[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Karabuk University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":517},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,20,0,[8,49,74,98,124,146,163,184,211,236,266,290,319,350,369,389,418,438,462,490],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":31,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":48},"100641992","effects-of-music-therapy-in-chronic-neck-pain-100641992",false,"NCT07658729","Effects of Music Therapy in Chronic Neck Pain","The Effects of Music Therapy on Pain, Cervical Position Sense, and Balance in Individuals With Chronic Neck Pain","Inclusion Criteria:\n\n* Being between 20-50 years old\n* Having experienced neck pain for at least 3 months\n* Having a resting neck pain score of 3 or higher on the Numeric Pain Scale\n* Being willing to participate in the study\n\nExclusion Criteria:\n\n* Patients with surgical indications for and\u002For who have undergone surgery in the cervical region\n* Having received physiotherapy and\u002For other treatment for neck pain within the last year\n* Those with a history of trauma and systemic disease in the cervical region (malignant condition, systemic rheumatic disease, etc.)\n* Having additional musculoskeletal diseases that may also affect the cervical region (thoracic outlet and scoliosis, etc.)\n* Having a psychiatric illness\n* Being visually impaired",true,"ALL","20 Years","50 Years",{"count":21,"type":22},19,"ESTIMATED","INTERVENTIONAL",[25],"NA","This study aims to investigate the effects of music therapy on pain, cervical position sense, and balance in individuals with chronic neck pain. Chronic neck pain is a common musculoskeletal disorder that may impair proprioception and postural control, negatively affecting daily functioning and quality of life. Music therapy is a safe, low-cost, and non-pharmacological intervention with potential benefits for pain management and sensorimotor function; however, evidence regarding its effects in musculoskeletal rehabilitation is limited. In this study, nineteen individuals with chronic neck pain will listen to instrumental Turkish Classical Music in the Nihavend mode for 60 minutes. Pain intensity, cervical position sense, and static and dynamic balance will be assessed before and after the intervention. The findings are expected to provide evidence for the clinical use of music therapy as an adjunctive treatment in chronic neck pain rehabilitation.",[28,29,30],"Neck Pain","Pain","Music Therapy",[32,33,34,35],"neck pain","music therapy","proprioception","balance","NOT_YET_RECRUITING","2026-06-18",{"date":39,"type":40},"2026-06-23","ACTUAL",{"date":42,"type":22},"2026-07-01",{"date":44,"type":22},"2026-08-30",{"name":46,"class":47},"Karabuk University","OTHER",1,{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":4,"eligibilityCriteria":55,"healthyVolunteers":11,"sex":17,"minAge":56,"maxAge":57,"enrollmentInfo":58,"targetDuration":4,"studyType":60,"phases":4,"briefSummary":61,"conditions":62,"keywords":4,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":68,"startDateStruct":70,"completionDateStruct":71,"leadSponsor":73,"locationsCount":4},"100641843","symptom-severity-posture-pain-and-physical-activity-in-gastroesophageal-reflux-disease-100641843","NCT07643779","Symptom Severity, Posture, Pain, and Physical Activity in Gastroesophageal Reflux Disease","Investigation of Symptom Severity, Posture, Musculoskeletal Pain, and Physical Activity Levels in Patients With Gastroesophageal Reflux Disease","Inclusion Criteria:\n\n* Being diagnosed with gastroesophageal reflux disease (GERD)\n* Age between 18 and 65 years\n* Willingness to participate in the study assessments\n\nExclusion Criteria:\n\n* Presence of a diagnosed psychiatric disorder\n* Pregnancy or breastfeeding status","18 Years","65 Years",{"count":59,"type":22},51,"OBSERVATIONAL","This study is a cross-sectional research designed to investigate symptom severity, posture, musculoskeletal pain, and physical activity levels in individuals with gastroesophageal reflux disease (GERD).",[63,64,65,66],"Gastroesophageal Reflux Disease (GERD)","Symptom","Musculoskeletal Pain","Physical