[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Toros University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":292},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,10,0,[8,47,75,104,129,149,185,210,238,266],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":29,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":46},"100647777","blood-flow-restriction-during-nordic-hamstring-exercise-in-elite-adolescent-athletes-100647777",false,"NCT07715786","Blood Flow Restriction During Nordic Hamstring Exercise in Elite Adolescent Athletes","Comparison of Hamstring Muscle Oxygenation Responses During Nordic Hamstring Exercise and Blood Flow Restriction Nordic Hamstring Exercise in Elite Adolescent Athletes: A Crossover Experimental Study","Inclusion Criteria:\n\n* Elite adolescent athletes aged 14 to 18 years.\n* Licensed athletes with at least 3 years of regular sports participation.\n* Currently participating in a regular weekly training program.\n* Physically able to complete the Nordic Hamstring Exercise and study testing protocol.\n* Willing to participate in the study.\n* Able to provide written informed consent.\n* For participants younger than 18 years, written informed consent provided by a parent or legal guardian and assent provided by the participant.\n\nExclusion Criteria:\n\n* Hamstring injury within the previous 6 months.\n* Lower extremity surgery within the previous 6 months.\n* Current lower extremity pain or musculoskeletal injury that may interfere with exercise performance.\n* Cardiovascular, vascular, neurological, or other medical conditions that may contraindicate blood flow restriction exercise.\n* Presence of skin lesions or conditions preventing placement of the blood flow restriction cuff or MOXY sensor.\n* Inability to complete either exercise condition or follow the study protocol.",true,"ALL","14 Years","18 Years",{"count":21,"type":22},24,"ESTIMATED","INTERVENTIONAL",[25],"NA","This crossover experimental study aims to compare acute hamstring muscle oxygenation responses during Nordic Hamstring Exercise (NHE) and Blood Flow Restriction Nordic Hamstring Exercise (BFR-NHE) in elite adolescent athletes. Participants will complete both exercise conditions in a randomized order separated by a 7-day washout period. Muscle oxygen saturation will be assessed using near-infrared spectroscopy (MOXY), together with total hemoglobin responses, blood lactate concentration, perceived exertion, and exercise performance variables. The findings may improve understanding of the physiological effects of blood flow restriction during eccentric hamstring exercise in adolescent athletes.",[28],"Healthy Volunteers (HV)",[30,31,32,33],"Nordic Hamstring Exercise","Blood Flow Restriction","Elite Adolescent Athletes","Muscle Oxygenation","RECRUITING","2026-07-13",{"date":37,"type":38},"2026-07-20","ACTUAL",{"date":40,"type":38},"2026-07-01",{"date":42,"type":22},"2027-08",{"name":44,"class":45},"Toros University","OTHER",1,{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":4,"eligibilityCriteria":53,"healthyVolunteers":11,"sex":17,"minAge":19,"maxAge":54,"enrollmentInfo":55,"targetDuration":4,"studyType":23,"phases":57,"briefSummary":58,"conditions":59,"keywords":61,"overallStatus":66,"whyStopped":4,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":68,"startDateStruct":70,"completionDateStruct":72,"leadSponsor":74,"locationsCount":4},"100647225","acute-effects-of-classical-vs-percussive-massage-on-text-neck-syndrome-100647225","NCT07705711","Acute Effects of Classical vs. Percussive Massage on Text Neck Syndrome","Comparison of the Acute Effects of Classical Massage and Percussive Massage in Young Adults With Text Neck Syndrome","Inclusion Criteria:\n\n* University students aged between 18 and 30 years.\n* Willing to participate in the study and provide informed consent.\n* Have been using a mobile device for at least 1 year.\n* Have no communication impairments.\n* Use a mobile device for at least 3 hours per day.\n* Report at least three of the six core symptoms of Mobile Neck Syndrome (MNS): neck pain, upper back pain, shoulder pain, headache, insomnia, and tingling or numbness in the hands.\n* Have a Neck Disability Index (NDI) score of 10 or higher.\n\nExclusion Criteria:\n\n* History of generalized joint disorders affecting the head, neck, or shoulder region.\n* History of radiotherapy involving the head, neck, or shoulder region.