[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"kinesiophobia-fear-of-movement\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:kinesiophobia-fear-of-movement":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,8,0,[8,54,86,116,149,181,212,238],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":29,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":42,"lastUpdatePostDateStruct":43,"startDateStruct":46,"completionDateStruct":48,"leadSponsor":50,"locationsCount":53},"100649215","impact-of-the-receptive-music-intervention-tool-music-care-on-changes-in-the-functional-abilities-of-patients-with-chronic-low-back-pain-100649215",false,"NCT07731204","Impact of the Receptive Music Intervention Tool (MUSIC CARE©) on Changes in the Functional Abilities of Patients With Chronic Low Back Pain","LOMBALZIC'","Inclusion Criteria:\n\n* Diagnosed with chronic low back pain by a Physical Medicine and Rehabilitation (PMR) physician, defined as lumbar pain and\u002For pain radiating to the lower limb that affects daily and professional activities and has lasted more than 3 months\n* If surgery was performed, it must have been done at least 3 months before entering the study\n* Adult (18 years of age or older) admitted to the day hospital at Clinique Saint-Roch for a chronic low back pain rehabilitation program\n* Considered able to return to work, as assessed by the PMR physician during the pre-admission consultation, with no medical contraindication to resuming professional activity\n* Affiliated with a French social security scheme\n* Has given written informed consent to participate in the study\n\nExclusion Criteria:\n\n* Hearing impairment that would prevent the use of the MUSIC CARE© device\n* Medical contraindication to hydrotherapy (balneotherapy)\n* Symptomatic disc herniation\n* Vertebral fracture or history of recent vertebral fracture within the past 2 years\n* Unstable spondylolisthesis\n* Disc-vertebral infection (spondylodiscitis)\n* Inflammatory rheumatic disease such as ankylosing spondylitis (spondyloarthritis) or rheumatoid arthritis\n* Constitutional connective tissue disorder such as Ehlers-Danlos syndrome or Marfan syndrome\n* Severe, unstabilized, or decompensated psychiatric disorder, including psychotic disorders, acute-phase bipolar disorder, or severe major depressive episode\n* Central nervous system neurological disease such as multiple sclerosis, stroke, or Parkinson's disease\n* Peripheral neuropathy of the lower limbs\n* Unstabilized cardiovascular disease\n* Active cancer treatment or cancer diagnosis within the past 2 years\n* Surgery for a reason other than low back pain within the past 6 months\n* Currently retired (not in active employment)\n* Currently enrolled in another interventional research study\n* Persons under legal protection as defined by Articles L.1121-5 to L.1121-8 of the French Public Health Code, including:\n* Persons under guardianship, curatorship, or judicial protection\n* Minors (under 18 years of age)\n* Pregnant or breastfeeding women\n* Any person subject to a legal protection measure or unable to freely provide informed consent","ALL","18 Years",{"count":19,"type":20},34,"ESTIMATED","INTERVENTIONAL",[23],"NA","Brief Summary The goal of this clinical trial is to learn if MUSIC CARE©, a music-based therapy tool, can improve the physical abilities of people with chronic low back pain (back pain that lasts more than 3 months).\n\nThe main questions it aims to answer are:\n\nDoes MUSIC CARE© help participants better perform their daily activities? Does MUSIC CARE© lower the fear of movement in participants? Does MUSIC CARE© help participants return to work?\n\nWhy this study? Chronic low back pain is a leading cause of disability and absence from work. Physical rehabilitation is the recommended treatment. However, many participants develop a fear of movement. This fear slows down their recovery and limits the benefits of rehabilitation.\n\nMUSIC CARE© is a digital music tool. It uses specially designed music to help participants relax and feel less pain. Researchers believe that using MUSIC CARE© before rehabilitation sessions may help participants move more freely and recover better.