[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Acibadem University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":649},{"pageToken":4,"total":5,"offset":6,"count":7,"results":8},null,40,0,25,[9,48,79,99,133,162,182,217,249,277,308,331,352,369,384,405,436,466,488,515,543,572,594,611,634],{"id":10,"slug":11,"hasResults":12,"nctId":13,"briefTitle":14,"officialTitle":15,"acronym":4,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":20,"enrollmentInfo":21,"targetDuration":4,"studyType":24,"phases":25,"briefSummary":27,"conditions":28,"keywords":31,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":39,"startDateStruct":42,"completionDateStruct":44,"leadSponsor":45,"locationsCount":4},"100642656","eda-based-adaptive-support-in-vr-als-training-100642656",false,"NCT07650019","EDA-Based Adaptive Support in VR ALS Training","Effects of Electrodermal Activity-Based Adaptive Support Systems on Performance in VR-Based Advanced Life Support Training: A Randomized Controlled Study","Inclusion Criteria:\n\n* Being older than 18\n\nExclusion Criteria:\n\n* prior completion of ALS training\n* history of virtual reality (VR)-induced motion sickness\n* medical conditions such as vertigo or the use of medications known to cause vertigo-like symptoms",true,"ALL","18 Years","25 Years",{"count":22,"type":23},72,"ESTIMATED","INTERVENTIONAL",[26],"NA","This randomized controlled study aims to investigate the effects of an electrodermal activity (EDA)-based adaptive support system on performance during virtual reality (VR)-based advanced life support (ALS) training. Participants' stress levels will be continuously monitored through EDA during the simulation. When stress exceeds a predefined threshold, the adaptive system will automatically activate a support mode that provides additional guidance and time. The performance outcomes of participants receiving adaptive support will be compared with those receiving standard VR training. The study will also examine the role of presence, anxiety, social anxiety, and personality traits in the relationship between stress and performance.",[29,30],"Adaptive Support Condition","Standard Training Condition",[32,33,34,35,36],"virtual reality","adaptive training","stress","Adaptive Life Support Training","electrodermal activity","NOT_YET_RECRUITING","2026-07-01",{"date":40,"type":41},"2026-07-02","ACTUAL",{"date":43,"type":23},"2026-07",{"date":43,"type":23},{"name":46,"class":47},"Acibadem University","OTHER",{"id":49,"slug":50,"hasResults":12,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":4,"eligibilityCriteria":54,"healthyVolunteers":12,"sex":55,"minAge":56,"maxAge":57,"enrollmentInfo":58,"targetDuration":4,"studyType":24,"phases":60,"briefSummary":61,"conditions":62,"keywords":65,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":73,"completionDateStruct":75,"leadSponsor":77,"locationsCount":78},"100546749","the-effect-of-cognitive-exercise-therapy-approach-and-yoga-in-adolescents-with-dysmenorrhoea-100546749","NCT06398990","The Effect of Cognitive Exercise Therapy Approach and Yoga in Adolescents With Dysmenorrhoea","The Effect of Telerehabilitation-Based Cognitive Exercise Therapy Approach and Yoga on Pain, Physical Function and Quality of Life in Adolescents With Dysmenorrhoea","Inclusion Criteria:\n\n* Between the ages of 10 and 19,\n* Having had a menstrual cycle for at least 6-12 months (ACOG, 2018),\n* Having menstrual pain intensity of ≥4 cm according to the Visual Analog Scale (VAS, 0-10 cm) (Kannan, P. 2015; Yonglitthipagon, P. 2017),\n* To have been diagnosed with primary dysmenorrhea according to the clinical characteristics and diagnostic approach defined in international dysmenorrhea guidelines (ACOG 2018; JOGC 2017),\n* Nulliparous (having never given birth),\n* Able to read and write in Turkish,\n* Willing to participate in the study and having provided informed consent.\n\nExclusion Criteria:\n\n* History or clinical findings suggestive of secondary dysmenorrhea,\n* Presence of serious comorbidities, including neurological, cardiovascular, musculoskeletal, psychiatric, gastrointestinal, or autoimmune disorders,\n* History of surgery involving the abdominal, pelvic, or spinal regions within the past 12 months,\n* Current pregnancy or suspected pregnancy,\n* Use of intrauterine devices (IUDs),\n* Having participated in a regular exercise, sports, or physiotherapy program within the last 6 months,\n* Concurrent participation in another clinical study.","FEMALE","10 Years","19 Years",{"count":59,"type":23},42,[26],"Dysmenorrhoea is a condition that negatively affects the quality of life in women of many age groups. In girls with dysmenorrhoea in adolescence, there is an effect on school performance, self-confidence-depression problems and a decrease in quality of life due to pain. In order to eliminate these negative effects, they should receive a good treatment. Medical treatment usually tries to minimise and balance this situation. Considering the fact that families do not want to use drugs such as oral contraceptives in their children at this age and the risks of oral contraceptives, parents are in different searches. Considering that the approach to pain should always be from a holistic perspective, yoga and cognitive exercise therapy approaches are both biopsychosocial treatment methods within the scope of mind-body integrity. Yoga and cognitive exercise therapy approach is thought to reduce symptoms, improve physical functions and quality of life in adolescent girls. With these positive effects, school absenteeism decreases, depression and self-confidence improve. Health costs will also be reduced to some extent.",[63,64],"Dysmenorrhea","Primary Dysmenorrhea",[66,67,68,69],"dysmenorrhea","mind-body exercises","cognitive exercise therapy approach","yoga","RECRUITING","2026-06-30",{"date":40,"type":41},{"date":74,"type":41},"2025-12-01",{"date":76,"type":23},"2026-12",{"name":46,"class":47},1,{"id":80,"slug":81,"hasResults":12,"nctId":82,"briefTitle":83,"officialTitle":84,"acronym":4,"eligibilityCriteria":85,"healthyVolunteers":12,"sex":18,"minAge":56,"maxAge":57,"enrollmentInfo":86,"targetDuration":4,"studyType":88,"phases":4,"briefSummary":89,"conditions":90,"keywords":4,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":93,"lastUpdatePostDateStruct":94,"startDateStruct":95,"completionDateStruct":96,"leadSponsor":98,"locationsCount":78},"100645027","psychometric-properties-of-the-turkish-version-of-the-staffordshire-adolescent-idiopathic-scoliosis-questionnaire-100645027","NCT07676019","Psychometric Properties of the Turkish Version of the Staffordshire Adolescent Idiopathic Scoliosis Questionnaire","Psychometric Properties of the Turkish Version of the Staffordshire Adolescent Idiopathic Scoliosis Questionnaire (SQAIS)","Inclusion Criteria\n\n* Aged between 10 and 19 years.\n* Diagnosed with Adolescent Idiopathic Scoliosis (AIS) by an orthopedic surgeon or spine specialist.\n* Able to read and understand Turkish.\n\nExclusion Criteria\n\n* Diagnosis of congenital, neuromuscular, or syndromic scoliosis.\n* History of severe neurological, psychiatric, or cognitive disorders.\n* Presence of communication impairments that may interfere with understanding or completing the questionnaires.\n* History of major trauma or spinal surgery within the previous 6 months.",{"count":87,"type":23},100,"OBSERVATIONAL","Patient-Reported Outcome Measures (PROMs) have gained increasing importance in scoliosis research in recent years. Although widely used instruments such as the Scoliosis Research Society-22 (SRS-22) include domains related to body image, their primary purpose is to assess overall health-related quality of life and functional outcomes. In contrast, the Staffordshire Questionnaire for Adolescent Idiopathic Scoliosis (SQAIS) was specifically developed to provide a more detailed and patient-centered evaluation of body image and perceived deformity in individuals with adolescent idiopathic scoliosis (AIS). However, a Turkish version of the questionnaire with established validity and reliability is not currently available.