\n* History of surgery involving the head or neck region.\n* Diagnosis of cervical disc herniation, cervical radiculopathy, or cervical myelopathy.\n* History of inflammatory, neuromuscular, or congenital disorders affecting the head or neck region.\n* Presence of a metal implant in the treatment area.\n* Current use of analgesics, muscle relaxants, anticoagulants, or other medications that may influence the study outcomes.\n* History of systemic disease.\n* Receipt of any treatment targeting the cervical region within the previous 3 months.\n* Pregnancy.","30 Years",{"count":56,"type":22},34,[25],"The aim of our study is to compare the short-term effects of traditional classical massage and percussive massage on neck pain, patient satisfaction level, and upper extremity flexibility in young adults with MBS. Another aim of the study is to contribute to the literature, as there are a limited number of studies that directly evaluate the effectiveness of popular vibration devices (Theragun, etc.) compared to classical massage. Original value: With the development of technology and the increase in mobile device usage times, MBS is increasingly common, especially among young adults and university students. There are limited studies in the literature on the treatment of MBS. No studies comparing the acute effects of classical massage and percussion therapy in the treatment of this syndrome have been found. Therefore, our study has the potential to make a unique contribution to the literature by offering a direct comparison between both traditional classical massage and the modern technological method of percussion gun.\n\nSociodemographic Assessment Form: The form to be prepared before the study will record information such as age (years), gender, body weight (kg) and height (cm) of the participants, as well as trauma-surgery history, systemic problems, and average daily mobile device usage time. Six symptoms reporting MBS diagnostic criteria (neck pain, back pain, shoulder pain, headache, insomnia, tingling and numbness in the hands) will be questioned .\n\nPain Assessment: The pain intensity of individuals with MBS will be assessed using the Visual Analog Scale, which is reported to be valid and reliable. Individuals included in the study will be asked to indicate the pain intensity they experienced in the last week on a vertically positioned 100 mm long line. The marked points will be measured and recorded in millimeters.\n\nNeck Disability Index (NDI): It is planned to use the Neck Disability Index, which has Turkish validity and reliability, to determine neck disability. The first four items of the ten-item questionnaire are related to subjective symptoms, while the other six items are related to daily life activities. When the total score of the questionnaire is examined, 0 points indicate no disability, 5-14 points indicate mild disability, 15-24 points indicate moderate disability, 25-34 points indicate severe disability, and 35 points and above indicate complete disability.\n\nEvaluation of Patient Satisfaction Level: The treatment satisfaction levels of the participants included in the study will be evaluated with the Patient Satisfaction Scale developed for physical therapy outpatient clinics.\n\nThe Turkish validity and reliability study of this 24-item scale was carried out by Tüzün et al. (2009) (Cronbach alpha: 0.88). The scale is scored between 0 (strongly disagree) and 4 (strongly agree), and higher scores indicate higher satisfaction. Assessment of Upper Extremity Balance: Participants' upper extremity balance and performance will be assessed using the Upper Extremity Balance Test.\n\nWhile maintaining a push-up position with feet no more than twelve inches (30.5 cm) apart, the individual will reach with maximum effort in three directions (medial, superolateral, and inferolateral) with their free hand relative to the fixed hand, and the distance reached in each direction will be recorded. Each individual will be allowed to make 3 practice trials before the test, and the average of 3 trials will be used for analysis.