\n\nHow does the study work?\n\nResearchers will compare two groups of participants:\n\nGroup 1: follows a standard rehabilitation program with MUSIC CARE© Group 2: follows a standard rehabilitation program without MUSIC CARE© This comparison will show whether MUSIC CARE© brings added benefits.\n\nParticipants will:\n\nTake part in a rehabilitation program for 5 to 6 weeks Use MUSIC CARE© before each therapy session (Group 1 only). Complete questionnaires about their pain, fear of movement, and ability to perform daily activities.\n\nBe followed for 6 months after the program ends, including an assessment of their return to work.\n\nWhat could this study change? If results are positive, this study could confirm that MUSIC CARE© is a useful non-drug tool to support rehabilitation for people with chronic low back pain. It could help bring this approach into standard care programs, with no additional medication.",[26,27,28],"Low Back Pain","Kinesiophobia (Fear of Movement)","Chronic Low-back Pain (cLBP)",[26,30,31,32,33,34,35,36,37,38,39,40],"Chronic Pain","Music Therapy","Physical Functional Performance","Kinesiophobia","Fear of Movement","Rehabilitation","Exercise Therapy","Return to Work","Non-Pharmacological Intervention","Patient Reported Outcome Measures","Functional Capacity","NOT_YET_RECRUITING","2026-07-23",{"date":44,"type":45},"2026-07-28","ACTUAL",{"date":47,"type":20},"2026-10-01",{"date":49,"type":20},"2027-12",{"name":51,"class":52},"LNA SANTE","OTHER",1,{"id":55,"slug":56,"hasResults":11,"nctId":57,"briefTitle":58,"officialTitle":59,"acronym":4,"eligibilityCriteria":60,"healthyVolunteers":61,"sex":16,"minAge":17,"maxAge":62,"enrollmentInfo":63,"targetDuration":4,"studyType":21,"phases":65,"briefSummary":66,"conditions":67,"keywords":69,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":77,"lastUpdatePostDateStruct":78,"startDateStruct":80,"completionDateStruct":82,"leadSponsor":84,"locationsCount":53},"100646708","pain-beliefs-and-intracortical-excitability-during-experimental-pain-100646708","NCT07688525","Pain Beliefs and Intracortical Excitability During Experimental Pain","Influence Of Pain-Related Beliefs On The Modulation Of Intracortical Circuits During Experimental Pain Induced By Topical Capsaicin","Inclusion Criteria:\n\n* Aged 18 to 35 years, inclusive\n* Healthy\n* Able to understand the study information and experimental procedures\n* Able to provide informed consent\n\nExclusion Criteria:\n\n* History of psychiatric disorders (including intellectual disability or severe cognitive, behavioral, or affective impairment) that could interfere with understanding the study or providing informed consent.\n* History of neurological disorders, including epilepsy, stroke, brain or spinal cord surgery, or any neurological disease affecting motor or sensory function.\n\nInability to provide informed consent (e.g., dementia, significant hearing impairment, insufficient language proficiency).\n\n* Any pain condition within the past 3 months, regardless of origin.\n* Recent musculoskeletal injury or surgery within the past 3 months.\n* Contraindications to transcranial magnetic stimulation (TMS), including a history of epilepsy or the presence of intracranial metallic objects, cochlear implants, or other non-removable metallic implants in or near the head.\n* Use of analgesic or psychotropic medications.\n* Individuals under legal guardianship or curatorship.\n* Pregnant or breastfeeding women.\n* Presence of a cardiac pacemaker or other implanted electronic medical device.\n* Known allergy or previous skin reaction to capsaicin",true,"35 Years",{"count":64,"type":20},30,[23],"Pain can influence the way the motor system functions. However, responses to pain vary widely between individuals, and this variability may be partly related to pain-related beliefs such as kinesiophobia.