\n\nTherefore, the aim of the planned master's thesis is to conduct the cultural adaptation of the Staffordshire Questionnaire for Adolescent Idiopathic Scoliosis into Turkish and to evaluate its psychometric properties in adolescents with AIS. The study will involve a systematic process of linguistic translation and cross-cultural adaptation. Subsequently, the validity and reliability of the Turkish version will be assessed through analyses of internal consistency, test-retest reliability, construct validity, and criterion validity.\n\nThe findings of this study are expected to provide a valid and reliable instrument for assessing body image and deformity perception among Turkish adolescents with idiopathic scoliosis, thereby contributing an important patient-centered outcome measure to both clinical practice and research.",[91,92],"Scoliosis","Quality of Life","2026-06-24",{"date":71,"type":41},{"date":40,"type":23},{"date":97,"type":23},"2027-03-02",{"name":46,"class":47},{"id":100,"slug":101,"hasResults":12,"nctId":102,"briefTitle":103,"officialTitle":104,"acronym":4,"eligibilityCriteria":105,"healthyVolunteers":12,"sex":18,"minAge":19,"maxAge":106,"enrollmentInfo":107,"targetDuration":4,"studyType":24,"phases":109,"briefSummary":110,"conditions":111,"keywords":114,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":125,"lastUpdatePostDateStruct":126,"startDateStruct":128,"completionDateStruct":130,"leadSponsor":132,"locationsCount":78},"100644569","quadriceps-tendon-vs-peroneus-longus-tendon-in-acl-reconstruction-100644569","NCT07671729","Quadriceps Tendon vs Peroneus Longus Tendon in ACL Reconstruction","A Prospective Randomized Clinical Trial Comparing Quadriceps Tendon and Peroneus Longus Tendon Autografts in Anterior Cruciate Ligament Reconstruction: Clinical, Functional, and Gait Analysis Outcomes","Inclusion Criteria:\n\n* Patients diagnosed with anterior cruciate ligament rupture\n* Patients scheduled for primary anterior cruciate ligament reconstruction\n* Age between 18 and 50 years\n* Ability to provide informed consent\n* Willingness to comply with postoperative rehabilitation and follow-up evaluations\n\nExclusion Criteria:\n\n* Previous ligament reconstruction surgery on the affected knee\n* Multi-ligament knee injuries requiring additional ligament reconstruction\n* Severe osteoarthritis of the knee\n* Revision anterior cruciate ligament reconstruction\n* Neuromuscular disorders affecting lower extremity function\n* Active infection\n* Inability to comply with follow-up protocol","50 Years",{"count":108,"type":23},60,[26],"This prospective randomized clinical trial aims to compare quadriceps tendon and peroneus longus tendon autografts in anterior cruciate ligament reconstruction. Patients with anterior cruciate ligament injury undergoing primary reconstruction surgery will be randomly assigned to one of the two graft groups. Clinical examination findings, return-to-sport outcomes, ankle muscle strength, ankle-related functional scores, and gait analysis parameters will be evaluated at 6 months and 12 months postoperatively. The study aims to investigate both knee-related functional outcomes and donor site morbidity associated with graft harvesting techniques.",[112,113],"Anterior Cruciate Ligament Injury","Anterior Cruciate Ligament Rupture",[115,116,117,118,119,120,121,122,123,124],"ACL reconstruction","Anterior cruciate ligament","Quadriceps tendon autograft","Peroneus longus tendon autograft","Gait analysis","Return to sport","Knee stability","Ankle muscle strength","Functional outcomes","Randomized controlled trial","2026-06-23",{"date":127,"type":41},"2026-06-26",{"date":129,"type":41},"2026-05-01",{"date":131,"type":23},"2027-12",{"name":46,"class":47},{"id":134,"slug":135,"hasResults":12,"nctId":136,"briefTitle":137,"officialTitle":138,"acronym":4,"eligibilityCriteria":139,"healthyVolunteers":12,"sex":18,"minAge":19,"maxAge":140,"enrollmentInfo":141,"targetDuration":4,"studyType":24,"phases":143,"briefSummary":144,"conditions":145,"keywords":149,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":154,"lastUpdatePostDateStruct":155,"startDateStruct":157,"completionDateStruct":159,"leadSponsor":161,"locationsCount":4},"100639469","effectiveness-of-combined-glp-1gip-dual-agonist-therapy-and-structured-exercise-on-skeletal-muscle-morphology-quality-and-physical-function-in-overweight-and-obese-individuals-100639469","NCT07609160","Effectiveness of Combined GLP-1\u002FGIP Dual Agonist Therapy and Structured Exercise on Skeletal Muscle Morphology, Quality, and Physical Function in Overweight and Obese Individuals","Effectiveness of Combined GLP-1\u002FGIP Dual Agonist Therapy and Structured Exercise on Skeletal Muscle Morphology, Quality, and Physical Function in Overweight and Obese Individuals: a Randomized Controlled Trial Protocol","Inclusion Criteria:\n\n* initiation of tirzepatide-based pharmacological treatment as prescribed by an endocrinology and metabolism specialist,\n* body mass index (BMI) ≥27 kg\u002Fm² and the presence of a comorbidity condition or BMI≥30 kg\u002Fm²\n* age between 18 and 65 years\n\nExclusion Criteria:\n\n* diagnosis of type 1 or type 2 diabetes mellitus\n* presence of cerebrovascular, hematological, pulmonary, rheumatological, or neurological disorders\n* current participation in a structured diet or exercise program\n* use of weight-loss medications within the past 12 months\n* history of upper or lower extremity surgery or injury within the past 6 months\n* any contraindication to resistance exercise as determined by the treating physician.","65 Years",{"count":142,"type":23},108,[26],"This randomized controlled trial aims to investigate the effects of a 24-week home-based progressive resistance exercise program combined with tirzepatide treatment on skeletal muscle mass, muscle quality, and functional capacity in overweight and obese individuals. A total of 108 participants initiating tirzepatide therapy will be randomized to either exercise plus pharmacotherapy or pharmacotherapy alone. The primary outcome is change in thigh muscle thickness and echo intensity assessed by ultrasonography.",[146,147,148],"Obesity","Sarcopenia","Overweight (Without Type 2 Diabetes) With Weight-related Comorbidities",[150,151,152,153],"exercise","physical activity","muscle","physical function","2026-06-03",{"date":156,"type":41},"2026-06-04",{"date":158,"type":23},"2026-11-01",{"date":160,"type":23},"2028-01-01",{"name":46,"class":47},{"id":163,"slug":164,"hasResults":12,"nctId":165,"briefTitle":166,"officialTitle":166,"acronym":167,"eligibilityCriteria":168,"healthyVolunteers":17,"sex":18,"minAge":4,"maxAge":4,"enrollmentInfo":169,"targetDuration":4,"studyType":24,"phases":171,"briefSummary":172,"conditions":173,"keywords":4,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":129,"lastUpdatePostDateStruct":175,"startDateStruct":177,"completionDateStruct":179,"leadSponsor":181,"locationsCount":78},"100637030","the-effect-of-preoperative-patient-preparation-video-shown-through-virtual-reality-goggles-on-empathy-levels-in-nursing-students-100637030","NCT07573384","The Effect of Preoperative Patient Preparation Video Shown Through Virtual Reality Goggles on Empathy Levels in Nursing Students","PPP-VR","Inclusion Criteria:\n\n* Being enrolled in and attending the Surgical Nursing course at the institution where the research is being conducted, and taking the course for the first time\n\nExclusion Criteria:\n\n* Having worked or currently working in an operating room.",{"count":170,"type":23},50,[26],"This study was planned to evaluate the effect of a preoperative patient preparation video, shown to nursing students via virtual reality glasses, on the development of empathy skills towards the perioperative process.",[174],"Empathy Skills",{"date":176,"type":41},"2026-05-07",{"date":178,"type":41},"2026-02-25",{"date":180,"type":23},"2026-06-15",{"name":46,"class":47},{"id":183,"slug":184,"hasResults":12,"nctId":185,"briefTitle":186,"officialTitle":187,"acronym":188,"eligibilityCriteria":189,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":20,"enrollmentInfo":190,"targetDuration":4,"studyType":24,"phases":192,"briefSummary":193,"conditions":194,"keywords":197,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":209,"lastUpdatePostDateStruct":210,"startDateStruct":212,"completionDateStruct":214,"leadSponsor":216,"locationsCount":78},"100633018","acute-effects-of-smartphone-delivered-local-vibration-on-hand-sensorimotor-performance-100633018","NCT07521228","Acute Effects of Smartphone-Delivered Local Vibration on Hand Sensorimotor Performance","Acute