Activity","2026-06-11",{"date":69,"type":40},"2026-06-15",{"date":42,"type":22},{"date":72,"type":22},"2026-12-30",{"name":46,"class":47},{"id":75,"slug":76,"hasResults":11,"nctId":77,"briefTitle":78,"officialTitle":79,"acronym":4,"eligibilityCriteria":80,"healthyVolunteers":16,"sex":81,"minAge":56,"maxAge":82,"enrollmentInfo":83,"targetDuration":4,"studyType":23,"phases":84,"briefSummary":85,"conditions":86,"keywords":4,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":92,"startDateStruct":94,"completionDateStruct":95,"leadSponsor":97,"locationsCount":4},"100641838","the-effect-of-foot-reflexology-in-women-with-migraine-100641838","NCT07651839","The Effect of Foot Reflexology in Women With Migraine","The Effect of Foot Reflexology on Pain, Anxiety, Kinesiophobia, and Postural Control in Women With Migraine","Inclusion Criteria:\n\n* Being a woman between the ages of 18 and 45\n* Having been diagnosed with migraine by a neurologist according to the International Headache Society (IHS) criteria\n* Volunteering to participate in the study\n* Being literate\n* Not having entered menopause\n\nExclusion Criteria:\n\n* Having any neurological disease other than migraine\n* Having a psychiatric illness\n* Smoking\n* Having a musculoskeletal disease affecting the head and neck area\n* Having a history of cervical or cranial surgery\n* Having irritation or ulceration in the skin area to be massaged\n* Receiving migraine treatment other than pharmacological treatment (acupuncture, dry needling, cupping, etc.)\n* Having diabetic foot\n* Having open wounds on the foot\n* Pregnant individuals or individuals who become pregnant during the study period","FEMALE","45 Years",{"count":5,"type":22},[25],"This prospective randomized controlled study aims to investigate the effects of foot massage on pain, anxiety, kinesiophobia, and postural control in women aged 18-45 years diagnosed with migraine who attend the Neurology Outpatient Clinic of Karabük University Karabük Training and Research Hospital. Participants who meet the inclusion and exclusion criteria will be randomly allocated into either a foot massage group or a control group using a simple randomization method. The foot massage group will receive a total of 10 sessions of foot massage over 5 weeks, with two sessions per week, while no massage intervention will be applied to the control group. All participants will be assessed at baseline, immediately after the intervention period, and two weeks following the completion of treatment. The findings of this study are expected to provide evidence regarding the effectiveness of foot massage in the management of symptoms in women with migraine.",[87,88,29,89,90,91],"Migraine","Reflexology","Anxiety","Kinesiophobia","Postural Control",{"date":93,"type":40},"2026-06-16",{"date":37,"type":22},{"date":96,"type":22},"2026-07-30",{"name":46,"class":47},{"id":99,"slug":100,"hasResults":11,"nctId":101,"briefTitle":102,"officialTitle":103,"acronym":4,"eligibilityCriteria":104,"healthyVolunteers":16,"sex":81,"minAge":105,"maxAge":106,"enrollmentInfo":107,"targetDuration":4,"studyType":60,"phases":4,"briefSummary":109,"conditions":110,"keywords":4,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":117,"lastUpdatePostDateStruct":118,"startDateStruct":119,"completionDateStruct":121,"leadSponsor":123,"locationsCount":4},"100642517","balance-fall-risk-and-gait-in-women-with-total-knee-arthroplasty-100642517","NCT07650175","Balance, Fall Risk, and Gait in Women With Total Knee Arthroplasty","Investigation of Balance, Fall Risk, Gait Performance, and Quality of Life in Postmenopausal Women Undergoing Total Knee Arthroplasty","Inclusion Criteria:\n\n* Volunteering to participate in the study.\n* Being 60 years of age or older.\n* Having a Mini Mental Test score of 24 or higher.\n* Not having undergone previous arthroplasty surgery on the knee where surgery is planned.\n* Having experienced unilateral TDA.\n* Being a postmenopausal woman\n\nExclusion Criteria:\n\n* Individuals whose vital signs are unstable after surgery, or who develop any major complications such as deep vein thrombosis, pulmonary embolism, wound infection, or prolonged anesthesia side effects.\n* Presence of any neurological, vestibular, visual, cardiopulmonary, auditory, or cognitive deficits that may affect measurements.