[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"postural-control\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:postural-control":25},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,11,0,[8,47,79,107,139,170,194,220,261,288,334],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":17,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":22,"conditions":23,"keywords":30,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":46},"100645113","the-relationship-between-lost-extremity-percentage-and-postural-control-neck-and-low-back-pain-daily-living-activities-and-reaction-time-in-individuals-with-unilateral-upper-limb-amputation-100645113",false,"NCT07677969","The Relationship Between Lost Extremity Percentage and Postural Control, Neck and Low Back Pain, Daily Living Activities, and Reaction Time in Individuals With Unilateral Upper Limb Amputation","Inclusion Criteria:\n\n* Adults aged 18-65 years\n* Unilateral upper limb amputation\n* Use of a myoelectric or bionic prosthesis for at least 1 year\n* Current prosthesis use for a minimum of 3 months\n\nExclusion Criteria:\n\n* Bilateral upper limb amputation\n* Additional amputation of another limb\n* Use of passive or cosmetic prosthesis\n* Presence of neurological or other significant orthopedic disorders unrelated to amputation","ALL","18 Years","65 Years",{"count":19,"type":20},15,"ESTIMATED","OBSERVATIONAL","This observational study aims to examine the relationship between the percentage of limb loss and functional outcomes in individuals with unilateral upper limb amputation. Upper limb amputation can affect posture, balance control, pain levels, daily living activities, hand function, and reaction time. However, limited research has investigated how the amount of limb loss influences these outcomes.\n\nParticipants between 18 and 65 years of age who use a myoelectric or bionic prosthesis will undergo a series of assessments. These assessments include measurements of postural control using a force platform, posture analysis, evaluation of neck and low back pain using a visual analog scale, daily living activities using a validated questionnaire, hand dexterity using the Box and Block Test, and reaction time using a visual stimulus device.\n\nThe study does not involve any intervention or treatment. All evaluations will be performed during a single assessment session. The results of this study may help improve rehabilitation planning and provide better understanding of functional changes associated with different levels of limb loss in people with upper limb amputation.",[24,25,26,27,28,29],"Upper Limb Amputation","Postural Control","Neck Pain","Low Back Pain","Daily Activities","Reaction Time",[24,25,26,31,32,33],"low back pain","Daily Living Activities","reaction time","RECRUITING","2026-06-30",{"date":37,"type":38},"2026-07-01","ACTUAL",{"date":40,"type":38},"2026-01-01",{"date":42,"type":20},"2026-12-01",{"name":44,"class":45},"Hacettepe University","OTHER",1,{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":4,"eligibilityCriteria":53,"healthyVolunteers":54,"sex":55,"minAge":16,"maxAge":56,"enrollmentInfo":57,"targetDuration":4,"studyType":59,"phases":60,"briefSummary":62,"conditions":63,"keywords":4,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":70,"lastUpdatePostDateStruct":71,"startDateStruct":73,"completionDateStruct":75,"leadSponsor":77,"locationsCount":4},"100641838","the-effect-of-foot-reflexology-in-women-with-migraine-100641838","NCT07651839","The Effect of Foot Reflexology in Women With Migraine","The Effect of Foot Reflexology on Pain, Anxiety, Kinesiophobia, and Postural Control in Women With Migraine","Inclusion Criteria:\n\n* Being a woman between the ages of 18 and 45\n* Having been diagnosed with migraine by a neurologist according to the International Headache Society (IHS) criteria\n* Volunteering to participate in the study\n* Being literate\n* Not having entered menopause\n\nExclusion Criteria:\n\n* Having any neurological disease other than migraine\n* Having a psychiatric illness\n* Smoking\n* Having a musculoskeletal disease affecting the head and neck area\n* Having a history of cervical or cranial surgery\n* Having irritation or ulceration in the skin area to be massaged\n* Receiving migraine treatment other than pharmacological treatment (acupuncture, dry needling, cupping, etc.)