Effects of Smartphone-Delivered Local Vibration at Three Frequencies on Hand Grip Strength, Two-Point Discrimination, Pressure Pain Threshold, and Reaction Time in Healthy Young Adults: A Randomized Crossover Study","SmartVib","Inclusion Criteria:\n\n* Healthy university students aged 18-25 years\n* Willing to participate and provide written informed consent\n* Able to attend three separate measurement sessions\n\nExclusion Criteria:\n\n* Surgical intervention on the hand or wrist within the past 6 months\n* Serious upper extremity injury or trauma within the past 6 months\n* Diagnosis of carpal tunnel syndrome or peripheral nerve entrapment\n* Numbness, paresthesia, or sensory impairment in the hand or wrist\n* History of neurological disease (e.g., stroke, multiple sclerosis, peripheral neuropathy)\n* Active pain, infection, open wound, or dermatological condition at the measurement site\n* Reported hypersensitivity or intolerance to vibration\n* Pregnancy",{"count":191,"type":23},20,[26],"This study investigates the acute effects of smartphone-delivered local vibration on hand sensorimotor performance in healthy young adults. Using a custom-developed iPhone application, three vibration frequencies (80 Hz, 150 Hz, and 220 Hz) are applied to the dominant hand in a randomized crossover design with a minimum 48-hour washout between sessions.\n\nThe primary aim is to evaluate frequency-dependent dose-response effects on hand grip strength. Secondary aims include assessment of two-point discrimination (tactile spatial acuity), pressure pain threshold, and hand reaction time before and immediately after each vibration condition.\n\nThe study seeks to generate evidence on optimal application parameters for smartphone vibration as an accessible and portable local vibration source in clinical and educational settings.",[195,196],"Healthy Volunteers","Vibration; Adverse Effect",[198,199,200,201,202,203,204,205,206,207,208],"local vibration","smartphone vibration","haptic feedback","grip strength","two-point discrimination","pressure pain threshold","reaction time","sensorimotor performance","dose-response","crossover","hand function","2026-04-03",{"date":211,"type":41},"2026-04-09",{"date":213,"type":23},"2026-04",{"date":215,"type":23},"2026-11",{"name":46,"class":47},{"id":218,"slug":219,"hasResults":12,"nctId":220,"briefTitle":221,"officialTitle":222,"acronym":223,"eligibilityCriteria":224,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":225,"targetDuration":4,"studyType":24,"phases":226,"briefSummary":227,"conditions":228,"keywords":232,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":209,"lastUpdatePostDateStruct":245,"startDateStruct":246,"completionDateStruct":247,"leadSponsor":248,"locationsCount":78},"100633017","evaluation-of-injury-risk-factors-and-effects-of-individualized-exercise-program-in-basketball-and-volleyball-athletes-100633017","NCT07521215","Evaluation of Injury Risk Factors and Effects of Individualized Exercise Program in Basketball and Volleyball Athletes","Evaluation of Injury Risk Factors With Clinical\u002FFunctional Tests and Effects of Individualized Exercise Program in University Basketball and Volleyball Athletes: A Non-Randomized Parallel-Group Study","IRISPORT","Inclusion Criteria:\n\n* Active member of Acibadem University basketball or volleyball team\n* Regular training within the past 6 months\n* Age 18 years or older\n* Willing to participate and provide written informed consent\n* Physical and cognitive capacity to complete test protocols\n\nExclusion Criteria:\n\n* Surgical intervention within the past 6 months\n* Acute musculoskeletal injury within the past 2 weeks (acute sprain\u002Fstrain\u002Fcontusion etc.) that would preclude testing\n* History of vestibular disorder, neurological disease, or systemic condition that may affect balance testing\n* Uncontrolled cardiovascular disease\u002Fhypertension or other medical condition contraindicating exercise\n* Pregnancy or within the first 6 months postpartum (female athletes)\n* Refusal to provide informed consent",{"count":87,"type":23},[26],"This study aims to identify injury risk factors using a clinical\u002Ffunctional test battery in university basketball and volleyball athletes, to develop individualized exercise prescriptions for athletes scoring below established cut-off values on each test, and to evaluate the effects of an 8-week intervention program on test parameters.\n\nAs a secondary aim, all participants will be monitored prospectively over a 6-month season to assess the incidence of injuries and health problems, and to evaluate the contribution of the individualized program to injury-related health outcomes.\n\nThe study consists of four phases: (1) baseline cross-sectional assessment (T0), (2) 8-week individualized exercise intervention for athletes below cut-off thresholds, (3) post-intervention reassessment (T1), and (4) 6-month prospective injury surveillance (T2).",[229,230,231],"Athletic Injuries","Sports Injury Prevention","Musculoskeletal Injury",[233,234,235,236,237,238,239,240,241,242,243,244],"injury prevention","individualized exercise","Y-Balance Test","Hop Test","Limb Symmetry Index","GIRD","CKCUEST","university athletes","basketball","volleyball","functional screening","neuromuscular training",{"date":211,"type":41},{"date":213,"type":23},{"date":215,"type":23},{"name":46,"class":47},{"id":250,"slug":251,"hasResults":12,"nctId":252,"briefTitle":253,"officialTitle":254,"acronym":4,"eligibilityCriteria":255,"healthyVolunteers":12,"sex":18,"minAge":19,"maxAge":140,"enrollmentInfo":256,"targetDuration":4,"studyType":24,"phases":258,"briefSummary":259,"conditions":260,"keywords":262,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":269,"lastUpdatePostDateStruct":270,"startDateStruct":272,"completionDateStruct":274,"leadSponsor":276,"locationsCount":78},"100631980","occlusal-splint-and-exercise-therapy-for-temporomandibular-disorders-100631980","NCT07507734","Occlusal Splint and Exercise Therapy for Temporomandibular Disorders","The Effects of Occlusal Splint and Exercise in Individuals With Temporomandibular Disorders","Inclusion Criteria:\n\n* Clinical and radiological diagnosis of TMD\n* Being between 18-65 years of age\n* Presence of Temporomandibular Joint (TMJ) pain for the last 3 months.\n\nExclusion Criteria:\n\n* Intra-articular or degenerative joint disorders and subluxation requiring immediate treatment,\n* A history of TMJ or cervical region surgery in the last 3 months,\n* A history of treatment from related regions,\n* The presence of rheumatic diseases, including TMJ diseases,\n* TMJ instability or fracture,\n* The presence of perception-cognition disorder,\n* The presence of chronic pain, such as trigeminal neuralgia.",{"count":257,"type":23},38,[26],"The goal of this clinical trial is to learn if an exercise protocol can improve temporomandibular pain, jaw function and muscle mechanical properties in individuals with Temporomandibular Disorders (TMD). This study focuses on patients who are already receiving occlusal splint therapy.\n\nThe main question it aims to answer is:\n\nHow does the addition of an exercise protocol to occlusal splint therapy affect temporomandibular pain, jaw function and muscle mechanical properties of the masticatory and neck muscles? Researchers will compare the group receiving both occlusal splint therapy and the exercise protocol to a group only occlusal splint therapy to see if the combined approach is more effective.\n\nParticipants will:\n\n* Undergo an initial assessment of the Jaw Functional Limitation Scale-20 (JLFS-20), Craniofacial Pain and Disability Inventory (CF-PDI), Graded Chronic Pain Scale Version 2.0 (GCPS-2.0), jaw range of motion, pain pressure threshold and muscle mechanical properties.\n* Receive occlusal splint therapy as a part of their treatment.