\n* Individuals diagnosed with diabetes.","60 Years","85 Years",{"count":108,"type":22},30,"Total knee arthroplasty (TKA) is a commonly performed surgical procedure aimed at reducing pain, restoring joint function, and improving quality of life, particularly among older women. Despite improvements in pain and functional outcomes following TKA, findings regarding balance, fall risk, and gait performance remain inconsistent. Impairments in these parameters may adversely affect daily activities, independence, and overall quality of life.\n\nUnlike previous studies that have primarily focused on one or two outcomes, this study will comprehensively evaluate balance, fall risk, gait performance, and quality of life in postmenopausal women who have undergone TKA. The findings are expected to provide a more holistic understanding of long-term functional outcomes following TKA and contribute to the planning of rehabilitation programs. Therefore, the aim of this study is to compare balance, fall risk, gait performance, and quality of life between postmenopausal women who have undergone TKA and healthy postmenopausal women.",[111,112,113,114,115,116],"Total Knee Arthroplasty","Postmenopausal Women","Quality of Life (QOL)","Balance","Risk of Falling","Walking","2026-06-10",{"date":93,"type":40},{"date":120,"type":22},"2026-06-20",{"date":122,"type":22},"2026-07-22",{"name":46,"class":47},{"id":125,"slug":126,"hasResults":11,"nctId":127,"briefTitle":128,"officialTitle":129,"acronym":4,"eligibilityCriteria":130,"healthyVolunteers":11,"sex":17,"minAge":56,"maxAge":4,"enrollmentInfo":131,"targetDuration":4,"studyType":23,"phases":133,"briefSummary":134,"conditions":135,"keywords":4,"overallStatus":137,"whyStopped":4,"lastUpdateSubmitDate":138,"lastUpdatePostDateStruct":139,"startDateStruct":141,"completionDateStruct":143,"leadSponsor":145,"locationsCount":48},"100642779","the-effect-of-action-observation-therapy-including-unimanual-and-bimanual-activities-in-chronic-stroke-100642779","NCT07631169","The Effect of Action Observation Therapy Including Unimanual and Bimanual Activities in Chronic Stroke","Investigation of the Effects of Action Observation Therapy Including Unimanual and Bimanual Activities on Upper Extremity Functions, Activities of Daily Living, and Quality of Life in Chronic Stroke","Inclusion Criteria:\n\n* Being over 18 years of age,\n* Diagnosis of left hemiparetic stroke,\n* Having passed between 6 months since the onset of stroke,\n* Being in stage 4 or 5 of the hand and stage 4, 5 or 6 of the upper extremity --according to Brunnstrom staging,\n* Being able to sit on a chair for 30 minutes without support (patients who scored 20 or more points in total from the Trunk Impairment Scale),\n* Scoring 24 or more points from the Mini Mental Test\n\nExclusion Criteria:\n\n* Unwillingness to participate in the study,\n* Having spasticity that prevents grasping and releasing an object (levels 3 and 4 on the Modified Ashworth Scale),\n* Having a contracture in any of the affected upper extremity joints,\n* Having severe neglect disorder (scoring 21 or higher on the Catherine Bergego Scale),\n* Having impaired cooperation, compliance, and behavior during the administration of tests used to obtain data,\n* Having a mental impairment that prevents communication and following basic commands (scoring less than 24 on the Mini-Mental Test),\n* Having additional neurological and\u002For orthopedic problems that may affect motor performance and sitting balance,\n* Having severe visual and hearing problems (if any, these problems not corrected with assistive devices such as glasses, contact lenses, hearing aids, etc.)",{"count":132,"type":22},45,[25],"Functional impairments in the upper extremities following a stroke significantly restrict individuals' activities of daily living and overall quality of life; in this context, Action Observation Training (AOT) has emerged in recent years as an effective rehabilitation method that promotes motor learning processes and cortical activity by activating the mirror neuron system. Although the literature acknowledges the positive effects on neural mechanisms of both unimanuel approaches, which focus on the paretic hand alone, and bimanual approaches, which involve the simultaneous use of both hands, there remains a gap regarding which method yields superior outcomes. This study aims to compare the effectiveness of AOT interventions consisting