[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Mardin Artuklu University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":136},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,50,79,108],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":30,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":39,"lastUpdatePostDateStruct":40,"startDateStruct":43,"completionDateStruct":45,"leadSponsor":47,"locationsCount":4},"100633079","daytime-vs-evening-rehabilitation-in-lumbar-disc-herniation-patients-at-high-risk-for-obstructive-sleep-apnea-100633079",false,"NCT07522021","Daytime vs Evening Rehabilitation in Lumbar Disc Herniation Patients at High Risk for Obstructive Sleep Apnea","Effects of Daytime and Evening Rehabilitation Programs on Sleep Quality and Daytime Sleepiness in Patients With Lumbar Disc Herniation at High Risk for Obstructive Sleep Apnea: A Randomized Controlled Trial","REHAB-TIME","Inclusion Criteria:\n\n* Individuals aged 18-65 years\n* High risk for obstructive sleep apnea, defined as a score \\>4 on the STOP-Bang questionnaire (Snoring, Tiredness, Observed apnea, high blood pressure, Body mass index, Age, Neck circumference, and Gender)\n* Presence of lumbar disc herniation (bulging, protrusion, or extrusion) at L1-S1 levels confirmed by magnetic resonance imaging (MRI)\n* Chronic low back pain lasting at least 3 months with clinical symptoms consistent with imaging findings\n* Mild to moderate radicular symptoms For participants over 55 years of age: single-level or dominant-level protrusion or extrusion-type disc herniation to minimize confounding effects of multilevel degeneration\n* Pain intensity ≥4 on the Visual Analog Scale (VAS) within the last week\n* Ability to participate regularly in the physiotherapy and rehabilitation program\n* Willingness to provide written informed consent Exclusion Criteria:\n* Presence of sequestrated disc herniation or cauda equina compression confirmed by magnetic resonance imaging (MRI)\n* Progressive motor deficit or significant muscle weakness\n* Indication for urgent surgical intervention\n* History of previous lumbar spine surgery\n* Low back pain due to specific causes (e.g., spinal tumor, infection such as spondylodiscitis, inflammatory rheumatic diseases, or traumatic fracture)\n* Previous use of continuous positive airway pressure (CPAP) or bilevel positive airway pressure (BiPAP) therapy\n* Shift work or irregular sleep patterns\n* Major changes in sleep medication within the last 4 weeks\n* Contraindications to electrotherapy (e.g., pacemaker or implanted electronic devices, suspected malignancy, sensory loss in the treatment area, open wounds, or infection)\n* Cardiopulmonary conditions that contraindicate exercise\n* Uncontrolled hypertension or advanced heart failure\n* Pregnancy\n* Severe psychiatric disorders or cognitive impairment\n* Neurological disorders (e.g., multiple sclerosis, stroke sequelae)\n* Epidural or facet joint injection within the last 3 months\n* Diagnosed severe obesity hypoventilation syndrome or severe chronic obstructive pulmonary disease (COPD)\n* Refusal to provide informed consent","ALL","18 Years","65 Years",{"count":21,"type":22},60,"ESTIMATED","INTERVENTIONAL",[25],"NA","Lumbar disc herniation is a common musculoskeletal condition that negatively affects quality of life, physical function, and daily activities. Previous studies have shown that individuals with lumbar disc herniation often experience poor sleep quality, which is closely related to pain severity and functional limitations. In addition, a bidirectional relationship exists between chronic pain and sleep disturbances, where poor sleep can increase pain perception, and pain can further impair sleep.\n\nObstructive sleep apnea (OSA) is a common sleep-related breathing disorder associated with reduced sleep quality, daytime dysfunction, and adverse health outcomes. The STOP-Bang questionnaire (Snoring, Tiredness, Observed apnea, high blood Pressure, Body mass index, Age, Neck circumference, and Gender) is a widely used and practical screening tool to identify individuals at high risk for OSA in clinical settings.\n\nPhysiotherapy and rehabilitation programs are commonly used in the conservative management of lumbar disc herniation and have been shown to improve pain and functional outcomes. However, the effect of the timing of rehabilitation (daytime versus evening) on sleep-related outcomes has not been sufficiently investigated. Considering that circadian rhythms influence pain perception, physiological processes, and sleep regulation, the timing of rehabilitation interventions may play an important role in clinical outcomes.