\n\nAssessment of Upper Extremity Flexibility: To assess the upper extremity flexibility of the participants, the Apley Scratch Test will be used. Also called the Dawbarn Test, the Apley Scratch Test provides a rapid assessment of the patient's active range of motion, including internal rotation, extension, and adduction. During the Apley scratch test, the patient attempts to reach upwards from their back, starting from below and aiming to place their hand between their shoulder blades. Then the distance between the two hands is measured with the help of a tape measure.\n\nInterventions Percussive Massage Therapy: Percussive massage therapy will be applied with the TheraGun Relief Navy massage gun, which is planned to be supplied within the scope of the project. Percussive massage application will be applied from distal to proximal along the starting points of the trapezius, levator scapulae and cervical paravertebral muscles at a medium speed (level 2, range: 33-40 Hz) and 12 mm amplitude. Percussive therapy will be performed using the soft head of the massage gun with a treatment time of five minutes for each muscle group.\n\nClassic Massage Therapy: After carefully protecting patient privacy in a prone position, general stroking is applied to the neck area, followed by massage oil using the 3 Stroking-3 Kneading-3 Stroking technique on the erector spinae, trapezius and levator scapulae muscles, from distal to proximal.",[60],"Text Neck Syndrome",[62,63,64,65],"text neck syndrome","neck pain","pain","massage therapy","NOT_YET_RECRUITING","2026-07-10",{"date":69,"type":38},"2026-07-15",{"date":71,"type":22},"2026-08-03",{"date":73,"type":22},"2026-11-20",{"name":44,"class":45},{"id":76,"slug":77,"hasResults":11,"nctId":78,"briefTitle":79,"officialTitle":80,"acronym":4,"eligibilityCriteria":81,"healthyVolunteers":16,"sex":82,"minAge":83,"maxAge":19,"enrollmentInfo":84,"targetDuration":4,"studyType":23,"phases":86,"briefSummary":87,"conditions":88,"keywords":93,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":98,"startDateStruct":99,"completionDateStruct":101,"leadSponsor":103,"locationsCount":46},"100647218","nordic-vs-blood-flow-restriction-nordic-exercise-in-elite-female-pole-vaulters-100647218","NCT07705698","Nordic vs Blood Flow Restriction Nordic Exercise in Elite Female Pole Vaulters","Effects of Nordic Hamstring Exercise and Blood Flow Restriction-Assisted Nordic Hamstring Exercise on Hamstring Strength, Muscle Morphology and Functional Performance in Elite Adolescent Female Pole Vaulters: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Female athletes aged between 12 and 18 years.\n* Elite pole vault athletes actively participating in organized training and competition.\n* Minimum of 1 year of regular pole vault training experience.\n* Participation in regular training at least 3 times per week.\n* Ability to participate in an 8-week exercise program.\n* Written informed assent from the athlete and written informed consent from a parent or legal guardian.\n\nExclusion Criteria:\n\n* Any lower extremity musculoskeletal injury within the previous 6 months.\n* Previous hamstring muscle surgery.\n* Current pain or injury limiting sports participation.\n* Neurological disorders affecting movement or balance.\n* Cardiovascular conditions contraindicating exercise training or blood flow restriction.\n* Any contraindication to blood flow restriction training.\n* Participation in another structured hamstring strengthening program during the study period.\n* Inability or unwillingness to comply with study procedures.","FEMALE","12 Years",{"count":85,"type":22},36,[25],"The purpose of this randomized controlled trial is to compare the effects of Nordic Hamstring Exercise (NHE) and Blood Flow Restriction-assisted Nordic Hamstring Exercise (BFR-NHE) on hamstring muscle strength, muscle morphology, and functional performance in elite adolescent female pole vaulters. Thirty-six athletes aged 12-18 years will be randomly assigned to a Nordic Hamstring Exercise group, a Blood Flow Restriction-assisted Nordic Hamstring Exercise group, or a control group. Intervention groups will participate in supervised exercise training three times per week for eight weeks, while the control group will continue routine sports training. Outcomes will be assessed before and after the intervention period.",[89,90,91,92],"Muscle Strength","Athletic Performance","Hamstring Adaptation","Sports Injury Prevention",[30,94,95,96,97],"Blood Flow Restriction Training","Ultrasonography","Functional Performance","Adolescent