[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Gulhane School of Medicine\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":190},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,7,0,[8,44,73,100,124,143,167],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":22,"studyType":23,"phases":4,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100620344","associations-of-cranial-outcomes-and-parental-expectations-and-satisfaction-100620344",false,"NCT07356401","Associations of Cranial Outcomes and Parental Expectations and Satisfaction","Association Between Cranial Morphological Changes, Parental Expectations, and Satisfaction Following Cranial Remolding Orthosis Treatment in Infants","Inclusion Criteria:\n\n* Infants diagnosed with positional cranial deformities (e.g., plagiocephaly, brachycephaly, or asymmetrical cranial shape)\n* Infants who received cranial remolding orthosis treatment\n* Use of a custom-made cranial remolding orthosis\n* Availability of pre-treatment and post-treatment cranial measurements\n* Parents or legal guardians who provided informed consent and were able to complete expectation and satisfaction questionnaires\n* Infants who completed the planned cranial remolding orthosis treatment and follow-up period\n\nExclusion Criteria:\n\n* Infants with neurological disorders, genetic syndromes, or congenital conditions affecting cranial growth\n* Infants who underwent previous cranial surgery or other cranial interventions\n* Infants who received non-custom-made or prefabricated cranial orthoses\n* Incomplete clinical records or missing pre- or post-treatment cranial measurements\n* Parents or caregivers unable to complete the questionnaires due to language or cognitive limitations\n* Infants with a diagnosis of microcephaly or macrocéphaly.","ALL","3 Months","18 Months",{"count":20,"type":21},20,"ESTIMATED","1 Month","OBSERVATIONAL","This study aims to investigate the association between objective cranial morphological changes and parental expectations and satisfaction in infants undergoing treatment with a cranial remolding orthosis (CRO). Infants diagnosed with positional cranial deformities and prescribed CRO treatment will be included. Cranial morphological outcomes will be assessed using standardized cranial measurements obtained before and after the treatment period.\n\nParental treatment expectations will be evaluated prior to the initiation of CRO therapy using the Treatment Expectation Questionnaire (TR.TEX-Q), while parental satisfaction with the device and treatment process will be assessed at the end of treatment using the Quebec User Evaluation of Satisfaction with Assistive Technology (QUEST).\n\nThe primary objective of the study is to examine the relationships between changes in cranial morphology and parental expectations and satisfaction scores. Secondary objectives include exploring the association between baseline expectations and post-treatment satisfaction. The findings are expected to provide insight into how objective treatment outcomes align with family-reported perceptions in cranial remolding orthosis therapy.",[26,27,28,29,30],"Plagiocephaly","Cranial Defect","Orthosis","Expectancy","Satisfaction","RECRUITING","2026-01-22",{"date":34,"type":35},"2026-01-26","ACTUAL",{"date":37,"type":35},"2025-11-25",{"date":39,"type":21},"2026-03-15",{"name":41,"class":42},"Gulhane School of Medicine","OTHER",1,{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":49,"acronym":4,"eligibilityCriteria":50,"healthyVolunteers":11,"sex":16,"minAge":51,"maxAge":52,"enrollmentInfo":53,"targetDuration":54,"studyType":23,"phases":4,"briefSummary":55,"conditions":56,"keywords":60,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":72,"locationsCount":43},"100619664","a-comparison-of-myoelectric-and-bionic-hands-100619664","NCT07347561","A Comparison of Myoelectric and Bionic Hands","Myoelectric and Bionic Hands in Upper Limb Amputations: A Comparison of Body Image, Function and User Satisfaction","Inclusion Criteria:\n\n* Aged 18 to 65 years\n* Individuals with unilateral upper