[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Izmir Bakircay University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":353},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,13,0,[8,48,77,99,126,150,180,203,231,257,279,304,332],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":29,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100644655","vr-simulation-based-implanted-port-catheter-training-in-nursing-students-100644655",false,"NCT07674108","VR Simulation-Based Implanted Port Catheter Training in Nursing Students","Effectiveness of Virtual Reality Simulation-Based Implanted Port Catheter Training on Knowledge, Learning Satisfaction and Motivation in Nursing Students: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Being 18 years of age or older\n* Being an undergraduate nursing student\n* Having completed the Internal Medicine Nursing course\n* Voluntarily agreeing to participate in the study\n* Providing written informed consent\n\nExclusion Criteria:\n\n* Having any communication barrier that may prevent participation in the study or completion of the study forms\n* Having neck pain or neck injury severe enough to prevent head movement\n* Having a visual problem that prevents safe use of the virtual reality application\n* Experiencing severe nausea or dizziness during the virtual reality application\n* Having a diagnosed history of epilepsy",true,"ALL","18 Years",{"count":20,"type":21},80,"ESTIMATED","INTERVENTIONAL",[24],"NA","Implanted port catheter care is a critical clinical skill in oncology nursing, requiring accurate knowledge, aseptic technique, safe procedural practice, and early recognition of potential complications. This parallel group randomized controlled study aims to evaluate the effectiveness of virtual reality simulation-based implanted port catheter training in undergraduate nursing students. Eligible second-year nursing students will be randomly assigned to either an intervention group or a control group. All students will receive a two-hour traditional implanted port catheter training session in the classroom setting. In addition to traditional training, students in the intervention group will receive virtual reality simulation-based training consisting of two scenarios: safe implanted port catheter access and extravasation\u002Fcomplication management. The control group will receive only traditional training.",[27,28],"Nursing Education","Clinical Competence",[30,31,32,33,34],"Virtual reality","Simulation-based education","Implanted port catheter","Clinical skills","Nursing students","NOT_YET_RECRUITING","2026-06-25",{"date":38,"type":39},"2026-06-29","ACTUAL",{"date":41,"type":21},"2026-09-21",{"date":43,"type":21},"2027-06-28",{"name":45,"class":46},"Izmir Bakircay University","OTHER",1,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":4,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":55,"minAge":18,"maxAge":4,"enrollmentInfo":56,"targetDuration":4,"studyType":22,"phases":58,"briefSummary":59,"conditions":60,"keywords":62,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":70,"startDateStruct":72,"completionDateStruct":74,"leadSponsor":76,"locationsCount":47},"100644512","nurse-led-self-management-program-on-taste-alteration-in-women-with-breast-cancer-100644512","NCT07670221","Nurse-Led Self-Management Program on Taste Alteration in Women With Breast Cancer","The Effect of a Nurse-Led Self-Management Program on Taste Alteration, Nutritional Status, and Quality of Life in Women With Breast Cancer Receiving Taxane-Based Chemotherapy: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Aged 18 years or older\n* Literate\n* Diagnosed with breast cancer\n* Receiving taxane-based chemotherapy\n* Having a score of 1 or 2 for taste alteration according to the Common Terminology Criteria for Adverse Events version 4.0 (CTCAE v4.0) after the first cycle of chemotherapy\n* Willing to participate in the study and providing written informed consent\n\nExclusion Criteria:\n\n* Having any communication barrier that prevents participation in the study\n* Having a diagnosed psychiatric disorder\n* Receiving radiotherapy\n* Having metastasis\n* Having a diagnosed physical disease that may affect food intake, such as ulcerative colitis or Crohn's disease\n* Receiving enteral or parenteral nutrition