\n\nTherefore, this randomized controlled trial aims to investigate the effects of daytime versus evening rehabilitation programs on sleep quality and daytime sleepiness in patients with lumbar disc herniation who are at high risk for obstructive sleep apnea.",[28,29],"Lumbar Disc Herniation","Obstructive Sleep Apnea Risk Management",[28,31,32,33,34,35,36,37],"Obstructive Sleep Apnea risk management","Sleep Quality","Daytime Sleepiness","Rehabilitation","Physiotherapy","Exercise Therapy","Randomized Controlled Trial","NOT_YET_RECRUITING","2026-04-03",{"date":41,"type":42},"2026-04-13","ACTUAL",{"date":44,"type":22},"2026-04-10",{"date":46,"type":22},"2026-11-12",{"name":48,"class":49},"Mardin Artuklu University","OTHER",{"id":51,"slug":52,"hasResults":11,"nctId":53,"briefTitle":54,"officialTitle":55,"acronym":4,"eligibilityCriteria":56,"healthyVolunteers":57,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":58,"targetDuration":4,"studyType":60,"phases":4,"briefSummary":61,"conditions":62,"keywords":65,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":70,"lastUpdatePostDateStruct":71,"startDateStruct":73,"completionDateStruct":75,"leadSponsor":77,"locationsCount":78},"100628763","validity-and-reliability-of-the-6-minute-pegboard-and-ring-test-6pbrt-in-adults-with-obstructive-sleep-apnea-syndrome-100628763","NCT07465874","Validity and Reliability of the 6-Minute Pegboard and Ring Test (6PBRT) in Adults With Obstructive Sleep Apnea Syndrome","Validity and Reliability of the 6-Minute Pegboard and Ring Test (6PBRT) in Adults With Obstructive Sleep Apnea: A Polysomnography-Based Methodological Study","Inclusion Criteria:\n\n* Being between 18 and 65 years of age\n\nHaving a diagnosis of obstructive sleep apnea (OSA) confirmed by polysomnography\n\nHaving sufficient cognitive ability to understand and follow the test instructions\n\nHaving adequate shoulder range of motion to elevate the upper extremities above head level for performing the 6PBRT\n\nVoluntarily agreeing to participate in the study and providing written informed consent\n\nExclusion Criteria:\n\n* Presence of neurological diseases that may significantly affect upper extremity function (e.g., stroke, multiple sclerosis, peripheral neuropathy)\n\nSevere orthopedic conditions limiting upper extremity movement (e.g., advanced shoulder pathology, recent surgery, severe contracture)\n\nUnstable cardiopulmonary conditions (e.g., recent myocardial infarction, decompensated heart failure, uncontrolled arrhythmia, acute COPD\u002Fasthma exacerbation)\n\nAcute infection, febrile illness, or severe clinical exacerbation within the last 4 weeks\n\nPain severe enough to interfere with the test or any clinical condition preventing the safe administration of the test",true,{"count":59,"type":22},80,"OBSERVATIONAL","Obstructive sleep apnea (OSA) is a common sleep-related breathing disorder characterized by recurrent upper airway obstruction during sleep, leading to intermittent hypoxia and sleep fragmentation. In addition to its well-known cardiometabolic consequences, OSA may negatively affect functional capacity and daily activity performance. However, upper extremity functional capacity in individuals with OSA has not been adequately evaluated.\n\nThe 6-Minute Pegboard and Ring Test (6PBRT) is a functional test designed to assess upper extremity functional capacity during unsupported arm activity. Although the test has been widely used in respiratory diseases, its measurement properties have not yet been evaluated in patients with OSA.\n\nThe aim of this study is to investigate the validity and reliability of the 6PBRT in adults diagnosed with obstructive sleep apnea using polysomnography. Participants with OSA will undergo polysomnographic evaluation and complete the 6PBRT. Test-retest reliability will be assessed by repeating the test under the same conditions. The relationship between 6PBRT performance and polysomnographic parameters (AHI, ODI, minimum SpO₂ and T90) will also be examined. In addition, associations between 6PBRT performance and clinical scales such as the Epworth Sleepiness Scale and Functional Outcomes of Sleep Questionnaire will be analyzed.\n\nThe findings of this study are expected to provide evidence regarding the measurement properties of the 6PBRT in individuals with OSA and contribute to the clinical assessment of upper extremity functional capacity in this population.",[63,64],"Obstructive Sleep Apnea","Sleep Apnea",[66,67,68,63,69],"6-Minute Pegboard and Ring Test","Upper Extremity Functional Capacity","Polysomnography","Functional Performance","2026-03-06",{"date":72,"type":42},"2026-03-12",{"date":74,"type":22},"2026-03-23",{"date":76,"type":22},"2026-11-15",{"name":48,"class":49},1,{"id":80,"slug":81,"hasResults":11,"nctId":82,"briefTitle":83,"officialTitle":84,"acronym":4,"eligibilityCriteria":85,"healthyVolunteers":57,"sex":86,"minAge":87,"maxAge":88,"enrollmentInfo":89,"targetDuration":4,"studyType":23,"phases":91,"briefSummary":92,"conditions":93,"keywords":95,"overallStatus":99,"whyStopped":4,"lastUpdateSubmitDate":100,"lastUpdatePostDateStruct":101,"startDateStruct":103,"completionDateStruct":105,"leadSponsor":107,"locationsCount":78},"100611255","mixed-reality-training-for-teaching-cervical-effacement-and-dilation-100611255","NCT07238205","Mixed