Athletes",{"date":69,"type":38},{"date":100,"type":38},"2026-05-27",{"date":102,"type":22},"2027-04",{"name":44,"class":45},{"id":105,"slug":106,"hasResults":11,"nctId":107,"briefTitle":108,"officialTitle":109,"acronym":4,"eligibilityCriteria":110,"healthyVolunteers":11,"sex":82,"minAge":19,"maxAge":111,"enrollmentInfo":112,"targetDuration":4,"studyType":23,"phases":114,"briefSummary":115,"conditions":116,"keywords":118,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":123,"startDateStruct":124,"completionDateStruct":126,"leadSponsor":128,"locationsCount":46},"100645933","scapulothoracic-stabilization-and-postural-training-in-upper-extremity-lymphedema-100645933","NCT07697495","Scapulothoracic Stabilization and Postural Training in Upper Extremity Lymphedema","Effects of Scapulothoracic Stabilization and Postural Training Added to Standard Lymphedema Care on Muscle Strength, Posture and Functional Outcomes in Secondary Upper Extremity Lymphedema: A Single-Center Randomized Controlled Trial","Inclusion Criteria:\n\n* Female patients aged 18 to 65 years.\n* Diagnosed with secondary upper extremity lymphedema following breast cancer surgery (mastectomy).\n* Willing to participate in the study.\n* Able to provide written informed consent.\n\nExclusion Criteria:\n\n* Active infection (e.g., cellulitis or lymphangitis).\n* Advanced shoulder or cervical pathology.\n* Neurological disorders affecting upper extremity function.\n* Metastatic disease.\n* Receiving active chemotherapy.\n* Participation in another intensive lymphedema rehabilitation program within the previous 3 months.","65 Years",{"count":113,"type":22},60,[25],"This single-center randomized controlled trial aims to investigate the effects of adding scapulothoracic stabilization and postural training to standard lymphedema care in women with secondary upper extremity lymphedema following breast cancer surgery. Participants will be randomly assigned to receive either standard lymphedema care alone or standard care combined with scapulothoracic stabilization and postural training. Outcomes including scapular muscle strength, posture, upper extremity function, limb volume, and neck awareness will be assessed at baseline, immediately after treatment, and at a 2-month follow-up. The findings are expected to provide evidence regarding the effectiveness of incorporating targeted stabilization and postural exercises into conventional lymphedema rehabilitation.",[117],"Secondary Lymphedema",[119,120,121,89,122],"Upper Extremity Lymphedema","Scapulothoracic Stabilization","Postural Training","Posture",{"date":35,"type":38},{"date":125,"type":38},"2026-03-01",{"date":127,"type":22},"2027-03",{"name":44,"class":45},{"id":130,"slug":131,"hasResults":11,"nctId":132,"briefTitle":133,"officialTitle":134,"acronym":4,"eligibilityCriteria":135,"healthyVolunteers":11,"sex":82,"minAge":19,"maxAge":111,"enrollmentInfo":136,"targetDuration":4,"studyType":23,"phases":137,"briefSummary":138,"conditions":139,"keywords":141,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":145,"startDateStruct":146,"completionDateStruct":147,"leadSponsor":148,"locationsCount":46},"100645896","respiratory-and-relaxation-training-in-lower-extremity-lymphedema-100645896","NCT07697482","Respiratory and Relaxation Training in Lower Extremity Lymphedema","Effect of Respiratory and Relaxation Training Added to Complex Decongestive Therapy on Functional Capacity and Muscle Oxygenation in Patients With Lower Extremity Lymphedema: A Single-Center Randomized Controlled Trial","Inclusion Criteria:\n\n* Female patients aged 18 years or older.\n* Clinically diagnosed with secondary lower extremity lymphedema.\n* Presence of lower extremity lymphedema for at least 3 months.\n* Able to stand and walk independently to complete the Six-Minute Walk Test.\n* Willing and able to provide written informed consent.\n\nExclusion Criteria:\n\n* Acute cellulitis or other active infection within the previous 2-4 weeks.\n* Current or recent deep vein thrombosis (DVT) or uncontrolled peripheral vascular disease.\n* Severe cardiovascular, pulmonary, orthopedic, or neurological conditions that could interfere with participation or outcome assessments.\n* Pregnancy.\n* Skin lesions or irritation preventing placement of the near-infrared spectroscopy (MOXY) sensor.