and minimal detectable change (MDC) of the Figure-of-8 backward walking test in healthy elderly adults.",[137,28,138,139],"Elderly (People Aged 65 or More)","Dynamic Balance","Backward Walking","2026-07-12",{"date":120,"type":43},{"date":143,"type":43},"2025-05-01",{"date":145,"type":22},"2026-09-30",{"name":147,"class":50},"Kahramanmaras Sutcu Imam University",{"id":149,"slug":150,"hasResults":12,"nctId":151,"briefTitle":152,"officialTitle":153,"acronym":154,"eligibilityCriteria":155,"healthyVolunteers":58,"sex":17,"minAge":59,"maxAge":4,"enrollmentInfo":156,"targetDuration":4,"studyType":23,"phases":158,"briefSummary":159,"conditions":160,"keywords":161,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":164,"lastUpdatePostDateStruct":165,"startDateStruct":167,"completionDateStruct":169,"leadSponsor":171,"locationsCount":4},"100647095","otago-exercises-in-diabetes-mellitus-examining-its-effectiveness-100647095","NCT07705958","OTAGO Exercises in Diabetes Mellitus Examining Its Effectiveness","OTAGO Exercises in Individuals Diagnosed With Diabetes Mellitus Examining Its Effectiveness","OTAGO in DM","Inclusion Criteria:\n\n* Cases diagnosed with Diabetes Mellitus,\n* Cases that do not have any orthopedic\u002Fneurological\u002Fcardiopulmonary disease other than Diabetes Mellitus that will directly affect the evaluation results,\n* Having agreed to participate in the study voluntarily,\n* Having been diagnosed with Type 2 DM for at least 1 year\n\nExclusion Criteria:\n\n* Not agreeing to participate in the study,\n* Individuals with additional diseases other than DM that will affect the evaluations,\n* Having a smoking habit or history\n* Restriction in joint movements or any orthopedic\u002Fneurological\u002Fcardiopulmonary disease that may cause this,\n* Not being able to cooperate,\n* Having vision loss,\n* Having hearing loss,\n* Having a diabetic ulcer on the foot,",{"count":157,"type":22},56,[25],"Diabetes Mellitus (DM) is a chronic metabolic disease characterized by hyperglycemia, which occurs in insulin deficiency or when the body cannot effectively use the insulin produced. Moreover, according to the \"Global Report on Diabetes\" data published by the World Health Organization (WHO) in 2016, it is an important public health problem, one of the four priority non-communicable diseases (1, 2). In addition to the high mortality rates caused by complications due to DM, it is also known that it can cause low quality of life and many other additional problems in individuals. Possible complications are chronic and serious problems such as heart attack, risk of stroke, kidney failure, vision loss and nerve damage. One of the most common and most disabling complications is neuropathy. It should also be noted that approximately half of diabetic neuropathy is asymptomatic and patients diagnosed with DM may have neuropathy due to causes other than diabetes (2). These complications and damage that DM can cause can lead to decreased blood flow combined with neuropathy; As a result, foot ulcers and infections may occur; Amputation rates may increase. In addition to such additional complications that diabetic neuropathy may cause, due to all these; Loss of protective plantar sensation may also occur (3). This loss of protective sensation may lead to cutaneous deficits in the lower extremities, loss of muscle strength and reflexes, and gait and balance disorders (4). The mechanism that makes an important contribution to functional joint stability and the continuity of this stability, along with the feedback mechanisms required to ensure neuromuscular control, is proprioception, which includes joint movement (kinesthesia) and joint position sense (EPH) and is a subunit of the somatosensory system (5-7). . Rehabilitation with various injuries and other clinical conditions; Clinical studies to determine its effects on joint proprioception, neuromuscular control and balance have mostly focused on knee and ankle joints (5). The main reason for this can be attributed to the great importance of the knee and ankle joints in the lower extremities in maintaining general body kinematics and balance (8). Additionally, it has been reported in the literature that EPH and plantar sensory loss are observed in individuals diagnosed with DM, and these complications may cause additional problems (10, 12, 18-22). Additionally, many studies in the literature on this subject have been conducted in individuals with diabetic neuropathy, and changes in functional parameters such as plantar sensation, proprioception, muscle strength and balance have been examined (10, 19, 20, 22, 23). However, it has been found that not only individuals with neuropathy but also individuals diagnosed with DM without neuropathy have balance disorders (24).\n\nThere are many studies in the literature about the effects of different exercise training on proprioception. In general, studies have reported that exercise training without weight bearing on the extremity has no effect on proprioception, but as a result of exercises performed with weight bearing on the extremity, a significant improvement was noted in both proprioceptive performance and muscle strength (25). In one of the most recent studies on this subject, it was stated that proprioceptive sensitivity increased in individuals with knee osteoarthritis with 8-week squat strengthening training performed by transferring weight to the extremity (26). Additionally, there are studies in the literature reporting different results regarding the effects of stretching exercises on proprioceptive performance. Some studies have reported that static stretching has no effect on proprioception, while others have reported that it has a positive effect on proprioception (27,28).\n\nThe Otago Exercise Program is an evidence-based, home-based, individually tailored strength and balance retraining program. Research shows that the Otago Exercise Program is effective in reducing the risk of death and the incidence of falls in older adults over a one-year period. In one study, falls were reduced by 35% in older adults has been reported(29)\n\nThis study was planned to examine the effectiveness of balance exercises given as a home program to individuals diagnosed with Type 2 DM.",[30,28],[162,32,163],"balance","Diabetes mellitus","2026-07-10",{"date":166,"type":43},"2026-07-15",{"date":168,"type":22},"2026-08-01",{"date":170,"type":22},"2026-12-01",{"name":172,"class":50},"Pamukkale University",{"id":174,"slug":175,"hasResults":12,"nctId":176,"briefTitle":177,"officialTitle":178,"acronym":4,"eligibilityCriteria":179,"healthyVolunteers":12,"sex":17,"minAge":180,"maxAge":4,"enrollmentInfo":181,"targetDuration":4,"studyType":23,"phases":183,"briefSummary":184,"conditions":185,"keywords":191,"overallStatus":87,"whyStopped":4,"lastUpdateSubmitDate":195,"lastUpdatePostDateStruct":196,"startDateStruct":198,"completionDateStruct":199,"leadSponsor":201,"locationsCount":51},"100635573","wearable-sensory-prosthesis-to-improve-coordination-walking-and-physical-activity-100635573","NCT07554443","Wearable Sensory Prosthesis to Improve Coordination, Walking, and Physical Activity","Wearable Sensory Prostheses to Improve Neuromuscular Coordination, Walking Function, and Real-World Physical Activity","Inclusion Criteria:\n\n* Be 60 years of age or older\n* Have a diagnosis of PN with plantar sensory loss\n* Demonstrate balance impairment, defined as a Single-Leg Stance time of \\\u003C23 seconds\n* Be able to walk independently for at least 6 minutes without the use of an assistive device (rest breaks permitted)\n* Be willing to use the Walkasins device as recommended\n* Be willing to participate in all aspects of physical activity monitoring and study assessments\n\nExclusion Criteria:\n\n* Under 60 years old\n* Do not have a diagnosis of PN with plantar sensory loss\n* Self-reported acute thrombophlebitis, including deep vein thrombosis\n* Self-reported severe peripheral vascular disease\n* Untreated lymphedema\n* Untreated lesion of any kind, swelling, infection, inflamed area of skin or eruptions on the lower leg near product use\n* Self-reported, untreated fractures in the foot and ankle\n* Other neurological or musculoskeletal conditions that moderately or severely impact walking\n* Use of ankle-foot orthosis for ambulation that prevents donning of Walkasins\n* Weight of more than 300 pounds\n* Inability to perceive vibration from Walkasins Haptic Module\n* Do not demonstrate balance impairments, defined as a Single-Leg Stance time of \\\u003C23 seconds","60 Years",{"count":182,"type":22},18,[25],"The goal of this clinical trial is to investigate whether sensory stimulations from a neuroprosthesis device (Walkasins®) can increase physical activity and improve gait quality in persons with peripheral neuropathy (PN). The main question it aims to answer is whether Walkasins enhances habitual activity patterns in adults with peripheral neuropathy.