of exclusively unimanual versus exclusively bimanual activities on upper extremity functions, activities of daily living, and quality of life in chronic stroke patients, while investigating the potential differences between the outcomes of these two distinct approaches.",[136],"Chronic Stroke","RECRUITING","2026-06-05",{"date":140,"type":40},"2026-06-09",{"date":142,"type":22},"2026-05-18",{"date":144,"type":22},"2027-05-18",{"name":46,"class":47},{"id":147,"slug":148,"hasResults":11,"nctId":149,"briefTitle":150,"officialTitle":151,"acronym":4,"eligibilityCriteria":152,"healthyVolunteers":11,"sex":17,"minAge":56,"maxAge":4,"enrollmentInfo":153,"targetDuration":4,"studyType":23,"phases":154,"briefSummary":155,"conditions":156,"keywords":4,"overallStatus":137,"whyStopped":4,"lastUpdateSubmitDate":138,"lastUpdatePostDateStruct":157,"startDateStruct":158,"completionDateStruct":159,"leadSponsor":161,"locationsCount":162},"100643482","action-observation-therapy-in-chronic-stroke-via-telerehabilitation-100643482","NCT07631182","Action Observation Therapy in Chronic Stroke Via Telerehabilitation","Investigation of the Effect of Action Observation Therapy Via Telerehabilitation Method on Upper Extremity Functions, Daily Living Activities and Quality of Life in Chronic Stroke Patients","Inclusion Criteria:\n\n* Being over 18 years of age,\n* Diagnosis of left hemiparetic stroke,\n* Having passed between 6 months since the onset of stroke,\n* Being in stage 4 or 5 of the hand and stage 4, 5 or 6 of the upper extremity according to Brunnstrom staging,\n* Being able to sit on a chair for 30 minutes without support (patients who scored 20 or more points in total from the Trunk Impairment Scale),\n* Scoring 24 or more points from the Mini Mental Test\n\nExclusion Criteria:\n\n* Unwillingness to participate in the study,\n* Having spasticity that prevents grasping and releasing an object (levels 3 and 4 on the Modified Ashworth Scale),\n* Having a contracture in any of the affected upper extremity joints,\n* Having severe neglect disorder (scoring 21 or higher on the Catherine Bergego Scale),\n* Having impaired cooperation, compliance, and behavior during the administration of tests used to obtain data,\n* Having a mental impairment that prevents communication and following basic commands (scoring less than 24 on the Mini-Mental Test),\n* Having additional neurological and\u002For orthopedic problems that may affect motor performance and sitting balance,\n* Having severe visual and hearing problems (if any, these problems not corrected with assistive devices such as glasses, contact lenses, hearing aids, etc.)",{"count":108,"type":22},[25],"Stroke, a leading cause of disability worldwide, particularly affects upper extremity function, rendering individuals dependent on others for daily living activities and reducing their quality of life. To mitigate these effects, Action Observation Therapy (AOT), which has gained prominence in recent years, activates the mirror neuron system, triggering learning processes in the motor cortex and supporting functional recovery through the imitation of observed movements. Furthermore, telerehabilitation offers a significant advantage in facilitating access to rehabilitation services for these patients requiring long-term treatment, eliminating barriers such as transportation and cost. The absence of studies in the literature comparing the effectiveness of combining these two methods on hand skills and quality of life in individuals with chronic stroke with conventional physiotherapy makes investigating the clinical value of this approach academically unique and necessary.",[136],{"date":140,"type":40},{"date":69,"type":22},{"date":160,"type":22},"2026-10-01",{"name":46,"class":47},2,{"id":164,"slug":165,"hasResults":11,"nctId":166,"briefTitle":167,"officialTitle":168,"acronym":4,"eligibilityCriteria":169,"healthyVolunteers":16,"sex":17,"minAge":56,"maxAge":170,"enrollmentInfo":171,"targetDuration":4,"studyType":23,"phases":173,"briefSummary":174,"conditions":175,"keywords":4,"overallStatus":137,"whyStopped":4,"lastUpdateSubmitDate":177,"lastUpdatePostDateStruct":178,"startDateStruct":180,"completionDateStruct":182,"leadSponsor":183,"locationsCount":48},"100639536","core-training-in-amateur-soccer-players-100639536","NCT07577362","Core Training in Amateur Soccer Players","The Effect of Core Muscle Strengthening Training on Performance in Soccer Players","Inclusion Criteria:\n\n* Being between 18-35 years old\n* Being able to communicate in Turkish\n* Willing to participate in the training.