\n* Inability to comply with the study protocol or follow-up assessments.",{"count":113,"type":22},[25],"This randomized controlled trial aims to investigate the effectiveness of respiratory and relaxation training added to standard complex decongestive therapy (CDT) on muscle oxygenation, functional capacity, and limb volume in patients with lower extremity lymphedema. Participants will be randomly assigned to receive either standard CDT alone or CDT combined with respiratory and relaxation exercises. Outcomes will be assessed before treatment, immediately after treatment, and two months after completion.",[140],"Lower Extremity Lymphedema",[140,142,143,144,33],"Complex Decongestive Therapy","Respiratory Training","Relaxation Training",{"date":35,"type":38},{"date":125,"type":38},{"date":127,"type":22},{"name":44,"class":45},{"id":150,"slug":151,"hasResults":11,"nctId":152,"briefTitle":153,"officialTitle":154,"acronym":155,"eligibilityCriteria":156,"healthyVolunteers":11,"sex":17,"minAge":157,"maxAge":158,"enrollmentInfo":159,"targetDuration":4,"studyType":161,"phases":4,"briefSummary":162,"conditions":163,"keywords":169,"overallStatus":66,"whyStopped":4,"lastUpdateSubmitDate":178,"lastUpdatePostDateStruct":179,"startDateStruct":181,"completionDateStruct":182,"leadSponsor":184,"locationsCount":46},"100643167","evaluation-of-metabolic-parameters-intestinal-permeability-and-gastrointestinal-symptoms-after-bariatric-surgery-in-body-weight-management-100643167","NCT07643376","Evaluation of Metabolic Parameters, Intestinal Permeability and Gastrointestinal Symptoms After Bariatric Surgery in Body Weight Management","Evaluation of Postoperative Metabolic Parameters, Intestinal Permeability and Gastrointestinal Symptoms in Body Weight Management After Laparoscopic Sleeve Gastrectomy","METABAR","Inclusion Criteria:\n\n* Underwent Laparoscopic Sleeve Gastrectomy (LSG) within the last 1 month\n* Aged between 19-50 years\n* BMI ≥40 kg\u002Fm² or BMI ≥35 kg\u002Fm² with obesity-related comorbidities\n* Signed informed consent form\n* Non-smoker and non-alcohol dependent\n\nExclusion Criteria:\n\n* Did not undergo or is not planned to undergo LSG\n* Outside the age range of 19-50 years\n* Did not sign the informed consent form\n* BMI \\\u003C40 kg\u002Fm² or BMI \\\u003C35 kg\u002Fm² without obesity-related comorbidities\n* Smoker or alcohol dependent\n* Has an inflammatory disease\n* Currently using probiotics, antibiotics, or fiber supplements\n* Has a psychiatric disorder","19 Years","50 Years",{"count":160,"type":22},40,"OBSERVATIONAL","This study aims to evaluate the changes in metabolic parameters, intestinal permeability, and gastrointestinal symptoms in individuals who have undergone bariatric surgery (Laparoscopic Sleeve Gastrectomy - LSG) for obesity treatment.\n\nObesity is a chronic disease associated with serious health complications including type 2 diabetes, hypertension, cardiovascular disease, and metabolic disorders. Bariatric surgery is currently the most effective treatment method for morbid obesity. However, monitoring patients after surgery in terms of metabolic health, gut permeability, and gastrointestinal symptoms is crucial for long-term success.\n\nIn this study, 40 volunteers (aged 19-50) who have undergone LSG surgery within the last month will be followed for 6 months. At the beginning of the study and 6 months later, the following will be assessed:\n\n* Metabolic parameters: fasting blood glucose, total cholesterol, triglycerides, high-density lipoprotein (HDL), low-density lipoprotein (LDL), very low-density lipoprotein (VLDL) cholesterol, and insulin levels\n* Intestinal permeability markers: zonulin, secretory immunoglobulin A (IgA), and lipopolysaccharide (LPS) levels\n* Gastrointestinal symptoms: assessed using the Gastrointestinal Symptom Rating Scale (GSRS)\n* Anthropometric measurements: body weight, height, waist and hip circumference, BMI\n* Nutritional intake: 3-day dietary records\n\nThe study will be conducted at Bursa Yıldırım Doruk Hospital, General Surgery Clinic. Results will contribute to understanding the relationship between bariatric surgery and gut health, potentially helping to prevent postoperative complications.",[164,165,166,167,168],"Obesity, Morbid","Bariatric Surgery","Intestinal Permeability","Gastrointestinal Symptoms","Metabolic Syndrome",[170,171,172,173,174,175,176,177],"Laparoscopic Sleeve Gastrectomy","Zonulin","Secretory IgA","Lipopolysaccharide","GSRS","Body Weight Management","Gut microbiota","Postoperative Metabolic