\n\nThis study examines whether temporary experimental pain changes intracortical excitability in the motor cortex, and whether this response differs according to baseline kinesiophobia. Healthy adults will complete one experimental session. Motor cortex excitability will first be assessed at baseline using transcranial magnetic stimulation, a non-invasive brain stimulation technique. A topical capsaicin cream will then be applied to the forearm to induce temporary, moderate experimental pain. Once pain is established, the same neurophysiological assessments will be repeated.\n\nThe main objective is to measure changes in short-interval intracortical inhibition before and during capsaicin-induced pain, with particular attention to whether these changes are associated with baseline kinesiophobia.\n\nSecondary objectives are to characterize other markers of motor cortex excitability, including long-interval intracortical inhibition, short-interval intracortical facilitation, intracortical facilitation, and corticospinal excitability assessed using input-output recruitment curves. Pain intensity will be monitored using a visual analog scale to characterize the experimental pain response. Baseline kinesiophobia will be assessed using the Tampa Scale of Kinesiophobia and examined as a factor associated with interindividual variability in neurophysiological responses to experimental pain.\n\nThe researchers expect that changes in motor cortex excitability during experimental pain will vary between individuals, and that individuals with higher kinesiophobia may show smaller changes in motor cortex excitability during capsaicin-induced pain.",[27,68],"Experimental Pain",[70,71,33,72,73,74,75,76],"Experimental pain","Topical capsaicin","Fear of movement","Motor cortex excitability","Intracortical excitability","Corticospinal excitability","Transcranial magnetic stimulation","2026-07-02",{"date":79,"type":45},"2026-07-07",{"date":81,"type":20},"2026-08-01",{"date":83,"type":20},"2026-12-31",{"name":85,"class":52},"Université de Sherbrooke",{"id":87,"slug":88,"hasResults":11,"nctId":89,"briefTitle":90,"officialTitle":91,"acronym":92,"eligibilityCriteria":93,"healthyVolunteers":11,"sex":16,"minAge":94,"maxAge":4,"enrollmentInfo":95,"targetDuration":4,"studyType":21,"phases":97,"briefSummary":98,"conditions":99,"keywords":100,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":107,"lastUpdatePostDateStruct":108,"startDateStruct":110,"completionDateStruct":112,"leadSponsor":114,"locationsCount":4},"100642654","virtual-reality-for-pain-and-well-being-in-older-adults-100642654","NCT07607899","Virtual Reality for Pain and Well-Being in Older Adults","Moving Without Fear or Pain: Use of Immersive Virtual Reality to Reduce Pain and Improve Well-Being in Older Adults","VitaMove","Inclusion Criteria:\n\n* Age 65 years or older\n* Able to understand and communicate in French\n* Chronic pain lasting 6 months or longer\n* Average pain intensity of 3 or greater on a 0-10 Numeric Rating Scale during the week prior to enrollment\n* Score greater than 25 on the 11-item Tampa Scale of Kinesiophobia (TSK-11)\n* No neurocognitive impairment (Mini-Mental State Examination \\[MMSE\\] ≥ 24), or mild neurocognitive impairment (MMSE 18-24) with preserved capacity to consent (University of California Brief Assessment of Capacity to Consent \\[UBACC\\] score ≥ 12)\n* Normal or corrected-to-normal visual acuity\n\nExclusion Criteria:\n\n* Severe motion sickness or intolerance that would prevent safe use of a virtual reality headset (experimental group only)\n* Medical condition that would prevent safe participation in rehabilitation activities\n* Presence of open wounds or infection at painful or contralateral sites","65 Years",{"count":96,"type":20},24,[23],"Chronic pain is common among adults aged 65 and older and can reduce mobility, independence, mood, and quality of life. Many older adults also develop a fear of movement because they worry that physical activity will increase their pain or cause injury. This fear can lead to reduced activity, physical deconditioning, and further loss of independence. This study aims to evaluate the feasibility, acceptability, and potential impact of Moving Without Fear or Pain, a program combining structured pain education (Empowered Relief) with immersive virtual reality rehabilitation to gradually reintroduce movement in a safe and engaging way. Empowered Relief is a single-session, two-hour online pain education class delivered by a trained health professional. It explains how chronic pain affects the brain and nervous system and teaches strategies to calm the nervous system, manage pain flare-ups, reduce pain-related worry and catastrophizing, and increase confidence in movement and daily activities.