limb amputation\n* Regular use of a prosthetic device for at least 6 months\n* Use of a semi-electronic elbow joint prosthetic component\n* Ability to understand and complete study assessments\n\nExclusion Criteria:\n\n* Presence of bilateral or multiple limb amputations\n* Proximal upper limb amputation at the shoulder level or above\n* Coexisting neurological or orthopedic disorders that may affect upper limb function or study outcomes","18 Years","65 Years",{"count":20,"type":21},"1 Day","This observational study aims to compare myoelectric and bionic hands in terms of upper extremity function, body image and satisfaction.\n\nThe main questions it aims to answer are:\n\n\\- Does upper extremity function differ between bionic and myoelectric hands?\n\nThe main questions it aims to answer are:\n\nDoes upper extremity function differ between bionic and myoelectric hands?",[57,58,59],"Amputation","Upper Limb Amputation","Prosthesis",[57,61,62,63,64,65],"bionic hand","myoelectric hand","prosthesis","trans-humeral","trnas-radial","2026-01-09",{"date":68,"type":35},"2026-01-16",{"date":70,"type":35},"2025-11-01",{"date":39,"type":21},{"name":41,"class":42},{"id":74,"slug":75,"hasResults":11,"nctId":76,"briefTitle":77,"officialTitle":78,"acronym":4,"eligibilityCriteria":79,"healthyVolunteers":11,"sex":80,"minAge":51,"maxAge":52,"enrollmentInfo":81,"targetDuration":4,"studyType":83,"phases":84,"briefSummary":86,"conditions":87,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":92,"lastUpdatePostDateStruct":93,"startDateStruct":95,"completionDateStruct":97,"leadSponsor":99,"locationsCount":43},"100589698","preoperative-pelvic-floor-muscle-training-in-female-urinary-incontinence-100589698","NCT06957795","Preoperative Pelvic Floor Muscle Training in Female Urinary Incontinence","Investigation of the Preoperative Effectiveness of Intensive Pelvic Floor Muscle Training in Women With Urinary Incontinence: a Randomized Controlled Trial.","Inclusion criteria for the study:\n\n* Being a woman between the ages of 18-65\n* Being diagnosed with SUI or SUI-predominant mixed type urinary incontinence by an obstetrician-gynecologist\n* Having active pelvic floor muscle contraction\n* No genital anatomical abnormality\n* Being able to understand and follow verbal and written instructions\n* The patient was referred to physiotherapy at least 6 weeks before the planned surgery date\n* Patients performed 75% or more of the given exercises (categorized as adequate compliance)\n\nExclusion criteria for the study:\n\n* Not volunteering to participate\n* Being pregnant\n* Having had previous pelvic floor surgery\n* Having received previous pelvic floor physiotherapy\n* Having a vaginal or urinary infection\n* Being unable to tolerate pelvic floor muscle function measurement\n* Having a neuromuscular or neurological disease that may affect muscle function","FEMALE",{"count":82,"type":21},60,"INTERVENTIONAL",[85],"NA","Pelvic floor muscles (PFM) play a crucial role in supporting pelvic organs and maintaining continence. Weakness in these muscles can lead to dysfunctions such as pelvic organ prolapse, urinary incontinence (UI), and sexual or anorectal disorders. UI, defined as the involuntary loss of urine, is common globally and classified as stress, urge, or mixed incontinence. Stress urinary incontinence (SUI) - the most prevalent type among women - occurs during activities that increase intra-abdominal pressure. Risk factors include female sex, aging, obesity, smoking, chronic constipation, previous gynecological surgeries, and childbirth. Treatment options for SUI include conservative and surgical methods. Pelvic floor training (PFT), first described by Arnold Kegel in 1948, is a conservative approach that strengthens PFM and alleviates symptoms. Although surgery is often used for SUI, with over 200 procedures described, this study aims to evaluate the preoperative effectiveness of intensive PFT in women with SUI. It will assess changes in muscle function and symptoms before surgery, guiding pelvic rehabilitation strategies to potentially reduce