\n* Having diabetic foot\n* Having open wounds on the foot\n* Pregnant individuals or individuals who become pregnant during the study period",true,"FEMALE","45 Years",{"count":58,"type":20},20,"INTERVENTIONAL",[61],"NA","This prospective randomized controlled study aims to investigate the effects of foot massage on pain, anxiety, kinesiophobia, and postural control in women aged 18-45 years diagnosed with migraine who attend the Neurology Outpatient Clinic of Karabük University Karabük Training and Research Hospital. Participants who meet the inclusion and exclusion criteria will be randomly allocated into either a foot massage group or a control group using a simple randomization method. The foot massage group will receive a total of 10 sessions of foot massage over 5 weeks, with two sessions per week, while no massage intervention will be applied to the control group. All participants will be assessed at baseline, immediately after the intervention period, and two weeks following the completion of treatment. The findings of this study are expected to provide evidence regarding the effectiveness of foot massage in the management of symptoms in women with migraine.",[64,65,66,67,68,25],"Migraine","Reflexology","Pain","Anxiety","Kinesiophobia","NOT_YET_RECRUITING","2026-06-11",{"date":72,"type":38},"2026-06-16",{"date":74,"type":20},"2026-06-18",{"date":76,"type":20},"2026-07-30",{"name":78,"class":45},"Karabuk University",{"id":80,"slug":81,"hasResults":11,"nctId":82,"briefTitle":83,"officialTitle":84,"acronym":4,"eligibilityCriteria":85,"healthyVolunteers":54,"sex":55,"minAge":16,"maxAge":17,"enrollmentInfo":86,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":88,"conditions":89,"keywords":94,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":99,"lastUpdatePostDateStruct":100,"startDateStruct":102,"completionDateStruct":104,"leadSponsor":105,"locationsCount":46},"100631416","postural-habits-body-awareness-and-functional-performance-across-bmi-categories-in-women-100631416","NCT07500389","Postural Habits, Body Awareness, and Functional Performance Across BMI Categories in Women","Investigation of Postural Habits and Body Awareness in Relation to Functional Performance Across Body Mass Index Categories in Women","Inclusion Criteria:\n\n* Female individuals aged 18-65 years\n* Classified into BMI categories (normal weight, overweight, obesity class I, obesity class II-III)\n* No obesity-related medical or surgical treatment in the last 6 months\n* Able to understand instructions and complete questionnaires\n\nExclusion Criteria:\n\n* Neurological disorders affecting mobility (e.g., stroke, Parkinson's disease, multiple sclerosis, peripheral neuropathy)\n* Rheumatologic or inflammatory diseases (e.g., rheumatoid arthritis, ankylosing spondylitis)\n* Severe orthopedic conditions limiting mobility (e.g., advanced osteoarthritis)\n* Major surgery within the last 12 months affecting mobility or physical performance\n* Pregnancy\n* Acute musculoskeletal injury within the last 4 weeks",{"count":87,"type":20},80,"This cross-sectional study aims to investigate the relationship between postural habits and body awareness with functional performance across different body mass index (BMI) categories in women. Participants will be categorized into four groups based on BMI (normal weight, overweight, obesity class I, and obesity class II-III). Postural habits and awareness, body awareness, and functional performance will be assessed using validated questionnaires and performance-based tests. The study also aims to explore the potential contribution of central adiposity (waist circumference) and psychological factors to these relationships. Findings are expected to provide a more comprehensive understanding of the biomechanical and perceptual factors associated with obesity.",[90,91,25,92,93],"Obesity & Overweight","Body Mass Index","Body Awareness","Functional Performance",[95,96,97,98],"Postural habits","body awareness","Functional mobility","Physical activity","2026-04-01",{"date":101,"type":38},"2026-04-07",{"date":103,"type":20},"2026-04-30",{"date":42,"type":20},{"name":106,"class":45},"Ondokuz Mayıs University",{"id":108,"slug":109,"hasResults":11,"nctId":110,"briefTitle":111,"officialTitle":112,"acronym":4,"eligibilityCriteria":113,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":114,"enrollmentInfo":115,"targetDuration":4,"studyType":59,"phases":117,"briefSummary":118,"conditions":119,"keywords":124,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":130,"lastUpdatePostDateStruct":131,"startDateStruct":133,"completionDateStruct":135,"leadSponsor":137,"locationsCount":46},"100628855","effectiveness-of-pilates-on-postural-correction-core-strength-and-flexibility-in-younger-individuals-with-non-specific-low-backache-100628855","NCT07467070","Effectiveness of Pilates on Postural Correction, Core Strength and Flexibility in Younger Individuals With Non-specific Low Backache","Effects of Pilates on Postural Correction, Core Strength and Flexibility in Young Individuals