\n\nParticipants will do the following as part of the study:\n\n* Complete a sensation and balance assessment to determine eligibility for the study.\n* Answer questions about their medical history, physical function, balance confidence, and sleep.\n* Perform various balance and walking tasks on three separate occasions. One of the tests involves walking for six minutes without a cane or walker.\n* Wear an activPAL activity monitor for ten days on three separate occasions and return it to the researcher as directed.\n* Wear Walkasins for ten weeks as part of their daily routine. Walkasins consists of two parts: 1) an insole that fits inside the shoe and 2) a strap that secures around the ankle.",[186,187,28,188,189,190],"Peripheral Neuropathy With Type 2 Diabetes","Peripheral Neuropathy Grade 2 or Greater","Balance Impairment, Gait Disorders, Fatigue","Balance Disorders","Physical Activities",[192,193,189,194],"Peripheral Neuropathy","Walkasins","Physical Activity","2026-06-22",{"date":197,"type":43},"2026-06-25",{"date":197,"type":22},{"date":200,"type":22},"2027-12",{"name":202,"class":203},"RxFunction Inc.","INDUSTRY",{"id":205,"slug":206,"hasResults":12,"nctId":207,"briefTitle":208,"officialTitle":209,"acronym":4,"eligibilityCriteria":210,"healthyVolunteers":58,"sex":17,"minAge":211,"maxAge":59,"enrollmentInfo":212,"targetDuration":4,"studyType":23,"phases":214,"briefSummary":215,"conditions":216,"keywords":221,"overallStatus":87,"whyStopped":4,"lastUpdateSubmitDate":225,"lastUpdatePostDateStruct":226,"startDateStruct":227,"completionDateStruct":229,"leadSponsor":231,"locationsCount":51},"100641968","the-effects-of-game-based-exercise-programs-100641968","NCT07660822","THE EFFECTS OF GAME-BASED EXERCISE PROGRAMS","THE EFFECTS OF VIRTUAL REALITY AND VIDEO GAME-BASED EXERCISE PROGRAMS ON PHYSICAL FITNESS AND ATTENTION LEVELS IN HEALTHY ADOLESCENTS","Inclusion Criteria:\n\n* Volunteering to participate in the study\n* Being an adolescent aged 10-18 years\n* Having a score below 4 on the Physical Activity Scale for Adolescents\n\nExclusion Criteria:\n\n* Having any physical disability that would prevent participation in the exercise program\n* Having upper or lower extremity orthopedic disease\n* Having a score above 4 on the Physical Activity Scale for Adolescents","10 Years",{"count":213,"type":22},48,[25],"Studies comparing aerobic exercise with virtual reality or video game technologies to traditional games and classical exercise have been conducted in healthy adolescents, but no studies comparing virtual reality and video game technologies have been found. Based on all this, we aimed to investigate the effect of virtual reality and video game-based exercise programs on physical fitness and attention levels in healthy adolescents. The study was planned as a quantitative experimental randomized controlled trial. Healthy individuals aged 10-18 years who meet the inclusion criteria will be evaluated during the dates of the study. Individuals will be divided into 3 groups: a classical physical activity group, a virtual reality group, and a video-based game group. Each program will be implemented for 20-30 minutes, three days a week for eight weeks. The Physical Activity Scale for Adolescents was used to evaluate the physical activity of the individuals, the Multidimensional Body-Self Relationship Scale was used to measure body image, and the Exercise Benefit\u002FBarrier Scale was used to measure exercise perception. To measure attention, balance, and reaction time, the D2 Attention Test, Y-Balance Test, and Nelson's Hand Reaction Test will be administered, respectively. In the virtual reality and video-based game group, the games played by participants will be similar to the physical activities performed in the classic exercise group. One or more games incorporating these physical activities will be selected.",[194,217,218,28,219,220],"Body Image","Exercise Perception","Reaction Time","Attention",[222,223,224],"Healthy adolescent","virtual reality","attention level)","2026-06-16",{"date":195,"type":43},{"date":228,"type":43},"2025-11-15",{"date":230,"type":22},"2026-08-30",{"name":232,"class":50},"Gaziantep Islam Science and Technology University",{"id":234,"slug":235,"hasResults":12,"nctId":236,"briefTitle":237,"officialTitle":238,"acronym":239,"eligibilityCriteria":240,"healthyVolunteers":12,"sex":17,"minAge":241,"maxAge":59,"enrollmentInfo":242,"targetDuration":4,"studyType":134,"phases":4,"briefSummary":244,"conditions":245,"keywords":250,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":252,"lastUpdatePostDateStruct":253,"startDateStruct":255,"completionDateStruct":257,"leadSponsor":259,"locationsCount":51},"100642191","core-stability-functional-capacity-balance-strength-and-fatigue-in-pediatric-demyelinating-diseases-100642191","NCT07654738","Core Stability, Functional Capacity, Balance, Strength, and Fatigue in Pediatric Demyelinating Diseases","Investigation of the Relationship Between Core Stability, Functional Capacity, Balance, Lower Extremity Strength, and Fatigue in Pediatric Demyelinating Diseases","PEDI-CORE","Inclusion Criteria:\n\n* Age between 6 and 18 years\n* Diagnosed with a pediatric demyelinating disease\n* No relapse within the last 3 months\n* No botulinum toxin (Botox) injections within the last 3 months\n* No corticosteroid treatment within the last 3 months\n* Ability to read and write\n\nExclusion Criteria:\n\n* History of concomitant autoimmune diseases\n* Refusal of the patient and\u002For caregiver to participate in the study\n* History of another primary neurological disease\n* Cognitive impairment that limits understanding of instructions and participation in assessments\n* Visual and\u002For hearing impairments that interfere with activities of daily living\n* Presence of additional rheumatological conditions that may interfere with assessments\n* Spasticity grade ≥2 according to the Modified Ashworth Scale in any muscle group","6 Years",{"count":243,"type":22},32,"This study aims to evaluate balance ability, core stability, functional capacity, lower extremity muscle strength, and fatigue levels in children diagnosed with central nervous system demyelinating diseases, in order to contribute to the development of evidence-based and individualized rehabilitation strategies.",[246,247,248,28,249],"Demyelinating Diseases of the Central Nervous System","Child","Core Stability","Fatigue",[251,248,28,249],"Pediatric Demyelinating Diseases","2026-06-12",{"date":254,"type":43},"2026-06-17",{"date":256,"type":22},"2026-07-30",{"date":258,"type":22},"2028-01-30",{"name":260,"class":50},"Istanbul University - Cerrahpasa",{"id":262,"slug":263,"hasResults":12,"nctId":264,"briefTitle":265,"officialTitle":266,"acronym":4,"eligibilityCriteria":267,"healthyVolunteers":58,"sex":17,"minAge":59,"maxAge":18,"enrollmentInfo":268,"targetDuration":270,"studyType":134,"phases":4,"briefSummary":271,"conditions":272,"keywords":4,"overallStatus":87,"whyStopped":4,"lastUpdateSubmitDate":274,"lastUpdatePostDateStruct":275,"startDateStruct":277,"completionDateStruct":279,"leadSponsor":281,"locationsCount":51},"100642542","spinal-alignment-spinal-mobility-and-balance-in-patients-with-multiple-sclerosis-100642542","NCT07648277","Spinal