Parameters","2026-06-08",{"date":180,"type":38},"2026-06-11",{"date":40,"type":22},{"date":183,"type":22},"2027-02-01",{"name":44,"class":45},{"id":186,"slug":187,"hasResults":11,"nctId":188,"briefTitle":189,"officialTitle":190,"acronym":191,"eligibilityCriteria":192,"healthyVolunteers":16,"sex":17,"minAge":111,"maxAge":4,"enrollmentInfo":193,"targetDuration":4,"studyType":161,"phases":4,"briefSummary":195,"conditions":196,"keywords":199,"overallStatus":66,"whyStopped":4,"lastUpdateSubmitDate":178,"lastUpdatePostDateStruct":203,"startDateStruct":205,"completionDateStruct":207,"leadSponsor":209,"locationsCount":46},"100604278","turkish-validation-of-the-aloc-screening-scale-in-older-adults-100604278","NCT07147439","Turkish Validation of the ALOC Screening Scale in Older Adults","Turkish Validity and Reliability of the Appetite Loss in Older Adults With and Without Cognitive Impairment (ALOC) Screening Scale","ALOC","Inclusion Criteria:\n\n* Elderly over 65 years, with or without cognitive impairment\n\nExclusion Criteria:\n\n\\-",{"count":194,"type":22},300,"As the elderly population increases, health problems related to aging are also increasing. Loss of appetite negatively affects public health by causing malnutrition and related health problems in elderly individuals. Loss of appetite is a common problem in older adults, both in individuals with and without cognitive impairment. This can lead to serious health problems such as malnutrition, weight loss, muscle loss, weakening of the immune system and decreased quality of life. Cognitive disorders such as Alzheimer's and dementia can trigger loss of appetite, or loss of appetite can be a symptom of these disorders. Factors such as metabolic changes during the aging process, decreased sense of taste and smell, loneliness and depression contribute to loss of appetite. However, there is no valid and reliable scale in Turkey for the early diagnosis and assessment of loss of appetite. A scale being valid and reliable means that it can measure the concept it is intended to measure accurately and consistently. The aim of this study was to determine the validity and reliability of the Turkish version of the Loss of Appetite Scale in older adults with and without cognitive impairment .",[197,198],"Elderly (People Aged 65 or More)","With or Without Cognitive Impairment",[200,191,201,202],"Elderly","SNAQ","TURKISH VALIDITY AND RELIABILITY",{"date":204,"type":38},"2026-06-10",{"date":206,"type":22},"2026-09-01",{"date":208,"type":22},"2026-12-01",{"name":44,"class":45},{"id":211,"slug":212,"hasResults":11,"nctId":213,"briefTitle":214,"officialTitle":215,"acronym":4,"eligibilityCriteria":216,"healthyVolunteers":11,"sex":17,"minAge":19,"maxAge":4,"enrollmentInfo":217,"targetDuration":4,"studyType":23,"phases":219,"briefSummary":220,"conditions":221,"keywords":226,"overallStatus":66,"whyStopped":4,"lastUpdateSubmitDate":232,"lastUpdatePostDateStruct":233,"startDateStruct":235,"completionDateStruct":236,"leadSponsor":237,"locationsCount":4},"100634547","cancer-awareness-among-syrian-migrants-100634547","NCT07541105","Cancer Awareness Among Syrian Migrants","A Theory-Driven Educational Intervention to Enhance Cancer Screening Uptake Among Syrian Migrants in Turkey: A Study Protocol","Inclusion Criteria:\n\n* over 18 years of age\n* hold Syrian citizenship\n* be registered with the Migrant Health Center in Mersin province\n* have proficiency in Turkish or Arabic\n* voluntarily agree to participate\n\nExclusion Criteria:\n\n* if they hold Turkish citizenship\n* have a diagnosed psychiatric disorder\n* have been diagnosed with cancer\n* wish to withdraw from the study",{"count":218,"type":22},30,[25],"This study aims to develop and evaluate a theory-based educational intervention to improve cancer screening participation among Syrian migrants in Turkey. The study will also develop a Cancer Protection Motivation Scale (CPMS) to measure individuals' motivation toward cancer screening. Using a mixed-methods design, the study will explore barriers, beliefs, and behaviors related to breast, cervical, and colorectal cancer screening. The effectiveness of the intervention will be assessed using a pretest-posttest design. The findings are expected to support culturally appropriate strategies to improve cancer screening uptake among migrant populations.",[222,223,224,225],"Breast Cancer Screening","Cervical Cancer Screening","Colorectal Cancer Screening","Cancer Prevention