\n* Perform a structured exercise protocol (only 1 group)\n* Attend follow up sessions at the 4th week to monitor changes in all initial assessment parameters.",[261],"Temporomandibular Disorders (TMD)",[263,264,265,266,267,268],"temporomandibular disorders","exercise therapy","occlusal splint","muscle mechanical properties","pain","jaw function","2026-03-27",{"date":271,"type":41},"2026-04-02",{"date":273,"type":41},"2025-07-10",{"date":275,"type":23},"2026-07-10",{"name":46,"class":47},{"id":278,"slug":279,"hasResults":12,"nctId":280,"briefTitle":281,"officialTitle":282,"acronym":283,"eligibilityCriteria":284,"healthyVolunteers":12,"sex":18,"minAge":285,"maxAge":286,"enrollmentInfo":287,"targetDuration":289,"studyType":88,"phases":4,"briefSummary":290,"conditions":291,"keywords":294,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":301,"lastUpdatePostDateStruct":302,"startDateStruct":303,"completionDateStruct":305,"leadSponsor":307,"locationsCount":78},"100631025","electrophysiologic-changes-after-extended-360-capsular-release-100631025","NCT07495306","Electrophysiologic Changes After Extended 360° Capsular Release","Electrophysiological Evidence of Neural Function Improvement After Extended Arthroscopic Circumferential Capsular Release for Adhesive Capsulitis","FROZEN-EMG","Inclusion Criteria:\n\n* Age between 21 and 70 years\n* Diagnosis of adhesive capsulitis (frozen shoulder)\n* Persistent symptoms despite conservative treatment (e.g., physical therapy, medication, or intra-articular injections)\n* Planned arthroscopic capsular release surgery\n* Ability to provide informed consent\n\nExclusion Criteria:\n\n* Known peripheral neuropathy\n* Previous brachial plexus injury\n* History of ipsilateral shoulder neurovascular surgery\n* Previous proximal brachial plexus surgery\n* Coagulation disorders\n* Active infection\n* Pregnancy","21 Years","70 Years",{"count":288,"type":23},15,"12 Weeks","Frozen shoulder (adhesive capsulitis) is a condition characterized by shoulder pain and restricted range of motion, significantly impairing daily living activities. In cases that do not respond to conservative treatment, arthroscopic capsular release is an effective surgical treatment option. The 360° capsular release technique, performed by some surgeons, involves release of the inferior capsule and therefore carries a potential risk of nerve injury due to the anatomical proximity of neurovascular structures such as the axillary nerve. In addition, surgical manipulations performed around the coracoid process may exert mechanical or compressive effects on the musculocutaneous nerve and its sensory continuation, the lateral antebrachial cutaneous nerve, due to their close relationship with the lateral cord of the brachial plexus.\n\nThe aim of this prospective, single-center observational clinical study is to objectively evaluate the morphological and functional effects of inferior capsular release and coracoid region dissection performed during arthroscopic 360° capsular release surgery on the axillary and musculocutaneous nerves, using electromyography (EMG) and nerve conduction studies (NCS) in patients with frozen shoulder.\n\nPatients aged 21-70 years with a diagnosis of frozen shoulder who have not responded to conservative treatments and are scheduled for arthroscopic capsular release will be included in the study. EMG and NCS assessments will be performed at the preoperative baseline, and at 12 weeks postoperatively. For the axillary nerve, the deltoid and teres minor muscles will be evaluated; for the musculocutaneous nerve, the biceps brachii and brachialis muscles will be assessed. Additionally, sensory conduction of the lateral antebrachial cutaneous nerve will be examined. Along with electrophysiological findings, shoulder range of motion (ROM), pain (VAS), muscle strength (MRC), and functional scores will also be recorded.\n\nThis study is expected to provide objective evidence regarding the effects of arthroscopic capsular release surgery on peripheral nerve function, thereby contributing new data on the safety of the surgical technique and enriching the currently limited literature on electromyographic evaluation in frozen shoulder surgery.",[292,293],"Adhesive Capsulitis","Frozen Shoulder",[292,295,296,297,298,299,300],"360° Capsular Release","Shoulder Arthroscopy","Electromyography","Axillary Nerve","Musculocutaneous Nerve","Peripheral Nerve Function","2026-03-23",{"date":269,"type":41},{"date":304,"type":41},"2026-02-26",{"date":306,"type":23},"2027-03-14",{"name":46,"class":47},{"id":309,"slug":310,"hasResults":12,"nctId":311,"briefTitle":312,"officialTitle":312,"acronym":4,"eligibilityCriteria":313,"healthyVolunteers":17,"sex":55,"minAge":19,"maxAge":4,"enrollmentInfo":314,"targetDuration":4,"studyType":88,"phases":4,"briefSummary":316,"conditions":317,"keywords":4,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":301,"lastUpdatePostDateStruct":324,"startDateStruct":326,"completionDateStruct":328,"leadSponsor":330,"locationsCount":78},"100624711","relationship-between-the-severity-of-sleep-deprivation-in-the-first-48-hours-postpartum-breastfeeding-motivation-and-breastfeeding-success-100624711","NCT07413185","Relationship Between the Severity of Sleep Deprivation in the First 48 Hours Postpartum, Breastfeeding Motivation, and Breastfeeding Success","Inclusion Criteria:\n\n* Primiparous or multiparous women aged 18 years and older\n* Having a healthy term delivery\n* Infant not admitted to the neonatal intensive care unit (NICU)\n* Initiated breastfeeding within the first 48 hours postpartum\n\nExclusion Criteria:\n\n* Complications requiring sedation\n* Severe postpartum hemorrhage\n* Severe postoperative pain or need for narcotic analgesics",{"count":315,"type":23},167,"The postpartum period is a critical time marked by significant physiological and psychosocial changes that can affect sleep, emotional well-being, and breastfeeding behaviors. Previous studies indicate that mode of delivery and sleep quality are closely associated with breastfeeding outcomes, with cesarean birth often linked to poorer sleep and lower breastfeeding success. Evidence also suggests that postpartum sleep disturbances are related to reduced breastfeeding self-efficacy, lower motivation, fatigue, depressive symptoms, and shorter breastfeeding duration.\n\nHowever, the literature lacks studies that evaluate insomnia severity, breastfeeding motivation, and breastfeeding success simultaneously-particularly during the first 48 hours after birth. This analytical study aims to assess insomnia severity, breastfeeding motivation, and breastfeeding success (LATCH) within the first 48 postpartum hours and to examine the relationships among these variables. Findings are expected to support early postpartum clinical interventions to improve maternal and infant health outcomes.",[318,319,320,321,322,323],"Postpartum Period","Sleep","Breastfeeding","Motivation","Cesarean Section","Lactation",{"date":325,"type":41},"2026-03-24",{"date":327,"type":41},"2026-03-12",{"date":329,"type":23},"2027-02-23",{"name":46,"class":47},{"id":332,"slug":333,"hasResults":12,"nctId":334,"briefTitle":335,"officialTitle":336,"acronym":4,"eligibilityCriteria":337,"healthyVolunteers":12,"sex":18,"minAge":338,"maxAge":339,"enrollmentInfo":340,"targetDuration":341,"studyType":88,"phases":4,"briefSummary":342,"conditions":343,"keywords":4,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":345,"lastUpdatePostDateStruct":346,"startDateStruct":347,"completionDateStruct":349,"leadSponsor":351,"locationsCount":4},"100630492","turkish-cognitive-self-efficacy-questionnaire-in-parkinsons-disease-100630492","NCT07488377","Turkish Cognitive Self-Efficacy Questionnaire in Parkinson's Disease","Validity and Reliability of the Turkish Version of the Cognitive Self-Efficacy Questionnaire in Individuals With Parkinson's Disease","Inclusion Criteria:\n\n* Clinically diagnosed with Parkinson's disease\n\nAged between 40 and 85 years\n\nMMSE score ≥ 24 (adequate cognitive level for communication)\n\nVoluntary participation with informed consent\n\nPatients attending the Movement Disorders Outpatient Clinic, Department of Neurology\n\nExclusion Criteria:\n\n* Presence of psychiatric disorders (major depression, psychotic disorders)\n\nDiagnosis of advanced dementia\n\nSevere visual or hearing impairment that may interfere with assessments\n\nInability to cooperate with the physiotherapist or complete the assessments","40 Years","85 Years",{"count":87,"type":23},"2 Months","This study aims to evaluate the validity and reliability of the Turkish version of the Cognitive Self-Efficacy Questionnaire in individuals with Parkinson's disease.",[344],"Parkinson