\n\nThe virtual reality intervention includes up to eight individualized sessions over approximately one month. Sessions last 5 to 30 minutes and are supervised by a trained clinician. Participants wear a virtual reality headset and are immersed in calming or engaging environments, such as nature settings. Depending on their comfort and abilities, sessions may begin with passive guided motor imagery and progress to active movement within interactive virtual environments. Some applications allow participants to control movement in the virtual world through gentle physical activity, such as stepping or upper-body movement. The intervention is personalized to each participant's physical capacity, preferences, and rehabilitation goals. The aim is to reduce fear of movement, increase confidence, and promote safe re-engagement in physical activity. In this pilot randomized controlled trial, 24 older adults with chronic pain will be randomly assigned to one of two groups: 1) Experimental Group: Participants will receive the Empowered Relief pain education course, usual care, and up to eight immersive virtual reality rehabilitation sessions. 2) Control Group: Participants will receive the Empowered Relief pain education course and usual care, without virtual reality sessions. The findings will inform a larger future study.",[30,27],[30,101,33,34,102,103,104,105,106],"Older Adults","Empowered Relief","Biopsychosocial Model","Motor Imagery","Virtual Reality Rehabilitation","Non-Pharmacological Pain Management","2026-06-12",{"date":109,"type":45},"2026-06-16",{"date":111,"type":20},"2026-06",{"date":113,"type":20},"2027-03",{"name":115,"class":52},"Laval University",{"id":117,"slug":118,"hasResults":11,"nctId":119,"briefTitle":120,"officialTitle":121,"acronym":122,"eligibilityCriteria":123,"healthyVolunteers":11,"sex":16,"minAge":124,"maxAge":125,"enrollmentInfo":126,"targetDuration":4,"studyType":128,"phases":4,"briefSummary":129,"conditions":130,"keywords":135,"overallStatus":139,"whyStopped":4,"lastUpdateSubmitDate":140,"lastUpdatePostDateStruct":141,"startDateStruct":143,"completionDateStruct":145,"leadSponsor":147,"locationsCount":53},"100584253","pain-education-after-rotator-cuff-surgery-100584253","NCT06886932","Pain Education After Rotator Cuff Surgery","The Effect of Pain Neuroscience Education on Patients Undergoing Surgical Repair of Moderate-Sized Rotator Cuff Tears","PNE-RCS","Eligibility Criteria\n\nInclusion Criteria:\n\nDiagnosis of a medium-sized rotator cuff tear (1-3 cm) confirmed by Magnetic Resonance Imaging (MRI) and scheduled for surgical repair Age between 40 and 75 years Sufficient Turkish language proficiency to understand and complete the informed consent form and assessment scales Mini-Mental State Examination (MMSE) score ≥ 24, indicating adequate cognitive function for study participation\n\nExclusion Criteria:\n\nCorticosteroid injection received within the last 6 weeks Adhesive capsulitis, defined as loss of passive external rotation greater than 50% or 30° History of previous cervical, thoracic, or shoulder surgery Presence of cervical radiculopathy, characterized by pain and tingling radiating to the arm due to nerve root involvement Acromioclavicular joint pathology or shoulder instability causing shoulder pain Full-thickness rotator cuff tear Calcific tendinitis Systemic diseases (e.g., inflammatory arthritis, malignancy) or neurological disorders (e.g., fibromyalgia, other neurological deficits) Fracture, labral lesion, or biceps tendon injury in the affected shoulder Prior participation in a chronic pain psychological management program or presence of generalized body pain","40 Years","75 Years",{"count":127,"type":20},45,"OBSERVATIONAL","Study Title: The Effect of Pain Neuroscience Education Combined with Conventional Rehabilitation on Pain Management and Functional Outcomes in Patients Undergoing Mini-Open Rotator Cuff Repair\n\nPurpose: This study aims to investigate whether adding Pain Neuroscience Education (PNE) to a conventional rehabilitation program improves pain management, physical function, and psychosocial outcomes in patients who have undergone mini-open surgery for rotator cuff tears (RCT). The study will also compare the effects of PNE when delivered before versus after surgery.