support","FEMALE",{"count":57,"type":21},68,[24],"Taste alteration is a common and distressing symptom experienced by women with breast cancer receiving taxane-based chemotherapy. This symptom may negatively affect food intake, nutritional status, psychological well-being, and quality of life. Although several approaches have been suggested for the management of chemotherapy-related taste alteration, evidence regarding structured nurse-led self-management interventions in this patient group remains limited.",[61],"Chemotherapy-Related Taste Alteration",[63,64,65,66,67,68],"Breast cancer","Taste alteration","Self-management","Nurse-led intervention","Nutritional status","Quality of life","RECRUITING",{"date":71,"type":39},"2026-06-26",{"date":73,"type":39},"2026-02-16",{"date":75,"type":21},"2026-08-24",{"name":45,"class":46},{"id":78,"slug":79,"hasResults":11,"nctId":80,"briefTitle":81,"officialTitle":82,"acronym":4,"eligibilityCriteria":83,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":84,"enrollmentInfo":85,"targetDuration":4,"studyType":22,"phases":87,"briefSummary":88,"conditions":89,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":91,"lastUpdatePostDateStruct":92,"startDateStruct":94,"completionDateStruct":96,"leadSponsor":98,"locationsCount":47},"100641749","effectiveness-of-matrix-rhythm-therapy-on-carpal-tunnel-syndrome-100641749","NCT07660913","Effectiveness of Matrix Rhythm Therapy on Carpal Tunnel Syndrome","Effectiveness of Matrix Rhythm Therapy on Symptom Severity and Function in Carpal Tunnel Syndrome: A Randomized, Placebo-Controlled, Assessor-Blinded Trial","Inclusion Criteria:\n\n* Having a diagnosis of unilateral carpal tunnel syndrome confirmed by an orthopedist based on clinical examination and electromyography (EMG) testing.\n* Being classified with mild-to-moderate carpal tunnel syndrome severity.\n* Having symptoms persisting for at least 12 weeks.\n* Having a Mini-Mental State Examination (MMSE) score greater than 24.\n* Being literate (able to read and write).\n\nExclusion Criteria:\n\n* History of prior carpal tunnel release surgery.\n* History of corticosteroid injection into the affected hand\u002Fwrist.\n* Having received physiotherapy for carpal tunnel syndrome within the last 6 months.\n* Presence of any neurological signs or symptoms in the upper extremity other than carpal tunnel syndrome.\n* History of prior surgery in the hand or wrist region due to other conditions.\n* Diagnosis of any systemic neurological disease.\n* Diagnosis of rheumatic diseases (e.g., rheumatoid arthritis, systemic lupus erythematosus).\n* Having ongoing pain in the arm or hand due to any other underlying cause.","60 Years",{"count":86,"type":21},84,[24],"The purpose of this study is to investigate the effects of matrix rhythm therapy, applied in addition to conventional treatment, on symptom severity, function, grip and pinch strength, and quality of life in patients with carpal tunnel syndrome.",[90],"Carpal Tunnel Syndrome","2026-06-16",{"date":93,"type":39},"2026-06-22",{"date":95,"type":21},"2026-07-01",{"date":97,"type":21},"2027-09-01",{"name":45,"class":46},{"id":100,"slug":101,"hasResults":11,"nctId":102,"briefTitle":103,"officialTitle":104,"acronym":4,"eligibilityCriteria":105,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":106,"enrollmentInfo":107,"targetDuration":4,"studyType":22,"phases":109,"briefSummary":110,"conditions":111,"keywords":113,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":120,"lastUpdatePostDateStruct":121,"startDateStruct":122,"completionDateStruct":123,"leadSponsor":125,"locationsCount":47},"100642588","mental-fatigue-effects-on-posture-and-spinal-reflexes-100642588","NCT07650903","Mental Fatigue Effects on Posture and Spinal Reflexes","Effects of Mental Fatigue on Posture and Spinal Reflexes Modulations","Inclusion Criteria:\n\n* Healthy participants aged between 18 and 35 years\n* Recreational active\n\nExclusion Criteria:\n\n* Previous major lower limb injury (last 6 months)\n* Present neurological or musculoskeletal disorders\n* Involvement in another concurrent physical or cognitive intervention study","35 Years",{"count":108,"type":21},26,[24],"This randomized crossover study investigates the effects of mental fatigue on postural control and spinal reflex excitability in healthy physically active adults aged 18-35 years. Participants will complete two experimental conditions: a mentally fatiguing Stroop task and a control condition involving passive documentary watching, separated by at least 48 hours. Postural control will be assessed using force plate measures of center of pressure displacement during bipedal and unipedal stance, with and without concurrent cognitive dual-tasking. In parallel, spinal reflex excitability will be evaluated using H-reflex recordings from the triceps surae muscles across sitting and standing postures.