\n* Being a licensed football player\n\nExclusion Criteria:\n\n* Body mass index of 30 kg\u002Fm² or higher\n* History of lower extremity surgery in the last 6 months\n* Cardiac, musculoskeletal, vestibular, and neurological problems","35 Years",{"count":172,"type":22},40,[25],"The core region is a part of the body composed of axes surrounding the torso and plays a crucial role in maintaining stability. Therefore, it is considered important for maintaining athletic performance in athletes. This study aims to investigate the effects of core strength training, in addition to routine training programs, on jumping, agility, speed, balance, and shooting speed performance in amateur football players.",[176],"Sports Physical Therapy","2026-05-03",{"date":179,"type":40},"2026-05-11",{"date":181,"type":40},"2026-05-01",{"date":72,"type":22},{"name":46,"class":47},{"id":185,"slug":186,"hasResults":11,"nctId":187,"briefTitle":188,"officialTitle":189,"acronym":4,"eligibilityCriteria":190,"healthyVolunteers":16,"sex":81,"minAge":56,"maxAge":4,"enrollmentInfo":191,"targetDuration":4,"studyType":23,"phases":193,"briefSummary":194,"conditions":195,"keywords":199,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":204,"lastUpdatePostDateStruct":205,"startDateStruct":207,"completionDateStruct":208,"leadSponsor":210,"locationsCount":4},"100633746","video-supported-flipped-learning-for-episiotomy-training-in-midwifery-students-100633746","NCT07530692","Video-Supported Flipped Learning for Episiotomy Training in Midwifery Students","The Effect of Video-Supported Flipped Learning Model in Episiotomy Education on Anxiety and Skill Levels of Midwifery Students","Inclusion Criteria:\n\n* Midwifery 3rd-year student who is taking the Normal Birth course\n* Willing to participate and provides informed consent\n* Has not received prior education in the health field during associate or undergraduate education\n* Has access to the internet and has a computer and\u002For smartphone\n\nExclusion Criteria:\n\n* Incomplete completion of data collection forms\n* Has received prior education in the health field during associate or undergraduate education\n* No access to the internet, computer, or smartphone\n* Does not participate in the study procedures\u002Fintervention sessions\n* Requests to withdraw from the study at any time",{"count":192,"type":22},60,[25],"This study aims to evaluate the effect of a video-supported flipped learning model on anxiety and skill levels of midwifery students in episiotomy education. Episiotomy is an important clinical skill in midwifery education, and the method used to teach this skill may influence students' anxiety and performance.\n\nThis randomized controlled educational study will be conducted with midwifery students who are enrolled in the episiotomy course. Participants will be randomly assigned to either an intervention group or a control group. Students in the intervention group will receive episiotomy education using a video-supported flipped learning model, in which theoretical content is provided through instructional videos prior to in-class activities. The control group will receive traditional classroom-based education.\n\nStudents' anxiety levels and episiotomy skill performance will be assessed using validated measurement tools before and after the educational intervention. The findings of this study are expected to contribute to evidence-based teaching strategies in midwifery education and support the use of innovative learning models to improve student outcomes.",[89,196,197,198],"Episiotomy","Midwifery","Clinical Competence",[196,200,201,202,203],"Video-Based Learning","Midwifery Students","Simulation Training","Randomized Controlled