\n\nWho Can Participate: Adults aged 40-75 who have been diagnosed with a medium-sized rotator cuff tear and are scheduled for mini-open surgical repair. Participants must meet specific health criteria and be willing to participate in the rehabilitation program.\n\nStudy Details:\n\nParticipants will be randomly assigned to one of three groups:\n\nGroup 1: Conventional rehabilitation only. Group 2: Conventional rehabilitation + PNE before surgery. Group 3: Conventional rehabilitation + PNE after surgery. PNE involves educational sessions that explain the biology of pain, how the nervous system processes pain, and strategies to reduce fear and catastrophizing related to pain.\n\nThe study will last approximately 12 weeks, with regular assessments of pain levels, physical function, and psychosocial factors (e.g., fear of movement, depression, sleep quality).\n\nPotential Benefits:\n\nParticipants may experience reduced pain, improved shoulder function, and better overall recovery.\n\nThe study may provide valuable insights into how PNE can enhance rehabilitation outcomes for patients with rotator cuff tears.\n\nPotential Risks:\n\nSome participants may find the educational sessions time-consuming or mentally challenging.\n\nThere is a small risk of discomfort during physical assessments or rehabilitation exercises.\n\nWhy is this study important?:\n\nRotator cuff tears are a common cause of shoulder pain and disability, especially in older adults. Post-surgical pain and fear of movement can slow recovery and reduce quality of life. This study will help determine whether PNE, when combined with conventional rehabilitation, can improve recovery outcomes and provide a better understanding of how timing (before or after surgery) affects its effectiveness.",[131,132,133,27,134],"Rotator Cuff Tears","Postoperative Pain Management","Shoulder Dysfunction","Postoperative Rehabilitation",[136,134,137,33,138,132],"Pain Neuroscience Education","Rotator Cuff Tear","Shoulder Surgery Outcomes","RECRUITING","2026-04-18",{"date":142,"type":45},"2026-04-22",{"date":144,"type":45},"2025-04-01",{"date":146,"type":20},"2026-09-30",{"name":148,"class":52},"Elif Dilara Durmaz",{"id":150,"slug":151,"hasResults":11,"nctId":152,"briefTitle":153,"officialTitle":154,"acronym":155,"eligibilityCriteria":156,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":94,"enrollmentInfo":157,"targetDuration":4,"studyType":21,"phases":159,"briefSummary":160,"conditions":161,"keywords":165,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":172,"lastUpdatePostDateStruct":173,"startDateStruct":175,"completionDateStruct":177,"leadSponsor":179,"locationsCount":53},"100633740","effects-of-music-listening-and-relaxation-interventions-on-postoperative-recovery-after-knee-surgery-100633740","NCT07530614","Effects of Music Listening and Relaxation Interventions on Postoperative Recovery After Knee Surgery","Effects of Music Listening and Emotional Freedom Techniques on Fall Risk, Kinesiophobia, and Pain Following Knee Arthroscopy","EFT","Inclusion Criteria:\n\n* Aged between 18 and 65 years\n* Scheduled for elective knee arthroscopy\n* Anxiety-fear intensity score ≥2 on the Subjective Units of Distress (SUD) scale\n* No hearing or speech problems that would prevent communication\n* No cognitive or mental impairments\n* No psychiatric disorders\n* No pain, tenderness, or wounds at the meridian points where Emotional Freedom Techniques (EFT) will be applied\n* Have not received prior training in coping with anxiety or fear\n* Have