Behavior",[227,228,229,230,231],"Breast cancer","Colon cancer","Cervical cancer","Protection motivation","Reduced inequalities","2026-04-20",{"date":234,"type":38},"2026-04-24",{"date":232,"type":22},{"date":69,"type":22},{"name":44,"class":45},{"id":239,"slug":240,"hasResults":11,"nctId":241,"briefTitle":242,"officialTitle":243,"acronym":4,"eligibilityCriteria":244,"healthyVolunteers":11,"sex":17,"minAge":245,"maxAge":83,"enrollmentInfo":246,"targetDuration":4,"studyType":23,"phases":248,"briefSummary":249,"conditions":250,"keywords":252,"overallStatus":66,"whyStopped":4,"lastUpdateSubmitDate":258,"lastUpdatePostDateStruct":259,"startDateStruct":261,"completionDateStruct":263,"leadSponsor":265,"locationsCount":4},"100602712","intravenous-catheter-application-100602712","NCT07127081","Intravenous Catheter Application","The Effect of Stress Ball and Watching Cartoons on Pain and Fear During Intravenous Catheter Application in Children: A Randomised Controlled Study","Inclusion Criteria:\n\n* Those who were admitted to Toros State Hospital, Child service on 01 September 2025- 01.02.2026,\n* Children aged 6 to 12 years,\n* Children scheduled for intravenous catheterisation,\n* Children without mental and developmental retardation,\n* Children who can speak and understand Turkish,\n* Children and parents who signed an informed consent form.\n\nExclusion Criteria:\n\n* Children who cannot speak or communicate in Turkish,\n* Children whose first attempt to insert an intravenous catheter failed,\n* Children and parents who did not sign the informed consent form.","6 Years",{"count":247,"type":22},90,[25],"The study was a randomised controlled trial showing the effect of watching cartoons and squeezing a stress ball on pain and fear in children admitted for intravenous catheter insertion. Hypotheses of the Study Hypothesis 1: Children who watch cartoons during intravenous catheter insertion have lower pain and fear scores than the control group.\n\nHypothesis 2: The pain and fear of children who squeeze a stress ball during intravenous catheter insertion are lower than the control group Hypothesis 3: There is a difference between the pain and fear scores of children who watch cartoons and squeeze a stress ball.",[251],"6-12 Years Old",[253,254,255,256,257],"Children","intravenous catheter","stress ball","cartoons","nursing","2025-08-20",{"date":260,"type":38},"2025-08-27",{"date":262,"type":22},"2025-09-01",{"date":264,"type":22},"2026-05-01",{"name":44,"class":45},{"id":267,"slug":268,"hasResults":11,"nctId":269,"briefTitle":270,"officialTitle":271,"acronym":4,"eligibilityCriteria":272,"healthyVolunteers":11,"sex":17,"minAge":19,"maxAge":111,"enrollmentInfo":273,"targetDuration":4,"studyType":23,"phases":274,"briefSummary":275,"conditions":276,"keywords":278,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":284,"lastUpdatePostDateStruct":285,"startDateStruct":287,"completionDateStruct":289,"leadSponsor":291,"locationsCount":46},"100589075","effect-of-dual-task-training-and-cognitive-rehabilitation-in-individuals-with-multiple-sclerosis-100589075","NCT06949696","Effect of Dual-Task Training and Cognitive Rehabilitation in Individuals With Multiple Sclerosis.","Effects of Dual-Task Training and Cognitive Rehabilitation on Gait, Balance, Fatigue and Cognitive Performance in Individuals With Multiple Sclerosis","Inclusion Criteria:\n\n* Definite MS diagnosis by a neurologist\n* Can walk independently\n* Expanded Disability Status Scale (EDSS) score below 5\n* Has not had an attack in the last 3 months, has been medically stable for 6 months\n* Has not received a regular physiotherapy program in the last 6 months volunteer\n\nExclusion Criteria:\n\n* Scoring 26 or below on the Montreal Cognitive Assessment Scale (MoCA)\n* Having systemic, orthopedic and neurological problems that may affect walking and balance in the assessments\n* Having additional psychiatric disorders",{"count":218,"type":22},[25],"The purpose of this study is to examine the effects of dual-task training and cognitive rehabilitation on gait, balance, fatigue and cognitive performance in individuals with multiple sclerosis.",[277],"Multiple Sclerosis",[279,280,281,282,283],"multiple sclerosis","balance","gait","dual task","fatigue","2025-04-22",{"date":286,"type":38},"2025-04-29",{"date":288,"type":38},"2025-04-20",{"date":290,"type":22},"2026-06-01",{"name":44,"class":45},""]