\n\nThe primary aim is to determine whether mental fatigue increases postural sway, particularly in more challenging balance conditions such as single-leg stance. The secondary aim is to examine whether mental fatigue alters the normal modulation of spinal reflex excitability across progressively demanding postural tasks. Additional biomechanical and neuromuscular measures, including EMG activity and hip kinematics, will be recorded to provide insight into underlying control mechanisms.\n\nThe study will include approximately 26 participants, with each serving as their own control. Data will contribute to understanding how cognitive fatigue influences balance control and spinal-level neuromuscular regulation.",[112],"Mental Fatigue",[114,115,116,117,118,119],"Postural control","Center of pressure","Spinal reflex excitability","H-reflex","Stroop task","Electromyography","2026-06-15",{"date":91,"type":39},{"date":95,"type":21},{"date":124,"type":21},"2026-12-01",{"name":45,"class":46},{"id":127,"slug":128,"hasResults":11,"nctId":129,"briefTitle":130,"officialTitle":130,"acronym":4,"eligibilityCriteria":131,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":106,"enrollmentInfo":132,"targetDuration":4,"studyType":22,"phases":134,"briefSummary":135,"conditions":136,"keywords":137,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":145,"lastUpdatePostDateStruct":146,"startDateStruct":147,"completionDateStruct":148,"leadSponsor":149,"locationsCount":47},"100642911","the-effect-of-mental-fatigue-on-upper-extremity-functional-performance-100642911","NCT07645404","The Effect of Mental Fatigue on Upper Extremity Functional Performance","Inclusion Criteria:\n\n* Age between 18 and 35 years\n* Healthy (no neurological, cardiovascular or musculoskeletal disorders of any kind)\n* Male or female\n* No prior knowledge of the concept of mental fatigue\n* Not currently taking medications that affect cognition or neuromuscular performance\n* According to the International Physical Activity Questionnaire, being physically active at a minimum level of 1500 MET-min\u002Fweek\n\nExclusion Criteria:\n\n* Previous major upper limb injury (last 6 months)\n* Involvement in another concurrent physical or cognitive intervention study\n* Use of caffeine and heavy efforts 24 hours prior each trial\n* Suffering from colour vision deficiencies\n* Not eating a standardized meal, the morning of each trial and the evening before each trial",{"count":133,"type":21},16,[24],"Mental fatigue (MF) is known to impair cognitive performance and may negatively affect physical performance. While its effects on lower-extremity functional performance have been investigated, little is known about the influence of MF on upper-extremity physical performance tests commonly used in sports and rehabilitation settings. This randomized crossover study will investigate the effects of experimentally induced mental fatigue on upper-extremity physical performance in 16 healthy physically active adults. Participants will complete both a mental fatigue condition, involving a prolonged Stroop task, and a control condition consisting of watching an emotionally neutral documentary. Before and after each condition, participants will perform the Upper Quarter Y Balance Test, Reactive Upper Quarter Y Balance Test, Closed Kinetic Chain Upper Extremity Stability Test, and Seated Single-Arm Shot Put Test. Subjective mental fatigue, cognitive performance, motivation, and perceived exertion will also be assessed. The findings will improve understanding of whether mental fatigue influences upper-extremity physical performance test outcomes and may assist clinicians and researchers in interpreting these assessments in sports medicine and rehabilitation contexts.",[112],[112,138,139,140,141,142,143,144],"Upper