not previously attended courses related to energy therapy\n* Agree to participate in the study\n\nExclusion Criteria:\n\n* Currently using psychiatric medications\n* Receiving active psychological therapy\n* Experiencing postoperative surgical complications\n* Having traumatic lower extremity fractures\n* Undergoing simultaneous bilateral knee arthroscopy",{"count":158,"type":20},85,[23],"This study aims to evaluate whether listening to music and using Emotional Freedom Techniques (EFT) can help patients recover better after knee arthroscopy. After this type of surgery, many patients experience pain, fear of movement (kinesiophobia), balance problems, and an increased risk of falling.\n\nIn this study, patients will receive music listening and EFT as supportive, non-drug interventions during the postoperative period. The goal is to determine whether these simple and safe methods can reduce pain, decrease fear of movement, and lower fall risk, ultimately improving recovery.\n\nThe findings of this study may help healthcare professionals, especially nurses, provide more holistic and patient-centered care after knee surgery.",[162,27,163,164],"Knee Surgery","Postoperative Pain","Arthroscopic Surgery",[166,167,168,169,170,171],"Emotional Freedom Techniques","knee surgery","arthroscopy","listening to music","kinesiophobia","postoperative pain","2026-04-10",{"date":174,"type":45},"2026-04-15",{"date":176,"type":20},"2026-03-30",{"date":178,"type":20},"2027-01-28",{"name":180,"class":52},"Arzum ÇELİK BEKLEVİÇ",{"id":182,"slug":183,"hasResults":11,"nctId":184,"briefTitle":185,"officialTitle":185,"acronym":4,"eligibilityCriteria":186,"healthyVolunteers":61,"sex":16,"minAge":17,"maxAge":187,"enrollmentInfo":188,"targetDuration":4,"studyType":128,"phases":4,"briefSummary":190,"conditions":191,"keywords":195,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":204,"lastUpdatePostDateStruct":205,"startDateStruct":207,"completionDateStruct":209,"leadSponsor":210,"locationsCount":4},"100626410","kinesiophobia-in-rheumatoid-arthritis-associations-with-functional-disability-disease-activity-and-related-clinical-factors-100626410","NCT07435272","Kinesiophobia in Rheumatoid Arthritis: Associations With Functional Disability, Disease Activity, and Related Clinical Factors","Inclusion Criteria:\n\n* Age: adult population with RA (18-69)\n* Disease duration ≥ 6 months\n\nExclusion Criteria:\n\n1. Juvenile cases\n2. Other rheumatic diseases (SLE, AS, 1ry OA, etc.)\n3. Trauma\n4. Comorbidities that affect mobility, e.g., UMNL (including stroke), parkinsonism, multiple sclerosis, cerebral palsy, dementia, peripheral neuropathy, chronic pain conditions, etc.\n5. Previous history of psychiatric illness before onset of RA (anxiety, depression, etc.)\n6. Pregnancy and lactation","69 Years",{"count":189,"type":20},400,"Objectives: Impairment of physical function is a core feature of RA, particularly in patients with high disease activity where pain and inflammation directly limit movement. but, Reduced mobility in RA is not exclusively driven by inflammatory pathology. There are non-inflammatory factors, including kinesiophobia, fatigue, depression, and anxiety, may significantly contribute to functional limitation and may initiate a self-perpetuating cycle in which movement avoidance leads to physical deconditioning, muscle weakness, and progressive functional decline. The aim of this study is to examine the relationship between kinesiophobia and functional outcomes in patients with rheumatoid arthritis, and to investigate its associations with disease activity, pain, fatigue, depressive symptoms, anxiety, and sarcopenia, with a focus on factors relevant to functional assessment and rehabilitation.