With Non-Specific Low Backache","Inclusion Criteria:\n\n* Age 18-25\n* Non-specific low backache of pain severity less than and equal to 5\u002F10 on Brief Pain Inventory Scale\n* Ability to attend complete six-week program\n* Both genders\n\nExclusion Criteria:\n\n* prior history of trauma, fracture, spinal stenosis, severe comorbidities, spinal surgery and neurological disorders\n* Individuals suffering from specific causes of low backache like Infection and pregnancy","25 Years",{"count":116,"type":20},50,[61],"The aim of this clinical trial is to study the effects of Pilates intervention versus conventional therapy on postural correction, core strength and flexibility in young individuals with complaint of non-specific low backache. The main question is whether the Pilates has better improvement as compared to the conventional therapy on postural correction, core strength and flexibility moreover to compare the effectiveness of two intervention. Participants of age 18-25 years and with complaint of non-specific low backache will be recruited. 50 participants will be enrolled. Participants will perform Pilates and conventional therapy for 3 times per week for six weeks. Participants will be randomly allocated to two groups and assessor blinding will be done to take baseline assessment. Assessor blinding is done to minimize biasness. Pre and Post assessments will be taken by the assessor. SPSS will be used for the analysis of the data.",[27,25,120,121,122,123],"Core Strength","Flexibility","Pilates","Non-specific Low Back Pain",[122,125,126,127,128,129,31],"core strength","flexibility","postural correction","young individuals","Non-specific low backache","2026-03-07",{"date":132,"type":38},"2026-03-12",{"date":134,"type":38},"2026-03-03",{"date":136,"type":20},"2026-04-20",{"name":138,"class":45},"University of Health Sciences Lahore",{"id":140,"slug":141,"hasResults":11,"nctId":142,"briefTitle":143,"officialTitle":144,"acronym":4,"eligibilityCriteria":145,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":146,"enrollmentInfo":147,"targetDuration":4,"studyType":59,"phases":149,"briefSummary":150,"conditions":151,"keywords":155,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":161,"lastUpdatePostDateStruct":162,"startDateStruct":164,"completionDateStruct":166,"leadSponsor":168,"locationsCount":46},"100617770","effects-of-exercise-with-visual-feedback-in-parkinsons-disease-100617770","NCT07322939","Effects of Exercise With Visual Feedback in Parkinson's Disease","Effects of Visual Indicator Exercises for the Trunk and Lower Extremities on Activity and Participation in Parkinson's Disease","Inclusion Criteria\n\n* Individuals diagnosed with idiopathic Parkinson's disease\n* Disease severity classified as stage 1 to 3 according to the Modified Hoehn and Yahr Scale\n* Patients receiving oral antiparkinsonian treatment only\n\nExclusion Critera\n\n* Presence of musculoskeletal, cardiovascular, or vestibular disorders that may interfere with the completion of the assessments or treatment protocol\n* Presence of additional neurological or psychiatric disorders other than Parkinson's disease\n* Presence of visual impairment insufficient to perceive visual feedback","85 Years",{"count":148,"type":20},32,[61],"Patients with Parkinson's disease who apply to the Hasan Kalyoncu University Application and Research Center and meet the inclusion criteria will be included in the study. The included participants will be randomly assigned into either the intervention group or the control group using a sealed-envelope method. Both groups will undergo a standard exercise program, consisting of posture, strengthening, and balance training, under the supervision of a physiotherapist for 8 weeks, 3 days per week. In addition to this, the intervention group will receive an additional exercise program incorporating visual feedback using a laser pointer, targeting the trunk and lower extremities, also under the supervision of a physiotherapist for 8 weeks, 3 days per week.",[152,153,154,25],"Parkinson Disease","Balance Impairment","Exercise Training",[156,157,158,159,160],"parkinson disease","balance","postural control","visual feedback","exercise","2026-01-24",{"date":163,"type":38},"2026-01-27",{"date":165,"type":38},"2025-12-01",{"date":167,"type":20},"2026-05-05",{"name":169,"class":45},"Hasan Kalyoncu University",{"id":171,"slug":172,"hasResults":11,"nctId":173,"briefTitle":174,"officialTitle":175,"acronym":4,"eligibilityCriteria":176,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":177,"targetDuration":4,"studyType":59,"phases":179,"briefSummary":180,"conditions":181,"keywords":4,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":184,"lastUpdatePostDateStruct":185,"startDateStruct":187,"completionDateStruct":189,"leadSponsor":191,"locationsCount":4},"100618672","postural-kinesio-taping-in-stroke-rehabilitation-100618672","NCT07334665","Postural