Extremity","Physical Performance","Functional Testing","Sports Medicine","Cognitive Performance","Visuomotor Reaction Time","Upper Quarter Y Balance Test","2026-06-12",{"date":120,"type":39},{"date":95,"type":21},{"date":124,"type":21},{"name":45,"class":46},{"id":151,"slug":152,"hasResults":11,"nctId":153,"briefTitle":154,"officialTitle":155,"acronym":4,"eligibilityCriteria":156,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":157,"enrollmentInfo":158,"targetDuration":4,"studyType":160,"phases":4,"briefSummary":161,"conditions":162,"keywords":166,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":172,"lastUpdatePostDateStruct":173,"startDateStruct":175,"completionDateStruct":177,"leadSponsor":179,"locationsCount":47},"100624781","multidimensional-frailty-assessment-and-post-transplant-outcomes-in-liver-transplant-candidates-100624781","NCT07414095","Multidimensional Frailty Assessment and Post-Transplant Outcomes in Liver Transplant Candidates","Investigation of the Relationship Between Frailty, Sarcopenia, Malnutrition, and Psychosocial Parameters and Post-Transplant Outcomes in Liver Transplant Candidates","Inclusion Criteria:\n\n* Being listed as a liver transplant candidate\n* Age between 18 and 65 years\n* Ability to understand the Turkish language\n\nExclusion Criteria:\n\n* Presence of orthopedic and\u002For neurological problems severe enough to prevent completion of assessment tools\n* Inability to understand verbal commands\n* Being a recipient of multiple organ transplants\n* Presence of serious active extrahepatic malignancy","65 Years",{"count":159,"type":21},60,"OBSERVATIONAL","This study will evaluate frailty, nutrition, sarcopenia, and psychological health in people waiting for a liver transplant. The purpose is to understand how these factors affect outcomes before and after transplantation. By identifying patients at higher risk early, the study aims to support the development of better care programs in the future.\n\nParticipants will complete simple tests of physical strength, walking speed, and daily activity levels. Their nutrition and psychological well-being will also be assessed. The study will then look at how these results relate to medical scores used in liver disease and to outcomes after transplant, such as hospital stay, complications, or survival.\n\nAdults aged 18-65 years who are on the liver transplant waiting list and can understand Turkish are eligible to join.",[163,164,165],"End-Stage Liver Disease","Liver Transplantation","Cirrhosis",[167,168,169,170,171],"Liver Transplant Candidates","Frailty","Sarcopenia","Malnutrition","Psychosocial Health","2026-02-12",{"date":174,"type":39},"2026-02-17",{"date":176,"type":39},"2025-12-15",{"date":178,"type":21},"2026-08",{"name":45,"class":46},{"id":181,"slug":182,"hasResults":11,"nctId":183,"briefTitle":184,"officialTitle":185,"acronym":4,"eligibilityCriteria":186,"healthyVolunteers":11,"sex":17,"minAge":187,"maxAge":18,"enrollmentInfo":188,"targetDuration":4,"studyType":160,"phases":4,"briefSummary":190,"conditions":191,"keywords":193,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":172,"lastUpdatePostDateStruct":197,"startDateStruct":198,"completionDateStruct":200,"leadSponsor":202,"locationsCount":47},"100595248","baylor-continence-scale-validity-in-anorectal-malformation-100595248","NCT07029984","Baylor Continence Scale Validity in Anorectal Malformation","Baylor Continence Scale in Children With Anorectal Malformations: A Turkish Validity and Reliability Study","Inclusion Criteria:\n\n* Having undergone surgery due to anorectal malformation\n* Being between 6 and 18 years old\n* The child and caregiver are required to know Turkish\n\nExclusion Criteria:\n\n* The child and caregiver having comprehension, hearing, or vision problems","6 Years",{"count":189,"type":21},230,"The aim of this study is to evaluate the validity and reliability of the Baylor Continence Scale in Turkish-speaking children diagnosed with anorectal malformations. The scale is used to assess continence levels, helping healthcare providers make informed decisions regarding treatment and follow-up. The study includes a sample of children with confirmed anorectal malformations, and data collection consists of language adaptation, statistical validation, and reliability testing. Results will