\n\nPatients and Methods\n\nA case - control study will be conducted on Two hundred adult patients previously diagnosed with RA according to ACR\u002FEULAR 2010 criteria for RA and 200 apparently healthy volunteers with age and sex matching will be involved in the study. The study will be conducted in Rheumatology department, Minia university Hospital, Egypt. All patients will be subjected to history taking, clinical examination, and assessment of the following parameters:\n\n1. Kinesiophobia: using the Arabic version of TSK-17\n2. Disease activity: using DAS 28\n3. pain severity using the Visual Analogue Scale (VAS)\n4. Fatigue: using the Arabic version of the Fatigue Severity Scale (FSS)\n5. Depression: using the Arabic version of the BDI-2\n6. Anxiety: using the Arabic version of the BAI\n7. sarcopenia using the Arabic version of the SARC-F questionnaire\n8. Functional disability: using the Arabic version of the HAQ-DI\n9. Physical activity:using IPAQ-SF",[27,192,193,194],"Rhematoid Arthritis","Rheumatoid Arthritis (RA)","Rheumatoid",[33,34,196,197,198,199,200,201,202,203],"Rheumatoid Arthritis","Functional Disability","Disease Activity","Pain","Fatigue","Anxiety","Depression","sarcopenia","2026-02-27",{"date":206,"type":45},"2026-03-03",{"date":208,"type":20},"2026-03-01",{"date":47,"type":20},{"name":211,"class":52},"Minia University",{"id":213,"slug":214,"hasResults":11,"nctId":215,"briefTitle":216,"officialTitle":217,"acronym":4,"eligibilityCriteria":218,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":219,"enrollmentInfo":220,"targetDuration":4,"studyType":21,"phases":222,"briefSummary":223,"conditions":224,"keywords":226,"overallStatus":139,"whyStopped":4,"lastUpdateSubmitDate":229,"lastUpdatePostDateStruct":230,"startDateStruct":232,"completionDateStruct":234,"leadSponsor":236,"locationsCount":53},"100625832","effect-of-cognitive-behavioral-therapy-on-kinesiophobia-and-functional-outcomes-after-total-hip-arthroplasty-100625832","NCT07427758","Effect of Cognitive Behavioral Therapy on Kinesiophobia and Functional Outcomes After Total Hip Arthroplasty.","Effect of Cognitive Behavioral Therapy on Kinesiophobia and Clinical Outcomes After Total Hip Arthroplasty: A Randomized Controlled Trial.","Inclusion Criteria:\n\n((1) postoperative unilateral THA for the first time; (2) at least primary education; (3) ≥18 years of age ; (4) voluntary participation and close cooperation with the care plan; and (5) agreement to continue the intervention and the six-month follow-up after discharge,(6) high level of kinesiophobia on Tampa Scale of Kinesiophobia(TSK), (7)medically stable and cleared by their orthopedic surgeon.\n\nExclusion Criteria:\n\n(1) revision surgery, (2) severe osteoarthritis in the contralateral hip, (3) severe acute metabolic neuromuscular and cardiovascular disease, (4) body mass index above 40, (5) presence of malignancy, any other orthopedic or neurologic problem that might affect treatment and assessments, (6) any condition that might interfere with communication, (7) or lack of cooperation during the study.(9) Individuals with cognitive disorder,(10) individuals with any psychological disease or disorder,(10) Had previously participated in a CBT intervention,(11) pregnancy.","80 Years",{"count":221,"type":20},100,[23],"The goal of this clinical trial study is to evaluate the effectiveness of cognitive behavioral therapy in reducing kinesiophobia and improving Clinical outcomes in postoperative patients following total hip arthroplasty The main question it aims to answer is:\n\nDoes the addition of cognitive behavioral therapy to standard physical therapy rehabilitation exercise reduce kinesiophobia and pain while improving functional mobility and quality of life in postoperative patients after total hip arthroplasty ? Participants will be divided into two groups to be compared: the first group (Control group) will only receive standard physical therapy rehabilitation exercises , consistent with routine post-total hip arthroplasty care, while the second group ( experimental group) will receive the same program in addition to cognitive behavioral therapy.",[225,27],"Total Hip Arthroplasty (THA)",[227,228],"Total Hip Arthroplasty","Kinesiophobia (fear of movement)","2026-02-17",{"date":231,"type":45},"2026-02-23",{"date":233,"type":45},"2026-02-01",{"date":235,"type":20},"2026-09-01",{"name":237,"class":52},"Cairo