Trial","2026-04-08",{"date":206,"type":40},"2026-04-15",{"date":206,"type":22},{"date":209,"type":22},"2026-07-20",{"name":46,"class":47},{"id":212,"slug":213,"hasResults":11,"nctId":214,"briefTitle":215,"officialTitle":216,"acronym":4,"eligibilityCriteria":217,"healthyVolunteers":11,"sex":17,"minAge":56,"maxAge":57,"enrollmentInfo":218,"targetDuration":4,"studyType":23,"phases":220,"briefSummary":221,"conditions":222,"keywords":224,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":230,"lastUpdatePostDateStruct":231,"startDateStruct":233,"completionDateStruct":234,"leadSponsor":235,"locationsCount":4},"100631038","mobile-app-supported-exercise-program-for-mechanical-low-back-pain-100631038","NCT07495475","Mobile App-Supported Exercise Program For Mechanical Low Back Pain","Effect of a Mobile Application-Supported Home Exercise Program on Posture, Balance, Pain and Functionality in Individuals With Mechanical Low Back Pain","Inclusion Criteria:\n\n* Individuals aged between 18 and 65 years\n* Diagnosis of chronic mechanical low back pain lasting longer than 3 months\n* Ability to use a smartphone or mobile device\n* Willingness to participate in the study and provide informed consent\n\nExclusion Criteria:\n\n* Cauda equina syndrome\n* Long-term corticosteroid use\n* Presence of focal neurological deficits associated with disability\n* Previous spinal surgery\n* Severe neurological or systemic disorders affecting mobility",{"count":219,"type":22},50,[25],"Mechanical low back pain is one of the most common musculoskeletal disorders affecting daily activities and quality of life. Home exercise programs are frequently recommended in the management of low back pain; however, adherence to these programs is often limited. Mobile health applications may enhance adherence by providing exercise demonstrations, reminders, and monitoring tools.\n\nThe aim of this study is to investigate the effects of a mobile application-supported home exercise program on posture, balance, pain, and functional status in individuals with mechanical low back pain. Participants with chronic mechanical low back pain will be randomly assigned to two groups. Both groups will receive the same home exercise program. The control group will receive the exercises in printed format, while the experimental group will follow the program through the E-Exercise mobile application that includes exercise videos, reminders, and progress tracking.\n\nParticipants will be evaluated before the intervention and after six weeks of exercise training. Outcome measures will include flexibility, posture, balance, pain intensity, and functional disability. The results of this study may contribute to improving adherence to home exercise programs and promoting the use of digital health technologies in physiotherapy practice.",[223],"Mechanical Low Back Pain",[225,223,226,227,228,229],"Low Back Pain","Home Exercise Program","Mobile Health Application","Physiotherapy","Exercise Adherence","2026-03-26",{"date":232,"type":40},"2026-04-01",{"date":232,"type":22},{"date":42,"type":22},{"name":46,"class":47},{"id":237,"slug":238,"hasResults":11,"nctId":239,"briefTitle":240,"officialTitle":241,"acronym":4,"eligibilityCriteria":242,"healthyVolunteers":16,"sex":81,"minAge":4,"maxAge":4,"enrollmentInfo":243,"targetDuration":4,"studyType":23,"phases":245,"briefSummary":246,"conditions":247,"keywords":252,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":258,"lastUpdatePostDateStruct":259,"startDateStruct":261,"completionDateStruct":263,"leadSponsor":265,"locationsCount":48},"100628161","the-impact-of-a-infant-sleep-hygiene-training-program-on-infant-sleep-habits-and-parental-self-efficacy-100628161","NCT07458035","The Impact of a Infant Sleep Hygiene Training Program on Infant Sleep Habits and Parental Self-Efficacy","The Impact of a Comfort Theory-Based Infant Sleep Hygiene Training Program on Infant Sleep Habits and Parental Self-Efficacy","Inclusion Criteria:\n\n1. Being a primiparous pregnant woman (first pregnancy)\n2. Being between 24 and 32 weeks of pregnancy\n3. Having a risk-free pregnancy\n4. Not having a mental disorder\n5. Speaking and understanding Turkish as a native language\n6. Being literate\n7. Not having received training on infant sleep\n8. Agreeing to participate in the study\n\nExclusion Criteria:\n\n1. The baby being born outside of the 38th to 42nd week of pregnancy\n2. The baby having a birth weight of less than 2,500 grams or more than 4,000 grams\n3. The baby being admitted to the neonatal intensive care unit after birth\n4. The baby having a condition that affects sleep, such as colic or hernia\n5. The baby having a chronic illness\n6. The parent wanting to leave work",{"count":244,"type":22},48,[25],"This randomized controlled trial aims to evaluate the effectiveness of a structured, Infant Sleep Hygiene Education Program initiated during pregnancy on infant sleep habits and parental self-efficacy related to infant sleep in the postpartum period. The program is grounded in developmental science and attachment-sensitive principles and focuses on promoting healthy sleep habits through responsive caregiving, consistent bedtime routines, and evidence-based sleep hygiene practices.