Disease","2026-03-18",{"date":301,"type":41},{"date":348,"type":23},"2026-04-01",{"date":350,"type":23},"2027-04-01",{"name":46,"class":47},{"id":353,"slug":354,"hasResults":12,"nctId":355,"briefTitle":356,"officialTitle":357,"acronym":4,"eligibilityCriteria":358,"healthyVolunteers":12,"sex":18,"minAge":338,"maxAge":339,"enrollmentInfo":359,"targetDuration":360,"studyType":88,"phases":4,"briefSummary":361,"conditions":362,"keywords":4,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":345,"lastUpdatePostDateStruct":363,"startDateStruct":364,"completionDateStruct":366,"leadSponsor":368,"locationsCount":4},"100630491","determinants-of-physical-frailty-in-parkinsons-disease-a-multi-factorial-analysis-100630491","NCT07488364","Determinants of Physical Frailty in Parkinson's Disease: A Multi-Factorial Analysis","Investigation of the Relationship Between Motor Imagery, Body Awareness, Kinesiophobia, Physical Activity, Symptom Severity, and Physical Frailty in Patients With Parkinson's Disease","Inclusion Criteria:\n\n* Clinically diagnosed Parkinson's disease\n\nHoehn and Yahr stage 1-3\n\nAge between 40 and 85 years\n\nAdequate cognitive function (Mini-Mental State Examination \\[MMSE\\] score ≥ 24)\n\nPatients attending the Movement Disorders Outpatient Clinic of the Neurology Department\n\nAbility to understand study procedures and provide informed consent\n\nExclusion Criteria:\n\n* Presence of psychiatric disorders (major depression, psychotic disorders)\n\nDiagnosis of advanced dementia\n\nPresence of severe cardiovascular or respiratory disease, or uncontrolled chronic systemic conditions (diabetes mellitus, hypertension)\n\nPresence of additional neurological or orthopedic conditions that may affect assessment performance\n\nSevere visual or hearing impairments that could interfere with testing procedures\n\nInability to cooperate adequately with the physiotherapist during assessments",{"count":87,"type":23},"1 Day","The aim of this study is to examine the associations between motor imagery capacity, body awareness (interoceptive awareness), kinesiophobia, physical activity level, and symptom severity in individuals with Parkinson's disease. In addition, the study aims to evaluate the relationships between these variables and physical frailty. This cross-sectional observational study will provide insight into the biopsychosocial factors associated with frailty in Parkinson's disease.",[344],{"date":301,"type":41},{"date":365,"type":23},"2026-03-30",{"date":367,"type":23},"2027-03-30",{"name":46,"class":47},{"id":370,"slug":371,"hasResults":12,"nctId":372,"briefTitle":373,"officialTitle":374,"acronym":4,"eligibilityCriteria":375,"healthyVolunteers":12,"sex":18,"minAge":338,"maxAge":339,"enrollmentInfo":376,"targetDuration":360,"studyType":88,"phases":4,"briefSummary":377,"conditions":378,"keywords":4,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":345,"lastUpdatePostDateStruct":380,"startDateStruct":381,"completionDateStruct":382,"leadSponsor":383,"locationsCount":4},"100630490","self-compassion-and-self-efficacy-in-parkinsons-disease-associations-with-symptoms-function-and-quality-of-life-100630490","NCT07488351","\"Self-Compassion and Self-Efficacy in Parkinson's Disease: Associations With Symptoms, Function, and Quality of Life\"","\"Associations of Self-Compassion and Self-Efficacy With Symptom Severity, Functional Status, and Quality of Life in Individuals With Parkinson's Disease: A Cross-Sectional Study\"","Inclusion Criteria:\n\n* Clinically diagnosed Parkinson's disease\n\nHoehn and Yahr stage 1-3\n\nAge between 40 and 85 years\n\nSufficient cognitive function to communicate (Mini-Mental State Examination \\[MMSE\\] score ≥ 24)\n\nPatients attending the Movement Disorders Outpatient Clinic of the Neurology Department\n\nWillingness to participate and provide informed consent\n\nExclusion Criteria:\n\n* Presence of psychiatric disorders (e.g., major depression, psychotic disorders)\n\nDiagnosis of advanced dementia\n\nPresence of uncontrolled systemic chronic diseases (e.g., diabetes mellitus, hypertension) or severe cardiovascular or respiratory conditions\n\nPresence of additional orthopedic or neurological conditions that may affect test performance\n\nSevere visual or hearing impairments that could interfere with assessments\n\nInability to cooperate adequately with the physiotherapist during assessments",{"count":87,"type":23},"The aim of this study is to evaluate the associations of self-compassion and self-efficacy levels with symptom severity, functional status, and quality of life in individuals with Parkinson's disease.",[379],"Parkinson Disease, Symptom Severity, Functional Status, Quality of Life, Self-compassion, and Self-efficacy",{"date":301,"type":41},{"date":365,"type":23},{"date":367,"type":23},{"name":46,"class":47},{"id":385,"slug":386,"hasResults":12,"nctId":387,"briefTitle":388,"officialTitle":389,"acronym":4,"eligibilityCriteria":390,"healthyVolunteers":12,"sex":18,"minAge":391,"maxAge":140,"enrollmentInfo":392,"targetDuration":4,"studyType":24,"phases":393,"briefSummary":394,"conditions":395,"keywords":4,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":397,"lastUpdatePostDateStruct":398,"startDateStruct":400,"completionDateStruct":402,"leadSponsor":404,"locationsCount":4},"100629991","the-effect-of-early-phase-graded-motor-imagery-following-massive-rotator-cuff-repair-100629991","NCT07481864","The Effect of Early-Phase Graded Motor Imagery Following Massive Rotator Cuff Repair.","The Effect of Early-Phase Graded Motor Imagery Following Massive Rotator Cuff Repair","Inclusion Criteria:\n\n* Age between 30 and 65 years\n* Presence of an arthroscopically repaired anterior-superior rotator cuff tear, involving the supraspinatus and subscapularis tendons\n\nExclusion Criteria:\n\n* Age younger than 30 years or older than 65 years\n\n  * Presence of severe malignant, hematological, endocrine, metabolic, rheumatologic, or gastrointestinal diseases\n  * Diagnosis of glenohumeral osteoarthritis (Kellgren-Lawrence grade III or higher, with radiographic evidence of osteophytes)\n  * Current treatment with cytotoxic agents or systemic corticosteroids\n  * Alcohol dependence, history of substance abuse, or psychological\u002Femotional disorders that may compromise the validity of informed consent\n  * Previous surgery on the ipsilateral shoulder\n  * Multiple tendon tears, such as combined tears involving the supraspinatus together with the infraspinatus or subscapularis tendons","30 Years",{"count":257,"type":23},[26],"Massive rotator cuff tears are associated with significant pain, functional limitations, and prolonged rehabilitation following surgical repair. In the early postoperative phase, rehabilitation protocols are often limited due to surgical protection requirements, which may delay the restoration of motor control and shoulder function. Graded motor imagery (GMI), a movement representation technique that includes laterality recognition, motor imagery, and mirror therapy, has been shown to modulate cortical processing and improve pain and motor function in various musculoskeletal and neurological conditions. However, its potential role in early postoperative shoulder rehabilitation has not been adequately investigated.",[396],"Shoulder Pain","2026-03-16",{"date":399,"type":41},"2026-03-19",{"date":401,"type":23},"2026-08-15",{"date":403,"type":23},"2026-10-30",{"name":46,"class":47},{"id":406,"slug":407,"hasResults":12,"nctId":408,"briefTitle":409,"officialTitle":410,"acronym":4,"eligibilityCriteria":411,"healthyVolunteers":17,"sex":18,"minAge":412,"maxAge":413,"enrollmentInfo":414,"targetDuration":4,"studyType":24,"phases":416,"briefSummary":417,"conditions":418,"keywords":420,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":428,"lastUpdatePostDateStruct":429,"startDateStruct":431,"completionDateStruct":433,"leadSponsor":435,"locationsCount":78},"100616192","effect-of-paternal-touch-on-sucking-performance-comfort-and-glucose-levels-in-newborns-at-risk-for-hypoglycemia-100616192","NCT07302412","Effect of Paternal Touch on Sucking Performance, Comfort, and Glucose Levels in Newborns at Risk for Hypoglycemia","The Effect of Paternal Touch on Sucking Performance, Comfort, and Glucose Levels in Newborns at Risk for Hypoglycemia During the First Hours of Life","Inclusion Criteria:\n\n* Newborns identified as being at risk for hypoglycemia (see study population).\n* Newborns whose parents\u002Flegal guardians have provided written informed consent.