University",{"id":239,"slug":240,"hasResults":11,"nctId":241,"briefTitle":242,"officialTitle":243,"acronym":244,"eligibilityCriteria":245,"healthyVolunteers":61,"sex":16,"minAge":17,"maxAge":246,"enrollmentInfo":247,"targetDuration":4,"studyType":21,"phases":249,"briefSummary":250,"conditions":251,"keywords":253,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":262,"lastUpdatePostDateStruct":263,"startDateStruct":265,"completionDateStruct":267,"leadSponsor":269,"locationsCount":4},"100621439","binaural-beats-stimulation-on-the-autonomic-nervous-system-ans-kinesiophobia-and-fitness-levels-in-professional-athletes-with-musculoskeletal-msk-injuries-100621439","NCT07370636","Binaural Beats Stimulation on the Autonomic Nervous System (ANS), Kinesiophobia and Fitness Levels in Professional Athletes With Musculoskeletal (MSK) Injuries","The Effect of Binaural Beats Stimulation on the Autonomic Nervous System, Considering Kinesiophobia of Reinjuries and Fitness Levels in Professional Athletes With Musculoskeletal Injuries","ANS MSK HRV","Inclusion Criteria:\n\n* Professional athletes in open-skill sports\n* Age 18-25 years old\n* Participation in national and\u002For international professional championships for ≥ 5 years\n* Athletes with previous lower limb musculoskeletal injuries within the past three months or longer\n* Athletes with previous lower limb musculoskeletal injuries who have been fully rehabilitated.\n* Injuries sustained during any training period or competitive event\n* Provoke injuries during any training period or competitive event\n* Athletes with Kinesiophobia who have presented Tampa of Scale Kinesiophobia (TSK) questionnaire scores ranging from 17 to 37\n* Athletes with Anxiety who have presented Sport Competition Anxiety Test (SCAT) questionnaire scores more than 17\n* Frequency of engaging in sports 3-5 times per week (training, competitions)\n* Duration of each training session not exceeding 90 minutes\n* Athletes with adequate proficiency in the English language\n\nExclusion Criteria:\n\n* Amateur and recreational athletes in open-skill activities\n* Athletes ≤ 17 and ≥ 26 years old\n* Athletes in close-skill sports\n* Athletes with current musculoskeletal injuries (\\\u003C 3 months)\n* Athletes with poor rehabilitation of sport injuries\n* Athletes with musculoskeletal injuries of upper limbs and trunk\n* Athletes with musculoskeletal injuries during off-season periods\n* Athletes with recent surgery\n* Athletes with a concussion that occurred during training or competition\n* Athletes with psychological and neurological problems\n* Athletes with hearing impairment\n* Athletes with inadequate proficiency in the English language","25 Years",{"count":248,"type":20},66,[23],"The purpose of the current study is to investigate the effectiveness of binaural beat stimulation on the autonomic nervous system (ANS), taking into account kinesiophobia related to reinjury and fitness levels in professional athletes with musculoskeletal injuries. The study hypothesis is that binaural beats will have beneficial effects by reducing ANS activity, primarily through modulation of parasympathetic nervous system (PNS) activity, as well as by reducing kinesiophobia related to reinjury and enhancing fitness levels in this population.\n\nResearchers will compare binaural beat stimulation to a placebo condition and to a condition without binaural beats in order to evaluate and compare the effects of those three conditions on psychological and physiological parameters in professional athletes with musculoskeletal injuries.\n\nParticipants will:\n\n* Receive receive music intervention either with binaural beat stimulation or placebo or music without binaural beats before their training sessions and competitions for a period of four weeks.\n* Maintain a diary to document each session of the music-based intervention.",[27,252],"Musculoskeletal Injuries",[254,170,255,256,257,258,259,260,261],"Binaural beats","Autonomic nervous system","sympathetic skin response","VO2max","Heart rate variability","grip strength test","pain","anxiety","2026-02-05",{"date":264,"type":45},"2026-02-10",{"date":266,"type":20},"2026-02",{"date":268,"type":20},"2027-06",{"name":270,"class":52},"University of West Attica"]