Kinesio Taping in Stroke Rehabilitation","Effects of Posture-Oriented Kinesio Taping on Mobility, Balance, Coordination, and Activities of Daily Living in Patients With Stroke: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Adults aged 18 years or older\n* Diagnosis of ischemic or hemorrhagic stroke confirmed clinically and\u002For radiologically\n* In the subacute or chronic phase of stroke (≥1 month post-stroke) and clinically stable\n* Presence of postural control and\u002For trunk control impairment\n* Ability to participate in a standard neurological rehabilitation program\n* No severe cognitive impairment or communication disorder that would interfere with outcome assessments\n* Intact skin at the kinesio taping application sites\n* Willingness to participate and provision of written informed consent\n\nExclusion Criteria:\n\n* Acute stroke phase or clinical instability\n* Severe cognitive impairment, aphasia, or insufficient cooperation that would interfere with reliable outcome assessments\n* Known allergy or hypersensitivity to kinesio tape\n* Active dermatological conditions at taping sites (e.g., open wounds, dermatitis, infection)\n* Severe spasticity (Modified Ashworth Scale ≥3)\n* Presence of other neurological disorders affecting balance or mobility (e.g., Parkinson's disease, multiple sclerosis)\n* Severe orthopedic conditions or cardiopulmonary diseases limiting participation in rehabilitation\n* Receipt of posture-oriented kinesio taping within the previous 3 months\n* Concurrent participation in another interventional clinical study that could influence study outcomes",{"count":178,"type":20},60,[61],"Stroke often leads to postural asymmetry and impaired trunk control, which negatively affect mobility, balance, coordination, and activities of daily living. These impairments increase the risk of falls and reduce functional independence during the rehabilitation process.\n\nThe purpose of this randomized controlled trial is to investigate the effects of posture-oriented kinesio taping, applied in addition to standard neurological rehabilitation, on functional outcomes in patients with stroke. Participants will be randomly assigned to either an intervention group receiving kinesio taping plus standard rehabilitation or a control group receiving standard rehabilitation alone.\n\nFunctional outcomes including trunk control, postural stability, balance, mobility, and activities of daily living will be assessed using validated clinical scales at baseline and after the intervention period. The findings of this study are expected to provide evidence regarding the clinical effectiveness of posture-oriented kinesio taping as a non-invasive and easily applicable adjunct treatment in stroke rehabilitation.",[182,183,25],"Stroke","Hemiplegia","2026-01-10",{"date":186,"type":38},"2026-01-13",{"date":188,"type":20},"2026-01-30",{"date":190,"type":20},"2027-01-30",{"name":192,"class":193},"Bursa City Hospital","OTHER_GOV",{"id":195,"slug":196,"hasResults":11,"nctId":197,"briefTitle":198,"officialTitle":199,"acronym":4,"eligibilityCriteria":200,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":201,"enrollmentInfo":202,"targetDuration":4,"studyType":59,"phases":204,"briefSummary":205,"conditions":206,"keywords":4,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":211,"lastUpdatePostDateStruct":212,"startDateStruct":214,"completionDateStruct":216,"leadSponsor":218,"locationsCount":46},"100614721","effect-of-functional-core-stability-training-or-cognitive-training-on-balance-and-postural-control-in-chronic-ankle-instability-100614721","NCT07283276","Effect of Functional Core Stability Training or Cognitive Training on Balance and Postural Control in Chronic Ankle Instability","Effect of Adding Functional Core Stability Training or Cognitive Training on Balance and Postural Control in Rehabilitation of Chronic Ankle Instability","Inclusion Criteria:\n\nInclusion criteria will be based on the standard criteria outlined by the International Ankle Consortium\n\n1. History of chronic lateral ankle sprain and\u002For recurrent sprain and\u002For \"feelings of instability or giving way\" for 6 months or more before the study, with at least 2 episodes.\n2. Patients are between 18 and 30 years old. 3- Body mass index less than 30\n\n4\\. The patient has a history of at least one significant ankle sprain with associated inflammatory symptoms and at least one day of interrupted physical activity.