Alignment, Spinal Mobility, and Balance in Patients With Multiple Sclerosis","Relationship Between Spinal Alignment, Spinal Mobility, and Balance in Patients With Multiple Sclerosis","Inclusion Criteria:\n\n* Diagnosis of relapsing-remitting multiple sclerosis (RRMS)\n* Aged between 18 and 65 years\n* EDSS score between 0.5 and 4.5\n* Standardized Mini-Mental State Examination score ≥24\n\nExclusion Criteria:\n\n* Receipt of corticosteroid treatment within the previous 4 weeks\n* Presence of any additional neurological disorder\n* Spasticity defined as a Modified Ashworth Scale score ≥3\n* History of surgical intervention involving the lower extremities, spine, or abdominal region",{"count":269,"type":22},30,"2 Years","Multiple sclerosis (MS) is a chronic inflammatory autoimmune disease of the central nervous system characterized by demyelination and axonal degeneration. Neuromuscular impairments associated with MS, including muscle weakness, spasticity, fatigue, and proprioceptive deficits, may lead to alterations in spinal posture and reduced spinal mobility. These changes can negatively affect trunk control, balance, respiratory function, and functional independence.\n\nAlthough postural abnormalities and mobility limitations have been reported in individuals with MS, the relationship between spinal posture, spinal mobility, and balance remains insufficiently investigated. Therefore, this study aims to examine the associations between spinal posture, spinal mobility, and balance performance in individuals with multiple sclerosis. Improved understanding of these relationships may contribute to the development of targeted rehabilitation interventions aimed at enhancing postural control and functional outcomes in this population. This study further hypothesises that alterations in spinal posture and spinal mobility are associated with impaired balance performance in individuals with multiple sclerosis.",[273,28],"Multiple Sclerosis","2026-06-10",{"date":276,"type":43},"2026-06-15",{"date":278,"type":43},"2026-02-01",{"date":280,"type":22},"2026-06-30",{"name":282,"class":50},"Ankara Yildirim Beyazıt University",{"id":284,"slug":285,"hasResults":12,"nctId":286,"briefTitle":287,"officialTitle":288,"acronym":4,"eligibilityCriteria":289,"healthyVolunteers":58,"sex":290,"minAge":180,"maxAge":131,"enrollmentInfo":291,"targetDuration":4,"studyType":134,"phases":4,"briefSummary":292,"conditions":293,"keywords":4,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":274,"lastUpdatePostDateStruct":299,"startDateStruct":300,"completionDateStruct":302,"leadSponsor":304,"locationsCount":4},"100642517","balance-fall-risk-and-gait-in-women-with-total-knee-arthroplasty-100642517","NCT07650175","Balance, Fall Risk, and Gait in Women With Total Knee Arthroplasty","Investigation of Balance, Fall Risk, Gait Performance, and Quality of Life in Postmenopausal Women Undergoing Total Knee Arthroplasty","Inclusion Criteria:\n\n* Volunteering to participate in the study.\n* Being 60 years of age or older.\n* Having a Mini Mental Test score of 24 or higher.\n* Not having undergone previous arthroplasty surgery on the knee where surgery is planned.\n* Having experienced unilateral TDA.\n* Being a postmenopausal woman\n\nExclusion Criteria:\n\n* Individuals whose vital signs are unstable after surgery, or who develop any major complications such as deep vein thrombosis, pulmonary embolism, wound infection, or prolonged anesthesia side effects.\n* Presence of any neurological, vestibular, visual, cardiopulmonary, auditory, or cognitive deficits that may affect measurements.\n* Individuals diagnosed with diabetes.","FEMALE",{"count":269,"type":22},"Total knee arthroplasty (TKA) is a commonly performed surgical procedure aimed at reducing pain, restoring joint function, and improving quality of life, particularly among older women. Despite improvements in pain and functional outcomes following TKA, findings regarding balance, fall risk, and gait performance remain inconsistent. Impairments in these parameters may adversely affect daily activities, independence, and overall quality of life.\n\nUnlike previous studies that have primarily focused on one or two outcomes, this study will comprehensively evaluate balance, fall risk, gait performance, and quality of life in postmenopausal women who have undergone TKA. The findings are expected to provide a more holistic understanding of long-term functional outcomes following TKA and contribute to the planning of rehabilitation programs. Therefore, the aim of this study is to compare balance, fall risk, gait performance, and quality of life between postmenopausal women who have undergone TKA and healthy postmenopausal women.",[294,295,296,28,297,298],"Total Knee Arthroplasty","Postmenopausal Women","Quality of Life (QOL)","Risk of Falling","Walking",{"date":225,"type":43},{"date":301,"type":22},"2026-06-20",{"date":303,"type":22},"2026-07-22",{"name":305,"class":50},"Karabuk University",{"id":307,"slug":308,"hasResults":12,"nctId":309,"briefTitle":310,"officialTitle":311,"acronym":4,"eligibilityCriteria":312,"healthyVolunteers":12,"sex":17,"minAge":313,"maxAge":314,"enrollmentInfo":315,"targetDuration":4,"studyType":23,"phases":317,"briefSummary":318,"conditions":319,"keywords":324,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":329,"lastUpdatePostDateStruct":330,"startDateStruct":332,"completionDateStruct":334,"leadSponsor":335,"locationsCount":4},"100639537","theratogs-effects-on-balance-and-mobility-in-cerebral-palsy-100639537","NCT07618962","TheraTogs Effects on Balance and Mobility in Cerebral Palsy","The Effect of the Dynamic Orthotic Garment TheraTogs on Balance and Functional Mobility of Children and Adolescent With Cerebral Palsy: A Cross-Sectional Clinical Study","Inclusion Criteria\n\n* Diagnosis of unilateral or bilateral spastic Cerebral Palsy\n* GMFCS level I or II\n* MAS level lower than +1\n* Ability to understand and follow instructions\n* Ability to walk without assistive devices\n\nExclusion Criteria\n\n* Use of medications affecting balance\n* Hearing or visual impairments\n* Intellectual disability\n* Botulinum toxin (Botox) injection in the lower limbs within the previous 6 months\n* Severe musculoskeletal deformities\n* Surgery within the previous 6 months\n* Uncontrolled seizures during the previous 6 months","5 Years","15 Years",{"count":316,"type":22},12,[25],"Cerebral Palsy (CP) is the most common cause of childhood disability, with an estimated prevalence of 17 million individuals worldwide. Children and adolescents with CP present impaired postural control and balance, negatively affecting their mobility and functional performance. The use of dynamic orthotic garments may contribute to the improvement of postural control, balance, and functional mobility in children and adolescents with CP.\n\nThe aim of the present study is to investigate the immediate effect of the dynamic orthotic garment TheraTogs on balance and functional mobility in children and adolescents with CP.