contribute to the standardization of continence assessment in Turkish clinical settings, ensuring accurate evaluations for pediatric patients.",[192],"Anorectal Malformations",[194,195,196],"Anorectal Malformation","Baylor Continence Scale","Validity and Reliability",{"date":174,"type":39},{"date":199,"type":39},"2025-05-10",{"date":201,"type":21},"2026-06",{"name":45,"class":46},{"id":204,"slug":205,"hasResults":11,"nctId":206,"briefTitle":207,"officialTitle":208,"acronym":4,"eligibilityCriteria":209,"healthyVolunteers":16,"sex":210,"minAge":211,"maxAge":4,"enrollmentInfo":212,"targetDuration":4,"studyType":160,"phases":4,"briefSummary":214,"conditions":215,"keywords":219,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":223,"lastUpdatePostDateStruct":224,"startDateStruct":226,"completionDateStruct":228,"leadSponsor":230,"locationsCount":47},"100595064","the-relationship-between-training-dynamics-and-general-health-status-in-veteran-football-players-100595064","NCT07027592","The Relationship Between Training Dynamics and General Health Status in Veteran Football Players","The Relationship Between Training Dynamics and General Health Status With Injury Risk in Veteran Football Players","Inclusion Criteria:\n\n* Playing football as a veteran\n\nExclusion Criteria:\n\n* Not participating in a regular training program","MALE","40 Years",{"count":213,"type":21},130,"The goal of this observational study is to learn how training habits and general health status are related to injury risk in veteran football players (men over 35 years old who play recreational football). The main questions it aims to answer are:\n\nDo specific training patterns (such as frequency, intensity, and duration) increase or lower the risk of injury?\n\nHow does general health status (including factors like sleep, nutrition, and existing health conditions) affect injury risk?\n\nParticipants will:\n\nComplete questionnaires about their training habits, lifestyle, and general health\n\nReport any injuries they experience during the football season\n\nAttend periodic health assessments",[216,217,218],"Football","Injury","Veteran",[220,221,222],"FIFA 11+","Veteran Football Players","Injury risk","2026-01-28",{"date":225,"type":39},"2026-01-30",{"date":227,"type":39},"2025-06-01",{"date":229,"type":21},"2026-05",{"name":45,"class":46},{"id":232,"slug":233,"hasResults":11,"nctId":234,"briefTitle":235,"officialTitle":236,"acronym":4,"eligibilityCriteria":237,"healthyVolunteers":11,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":238,"targetDuration":4,"studyType":160,"phases":4,"briefSummary":239,"conditions":240,"keywords":244,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":248,"lastUpdatePostDateStruct":249,"startDateStruct":251,"completionDateStruct":253,"leadSponsor":255,"locationsCount":256},"100594728","reliability-and-validity-study-of-the-turkish-version-of-the-parkinsons-disease-dyskinesia-scale-pdys-26-100594728","NCT07023224","Reliability and Validity Study of the Turkish Version of the Parkinson's Disease Dyskinesia Scale (PDYS-26)","Adaptation Of The Parkinson's Disease Dyskinesia Questionnaire Into Turkish And Its Validity And Reliability In Parkinson's Patient","Inclusion Criteria:\n\n* Being diagnosed with idiopathic Parkinson's disease\n* H\\&Y stage 1-3\n* UPDRS dyskinesia item score ≥1\n* Accepting to participate in the study\n\nExclusion Criteria:\n\n* Diagnosis of atypical-secondary parkinsonism\n* Severe musculoskeletal, neurological and\u002For cardiopulmonary problems that may affect the results of the assessment\n* Mini Mental State Examination score \\\u003C 24",{"count":213,"type":21},"The aim of this methodological study was to investigate the Turkish validity and reliability of the Parkinson's Disease Dyskinesia Scale (PDYS-26).The scale evaluates choreic dyskinesia.Measures the impact of dyskinesia on activities of daily living in patients with Parkinson's disease.\n\nHypotheses of the Study:\n\n* Parkinson's Disease Dyskinesia Scale (PDYS-26) is reliable in Turkish.\n* Parkinson's Disease Dyskinesia Scale (PDYS-26) is valid in Turkish.