surgical burden and improve outcomes.",[88,89,90,91],"Women","Urinary Incontinence (UI)","Pelvic Floor Muscle Training","Preoperative Period","2025-05-05",{"date":94,"type":35},"2025-05-08",{"date":96,"type":35},"2025-01-01",{"date":98,"type":21},"2025-09-01",{"name":41,"class":42},{"id":101,"slug":102,"hasResults":11,"nctId":103,"briefTitle":104,"officialTitle":105,"acronym":4,"eligibilityCriteria":106,"healthyVolunteers":11,"sex":16,"minAge":107,"maxAge":52,"enrollmentInfo":108,"targetDuration":4,"studyType":83,"phases":110,"briefSummary":111,"conditions":112,"keywords":114,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":116,"lastUpdatePostDateStruct":117,"startDateStruct":119,"completionDateStruct":121,"leadSponsor":123,"locationsCount":43},"100584267","can-lumbar-mulligan-mobilization-improve-gait-balance-and-trunk-position-sense-after-stroke-100584267","NCT06887114","Can Lumbar Mulligan Mobilization Improve Gait, Balance, and Trunk Position Sense After Stroke?","Effects of Mulligan-Based Lumbar Mobilization on Trunk Position Sense, Balance, and Gait in Stroke Survivors: A Randomized Study","Inclusion Criteria:\n\n* Participants must meet all of the following conditions to be eligible for the study:\n\n  * Diagnosed with stroke by a neurologist.\n  * Aged 30 to 65 years.\n  * First-ever stroke (single episode).\n  * Stroke duration between 6 to 24 months.\n  * Score of ≤3 on the Modified Rankin Scale (mRS).\n  * Score of ≥24 on the Mini-Mental State Examination (MMSE).\n\nExclusion Criteria:\n\n* Participants will be excluded if they meet any of the following conditions:\n\n  * History of musculoskeletal disorders affecting the spine (e.g., cancer, scoliosis, spondylolisthesis, rheumatoid arthritis, ankylosing spondylitis).\n  * Previous lumbar spine surgery.\n  * Presence of neurological conditions other than stroke (e.g., Parkinson's disease, multiple sclerosis).\n  * Severe visual impairment affecting balance or walking.","30 Years",{"count":109,"type":21},40,[85],"Stroke is a pathology caused by disturbances in the brain's arterial circulation, leading to high morbidity rates. Individuals who experience a stroke often face neurological impairments such as motor, sensory, and cognitive dysfunctions, which negatively impact muscle strength, postural control, sensation, and gait, reducing their independence in daily activities. Balance deficits in stroke patients increase the risk of falls and contribute to a fear of falling. Improving balance control is a key goal in rehabilitation. The importance of the trunk in balance control and rehabilitation is well-established, as it plays a central role in maintaining stability. In individuals with restricted lumbar mobility, weakened trunk muscles and altered muscle activation can lead to a reduction in proprioception, hip strategy, and spinal stabilization, further impairing balance. Combining conventional exercise approaches with other rehabilitation techniques has been shown to yield more effective outcomes. This study aims to investigate the effects of Mulligan-based lumbar spine mobilization on balance, trunk position sense, and gait in individuals with stroke.",[113],"Balance Impairments in Stroke Patients",[115],"Stroke, Lumbar Mobilization, Mulligan, Balance, Trunk Position Sense and Gait.","2025-03-14",{"date":118,"type":35},"2025-03-20",{"date":120,"type":35},"2024-05-08",{"date":122,"type":21},"2025-06-10",{"name":41,"class":42},{"id":125,"slug":126,"hasResults":11,"nctId":127,"briefTitle":128,"officialTitle":129,"acronym":4,"eligibilityCriteria":130,"healthyVolunteers":11,"sex":80,"minAge":51,"maxAge":4,"enrollmentInfo":131,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":133,"conditions":134,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":136,"lastUpdatePostDateStruct":137,"startDateStruct":139,"completionDateStruct":140,"leadSponsor":142,"locationsCount":43},"100582709","examination-of-the-effect-of-nocturia-on-pelvic-floor-symptoms-sleep-parameters-and-quality-of-life-in-women-with-urinary-incontinence-100582709","NCT06866834","Examination of