\n\nIn this cross-sectional pilot study, children and adolescents with CP classified as levels I and II according to the Gross Motor Function Classification System (GMFCS), and with spasticity levels lower than +1 according to the Modified Ashworth Scale, will participate. Balance will be assessed using the Pediatric Balance Scale (PBS), while functional mobility will be evaluated with the Timed Up and Go (TUG) test and the 10 Meter Walk Test (10MWT). Each assessment will be performed twice by each participant, with and without the TheraTogs dynamic orthotic garment, in random order. Statistical analysis will be conducted using SPSS Statistics V29 software, with the level of significance set at p \\\u003C 0.05.",[320,321,322,323],"Cerebral Palsy","THERATOGS","BALANCE","FUCTIONAL MOBILITY",[320,325,326,162,327,328],"children","adolescents","functional mobility","TheraTogs","2026-05-30",{"date":331,"type":43},"2026-06-02",{"date":333,"type":22},"2026-06",{"date":333,"type":22},{"name":336,"class":50},"University of West Attica",{"id":338,"slug":339,"hasResults":12,"nctId":340,"briefTitle":341,"officialTitle":342,"acronym":343,"eligibilityCriteria":344,"healthyVolunteers":12,"sex":17,"minAge":59,"maxAge":4,"enrollmentInfo":345,"targetDuration":4,"studyType":23,"phases":346,"briefSummary":347,"conditions":348,"keywords":352,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":354,"lastUpdatePostDateStruct":355,"startDateStruct":357,"completionDateStruct":359,"leadSponsor":361,"locationsCount":51},"100638614","the-effects-of-high-intensity-interval-training-on-gait-balance-and-cognitive-functions-in-individuals-with-multiple-sclerosis-100638614","NCT07578740","The Effects of High-Intensity Interval Training on Gait, Balance, and Cognitive Functions in Individuals With Multiple Sclerosis","Investigating the Effects of High-Intensity Interval Training on Gait, Balance, and Cognition in Individuals With Multiple Sclerosis","HIIT-MS","Inclusion Criteria:\n\n* Diagnosed with Multiple Sclerosis by a neurologist (Hacettepe University Hospitals, Neurology Outpatient Clinic)\n* Age 18 years and older\n* EDSS score between 0 and 4\n* Score of 24 or above on the Standardized Mini Mental State Examination\n* No relapse in the past 3 months\n* Medically stable for at least 6 months\n\nExclusion Criteria:\n\n• Any additional cardiopulmonary, neurological, or systemic disease other than MS",{"count":62,"type":22},[25],"This study aims to comparatively investigate the effects of low-volume High-Intensity Interval Training (HIIT) versus Moderate-Intensity Continuous Training (MICT) on gait, balance, cognitive functions, and neurovascular biomarkers (BDNF, VEGF) in individuals with Multiple Sclerosis (MS). This randomized controlled trial will be conducted at Hacettepe University, Faculty of Physical Therapy and Rehabilitation.",[273,349,29,28,350,351],"High-intensity Interval Training","Cognition","Biomarkers",[353],"Multiple Sclerosis, High-Intensity Interval Training, HIIT, Gait, Balance, Cognition, BDNF, VEGF, Randomized Controlled Trial","2026-05-18",{"date":356,"type":43},"2026-05-20",{"date":358,"type":22},"2026-07",{"date":360,"type":22},"2028-06",{"name":362,"class":50},"Hacettepe University",{"id":364,"slug":365,"hasResults":12,"nctId":366,"briefTitle":367,"officialTitle":367,"acronym":4,"eligibilityCriteria":368,"healthyVolunteers":12,"sex":17,"minAge":59,"maxAge":19,"enrollmentInfo":369,"targetDuration":4,"studyType":23,"phases":371,"briefSummary":372,"conditions":373,"keywords":375,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":380,"lastUpdatePostDateStruct":381,"startDateStruct":383,"completionDateStruct":385,"leadSponsor":386,"locationsCount":4},"100638932","effects-of-a-combined-repetitive-transcranial-magnetic-stimulation-and-physical-therapy-protocol-on-motor-function-balance-and-quality-of-life-in-chronic-post-stroke-hemiplegia-a-case-series-100638932","NCT07597746","\"Effects of a Combined Repetitive Transcranial Magnetic Stimulation and Physical Therapy Protocol on Motor Function, Balance, and Quality of Life in Chronic Post-Stroke Hemiplegia: A Case Series\"","Inclusion Criteria:\n\n* Diagnosis of first-ever unilateral ischemic or hemorrhagic stroke confirmed by neuroimaging (CT or MRI)\n* Chronic post-stroke hemiplegia (≥ 6 months since stroke onset)\n* Moderate to severe motor impairment of the affected lower limb (FMA-LE score between 10 and 28 points)\n* Age between 18 and 75 years\n* Medically stable and able to participate in a rehabilitation program\n* Ability to understand study procedures and provide written informed consent\n* No contraindications to repetitive transcranial magnetic stimulation (rTMS), according to current safety guidelines.\n\nExclusion Criteria:\n\n* History of epilepsy or seizures\n* Presence of pacemakers, cochlear implants, intracranial metallic implants, or other contraindications to rTMS\n* Severe cognitive impairment or communication deficits preventing participation\n* Progressive neurological disorders or unstable medical conditions\n* Participation in other experimental neurorehabilitation interventions during the study period\n* Any condition judged by investigators to compromise safety or data valid",{"count":370,"type":22},20,[25],"Chronic post-stroke hemiplegia frequently results in persistent motor deficits, impaired balance, and reduced quality of life. Conventional physical therapy is fundamental for functional recovery; however, motor improvement often plateaus during the chronic phase. Repetitive transcranial magnetic stimulation (rTMS) is a non-invasive neuromodulation technique that has shown potential to enhance motor recovery by modulating cortical excitability and promoting neuroplasticity.\n\nThis case series aims to investigate the effects of a combined protocol of repetitive transcranial magnetic stimulation and conventional physical therapy on motor function, balance, and quality of life in individuals with chronic post-stroke hemiplegia. Participants will undergo rTMS applied to the motor cortex in conjunction with a structured physical therapy program. Clinical outcomes will be assessed before and after the intervention to explore feasibility, safety, and potential functional benefits of the combined approach.",[374,28],"Chronic Stroke",[376,377,378,162,379],"repetitive transcraneal magnetic stimulation","chronic stroke","motor recovery","physical therapy","2026-05-13",{"date":382,"type":43},"2026-05-19",{"date":384,"type":22},"2026-06-05",{"date":230,"type":22},{"name":387,"class":50},"Sierra Varona SL",{"id":389,"slug":390,"hasResults":12,"nctId":391,"briefTitle":392,"officialTitle":393,"acronym":394,"eligibilityCriteria":395,"healthyVolunteers":12,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":396,"targetDuration":4,"studyType":134,"phases":4,"briefSummary":398,"conditions":399,"keywords":4,"overallStatus":87,"whyStopped":4,"lastUpdateSubmitDate":401,"lastUpdatePostDateStruct":402,"startDateStruct":404,"completionDateStruct":406,"leadSponsor":408,"locationsCount":51},"100639177","figure-of-8-walk-test-in-individuals-with-motoric-cognitive-risk-syndrome-100639177","NCT07586553","Figure-of-8 Walk Test in Individuals With Motoric Cognitive Risk Syndrome","Validity and Reliability of the Figure-of-8 Walk Test (8FWT) in Individuals With Motoric Cognitive Risk Syndrome","8FWT-MCR","Inclusion Criteria:\n\nAged 65 years or older Presence of subjective cognitive complaints Gait speed ≤ 0.8 m\u002Fs (4-meter walk test) Able to walk independently without assistive devices No clinical diagnosis of dementia Able to understand and follow test instructions\n\nExclusion Criteria:\n\nMini-Mental State Examination (MMSE) score \\\u003C 24 Neurological diseases affecting gait (e.g., stroke, Parkinson's disease, multiple sclerosis) Severe musculoskeletal conditions affecting walking Lower extremity surgery within the last 6 months Severe visual or hearing impairment that interferes with testing Dependence on assistive walking devices",{"count":397,"type":22},52,"This observational study aims to investigate the validity and reliability of the Figure-of-8 Walk Test (8FWT) in individuals with Motoric Cognitive Risk Syndrome (MCRS). The study will evaluate test-retest reliability, measurement error (SEM, MDC), and construct validity by examining the relationship between 8FWT performance and functional mobility measures. The findings are expected to provide evidence for the clinical applicability of 8FWT in assessing dynamic balance, gait performance, and cognitive-motor interaction in older adults.",[400,29,28],"Motoric Cognitive Risk Syndrome","2026-05-07",{"date":403,"type":43},"2026-05-14",{"date":405,"type":43},"2026-04-07",{"date":407,"type":22},"2026-07-08",{"name":409,"class":50},"Balikesir University",{"id":411,"slug":412,"hasResults":12,"nctId":413,"briefTitle":414,"officialTitle":415,"acronym":4,"eligibilityCriteria":416,"healthyVolunteers":12,"sex":17,"minAge":59,"maxAge":417,"enrollmentInfo":418,"targetDuration":4,"studyType":23,"phases":420,"briefSummary":421,"conditions":422,"keywords":427,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":90,"lastUpdatePostDateStruct":432,"startDateStruct":434,"completionDateStruct":436,"leadSponsor":438,"locationsCount":51},"100640667","effectiveness-of-dance-therapy-in-stroke-patients-100640667","NCT07578493","Effectiveness of Dance Therapy in Stroke Patients.","Effectiveness of Proprioceptive Neuromuscular Facilitation-based Dance Therapy for Patients With Chronic Stroke.","Inclusion Criteria:\n\n* Chronic hemiparesis (≥ 6 months post-stroke).