\n\nTo determine the validity of dyskinesia;\n\n* Tampa Kinesiophobia Scale,\n* Mini BesTest,\n* Activity Specific Balance Safety Scale (ABC) and\n* Parkinson's Disease Questionnaire-39 will be evaluated.",[241,242,243],"Idiopathic Parkinson Disease","Dyskinesias","Quality of Life",[245,246,247],"Parkinson's disease","Dyskinesia","Parkinson's Disease Dyskinesia Scale","2025-09-16",{"date":250,"type":39},"2025-09-19",{"date":252,"type":39},"2024-11-14",{"date":254,"type":21},"2025-12-01",{"name":45,"class":46},2,{"id":258,"slug":259,"hasResults":11,"nctId":260,"briefTitle":261,"officialTitle":262,"acronym":4,"eligibilityCriteria":263,"healthyVolunteers":11,"sex":17,"minAge":264,"maxAge":18,"enrollmentInfo":265,"targetDuration":4,"studyType":22,"phases":267,"briefSummary":268,"conditions":269,"keywords":4,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":271,"lastUpdatePostDateStruct":272,"startDateStruct":274,"completionDateStruct":276,"leadSponsor":278,"locationsCount":47},"100590371","investigating-the-effectiveness-of-graded-motor-imagery-training-in-children-with-obstetric-brachial-plexus-injury-100590371","NCT06966544","Investigating the Effectiveness of Graded Motor Imagery Training in Children With Obstetric Brachial Plexus Injury","Investigating the Effectiveness of Graded Motor Imagery Training on Upper Limb Function, Proprioception, Functional Mobility, Balance and Quality of Life in Children With Obstetric Brachial Plexus Injury","Inclusion Criteria:\n\n* Obtaining family consent and the child's willingness\n* Being between the ages of 7-18\n* Being diagnosed with obstetric brachial plexus injury\n* Not having received physical therapy in the last 6 months\n\nExclusion Criteria:\n\n* Having a traumatic (postnatal) brachial plexus injury\n* Having undergone surgery for complications related to brachial plexus injury within the last six months (release, tendon transfer, osteotomy, etc.)\n* Having another neurological, neuromuscular, musculoskeletal or cardiopulmonary system disease in addition to OBPI","7 Years",{"count":266,"type":21},40,[24],"The aim of this study is to investigate the effect of graded motor imagery training on upper extremity motor function, proprioception, functional mobility, balance and quality of life in patients with obstetric brachial plexus injury in addition to conventional treatment. In this context, our aim is to identify new and potential physiotherapeutic approaches to address deficits in motor planning that have been shown to occur at the level of the central nervous system.",[270],"Obstetric Brachial Plexus Injury","2025-05-04",{"date":273,"type":39},"2025-05-12",{"date":275,"type":39},"2024-03-04",{"date":277,"type":21},"2025-07-20",{"name":45,"class":46},{"id":280,"slug":281,"hasResults":11,"nctId":282,"briefTitle":283,"officialTitle":284,"acronym":4,"eligibilityCriteria":285,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":286,"targetDuration":4,"studyType":160,"phases":4,"briefSummary":288,"conditions":289,"keywords":4,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":296,"lastUpdatePostDateStruct":297,"startDateStruct":299,"completionDateStruct":301,"leadSponsor":303,"locationsCount":47},"100588798","the-effect-of-upper-extremity-motor-function-trunk-control-and-motor-imagery-ability-on-turkish-language-skills-in-individuals-with-stroke-100588798","NCT06946082","The Effect of Upper Extremity Motor Function, Trunk Control and Motor Imagery Ability on Turkish Language Skills in Individuals With Stroke","It is to Examine the Relationship Between Upper Extremity Motor Function, Trunk Control, Motor Imagery.","Inclusion Criteria:\n\n* 18 years of age or older\n* Stroke onset more than 1 week\n* Not having practiced imagery before\n* Being a native speaker of Turkish\n* Standardized Mini Mental Test (SMMT) Score of 24 and above\n* History of cerebrovascular events\n* Not having any neurological disorder other than stroke\n* The ability to grasp and hold a 2.5 cm cube\n\nExclusion Criteria:\n\n* No consent from the family or person\n* Having had a stroke before\n* Severe hearing or vision loss\n* Individuals are excluded if they have other primary medical conditions that may affect language and motor functions (e.g. brain tumor, Parkinson's disease, severe post-stroke depression, Alzheimer's disease) or have undergone surgery.",{"count":287,"type":21},101,"A large number of people have a stroke each year and it is a major cause of disability worldwide. Upper limb motor impairments, aphasia, body control problems and decreased