\n\n5\\. Patients who have unilateral chronic ankle instability. 6. Self-reported ankle instability should be confirmed using a validated ankle instability questionnaire (greater than 24).\n\nExclusion Criteria:\n\nThose with a history of spine, pelvis, and lower extremity injury, fracture, or surgery 2- Those with low back pain that require medical or surgical intervention. 3- Having a history of an acute lower extremity injury or lower extremity surgery or fracture in the 3 months before the Study 4. Participation in formal ankle rehabilitation in the 3 months before the study.\n\n5\\. Being diagnosed with neurologic dysfunction, such as multiple sclerosis, Parkinson's disease, or head injury","30 Years",{"count":203,"type":20},45,[61],"The purpose of the study is to investigate dynamic core stability training versus cognitive training on balance, functional performance, postural control, ankle instability scores, ankle dorsiflexion range of motion, and mental workload in chronic ankle instability",[207,208,209,25,210],"Cognitive Training","Functional Core Stability Training","Balance; Distorted","Chronic Ankle Instability","2025-12-02",{"date":213,"type":38},"2025-12-15",{"date":215,"type":38},"2025-08-15",{"date":217,"type":20},"2026-03-01",{"name":219,"class":45},"Cairo University",{"id":221,"slug":222,"hasResults":11,"nctId":223,"briefTitle":224,"officialTitle":224,"acronym":4,"eligibilityCriteria":225,"healthyVolunteers":54,"sex":15,"minAge":16,"maxAge":226,"enrollmentInfo":227,"targetDuration":4,"studyType":59,"phases":228,"briefSummary":229,"conditions":230,"keywords":235,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":253,"lastUpdatePostDateStruct":254,"startDateStruct":256,"completionDateStruct":258,"leadSponsor":259,"locationsCount":46},"100599509","sensor-ankle-brace-for-special-operations-rehabilitation-100599509","NCT07085416","Sensor Ankle Brace for Special Operations Rehabilitation","Inclusion Criteria for both cohorts:\n\n* Healthy adults: ages 18 - 40 years\n* considered \"healthy to exercise\" as determined by the physical activity readiness questionnaire (PAR-Q)\n\nAdditional Inclusion Criteria specific to cohort 2 only:\n\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 for both cohorts:\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\nAdditional Exclusion Criteria specific to cohort 2 only:\n\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.","40 Years",{"count":178,"type":20},[61],"The primary purpose of this study is to conduct a clinical trial to test a prototype device for feasibility and not health outcomes. To do this, the investigators will evaluate the performance of commercially available inertial measurement unit sensors incorporated into an existing ankle brace (\"sXAB\") by TayCo Brace, Inc. We will compare the gait metrics calculated from the sensors incorporated into the brace with 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. The sensors in the ankle brace will be validated in the lab, first on healthy subjects walking in standard tennis shoes\u002Fsneakers (protocol 1), and secondarily in the lab on healthy subjects wearing combat boots performing walking, running, jumping, and stair climbing (protocol 2). These movements were selected because they simulate key movements performed during operational activities. Protocol 1 will take place first, then aspects of the sXAB will be evaluated and implemented, then protocol 2 will take place. Participants completing protocol 1 are eligible to complete protocol 2. The study includes two cohorts of participants completing different functional tasks. 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).",[231,232,233,25,234],"Gait","Balance","Biomechanical Data","Locomotion",[236,237,238,239,240,241,242,243,244,245,246,247,248,249,250,251,252],"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","2025-10-21",{"date":255,"type":38},"2025-10-23",{"date":257,"type":38},"2025-10-16",{"date":74,"type":20},{"name":260,"class":45},"Indiana University",{"id":262,"slug":263,"hasResults":11,"nctId":264,"briefTitle":265,"officialTitle":266,"acronym":4,"eligibilityCriteria":267,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":268,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":270,"conditions":271,"keywords":274,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":279,"lastUpdatePostDateStruct":280,"startDateStruct":282,"completionDateStruct":284,"leadSponsor":286,"locationsCount":46},"100597961","plantar-sensation-position-sense-and-weight-bearing-asymmetry-related-to-balance-and-mobility-post-stroke-100597961","NCT07065292","Plantar Sensation, Position Sense, and Weight-Bearing Asymmetry Related to Balance and Mobility Post-Stroke","Investigation