\n* Ability to maintain independent standing or with minimal assistance.\n* Clinical stability to perform moderate physical exercise.\n* Sufficient understanding to follow simple instructions.\n\nExclusion Criteria:\n\n* Severe aphasia or other cognitive disorders that limit comprehension.\n* Behavioral disorders that hinder group participation.\n* Severe musculoskeletal disorders or concomitant neurological conditions.","80 Years",{"count":419,"type":22},16,[25],"Hemiparesis following a stroke is associated with persistent deficits in postural control, balance, and social participation, especially in the chronic phase. Dance therapy, as a multisensory intervention based on movement, music, and body expression, could promote sensorimotor integration and improve postural stability, complementing conventional physiotherapy. The primary objective of this pilot study is to evaluate the effect of a therapeutic dance program on postural control in individuals with chronic hemiparesis. A secondary objective is to analyze changes in functional balance and gait, as well as subjective satisfaction with the therapy. A controlled study with two parallel groups will be conducted. Sixteen participants with chronic hemiparesis will be recruited (n=8 experimental group; n=8 control group). Both groups will receive standard physiotherapy, but the experimental group will also receive an 8-week therapeutic dance program, with one 30-minute session per week to complement their usual therapy. Pre- and post-intervention assessments will be performed. ThThe experimental group is expected to show a significantly greater improvement in posturographic and clinical parameters compared to the control group. The results could support the implementation of dance therapy as a complementary intervention in community neurorehabilitation programs.",[28,423,424,425,426],"Gait Analysis","Thermography","Range of Motion, Articular","Muscular Strength",[428,429,430,29,431],"Dance Therapy","Stroke","Postural balance","Physical Therapy Modalities",{"date":433,"type":43},"2026-05-11",{"date":435,"type":22},"2026-05-15",{"date":437,"type":22},"2026-11-30",{"name":439,"class":50},"University of Salamanca",{"id":441,"slug":442,"hasResults":12,"nctId":443,"briefTitle":444,"officialTitle":445,"acronym":4,"eligibilityCriteria":446,"healthyVolunteers":12,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":447,"targetDuration":4,"studyType":134,"phases":4,"briefSummary":449,"conditions":450,"keywords":4,"overallStatus":87,"whyStopped":4,"lastUpdateSubmitDate":452,"lastUpdatePostDateStruct":453,"startDateStruct":454,"completionDateStruct":456,"leadSponsor":457,"locationsCount":51},"100636998","dual-task-effects-on-gait-and-balance-in-mcrs-100636998","NCT07572968","Dual-Task Effects on Gait and Balance in MCRS","Effects of Cognitive Load on Gait and Balance Performance in Individuals With Motoric Cognitive Risk Syndrome: A Dual-Task Analysis","Inclusion Criteria:\n\nAge ≥ 65 years Subjective cognitive complaints Slow gait speed No dementia diagnosis\n\nExclusion Criteria:\n\nSevere visual\u002Fhearing impairment Neurological diseases (stroke, Parkinson) Acute orthopedic conditions affecting walking",{"count":448,"type":22},35,"This study aims to investigate the effects of cognitive load on gait and balance performance in individuals with Motoric Cognitive Risk Syndrome (MCRS). Participants will perform Timed Up and Go (TUG) and tandem walking tests under single-task and dual-task conditions. The study evaluates cognitive-motor interference and dual-task cost to better understand early markers of cognitive decline and fall risk.",[400,451,29,28],"Dual-Task Performance","2026-05-01",{"date":401,"type":43},{"date":455,"type":43},"2026-04-15",{"date":166,"type":22},{"name":409,"class":50},{"id":459,"slug":460,"hasResults":12,"nctId":461,"briefTitle":462,"officialTitle":463,"acronym":4,"eligibilityCriteria":464,"healthyVolunteers":12,"sex":17,"minAge":465,"maxAge":19,"enrollmentInfo":466,"targetDuration":4,"studyType":23,"phases":467,"briefSummary":468,"conditions":469,"keywords":472,"overallStatus":87,"whyStopped":4,"lastUpdateSubmitDate":475,"lastUpdatePostDateStruct":476,"startDateStruct":478,"completionDateStruct":480,"leadSponsor":482,"locationsCount":51},"100635252","body-weight-supported-and-virtual-reality-gait-training-in-stroke-patients-100635252","NCT07550270","Body Weight-Supported and Virtual Reality Gait Training in Stroke Patients","A Comparative Evaluation of the Effectiveness of Body Weight-Supported Forward and Backward Gait Training Versus Virtual Reality-Assisted Gait Training in Patients With Stroke","Inclusion Criteria:\n\n* Patients experiencing their first-ever stroke\n* Patients with a post-stroke duration of more than 2 weeks\n* Patients with plantar flexor muscle spasticity of the lower extremity less than grade 3 according to the Modified Ashworth Scale (MAS)\n* Patients with a Brunnstrom stage of the lower extremity greater than 2\n* Patients who are able to stand independently or under supervision for at least 2 minutes for standing assessments\n* Patients who are able to walk at least 10 meters independently or under supervision, with or without an assistive device, for walking assessments\n* Patients with sufficient cognitive function to understand study instructions (Mini-Mental State Examination \\[MMSE\\] score \\> 23)\n* Patients with stable medical and psychological conditions\n* Patients who are willing to participate in the study\n\nExclusion Criteria:\n\n* Patients with bilateral hemispheric lesions\n* Patients with severe cardiovascular or musculoskeletal conditions that prevent walking (e.g., fixed ankle contracture)\n* Patients using a permanent urinary catheter, or those with pressure ulcers or urinary and\u002For fecal incontinence\n* Patients with unilateral neglect\n* Patients with neurological conditions other than stroke that may affect balance performance (e.g., Parkinson's disease, epilepsy, meningitis, cerebellar disorders, vertigo, dizziness, polyneuropathy) or musculoskeletal disorders (e.g., severe low back pain, knee disorders)\n* Patients with severe visual, hearing, or speech impairments","45 Years",{"count":269,"type":22},[25],"The aim of this study is to compare the effects of body weight-supported gait training that includes virtual reality-assisted dual-task applications with body weight-supported forward and backward gait training on functional capacity, gait parameters (such as step length, gait speed, and balance), cognitive functions and psychological status in patients with stroke. The findings of this study are expected to contribute to the development of more effective rehabilitation strategies for improving mobility in patients with stroke",[429,470,28,471],"Walking Impairment","Gait Training",[473,474],"stroke","gait training","2026-04-19",{"date":477,"type":43},"2026-04-24",{"date":479,"type":43},"2026-03-26",{"date":481,"type":22},"2026-12",{"name":483,"class":50},"Gaziler Physical Medicine and Rehabilitation Education and Research Hospital",{"id":485,"slug":486,"hasResults":12,"nctId":487,"briefTitle":488,"officialTitle":489,"acronym":490,"eligibilityCriteria":491,"healthyVolunteers":12,"sex":290,"minAge":492,"maxAge":493,"enrollmentInfo":494,"targetDuration":4,"studyType":23,"phases":495,"briefSummary":496,"conditions":497,"keywords":503,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":506,"lastUpdatePostDateStruct":507,"startDateStruct":509,"completionDateStruct":511,"leadSponsor":513,"locationsCount":4},"100635050","virtual-reality-training-using-wii-fit-in-children-with-cerebral-palsy-100635050","NCT07547644","Virtual Reality Training Using Wii Fit in Children With Cerebral Palsy","EFFECTS OF VIRTUAL REALITY TRAINING USING WII FIT ON BALANCE, GROSS MOTOR FUNCTION, AND AGILITY IN CHILDREN WITH CEREBRAL PALSY -A RANDOMIZED CONTROLLED TRIAL","VR in CP","Inclusion Criteria:\n\n* ● Children aged 7 to 14 years\n\n  * Diagnosed cases of spastic diplegic CP, characterized by bilateral lower limb involvement\n  * Classified under GMFCS levels I to II.