the Effect of Nocturia on Pelvic Floor Symptoms, Sleep Parameters and Quality of Life in Women with Urinary Incontinence","Examination of the Effect of Nocturia on Pelvic Floor Symptoms, Chronotype, Sleepiness, Sleep Quality, Fatigue and Quality of Life in Women with Urinary Incontinence","Inclusion Criteria:\n\nInclusion Criteria for the Group with Nocturia:\n\n* Being 18 years of age or older\n* Being female\n* Have been diagnosed with urinary incontinence\n* Wake up during the main sleep period to relieve the need to urinate, with the intention of returning to sleep or falling asleep again after each urination\n\nInclusion Criteria for the Group without Nocturia:\n\n* Being 18 years of age or older\n* Being female\n* Have been diagnosed with urinary incontinence\n\nExclusion Criteria:\n\nExclusion Criteria for the Group with Nocturia:\n\n* Diagnosis of a sleep disorder\n* Diagnosis of any neurological disease\n* Chronic kidney disease\n* Diagnosis of diabetes\n* Use of sleep medications\n* Use of antidepressants\n* Use of diuretic medications\n* Use of any medication for urinary incontinence\n* Hormone replacement therapy\n* Pregnancy or having given birth within the last six months\n* Having had a urinary tract infection in the last three months\n* Presence of prolapse greater than stage 2\n* History of orthopedic trauma to the pelvic region\n* Pelvic surgery within the last six months\n* History of cancer\n\nExclusion Criteria for the Group without Nocturia:\n\n* Waking up during the main sleep period to relieve the need to urinate, with the intention of returning to sleep or falling asleep again after each urination\n* Diagnosis of a sleep disorder\n* Diagnosis of any neurological disease\n* Chronic kidney disease\n* Diagnosis of diabetes\n* Use of sleep medications\n* Use of antidepressants\n* Use of diuretic medications\n* Use of any medication for urinary incontinence\n* Hormone replacement therapy\n* Pregnancy or having given birth within the last six months\n* Having had a urinary tract infection in the last three months\n* Presence of prolapse greater than stage 2\n* History of orthopedic trauma to the pelvic region\n* Pelvic surgery within the last six months\n* History of cancer",{"count":132,"type":21},102,"Urinary incontinence (UI), a common issue, is the involuntary leakage of urine that negatively affects individuals socially, physically, and psychologically, leading to a decreased quality of life. Nocturia, which is often seen alongside UI, has similar adverse effects. Nocturia refers to the number of urinations during the main sleep period, and it should be accompanied by the intention to fall back asleep after waking up. Nocturia can arise from factors such as sleep disorders and circadian rhythm disturbances. The circadian rhythm regulates the body's biological functions, and this rhythm varies from person to person, creating chronotypes. There is a strong relationship between sleep and nocturia because nocturia leads to deep sleep loss, an increased risk of metabolic diseases, decreased sleep quality and sleep efficiency, and an increase in the number of awakenings after sleep onset. It is necessary to distinguish whether nocturia, which has a comprehensive impact, affects pelvic floor symptoms, chronotype, sleep quality, fatigue, sleepiness, and quality of life in women with UI. Therefore, the aim of this study is to examine the effect of nocturia on pelvic floor symptoms, chronotype, sleepiness, sleep quality, fatigue, and quality of life in women with UI.",[88,89,135],"Nocturia","2025-03-04",{"date":138,"type":35},"2025-03-10",{"date":96,"type":35},{"date":141,"type":21},"2025-06-01",{"name":41,"class":42},{"id":144,"slug":145,"hasResults":11,"nctId":146,"briefTitle":147,"officialTitle":147,"acronym":4,"eligibilityCriteria":148,"healthyVolunteers":11,"sex":16,"minAge":51,"maxAge":52,"enrollmentInfo":149,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":151,"conditions":152,"keywords":154,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":159,"lastUpdatePostDateStruct":160,"startDateStruct":162,"completionDateStruct":164,"leadSponsor":166,"locationsCount":43},"100581447","examining-the-relationship-between-physical-activity-levels-and-chronotype-tendencies-in-individuals-with-alcohol-dependence-100581447","NCT06850428","Examining the Relationship Between Physical Activity Levels and Chronotype Tendencies in Individuals With Alcohol Dependence","Inclusion Criteria:\n\n* Age: Being between 18-65 years old.