Reality Training for Teaching Cervical Effacement and Dilation","The Effect of Mixed Reality Application in Teaching Cervical Effacement and Dilatation on Cognitive Load, Sense of Presence, and Midwifery Professional Perception","Inclusion Criteria:\n\n* Enrolled in the Midwifery Department at Mardin Artuklu University,\n* Taking the course \"Normal Birth and Postpartum Care,\"\n* Who have not previously received any structured training (practical training, simulation, etc.) related to vaginal examination or cervical dilation\u002Feffacement procedures,\n* Who do not feel confident in assessing cervical effacement and dilation,\n* Who volunteer to participate in the study will be included,\n* Pregnant women who are in the first stage of labor and have no obstetric complications.\n\nExclusion Criteria:\n\n* Individuals who are graduates of health vocational high schools,\n* Have disabilities in their eyes, hands, arms, or fingers,\n* Those who do not complete the training will not be included.","FEMALE","18 Months","35 Years",{"count":90,"type":22},90,[25],"The aim of this educational research is to determine whether a mixed reality-based training program is effective in teaching midwifery students how to assess cervical effacement and dilation. The study also examines the impact of mixed reality on students' cognitive load, sense of presence, and midwifery professional perception.\n\nThe main questions the study seeks to answer are:\n\nDoes mixed reality training reduce students' cognitive load?\n\nDoes mixed reality increase the students' sense of presence?\n\nHow does mixed reality-based training influence students' professional perception of midwifery?\n\nDo students who receive mixed reality training perform better in assessing cervical effacement and dilation on real pregnant women compared with the control group?",[94],"Labor; Poor, Primary",[96,97,98],"Cervical Dilatation","Labor","First Stage","RECRUITING","2025-11-15",{"date":102,"type":42},"2025-11-20",{"date":104,"type":42},"2025-10-01",{"date":106,"type":22},"2026-02-01",{"name":48,"class":49},{"id":109,"slug":110,"hasResults":11,"nctId":111,"briefTitle":112,"officialTitle":113,"acronym":4,"eligibilityCriteria":114,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":115,"enrollmentInfo":116,"targetDuration":4,"studyType":23,"phases":118,"briefSummary":119,"conditions":120,"keywords":122,"overallStatus":99,"whyStopped":4,"lastUpdateSubmitDate":128,"lastUpdatePostDateStruct":129,"startDateStruct":131,"completionDateStruct":133,"leadSponsor":135,"locationsCount":78},"100610553","the-effectiveness-of-basic-body-awareness-therapy-in-individuals-with-pes-planus-100610553","NCT07229079","The Effectiveness of Basic Body Awareness Therapy in Individuals With Pes Planus","The Effectiveness of Basic Body Awareness Therapy Combined With Short Foot Exercises in Individuals With Pes Planus","Inclusion Criteria:\n\n* Aged 18-45 years\n* Willing to participate in the study\n* Flexible pes planus (Navicular Drop ≥10 mm and positive Jack's Toe Raise Test)\n\nExclusion Criteria:\n\n* Pain in lower extremity joints\n* Obesity (BMI \\>30)\n* Pregnancy\n* Systemic, neuromuscular, or neurological disorders\n* Posterior tibial tendon dysfunction (unable to perform heel-rise test)\n* History of lower limb surgery\n* Previous treatment for pes planus or use of foot orthoses\n* Lower extremity injury in past 6 months\n* Orthopedic conditions other than pes planus and mild hallux valgus (Manchester Scale C or D excluded)\n* Participation in regular exercise program in past 6 months\n* Prior personal experience with TBFT and\u002For short foot exercises","45 Years",{"count":117,"type":22},50,[25],"This study investigates whether adding Basic Body Awareness Therapy (BBAT) to Short Foot Exercises (SFE) improves pes planus, balance, and body awareness in adults with flexible pes planus. Fifty participants aged 18-45 will be randomly assigned to either a BBAT + SFE group or an SFE-only control group. The interventions will last eight weeks with supervised sessions twice weekly and additional home exercises. Outcomes will be measured before, after, and two months post-intervention.",[121],"Pes Planus",[123,124,121,125,126,127],"Short Foot Exercises (SFE)","Basic Body Awareness Therapy (BBAT)","Balance","Proprioception","Flatfoot","2025-11-14",{"date":130,"type":42},"2025-11-17",{"date":132,"type":42},"2025-01-01",{"date":134,"type":22},"2025-12",{"name":48,"class":49},""]