\n  * Having mild to moderate spasticity on Modified Ashworth Scale (MAS) scores ranging from 1, +1 or 2\n  * Mild level intellectual disability according to their health records\n  * Medically stable with no acute illness or uncontrolled comorbidities\n  * No major changes in medication or therapy planned during the study period.\n\nExclusion Criteria:\n\n* ● Orthopedic surgery or botulinum toxin injections in the past 16 months\n\n  * Hearing or visual impaired .\n  * Uncontrolled epilepsy or seizures\n  * Severe attention deficits or psychological issues interfering with task engagement such as attention deficit hyperactivity disorder (ADHD), Autism Spectrum Disorder (ASD) will be excluded from the study .","7 Years","14 Years",{"count":157,"type":22},[25],"The goal of this clinical trial is to determine whether virtual reality (VR) training using the Nintendo Wii Fit can improve balance, gross motor function, and agility in children aged 7-14 years with spastic cerebral palsy (GMFCS Levels I-II). The main questions it aims to answer are:\n\nDoes Wii Fit-based VR training improve balance more than conventional physiotherapy?\n\nDoes VR training enhance gross motor skills such as standing, walking, running, and jumping?\n\nDoes VR training improve agility in children with cerebral palsy?\n\nDoes VR training increase enjoyment and engagement during therapy?\n\nResearchers will compare Wii Fit-based VR training with conventional physiotherapy to determine which approach leads to greater improvements in motor function.\n\nParticipants will:\n\nAttend 18 sessions over 6 weeks (3 sessions per week).\n\nPerform either VR-based exercises using the Wii Fit Balance Board or traditional physiotherapy exercises.\n\nComplete pre- and post-intervention assessments using the Pediatric Balance Scale, GMFM-88 (domains D and E), BOT-2 agility subtest, and the PACES enjoyment scale.\n\nThis study aims to explore a fun, cost-effective, and engaging rehabilitation strategy that may improve functional independence and overall quality of life for children with cerebral palsy.",[498,499,28,500,501,502],"Cerebral Palsy (CP)","Virtual Reality","Gross Motor Function Classification System (GMFCS) Level I,II","Gross Motor Functions","Agility",[504,223,162,505],"cerebral palsy","GMFM","2026-04-16",{"date":508,"type":43},"2026-04-23",{"date":510,"type":22},"2026-04-25",{"date":512,"type":22},"2026-08-15",{"name":514,"class":50},"Ziauddin University",{"id":516,"slug":517,"hasResults":12,"nctId":518,"briefTitle":519,"officialTitle":519,"acronym":4,"eligibilityCriteria":520,"healthyVolunteers":12,"sex":17,"minAge":59,"maxAge":180,"enrollmentInfo":521,"targetDuration":4,"studyType":134,"phases":4,"briefSummary":522,"conditions":523,"keywords":525,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":530,"lastUpdatePostDateStruct":531,"startDateStruct":533,"completionDateStruct":534,"leadSponsor":536,"locationsCount":4},"100632603","loss-of-balance-experienced-by-industrial-workers-due-to-hearing-problems-100632603","NCT07515833","Loss of Balance Experienced by Industrial Workers Due to Hearing Problems","Inclusion Criteria:\n\n* Employment in industrial or heavy industrial settings\n* Age between 18 and 60 years\n* Presence of hearing problems diagnosed prior to or after starting industrial work\n\nExclusion Criteria:\n\n* Employment in office-based industrial positions\n* Working duration of less than one year",{"count":448,"type":22},"This study will investigate the balance performance and balance-related activities of daily living in 35 industrial workers with hearing problems exposed to occupational noise, using the Berg Balance Scale and the Vestibular Disorders Activities of Daily Living Scale. The research aims to determine whether there is a statistically significant association between hearing problems, balance performance, and daily noise exposure duration. It is hypothesized that while hearing problems related to occupational noise exposure may exist, they may not be directly associated with clinically significant balance impairment, potentially remaining at a tolerable level in daily life. Furthermore, the correlation between Berg Balance Scale and daily living activity scores will be evaluated to understand the functional impact of balance on these workers.",[28,524],"Hearing Problems",[162,526,527,528,529],"vestibular system","industrial workers","occupational noise","Hearing problems","2026-04-08",{"date":532,"type":43},"2026-04-13",{"date":452,"type":22},{"date":535,"type":22},"2027-01-01",{"name":537,"class":50},"Yeditepe University",{"id":539,"slug":540,"hasResults":12,"nctId":541,"briefTitle":542,"officialTitle":543,"acronym":544,"eligibilityCriteria":545,"healthyVolunteers":12,"sex":17,"minAge":103,"maxAge":180,"enrollmentInfo":546,"targetDuration":4,"studyType":23,"phases":547,"briefSummary":548,"conditions":549,"keywords":554,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":565,"lastUpdatePostDateStruct":566,"startDateStruct":568,"completionDateStruct":570,"leadSponsor":572,"locationsCount":4},"100632041","whole-body-vibration-on-balance-risk-of-falling-and-quality-of-life-in-chemotherapy-induced-peripheral-neuropathy-100632041","NCT07508527","Whole-Body Vibration on Balance, Risk of Falling and Quality of Life in Chemotherapy-Induced Peripheral Neuropathy","Effect of Whole Body Vibration on Balance, Risk of Falling, and Quality of Life in Patients With Chemotherapy Induced Peripheral Neuropathy","WBV\u002FQOL\u002FCIPN","Inclusion Criteria:\n\n* 30 patients diagnosed with chemotherapy-induced peripheral neuropathy from both genders.\n* Their ages will range from 30-60 years old.\n* All patients included in this study will be on chemotherapy from at least one cycle as a treatment of malignant tumor.\n* The patients will be mild to moderate neuropathy according to mTNS.\n* They were medically stable.\n\nExclusion Criteria:\n\n* History of other types of neuropathies (i.e., hereditry peripheral neuropathy associated with nutritional agents and paraneoplastic syndrome-related neuropathy…etc).\n* Unstable medical condition during chemotherapy\n* Patients who are starting new therapy or dose modification during study period\n* Morbid obesity body mass index \\>40%\n* History of non-surgically repaired nerve compression injuries such as carpal tunnel, brachial plexopathy, spinal stenosis, and spinal nerve root compression\n* History of central nervous system primary or metastatic malignancy.",{"count":269,"type":22},[25],"The goal of this clinical trial is to evaluate the efficacy of Whole-body vibration in improving postural control, risk of falling, and quality of life in patients with chemotherapy-induced peripheral neuropathy. The main questions it aims to answer are:\n\nDoes Whole-body vibration have a significant effect on postural control, risk of falling, and quality of life in patients with chemotherapy-induced peripheral neuropathy?