of the Relationship Between Plantar Sensation, Lower Extremity Position Sense, and Weight-Bearing Asymmetry With Posture, Balance, and Mobility in Individuals With Chronic Stroke","Inclusion Criteria:\n\n* Diagnosis of stroke confirmed by a physician (via official report)\n* Minimum of 6 months since stroke onset\n* Aged 18 years or older\n* Mini-Mental State Examination score ≥ 20\n* Brunnstrom lower extremity stage ≥ 3\n* Ability to complete assessments with or without walking aids\n* Voluntary participation\n\nExclusion Criteria:\n\n* Additional neurological, metabolic, or orthopedic conditions\n* Severe vision or hearing impairments\n* Modified Ashworth Score of 4 in any lower limb muscle",{"count":269,"type":20},22,"This study aims to examine how sensory deficits and weight-bearing asymmetry affect posture, balance, and mobility in individuals with chronic stroke. The research focuses on evaluating the relationships between plantar foot sensation, lower extremity position sense, and asymmetrical weight distribution with functional abilities such as walking and postural control.\n\nParticipants will undergo non-invasive assessments, including sensation tests, mobility and balance evaluations, and postural measurements. A total of 24 individuals with chronic stroke who are receiving physiotherapy at a rehabilitation center in Konya, Türkiye, will be included.\n\nThe results of this observational, cross-sectional study may contribute to a better understanding of the sensory-motor interactions in stroke survivors and support the development of more targeted rehabilitation strategies.",[272,273,25,232],"Chronic Stroke","Sensory Impairments",[272,275,276,277,278],"Somatosensory Function","Plantar Sensation","Balance Assessment","Weight-Bearing Asymmetry","2025-07-03",{"date":281,"type":38},"2025-07-15",{"date":283,"type":38},"2025-05-20",{"date":285,"type":20},"2026-01-20",{"name":287,"class":45},"Afyonkarahisar Health Sciences University",{"id":289,"slug":290,"hasResults":11,"nctId":291,"briefTitle":292,"officialTitle":293,"acronym":4,"eligibilityCriteria":294,"healthyVolunteers":11,"sex":15,"minAge":295,"maxAge":296,"enrollmentInfo":297,"targetDuration":4,"studyType":59,"phases":299,"briefSummary":300,"conditions":301,"keywords":312,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":325,"lastUpdatePostDateStruct":326,"startDateStruct":328,"completionDateStruct":330,"leadSponsor":332,"locationsCount":46},"100520408","the-effect-of-motor-image-training-on-balance-performance-in-geriatric-individuals-100520408","NCT06056180","The Effect of Motor Image Training on Balance Performance in Geriatric Individuals","Investigation of the Effects of Motor Imagery Training Given With Action Observation on Balance Performance in Geriatric Individuals","Inclusion Criteria:\n\n1. To be between 60-80 years old\n2. Having the ability to speak, read, understand and write Turkish\n3. To have the cognitive skills to understand and apply the trainings to be applied in the study (with ≥ 24 points from the Mini Mental State Test)\n4. Being able to do activities of daily living independently\n5. Being able to walk independently (without using a walking aid and at least 10 meters)\n6. Having a body mass index of \\\u003C35 kg\u002Fm2 (not being severely obese or morbidly obese)\n\nExclusion Criteria:\n\n1. Having visual, hearing and sensory impairment\n2. To have had a trauma, lesion or surgery that may affect balance and musculoskeletal system in the last 6 months\n3. Having a history of 2 ≥ falls in the last 6 months\n4. Having any chronic lower extremity pain\n5. Having an acute or chronic illness that may cause problems with balance and falling\n6. Being diagnosed with sensory, vestibular and cerebellar ataxia\n7. Being on any medication that may cause problems with balance, focus, attention and falling.\n8. Exercising regularly, which may affect performance results\n9. To stop participating in the study for any reason","60 Years","80 Years",{"count":298,"type":20},46,[61],"The goal of this study \\[type of study: clinical trial\\] is to was planned to investigate the effect of motor imagery training given to geriatric individuals with action observation on their balance performance and to compare these two methods.\n\nThe main questions it aims to answer are:\n\n1. Is virtual reality-based balance training given together with action observation and motor imagery for six weeks in geriatric individuals more effective in improving static balance than virtual reality-based balance training given alone?\n2. Is virtual reality-based balance training given together with action observation and motor imagery for six weeks in geriatric individuals more effective in improving dynamic balance than virtual reality-based balance training given alone?