\n* Clinically stable newborns who have no contraindications to breastfeeding during the first 6 hours after birth.\n* Newborns whose fathers are present during the first 6 hours after birth.\n\nExclusion Criteria:\n\n* Newborns who develop hypoglycemia during the study period or who require initiation of hypoglycemia treatment.\n* Newborns with congenital anomalies or a diagnosed genetic syndrome.","1 Hour","6 Hours",{"count":415,"type":23},98,[26],"This randomized controlled trial aims to examine the effects of Gentle Human Touch applied by fathers during the first hours of life on sucking performance, comfort level, and blood glucose values in newborns at risk for hypoglycemia. Eligible newborns will be randomly assigned to intervention and control groups.\n\nAfter the newborn is taken to the baby care room and routine care procedures are completed, comfort level will be assessed by the primary nurse and an independent second observer using the Neonatal Comfort and Behavior Scale (NCBS). In the intervention group, the first Gentle Human Touch application will begin after routine care and the initial comfort assessment are completed. Sucking performance will be assessed during the first breastfeeding session by the primary nurse and an independent observer using the LATCH Breastfeeding Assessment Tool.\n\nIn the intervention group, fathers will administer 15-minute Gentle Human Touch sessions every hour for six hours according to a structured protocol. In the control group, routine care will be provided without any additional touch.\n\nIn both the intervention and control groups, blood glucose levels will be measured at the 2nd hour according to clinical protocols. At the 6th hour, the newborn's comfort level (NCBS), sucking performance (LATCH), and blood glucose level will be reassessed and recorded.\n\nThis study aims to determine whether early paternal touch supports glucose stability, improves sucking performance, and enhances comfort in newborns at risk for hypoglycemia, and to contribute to the development of family-centered, non-invasive care practices in neonatal settings.",[419],"Infant, Newborn",[421,422,423,424,425,426,427],"Gentle Human Touch","Paternal Touch","Newborn Feeding Performance","Comfort","Infant,","Blood Glucose","Newborn","2026-03-10",{"date":430,"type":41},"2026-03-11",{"date":432,"type":41},"2026-01-05",{"date":434,"type":23},"2027-12-08",{"name":46,"class":47},{"id":437,"slug":438,"hasResults":12,"nctId":439,"briefTitle":440,"officialTitle":441,"acronym":4,"eligibilityCriteria":442,"healthyVolunteers":17,"sex":18,"minAge":140,"maxAge":4,"enrollmentInfo":443,"targetDuration":4,"studyType":88,"phases":4,"briefSummary":445,"conditions":446,"keywords":452,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":458,"lastUpdatePostDateStruct":459,"startDateStruct":461,"completionDateStruct":463,"leadSponsor":465,"locationsCount":78},"100621397","self-compassion-self-efficacy-and-health-outcomes-in-older-adults-100621397","NCT07370090","Self-Compassion, Self-Efficacy, and Health Outcomes in Older Adults","The Effect of Self-Compassion and Self-Efficacy on Postural Awareness, Pain, and Health-Promoting Lifestyle Behaviors in Older Adults","Inclusion Criteria:\n\n* Aged 65 years and older\n* Able to read and understand Turkish\n* Able to complete online questionnaires independently\n* Provided informed consent\n\nExclusion Criteria:\n\n* Diagnosis of severe cognitive impairment (e.g., dementia or Alzheimer's disease)\n* Severe psychiatric disorders (e.g., schizophrenia or bipolar disorder)\n* Inability to complete questionnaires independently\n* Incomplete or inconsistent questionnaire responses",{"count":444,"type":23},150,"This cross-sectional observational study aims to examine the relationship between self-compassion, self-efficacy, postural awareness, pain, quality of life, and health-promoting lifestyle behaviors in adults aged 65 years and older. Data will be collected using validated self-report questionnaires administered online. The findings are expected to contribute to a better understanding of psychological factors associated with physical and behavioral health outcomes in older adults.",[447,448,449,450,451],"Older Adults (65 Years and Older)","Health Behavior","Self-Compassion","Self-Efficacy","Pain",[453,454,455,456,457,451],"Self-compassion","Self-efficacy","Older adults","Postural awareness","Health-promoting lifestyle","2026-01-19",{"date":460,"type":41},"2026-01-27",{"date":462,"type":23},"2026-01-15",{"date":464,"type":23},"2026-03-01",{"name":46,"class":47},{"id":467,"slug":468,"hasResults":12,"nctId":469,"briefTitle":470,"officialTitle":470,"acronym":4,"eligibilityCriteria":471,"healthyVolunteers":12,"sex":55,"minAge":19,"maxAge":472,"enrollmentInfo":473,"targetDuration":4,"studyType":88,"phases":4,"briefSummary":475,"conditions":476,"keywords":4,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":480,"lastUpdatePostDateStruct":481,"startDateStruct":483,"completionDateStruct":485,"leadSponsor":487,"locationsCount":78},"100616665","the-relationship-between-quality-of-life-anxiety-levels-and-attitudes-toward-artificial-intelligence-among-women-undergoing-infertility-treatment-100616665","NCT07308561","The Relationship Between Quality of Life, Anxiety Levels, and Attitudes Toward Artificial Intelligence Among Women Undergoing Infertility Treatment","Inclusion Criteria:\n\n* Women aged 18-45 years diagnosed with infertility (primary or secondary infertility).\n* Women undergoing infertility treatment and those who have experienced various treatment modalities (IUI, IVF, ICSI).\n* Women who voluntarily agree to participate in the study.\n* Women who are able to understand and speak Turkish.\n\nExclusion Criteria:\n\n* Women with diagnosed psychological disorders (e.g., clinical depression, anxiety disorders).\n* Women who are not undergoing infertility treatment.","45 Years",{"count":474,"type":23},191,"Infertility affects approximately one in six individuals worldwide and is associated with significant psychological distress, particularly among women undergoing treatment. Increased anxiety levels are strongly linked to reduced quality of life during the infertility process. With the growing integration of artificial intelligence (AI) into healthcare, AI-based tools are increasingly used in infertility care to support decision-making and patient engagement. While many patients are familiar with AI technologies, individual attitudes toward AI may influence their acceptance and potential psychosocial benefits. This study aims to examine the relationship between attitudes toward artificial intelligence, anxiety levels, and quality of life among women undergoing infertility treatment.",[477,478,92,479],"Infertility, Female","Artificial Intelligence","Anxiety","2025-12-17",{"date":482,"type":41},"2025-12-29",{"date":484,"type":41},"2025-10-23",{"date":486,"type":23},"2026-10-23",{"name":46,"class":47},{"id":489,"slug":490,"hasResults":12,"nctId":491,"briefTitle":492,"officialTitle":493,"acronym":4,"eligibilityCriteria":494,"healthyVolunteers":17,"sex":18,"minAge":360,"maxAge":495,"enrollmentInfo":496,"targetDuration":4,"studyType":24,"phases":497,"briefSummary":498,"conditions":499,"keywords":502,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":507,"lastUpdatePostDateStruct":508,"startDateStruct":510,"completionDateStruct":512,"leadSponsor":514,"locationsCount":78},"100598214","effect-of-maternal-voice-on-physiological-indicators-and-feeding-performance-100598214","NCT07068581","Effect of Maternal Voice on Physiological Indicators and Feeding Performance","Effect of Maternal Voice on Physiological Indicators and Feeding Performance During Full Oral Feeding Transition in Preterm Infants: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Preterm infants born at gestational age ≥28 weeks and ≤34 weeks\n* Infants who are ≥30 postmenstrual weeks old at the time of enrollment\n* Infants weighing ≥1000 grams at the time of enrollment\n* Mothers aged 18 years or older\n* Preterm infants who have passed the hearing screening test\n* Infants whose mothers can provide an average of at least 30 ml of expressed breast milk daily during the study period.\n* Mothers who are Turkish speakers.