motor imagery ability are common after stroke. Although there are studies showing that these impairments may be related to each other, there is no comprehensive study examining the relationship between Turkish language skills and these motor functions. The aim of this study was to evaluate the relationship between Turkish language skills and upper extremity motor function, trunk control and motor imagery ability in stroke patients.",[290,291,292,293,294,295],"Hemiplegia","Aphasia","Stroke","Trunk","Upper Limbs","Motor Imagery","2025-04-19",{"date":298,"type":39},"2025-04-27",{"date":300,"type":39},"2024-12-10",{"date":302,"type":21},"2025-12-10",{"name":45,"class":46},{"id":305,"slug":306,"hasResults":11,"nctId":307,"briefTitle":308,"officialTitle":309,"acronym":310,"eligibilityCriteria":311,"healthyVolunteers":11,"sex":55,"minAge":18,"maxAge":312,"enrollmentInfo":313,"targetDuration":4,"studyType":22,"phases":314,"briefSummary":316,"conditions":317,"keywords":319,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":324,"lastUpdatePostDateStruct":325,"startDateStruct":327,"completionDateStruct":329,"leadSponsor":331,"locationsCount":47},"100562703","phase-2-cross-linked-hyaluronic-aciddextranomer-for-the-treatment-of-stress-urinary-incontinence-100562703","NCT06606613","Cross-linked Hyaluronic Acid\u002Fdextranomer for the Treatment of Stress Urinary Incontinence","Midurethral Sling Versus Cross-linked Hyaluronic Acid\u002Fdextranomer (CLHA\u002FDx) for the Treatment of Stress Urinary Incontinence","(CLHA\u002FDx)","Inclusion Criteria:\n\n* Diagnosis of Stress Urinary Incontinence.\n* Presence of incontinence during the Valsalva maneuver.\n* Positive Marshall-Marchetti test result.\n* Post-void residual urine volume of ≤100 mL.\n\nExclusion Criteria:\n\n* Temporary urinary incontinence.\n* Delirium.\n* Urinary tract infection.\n* Urethritis.\n* Pure urge incontinence.\n* Nocturnal enuresis.\n* Decreased bladder compliance or detrusor contraction observed in urodynamic -studies.\n* Leakage of urine with low bladder pressure.\n* Psychiatric conditions (severe depression and anxiety).\n* Body mass index (BMI) \\> 35 kg\u002Fm².\n* Use of medications that may influence bladder storage or emptying.","75 Years",{"count":159,"type":21},[315],"PHASE2","The investigators aimed to evaluate the effectiveness and safety of intraurethral cross-linked hyaluronic acid\u002Fdextranomer (CLHA\u002FDx) injection for the treatment of stress urinary incontinence (SUI) in women.",[318],"Urinary Stress Incontinence (SI)",[320,321,322,323],"Cross-linked hyaluronic acid\u002Fdextranomer","Mid-urethral sling","Female","Stress Urinary Incontinence","2024-09-24",{"date":326,"type":39},"2024-09-26",{"date":328,"type":21},"2024-10-10",{"date":330,"type":21},"2025-04-10",{"name":45,"class":46},{"id":333,"slug":334,"hasResults":11,"nctId":335,"briefTitle":336,"officialTitle":337,"acronym":4,"eligibilityCriteria":338,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":157,"enrollmentInfo":339,"targetDuration":4,"studyType":160,"phases":4,"briefSummary":341,"conditions":342,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":345,"lastUpdatePostDateStruct":346,"startDateStruct":348,"completionDateStruct":350,"leadSponsor":352,"locationsCount":4},"100560590","seating-posture-and-its-relation-to-pain-100560590","NCT06579131","Seating Posture and Its Relation to Pain","The Physiotherapeutic Perspective on","Inclusion Criteria:\n\n* Be between the ages of 18 and 65, Not having undergone any surgery affecting spinal posture in the last two years\n\nExclusion Criteria:\n\n* • Psikiyatrik hastalık tanısı olması ya da tedavi alıyor olması Omurganın duruşunun etkilenmesine sebep olabilecek nörolojik, romatizmal, ortopedik hastalık tanısı almış olmak",{"count":340,"type":21},300,"A study has been designed to evaluate pain levels experienced by subjects in relation to different sitting postures. The objective is to investigate how various ergonomic sitting positions affect pain intensity, by systematically assessing pain across a range of sitting postures to identify significant differences and correlations.",[343,344],"Posture; Myositis","Sitting Position","2024-08-28",{"date":347,"type":39},"2024-08-30",{"date":349,"type":21},"2025-01-30",{"date":351,"type":21},"2025-06-30",{"name":45,"class":46},""]