\n\nPregnant women will be randomly assigned to either an intervention group receiving a multi-session prenatal education program with postnatal follow-up support, or a control group receiving routine antenatal care. Primary outcomes include parental self-efficacy regarding infant sleep and infant sleep habits (e.g., night awakenings, sleep duration, sleep onset latency, and routine consistency), assessed at 1, 3, and 6 months postpartum.\n\nSecondary outcomes include adherence to recommended sleep-supportive parenting practices and infant sleep diary indicators. In addition, the mediating role of parental self-efficacy in the relationship between the intervention and infant sleep outcomes will be examined. Program evaluation outcomes will assess parental knowledge before and after the education, participation and adherence to the sessions, and parental satisfaction with the education program.\n\nThis study aims to provide evidence for an ethical, developmentally appropriate, and preventive infant sleep education model integrated into routine prenatal care.",[248,249,250,251],"Sleep Hygiene","Infant Sleeping Habits","Parent Education","Self Efficacy",[253,254,255,256,257],"infant sleep","sleep hygiene","parent education","educational program","comfort theory","2026-03-04",{"date":260,"type":40},"2026-03-09",{"date":262,"type":22},"2026-06",{"date":264,"type":22},"2027-03",{"name":46,"class":47},{"id":267,"slug":268,"hasResults":11,"nctId":269,"briefTitle":270,"officialTitle":271,"acronym":4,"eligibilityCriteria":272,"healthyVolunteers":16,"sex":17,"minAge":56,"maxAge":170,"enrollmentInfo":273,"targetDuration":4,"studyType":23,"phases":274,"briefSummary":275,"conditions":276,"keywords":278,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":283,"lastUpdatePostDateStruct":284,"startDateStruct":286,"completionDateStruct":288,"leadSponsor":289,"locationsCount":4},"100622882","grastion-and-percussion-therapy-100622882","NCT07389395","Grastion and Percussion Therapy","Comparison of the Effects of Pre-Exercise Instrument-Assisted Soft Tissue Mobilization and Percussion Therapy on Muscle Using a Crossover Design","Inclusion Criteria:\n\n* Aged 18-35 years\n* Healthy participants\n* Sedentary lifestyle as defined by the International Physical Activity Questionnaire (IPAQ) (low physical activity category)\n* Ability to understand the study procedures and provide written informed consent\n\nExclusion Criteria:\n\n* Upper extremity injury or surgery within the past 6 months\n* Presence of skin lesions, wounds, or dermatological diseases at the application site\n* Any diagnosed musculoskeletal disorder\n* History of cardiovascular, metabolic, or pulmonary disease\n* Presence of neurological disorders or cognitive impairment affecting cooperation\n* Use of medications affecting neuromuscular function or circulation\n* Participation in any upper extremity strength training within the past 3 months\n* Contraindications to percussion therapy or instrument-assisted soft tissue mobilization (Graston)",{"count":5,"type":22},[25],"The study aims to investigate the effects of percussion therapy and instrument-assisted soft tissue mobilization (AISM), commonly used in clinical settings, on muscle fatigue, maximum muscle strength, pain threshold, and muscle oxygenation.\n\nThe study will involve 20 volunteer participants. To achieve the study results, pre-exercise percussion therapy and instrument-assisted soft tissue mobilization (AISM) will be administered using a crossover design.