\n3. Is virtual reality-based balance training given together with motor imagery for six weeks in geriatric individuals more effective in increasing balance confidence than virtual reality-based balance training given alone?\n\n46 geriatric individuals will be randomized into 2 groups. Along with action observation, motor imagery training and virtual reality-based balance training will be given to the study group. On the other hand, only virtual reality-based balance training will be given to the control group. All assessments will be repeated before and after the trainings. The trainings will be applied 2 days a week for 6 weeks. Each training session; 25 minutes for the control group and 45 minutes for the study group.",[302,25,303,304,305,306,307,308,309,310,311],"Imagery (Psychotherapy)","Postural Balance","Virtual Reality Therapy","Surface Electromyography","Geriatric Assessment","Physical Therapy Techniques","Physical Therapy","Healthy Ageing","Healthy Aging","Falling",[313,314,158,315,316,317,318,319,320,321,322,323,324],"visual motor imagery","kinesthetic motor imagery","virtual reality therapy","interactive video games","balance platform with pressure sensor","surface electromyography","balance confidence","fall risk","mobility","cognitive processing speed","smartphone gyroscope sensor dataset","action observation","2025-05-05",{"date":327,"type":38},"2025-05-08",{"date":329,"type":38},"2023-11-01",{"date":331,"type":20},"2025-12",{"name":333,"class":45},"Muğla Sıtkı Koçman University",{"id":335,"slug":336,"hasResults":11,"nctId":337,"briefTitle":338,"officialTitle":339,"acronym":4,"eligibilityCriteria":340,"healthyVolunteers":54,"sex":15,"minAge":16,"maxAge":201,"enrollmentInfo":341,"targetDuration":4,"studyType":59,"phases":343,"briefSummary":344,"conditions":345,"keywords":4,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":349,"lastUpdatePostDateStruct":350,"startDateStruct":352,"completionDateStruct":354,"leadSponsor":356,"locationsCount":46},"100553832","the-relationship-between-pes-planus-diaphragm-postural-control-and-plantar-pressure-100553832","NCT06491212","The Relationship Between Pes Planus, Diaphragm, Postural Control, and Plantar Pressure","Examination of Diaphragm Function, Postural Control, and Plantar Pressure in Individuals With Pes Planus","Inclusion Criteria:\n\nInclusion criteria for individuals with Pes Planus Deformity\n\n* Willing to participate in the study voluntarily\n* Having a Navicular drop test value of 10mm or above\n* Being between the ages of 18-30\n* Having the physical capacity to perform assessments and tests\n* Having a body mass index of 18-25 kg\u002Fm²\n\nExclusion Criteria:\n\n* Exclusion criteria for individuals with Pes Planus Deformity:\n* Termination of voluntariness\n* Those with rigid flatfoot, pes cavus, hallux valgus, hallux rigidus, or calcaneal spur deformity\n* Those with chronic systematic and metabolic diseases (e.g., diabetes mellitus, rheumatoid arthritis, etc.) and musculoskeletal problems (e.g., pes planus) that may affect foot functions and gait\n* Those with any surgical history likely to affect balance, lower extremity strength, and postural control\n* Those with any visual\u002Fvestibular, musculoskeletal, or neurological problems\"\n\nInclusion criteria for healthy participants:\n\n* Willing to participate in the study voluntarily\n* Being between the ages of 18-30\n* Having the physical capacity to perform assessments and tests\n* Having a body mass index of 18-25 kg\u002Fm²\n* Having the ideal height of the medial longitudinal arch of the foot (not having pes planus)\n\nExclusion criteria for healthy participants:\n\n* Termination of voluntariness\n* Those with chronic systematic and metabolic diseases (e.g., diabetes mellitus, rheumatoid arthritis, etc.) and musculoskeletal problems (e.g., pes planus) that may affect foot functions and gait\n* Those with any surgical history likely to affect balance, lower extremity strength, and postural control\n* Those with any visual\u002Fvestibular, musculoskeletal, or neurological problems\"",{"count":342,"type":20},34,[61],"Our primary aim is to compare diaphragm function (resting thickness, activity\u002Fresting thickness ratio indicating contractility), postural control, and plantar pressure between individuals with pes planus and healthy controls without pes planus.",[346,347,348,25],"Pes Planus","Diaphragm Issues","Plantar Pressure","2024-06-30",{"date":351,"type":38},"2024-07-09",{"date":353,"type":38},"2024-05-01",{"date":355,"type":20},"2024-10-15",{"name":357,"class":45},"Alanya Alaaddin Keykubat University"]