\n\nResearchers will compare whole body vibration in addition to traditional exercise to traditional exercise alone to see if Whole-body vibration have a significant effect on postural control, risk of falling, and quality of life in patients with chemotherapy-induced peripheral neuropathy.\n\nParticipants will:\n\n* age between 30-60 years old.\n* be on chemotherapy for at least one cycle as a treatment of malignant tumors with peripheral neuropathy.\n* have mild to moderate neuropathy according to mTNS.\n* be assigned randomly into two equal groups (control group (A) and study group (B)).\n* Take three sessions per week for eight weeks.\n* The control group (A) will be treated by selected physical therapy treatment (Strength resistive training, Stretching \\& flexibility, Balance training)\n* The study group (B) will be treated with selected physical therapy treatment in addition to whole-body vibration therapy.",[550,551,552,28,553],"Whole Body Vibration","Chemotherapy Induced Peripheral Neuropathy (CIPN)","Fall Risk, Fall Prevention","Quality of Life",[555,556,557,558,28,559,560,561,562,563,564],"WBV","Whole body vibration","CIPN","Chemotherapy induced peripheral neuropathy","Risk of fall","falling","postural control","fall","QOL","Quality of life","2026-03-31",{"date":567,"type":43},"2026-04-02",{"date":569,"type":22},"2026-04",{"date":571,"type":22},"2027-06",{"name":49,"class":50},{"id":574,"slug":575,"hasResults":12,"nctId":576,"briefTitle":577,"officialTitle":578,"acronym":579,"eligibilityCriteria":580,"healthyVolunteers":12,"sex":17,"minAge":59,"maxAge":4,"enrollmentInfo":581,"targetDuration":4,"studyType":23,"phases":582,"briefSummary":583,"conditions":584,"keywords":589,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":593,"lastUpdatePostDateStruct":594,"startDateStruct":595,"completionDateStruct":597,"leadSponsor":599,"locationsCount":4},"100631702","the-effect-of-remotely-delivered-pilates-on-physical--and-psychological-outcomes-in-individuals-with-multiple-sclerosis-100631702","NCT07504120","The Effect of Remotely Delivered Pilates on Physical , and Psychological Outcomes in Individuals With Multiple Sclerosis","Does Remotely Delivered Pilates Influence Physical and Psychological Outcomes in Individuals With Multiple Sclerosis?","MS","Inclusion Criteria:\n\n* Age 18 years or older\n* Self-reported diagnosis of multiple sclerosis by a neurologist\n* Relapse-free for the past 30 days before screening\n* Able to speak and read English as the primary language\n* Access to the internet and e-mail,\n* Ability to use Zoom, and willingness to complete testing sessions and questionnaires\n* Ambulatory without an assistive device (for example, cane)\n* Low to moderate disability, defined as a score of 0-4 on the Patient-Determined Disease Steps (PDDS)\n* Insufficiently active, defined as a score \\\u003C 14 on the Godin Leisure-Time Exercise Questionnaire-Health Contribution Score (GLTEQ-HCS)\n* Adequate visual ability and literacy to read materials printed in 14-point font\n* Currently treated with a disease-modifying therapy\n\nExclusion Criteria:\n\n* Pregnant\n* Elevated risk for strenuous or maximal exercise, defined as more than one \"Yes\" response on the Physical Activity Readiness Questionnaire (PAR-Q) during screening",{"count":5,"type":22},[25],"Objectives Objective 1: To determine the effects of a 16-week remotely delivered Pilates intervention on walking endurance, walking speed, balance, fatigue, and pain compared to a waitlist control group in individuals with MS.\n\nObjective 2: To examine the impact of a 16-week remotely delivered Pilates intervention on depression \\& anxiety, cognitive function, and QOL compared to a waitlist control group in individuals with MS.\n\nAim Aim 1: To assess whether the 16-week remotely delivered Pilates intervention significantly improves walking endurance, walking speed, balance, fatigue, and pain compared to a waitlist control group in individuals with MS Aim 2: To investigate whether the 16-week remotely delivered Pilates intervention significantly improves depression \\& anxiety, cognitive function, and QOL compared to a waitlist control group in individuals with MS.\n\nHypothesis Hypothesis 1: The 16-week remotely delivered Pilates intervention will significantly improve walking endurance, walking speed, balance, fatigue, and pain compared to a waitlist control group in individuals with MS.\n\nHypothesis 2: Participants receiving the 16-week remotely delivered Pilates intervention will demonstrate significantly greater improvements in depression \\& anxiety, cognitive function, and QOL compared to a waitlist control group in individuals with MS.",[273,585,298,28,586,587,553,588,350,249],"Pilates Exercise","Fatigue in Multiple Sclerosis","Pain Management","Depression",[590,591,249,350,564,298,588,28,592],"multiple sclerosis","Pilates","Pain","2026-03-25",{"date":565,"type":43},{"date":596,"type":22},"2026-06-01",{"date":598,"type":22},"2027-12-01",{"name":600,"class":50},"University of Illinois at Chicago",{"id":602,"slug":603,"hasResults":12,"nctId":604,"briefTitle":605,"officialTitle":606,"acronym":4,"eligibilityCriteria":607,"healthyVolunteers":58,"sex":290,"minAge":180,"maxAge":608,"enrollmentInfo":609,"targetDuration":4,"studyType":23,"phases":610,"briefSummary":611,"conditions":612,"keywords":617,"overallStatus":87,"whyStopped":4,"lastUpdateSubmitDate":621,"lastUpdatePostDateStruct":622,"startDateStruct":624,"completionDateStruct":626,"leadSponsor":627,"locationsCount":51},"100626282","video-game-intervention-in-older-adults-100626282","NCT07433608","Video Game Intervention In Older Adults","The Effects Of A Video-Based Game Intervention On Cognitive, Physical And Psychosocial Outcomes In Older Adults","Inclusion Criteria:\n\nAge 60 years or older A score of 24 or higher on the Mini Mental State Examination (MMSE) Ability to understand and follow verbal instructions Willingness to participate voluntarily\n\nExclusion Criteria:\n\nPresence of a neurological, orthopedic, or psychiatric diagnosis Medical contraindications to exercise Diagnosis of dementia Acute orthopedic injury Visual or hearing impairment that would interfere with participation Inability to attend sessions regularly","69 Years",{"count":243,"type":22},[25],"The purpose of this clinical trial is to investigate the effects of a rehabilitative game-based intervention on self-efficacy, balance, and visual-motor integration in individuals aged 60 years and older.\n\nThe primary research questions are:\n\nDoes the rehabilitative game-based intervention improve balance and visual-motor integration? Does the rehabilitative game-based intervention improve self-efficacy levels?\n\nResearchers will compare a rehabilitative game intervention group with a control group. Participants will complete baseline and post-intervention assessments. Individuals in the intervention group will participate in rehabilitative game sessions twice per week for 6 weeks, while the control group will not receive any intervention.",[613,614,28,615,616],"Healhty","Aging","Self Efficacy","Visual Motor Integration",[499,618,619,28,620],"Visual-Motor Integration","Older Adults","Self-Efficacy","2026-03-03",{"date":623,"type":43},"2026-03-06",{"date":625,"type":43},"2026-02-17",{"date":405,"type":22},{"name":628,"class":50},"Biruni University",{"id":630,"slug":631,"hasResults":12,"nctId":632,"briefTitle":633,"officialTitle":633,"acronym":4,"eligibilityCriteria":634,"healthyVolunteers":58,"sex":17,"minAge":59,"maxAge":635,"enrollmentInfo":636,"targetDuration":4,"studyType":23,"phases":638,"briefSummary":640,"conditions":641,"keywords":642,"overallStatus":87,"whyStopped":4,"lastUpdateSubmitDate":644,"lastUpdatePostDateStruct":645,"startDateStruct":647,"completionDateStruct":649,"leadSponsor":651,"locationsCount":51},"100577916","early-phase-1-intermittent-visual-perturbations-to-enhance-balance-training-100577916","NCT06804512","Intermittent Visual Perturbations to Enhance Balance Training","Inclusion Criteria:\n\n* Ages 18-30 years, or 65-89 years.\n* Ability to walk independently for 10 minutes continuously.