\n* Alcohol Dependence: Having alcohol dependence and this condition being confirmed according to the Diagnostic and Statistical Manual of Mental Disorders (DSM)-5 criteria or stated based on self-report.\n* Remission Status: Being in remission for at least 1 month (i.e., no active alcohol use).\n\nExclusion Criteria:\n\n* Active Psychiatric Diseases: For example, individuals with active psychiatric diseases such as schizophrenia or bipolar disorder will not be included in the study.\n* Physical Disability: Individuals with any physical disability will also be excluded from the study.",{"count":150,"type":21},207,"Alcohol use disorders are characterized by excessive alcohol consumption and loss of control and are associated with high mortality and disease burden. The relationship between physical activity and alcoholism is complex, and low physical activity has been shown to be linked to alcohol consumption. Additionally, individuals' circadian rhythms (chronotypes) may influence alcohol consumption habits; Evening-type individuals are more likely to consume alcohol. This study aims to examine the relationship between physical activity levels and chronotype trends in individuals with alcohol addiction.",[153],"Alcohol Abuse\u002FDependence",[155,156,157,158],"chronotype","Alcohol abuse\u002FDependence","physical activity","physical activity level","2025-02-22",{"date":161,"type":35},"2025-02-27",{"date":163,"type":21},"2025-04-15",{"date":165,"type":21},"2025-09-15",{"name":41,"class":42},{"id":168,"slug":169,"hasResults":11,"nctId":170,"briefTitle":171,"officialTitle":172,"acronym":4,"eligibilityCriteria":173,"healthyVolunteers":11,"sex":80,"minAge":4,"maxAge":4,"enrollmentInfo":174,"targetDuration":4,"studyType":83,"phases":176,"briefSummary":177,"conditions":178,"keywords":4,"overallStatus":181,"whyStopped":4,"lastUpdateSubmitDate":182,"lastUpdatePostDateStruct":183,"startDateStruct":185,"completionDateStruct":187,"leadSponsor":189,"locationsCount":4},"100565606","acupressure-mat-on-perceived-stress-sleep-quality-and-premenstrual-symptoms-100565606","NCT06644365","Acupressure Mat on Perceived Stress, Sleep Quality and Premenstrual Symptoms","Examining the Effect of Acupressure Mat on Perceived Stress, Sleep Quality and Premenstrual Symptoms in Students Experiencing Premenstrual Syndrome: Randomized Controlled Study","Inclusion Criteria:\n\n* Using medication and\u002For non-medical methods to cope with PMS\n* Having any gynecological disease (abnormal uterine bleeding, myoma, ovarian cyst, etc.)\n* Using contraceptive medication.\n\nExclusion Criteria:\n\n* Participants wanting to withdraw from the study at any stage of the study\n* Participants not complying with the research plan\n* Diagnosed with a psychiatric or gynecological disease during the study\n* Participants starting to receive additional treatment for PMS during the study period",{"count":175,"type":21},42,[85],"Purpose of the study: To examine the effect of acupressure mat on perceived stress, sleep quality and premenstrual symptoms in students with premenstrual syndrome.\n\nHypotheses of the study;\n\nIn the post-test and follow-up test between students who were applied acupressure mat and those who were applied plain mat;\n\nH10: There is no difference in terms of severity of premenstrual symptoms.\n\nH20: There is no difference in terms of perceived stress.\n\nH30: There is no difference in terms of sleep quality.",[179,180],"Premenstrual Symptoms","Effect of Acupressure Mat","NOT_YET_RECRUITING","2024-10-15",{"date":184,"type":35},"2024-10-16",{"date":186,"type":21},"2024-11-15",{"date":188,"type":21},"2025-03-30",{"name":41,"class":42},""]