\n* Infants for whom the decision to transition from enteral feeding to full oral feeding has been made for the first time jointly by the physician and nurse\n\nExclusion Criteria:\n\n* Preterm infants with congenital anomalies.\n* Infants with a family history of congenital hearing loss.\n* Infants diagnosed with intraventricular hemorrhage (grade 3-4) or -periventricular leukomalacia.\n* Infants who have had necrotizing enterocolitis requiring treatment.\n* Infants whose mothers have a history of substance abuse or alcoholism","28 Days",{"count":170,"type":23},[26],"This study aimed to determine the effect of maternal voice on physiological indicators and oral feeding performance in preterm infants.\n\nHypothesis 1 (H1): Preterm infants who listen to their mother's voice throughout the full oral feeding process have higher oxygen saturation levels than those who do not.\n\nHypothesis 2 (H2): Preterm infants who listen to their mother's voice throughout the full oral feeding process have lower heart rates than those who do not.\n\nHypothesis 3 (H3): Preterm infants exposed to maternal voice throughout the full oral feeding process have lower respiratory rates than those who are not exposed.\n\nHypothesis 4 (H4): Preterm infants exposed to maternal voice throughout the full oral feeding process have better feeding maturation than those who are not exposed.\n\nHypothesis 5 (H5): The percentage of nutrient intake in preterm infants exposed to maternal voice throughout the entire oral feeding process is higher than in those not exposed.\n\nHypothesis 6 (H6): The feeding time of preterm infants exposed to the mother's voice throughout the entire oral feeding process is shorter than that of those not exposed.\n\nHypothesis 7 (H7): The amount of food consumed per minute by preterm infants exposed to the mother's voice throughout the entire oral feeding process is greater than that of those not exposed.",[500,501],"Preterm","Oral Feeding Performance",[503,504,505,506],"Preterm infants","Oral feeding performance","Maternal voice","NICU care","2025-12-11",{"date":509,"type":41},"2025-12-18",{"date":511,"type":41},"2025-08-10",{"date":513,"type":23},"2026-07-23",{"name":46,"class":47},{"id":516,"slug":517,"hasResults":12,"nctId":518,"briefTitle":519,"officialTitle":520,"acronym":4,"eligibilityCriteria":521,"healthyVolunteers":17,"sex":18,"minAge":522,"maxAge":495,"enrollmentInfo":523,"targetDuration":4,"studyType":24,"phases":525,"briefSummary":526,"conditions":527,"keywords":530,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":535,"lastUpdatePostDateStruct":536,"startDateStruct":538,"completionDateStruct":540,"leadSponsor":542,"locationsCount":78},"100613951","feeding-maturity-in-preterm-infants-100613951","NCT07273266","Feeding Maturity in Preterm Infants","The Effect of Routine Versus Random Pacifier Administration Methods on Feeding Maturity in Preterm Infants","Inclusion Criteria:\n\n* Preterm\n* who are clinically stable, and\n* who are within the first day of initiating enteral feeding.\n\nExclusion Criteria:\n\n* Newborns who have a contraindication to pacifier use\n* have comorbid medical conditions\n* who are intubated\n* have congenital anomalies","0 Days",{"count":524,"type":23},62,[26],"The aim of this study is to evaluate the effect of two pacifier-use strategies-routine 5-minute pacifier use prior to each feeding versus random 30-minute pacifier use at any time of day, independent of feeding-on feeding maturity in preterm infants. The hypotheses of the study are as follows: H1: The routine use of a pacifier prior to feeding has a positive effect on feeding maturity in preterm infants.\n\nH2: The routine use of a pacifier prior to feeding has a positive effect on discharge weight in preterm infants.\n\nH3: The routine use of a pacifier prior to feeding has a positive effect on the length of hospital stay in preterm infants.\n\nH4: The routine use of a pacifier prior to feeding has a positive effect on the gestational age at discharge in preterm infants.",[500,528,529],"Feeding","Non Nutritive Sucking",[531,532,533,534],"preterm","feeding","non nutritive sucking","feeding maturation","2025-12-07",{"date":537,"type":41},"2025-12-09",{"date":539,"type":41},"2025-03-04",{"date":541,"type":23},"2026-07-30",{"name":46,"class":47},{"id":544,"slug":545,"hasResults":12,"nctId":546,"briefTitle":547,"officialTitle":548,"acronym":549,"eligibilityCriteria":550,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":140,"enrollmentInfo":551,"targetDuration":4,"studyType":24,"phases":553,"briefSummary":554,"conditions":555,"keywords":559,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":563,"lastUpdatePostDateStruct":564,"startDateStruct":566,"completionDateStruct":568,"leadSponsor":570,"locationsCount":571},"100613612","effect-of-fan-application-in-preventing-ticagrelor-associated-dyspnea-100613612","NCT07268859","Effect of Fan Application in Preventing Ticagrelor-Associated Dyspnea","Effect of Fan Application in Preventing Ticagrelor-associated Dyspnea in Patients With Acute Coronary Syndrome.","ACS","Inclusion Criteria:\n\n* Between the ages of 18 and 65,\n* No severe hearing and vision problems,\n* Can speak and understand Turkish,\n* Easy to communicate with,\n* First-time sufferer of acute coronary syndrome (ACS) for the first time,\n* Decided to start ticagrelor therapy,\n* Able to adapt to treatment,\n* Individuals who volunteered to participate in the research.\n\nExclusion Criteria:\n\n* Having any problem that prevents you from communicating cognitively, emotionally and verbally,\n* Obstructive sleep abnormalities,\n* Have a disease that affects respiratory function (stage IV cancer, bronchial asthma, COVID-19, lung cancer, pulmonary edema, chronic obstructive pulmonary disease, pulmonary hypertension, pulmonary embolism, pneumonia or bronchitis, etc.),\n* With metabolic abnormalities,\n* Intubated after the procedure,\n* Previously treated with ticagrelor,\n* Individuals who did not volunteer to participate in the study. Losses to follow up\n* Individuals who wish to leave the study voluntarily.\n* Saturation value below 95%,\n* The one with the arrest,\n* Who will not be able to fulfill the requirements of the work,\n* Individuals with life-threatening conditions",{"count":552,"type":23},110,[26],"This study will be conducted in the coronary intensive care unit of Dr. Siyami Ersek Chest, Heart and Vascular Surgery Training and Research Hospital. It aims to investigate the effect of hand fan therapy on ticagrelor-associated dyspnea in patients receiving ticagrelor.",[556,557,558],"Acute Coronary Syndromes","Ticagrelor","Dyspnea",[560,557,561,558,562],"Nursing","Hand fan therapy","Non-pharmacological intervention","2025-12-04",{"date":565,"type":41},"2025-12-08",{"date":567,"type":41},"2025-03-15",{"date":569,"type":23},"2026-01-30",{"name":46,"class":47},2,{"id":573,"slug":574,"hasResults":12,"nctId":575,"briefTitle":576,"officialTitle":577,"acronym":4,"eligibilityCriteria":578,"healthyVolunteers":12,"sex":55,"minAge":19,"maxAge":472,"enrollmentInfo":579,"targetDuration":360,"studyType":88,"phases":4,"briefSummary":581,"conditions":582,"keywords":4,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":586,"lastUpdatePostDateStruct":587,"startDateStruct":589,"completionDateStruct":591,"leadSponsor":593,"locationsCount":78},"100602688","cyberchondria-and-stress-in-women-undergoing-infertility-treatment-100602688","NCT07126769","Cyberchondria and Stress in Women Undergoing Infertility Treatment","Virtual Knowledge, Real Stress: The Role of Cyberchondria Severity in Women Undergoing Infertility Treatment","Inclusion Criteria:\n\n* Women undergoing infertility treatment and those who have experienced various treatment methods (IUI, IVF, ICSI).\n* Women willing to participate in the study.\n* Women who understand and speak Turkish.\n\nExclusion Criteria:\n\n* Women with psychological disorders (e.g., clinical depression, anxiety disorders).