\n* Willingness to be randomized to any experimental group and to participate in all aspects of study assessment and intervention\n\nExclusion Criteria:\n\n-Major cognitive disorder that interferes with independence, based on affirmative response (always\u002Fusually\u002Fsometimes) to the following question: \"As a result of confusion or memory loss, how often do you need assistance with day-to-day activities such as cooking, cleaning, taking medications, driving, or paying bills? Would you say it is 1) Always; 2) Usually; 3) Sometimes; 4) Rarely; or 5) Never\".\n\n* Current or recent (within 6 months) lower limb musculoskeletal injury that causes pain during walking or limits walking ability.\n* History of neurological injury or disability (including spinal cord injury, stroke, Parkinson's disease, or multiple sclerosis).\n* Difficulty communicating with study personnel.\n* Current enrollment in any other clinical trial.\n* Low vision that cannot be corrected by wearing contact lens. Low vision will be operationally defined as visual acuity less than 20\u002F70 on standard eye chart, or difficulty perform complex walking tasks due to visual conditions affecting accurate navigation around and over obstacles (self-reported or observed by examiner). The goggles to be used in the study do not permit eyeglasses while using them.\n* Illiterate or non-English speaking, due to the likelihood of difficulties following protocol instructions.","89 Years",{"count":637,"type":22},540,[639],"EARLY_PHASE1","The purpose of this research study is to determine if intermittent visual perturbations can improve balance training. The investigators will quantify differences in body movement, muscle activity, and beam walking performance during and after practice walking on a balance beam that is 1\" high. The investigators will ask the participants to come to the laboratory twice (2 sessions). The first session will not last more than 3 hours. The second session will not last more than 1 hour and will be two weeks after the first session. In total, the maximum amount of time the participant would be asked to participate is 4 hours.",[28],[643,71],"walking balance","2026-02-09",{"date":646,"type":43},"2026-02-10",{"date":648,"type":43},"2024-08-20",{"date":650,"type":22},"2029-02-28",{"name":652,"class":50},"University of Florida",{"id":654,"slug":655,"hasResults":12,"nctId":656,"briefTitle":657,"officialTitle":658,"acronym":4,"eligibilityCriteria":659,"healthyVolunteers":58,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":660,"targetDuration":4,"studyType":23,"phases":661,"briefSummary":662,"conditions":663,"keywords":4,"overallStatus":87,"whyStopped":4,"lastUpdateSubmitDate":665,"lastUpdatePostDateStruct":666,"startDateStruct":668,"completionDateStruct":670,"leadSponsor":671,"locationsCount":51},"100618987","the-acute-effects-of-core-stabilization-exercises-on-balance-and-upper-extremity-functional-performance-in-archers-100618987","NCT07338760","The Acute Effects of Core Stabilization Exercises on Balance and Upper Extremity Functional Performance in Archers","Acute Effect of Core Stabilization Exercises Among Archers","Inclusion Criteria:\n\n* Have been involved in licensed archery for at least 1 year\n\n  * Be willing to participate in the program (both the athlete and their parent\u002Fguardian)\n  * Be an athlete without any illness or disability that prevents participation in sports (as determined by a current medical report submitted to the club for licensing purposes)\n  * Be able to read and write\n\nExclusion Criteria:\n\n* ● Those with diagnosed mental or cognitive problems\n\n  * Those who have undergone orthopedic surgery or received intra-articular steroid treatment within the last 6 months\n  * Those with a diagnosed medical condition that could affect balance and shooting performance\n  * Those with instability issues and associated joint movement restrictions\n  * Those with acute muscle spasms and pain complaints\n  * Those using painkillers, sedatives, alcohol, etc., or any other medication or substance that may affect shooting performance\n  * Those with any diagnosis of injury related to the musculoskeletal system\n  * Those actively involved in another sport besides archery",{"count":269,"type":22},[25],"This randomized controlled study aims to investigate the acute effects of a single session of core stabilization exercises on balance and upper extremity functional performance in competitive archers. Core stability is essential for postural control, neuromuscular coordination, and efficient force transfer during archery shooting. Understanding the immediate effects of core stabilization exercises may support their use as an effective warm-up and performance-enhancing strategy in archery athletes.",[664,248,28],"Archery","2026-01-04",{"date":667,"type":43},"2026-01-14",{"date":669,"type":43},"2025-06-03",{"date":278,"type":22},{"name":672,"class":50},"Atlas University",{"id":674,"slug":675,"hasResults":12,"nctId":676,"briefTitle":677,"officialTitle":678,"acronym":679,"eligibilityCriteria":680,"healthyVolunteers":12,"sex":17,"minAge":681,"maxAge":4,"enrollmentInfo":682,"targetDuration":4,"studyType":23,"phases":684,"briefSummary":685,"conditions":686,"keywords":688,"overallStatus":87,"whyStopped":4,"lastUpdateSubmitDate":697,"lastUpdatePostDateStruct":698,"startDateStruct":700,"completionDateStruct":702,"leadSponsor":703,"locationsCount":51},"100618651","impact-of-a-multicomponent-exercise-program-on-cognitive-and-functional-outcomes-in-patients-with-mild-cognitive-impairment-100618651","NCT07334392","Impact of a Multicomponent Exercise Program on Cognitive and Functional Outcomes in Patients With Mild Cognitive Impairment","Effectiveness of an Innovative Therapeutic Exercise Program on Physical and Cognitive Function in Mild Cognitive Impairment Due to Alzheimer's Disease","MExeProMCI","Inclusion Criteria:\n\n* individuals \\> 50 years old\n* people with confirmed cognitive impairment, as evidenced by values within normal limits on the Montreal Cognitive Assessment test (MOCA ) \\>20\n* stable medication in the last month\n* independent walking\n\nExclusion Criteria:\n\n* people with dementia\n* people suffering from chronic mental illness (e.g. schizophrenia, bipolar disorder)\n* people suffering from a neurological disorder or injuries (e.g. multiple sclerosis, Parkinson's, traumatic brain injury)\n* people with clinical depression (as determined by the Neuropsychiatric Inventory (NPI) assessment and medical diagnosis)\n* people who have had recent surgery\n* people with insufficient knowledge of the Greek language","50 Years",{"count":683,"type":22},45,[25],"The goal of this randomised clinical trial is to investigate the effectiveness of an innovative therapeutic exercise program emphasizing in dual-task exercises in people with amnestic Mild Cognitive Impairment. The main questions it aims to answer are:\n\nDoes the innovative therapeutic exercise program improve gait and balance? Does the innovative therapeutic exercise program improve cognition?\n\nResearchers will compare the innovative therapeutic exercise program emphasizing in dual-task exercises to a therapeutic exercise program without emphasizing in dual-task exercises and to a control group (given instruction about the benefits of exercise).\n\nParticipants will:\n\n* Perform the exercise program twice a week for three months.\n* Will be assessed before and after the intervention.\n* Will record The Borg Scale of Perceived Exertion every second week to monitor and assess the progression of exercise intensity.",[687,298,28,350],"Mild Cognitive Impairment",[689,162,690,691,692,693,694,695,696],"kinetic and kinematic","global cognition","executive function","attention","mci","multicomponent program","exercise","dual tasking","2025-12-30",{"date":699,"type":43},"2026-01-12",{"date":701,"type":43},"2025-12-01",{"date":437,"type":22},{"name":704,"class":50},"University of Patras"]