\n* Women not undergoing infertility treatment.",{"count":580,"type":23},201,"This study examines how searching for health information on the internet may affect stress and emotional well-being in women undergoing infertility treatment. Infertility is a common condition that impacts about 48 million couples worldwide and can cause not only physical challenges but also significant emotional strain, including anxiety, depression, and stress. Many women turn to the internet to seek answers about their condition and treatment. While online information can be helpful, it is not always accurate or consistent, which can increase worry and confusion. This repeated and sometimes excessive searching for health information, known as \"cyberchondria,\" has been linked in previous research to increased stress and anxiety. This study will assess women's online information-seeking patterns, infertility-related stress, and overall emotional and social well-being, aiming to better understand the role of cyberchondria in the infertility treatment process. The results may help healthcare professionals offer more targeted support and guidance to women facing these challenges.",[583,584,585],"Cyberchondria","Stress","Infertility","2025-09-25",{"date":588,"type":41},"2025-09-30",{"date":590,"type":41},"2025-09-01",{"date":592,"type":23},"2026-05-30",{"name":46,"class":47},{"id":595,"slug":596,"hasResults":12,"nctId":597,"briefTitle":598,"officialTitle":599,"acronym":4,"eligibilityCriteria":600,"healthyVolunteers":12,"sex":55,"minAge":19,"maxAge":4,"enrollmentInfo":601,"targetDuration":4,"studyType":88,"phases":4,"briefSummary":602,"conditions":603,"keywords":4,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":586,"lastUpdatePostDateStruct":606,"startDateStruct":607,"completionDateStruct":609,"leadSponsor":610,"locationsCount":78},"100598135","breastfeeding-myths-and-mothers-motivation-100598135","NCT07067554","Breastfeeding Myths and Mothers' Motivation","An Investigation of the Relationship Between Mothers' Susceptibility to Breastfeeding Myths and Their Motivation to Breastfeed","Inclusion Criteria:\n\n* Having an infant aged 0-6 months\n* Having breastfed the baby at least once\n* Voluntarily agreeing to participate in the study\n\nExclusion Criteria:\n\n* Having a physical or psychiatric health condition that prevents breastfeeding\n* Having had a multiple (twin or more) pregnancy\n* Exclusively formula-feeding the baby",{"count":474,"type":23},"Breast milk is a unique and irreplaceable source of nutrition for infants, offering protection against many common childhood diseases due to its natural sterility, accessibility, and immune-boosting antibodies. Exclusive breastfeeding for the first six months of life is critical for healthy growth, development, and immune support. Despite global recommendations by WHO and UNICEF, lack of knowledge and inadequate support continue to hinder optimal breastfeeding practices.\n\nOne major barrier is the persistence of cultural myths and misconceptions, such as \"colostrum should be discarded,\" or \"infants need water after every feeding.\" These unfounded beliefs may reduce mothers' confidence and lead to early cessation of breastfeeding or premature introduction of complementary foods.\n\nThis study aims to examine the relationship between mothers' belief in breastfeeding myths and their motivation to breastfeed. While prior research has explored each factor individually, no known studies have analyzed their interaction.",[320,604,605,321],"Maternal Behavior","Health Knowledge, Attitudes, Practice",{"date":588,"type":41},{"date":608,"type":41},"2025-09-09",{"date":541,"type":23},{"name":46,"class":47},{"id":612,"slug":613,"hasResults":12,"nctId":614,"briefTitle":615,"officialTitle":616,"acronym":4,"eligibilityCriteria":617,"healthyVolunteers":12,"sex":18,"minAge":338,"maxAge":4,"enrollmentInfo":618,"targetDuration":4,"studyType":24,"phases":620,"briefSummary":621,"conditions":622,"keywords":624,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":626,"lastUpdatePostDateStruct":627,"startDateStruct":629,"completionDateStruct":631,"leadSponsor":633,"locationsCount":78},"100565647","the-effect-of-gait-training-using-different-slope-types-on-balance-in-copd-patients-100565647","NCT06644898","The Effect of Gait Training Using Different Slope Types on Balance in COPD Patients","The Effect of Aerobic Exercise Training at Different Slope Types on Balance in COPD Patients","Inclusion Criteria:\n\n* Being diagnosed with COPD (A, B, E groups according to GOLD assessment)\n* Ambulate on your own\n* Not having any contraindications for exercise\n\nExclusion Criteria:\n\n* Being in GOLD 4 stage in spirometric evaluation\n* Presence of hypoxemia\n* Participation in another pulmonary rehabilitation program within the last 6 months\n* Having an exacerbation in the last 1 month\n* Being diagnosed with additional respiratory disease (asthma, bronchiectasis, etc.)\n* Having had pulmonary surgery\n* Having an orthopedic, neurological or cardiac disease that affects exercise\n* Having uncontrolled hypertension or diabetes\n* Presence of malignancy",{"count":619,"type":23},51,[26],"Although COPD is basically a respiratory system disease, its effects are not limited to the respiratory system. In this context, one parameter affected in COPD patients is balance. Recent studies have highlighted the importance of assessing balance and incorporating it into treatment options such as pulmonary rehabilitation. In this context, we aim to diversify the training by using different slope types (downhill, level, uphill) in aerobic exercise training, which is a strong component of pulmonary rehabilitation, and to evaluate the effect of slope type on balance. Testing different types of inclines in aerobic exercise training has the potential to result in different muscular gains. We anticipate that this may result in different balance gains.",[623],"Pulmonary Disease, Chronic Obstructive",[625],"aerobic exercise, slope, COPD","2025-06-10",{"date":628,"type":41},"2025-06-13",{"date":630,"type":41},"2025-04-09",{"date":632,"type":23},"2026-06-01",{"name":46,"class":47},{"id":635,"slug":636,"hasResults":12,"nctId":637,"briefTitle":638,"officialTitle":639,"acronym":4,"eligibilityCriteria":640,"healthyVolunteers":12,"sex":18,"minAge":338,"maxAge":4,"enrollmentInfo":641,"targetDuration":4,"studyType":24,"phases":642,"briefSummary":643,"conditions":644,"keywords":4,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":626,"lastUpdatePostDateStruct":645,"startDateStruct":646,"completionDateStruct":647,"leadSponsor":648,"locationsCount":78},"100537836","investigation-of-walking-training-with-different-slope-types-in-copd-patients-100537836","NCT06283004","Investigation of Walking Training With Different Slope Types in COPD Patients","The Effect of Aerobic Exercise Training in Different Slope Types on Exercise Capacity, Respiratory Functions, Muscle Strength, and Functional Status in COPD Patients","Inclusion Criteria:\n\n* Being diagnosed with COPD (A, B, E groups according to GOLD assessment)\n* Ambulate on your own\n* Not having any contraindications for exercise\n* To be mentally appropriate (score 24 points and above in the mini mental test)\n\nExclusion Criteria:\n\n* Being in GOLD 4 stage in spirometric evaluation\n* Presence of hypoxemia\n* Participation in another pulmonary rehabilitation program within the last 6 months\n* Having an exacerbation in the last 1 month\n* Being diagnosed with additional respiratory disease (asthma, bronchiectasis, etc.)\n* Having had pulmonary surgery\n* Having an orthopedic, neurological or cardiac disease that affects exercise\n* Having uncontrolled hypertension or diabetes\n* Presence of malignancy",{"count":619,"type":23},[26],"Chronic obstructive pulmonary disease (COPD) is a disease that continues to generate a great deal of research and this research must continue, both because it is not completely curable and because of the large patient population. The importance and benefits of exercise training in COPD patients are clear. One of the most preferred types of exercise training is the so-called aerobic exercise training, which typically takes the form of walking. A typical walking training does not use a slope or may include an uphill slope. However, recently there have been publications about downhill walking and its benefits in COPD. Walking on a level, uphill, and downhill slope may have the potential to result in different gains by using different muscle groups more. Therefore, this study aimed to compare the effects of walking training on exercise capacity, respiratory functions, muscle strength, and functional status in COPD patients with three different slope types: level, uphill, and downhill.",[623],{"date":628,"type":41},{"date":630,"type":41},{"date":632,"type":23},{"name":46,"class":47},""]