\n\nResults will be measured using a digital dynamometer, a moxy oxygen monitor, and a fatigue questionnaire.",[277],"Muscle Fatigue and Muscle Oxygenation",[279,280,281,282],"Muscle Oxygen Saturation","Muscle Strength","Instrument-Assisted Soft Tissue Mobilization (Graston Technique)","Percussion Therapy","2026-01-31",{"date":285,"type":40},"2026-02-05",{"date":287,"type":22},"2026-02-15",{"date":69,"type":22},{"name":46,"class":47},{"id":291,"slug":292,"hasResults":11,"nctId":293,"briefTitle":294,"officialTitle":295,"acronym":4,"eligibilityCriteria":296,"healthyVolunteers":16,"sex":81,"minAge":56,"maxAge":4,"enrollmentInfo":297,"targetDuration":4,"studyType":23,"phases":299,"briefSummary":300,"conditions":301,"keywords":306,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":312,"lastUpdatePostDateStruct":313,"startDateStruct":315,"completionDateStruct":317,"leadSponsor":318,"locationsCount":4},"100621266","qr-code-based-preoperative-education-for-cesarean-birth-anxiety-pain-and-comfort-100621266","NCT07368387","QR Code-Based Preoperative Education for Cesarean Birth: Anxiety, Pain, and Comfort","The Effect of QR Code-Based Preoperative Education on Anxiety, Postpartum Pain, and Comfort in Women Undergoing Cesarean Birth","Inclusion Criteria:\n\n* Pregnant women aged 18 years or older\n* Scheduled for elective (planned) cesarean birth\n* Able to read and understand Turkish and complete study questionnaires\n* Able to provide written informed consent\n* Has access to a smartphone and is able to use a QR code to view the educational materials (intervention arm)\n\nExclusion Criteria:\n\n* Emergency cesarean birth or unplanned change to emergency surgery\n* Presence of high-risk pregnancy or serious obstetric\u002Fmedical complications requiring intensive management (e.g., severe preeclampsia\u002Feclampsia, major hemorrhage risk, unstable systemic disease)\n* Known psychiatric disorder or current use of medications that may substantially affect anxiety assessment (as judged by the clinical team)\n* Communication barriers that prevent participation (e.g., severe visual\u002Fhearing impairment, cognitive impairment) or inability to complete questionnaires\n* No smartphone access or inability\u002Funwillingness to use QR code materials (for intervention delivery)\n* Refusal to participate or withdrawal of consent at any time",{"count":298,"type":22},88,[25],"This study aims to evaluate the effect of QR code-based preoperative education on anxiety, postpartum pain, and comfort levels in women undergoing cesarean birth. Cesarean delivery is a common surgical procedure, and insufficient preoperative information may increase anxiety and negatively affect postoperative recovery and comfort.\n\nIn this randomized controlled study, eligible pregnant women scheduled for elective cesarean birth will be assigned to either an intervention group or a control group. Women in the intervention group will receive preoperative education delivered through QR code-based digital materials, including information about the cesarean procedure, postoperative pain management, and comfort-enhancing strategies. The control group will receive routine care provided by the hospital.\n\nAnxiety levels will be assessed preoperatively, while postpartum pain and comfort levels will be evaluated after delivery using validated measurement tools. The findings of this study are expected to contribute to the development of accessible and effective educational interventions to improve maternal well-being and postoperative outcomes in cesarean birth.",[302,303,304,305],"Preoperative Anxiety","Postpartum Pain","Maternal Comfort","Cesarean Birth",[305,307,308,309,303,304,310,203,311],"Preoperative Education","QR Code-Based Education","Maternal Anxiety","Digital Health Education","Prenatal Education","2026-01-18",{"date":314,"type":40},"2026-01-26",{"date":316,"type":22},"2026-02-02",{"date":120,"type":22},{"name":46,"class":47},{"id":320,"slug":321,"hasResults":11,"nctId":322,"briefTitle":323,"officialTitle":324,"acronym":325,"eligibilityCriteria":326,"healthyVolunteers":16,"sex":327,"minAge":56,"maxAge":328,"enrollmentInfo":329,"targetDuration":4,"studyType":23,"phases":331,"briefSummary":332,"conditions":333,"keywords":337,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":342,"lastUpdatePostDateStruct":343,"startDateStruct":345,"completionDateStruct":347,"leadSponsor":349,"locationsCount":48},"100618096","bfr-rope-training-in-male-volleyball-players-100618096","NCT07327177","BFR Rope Training in Male Volleyball Players","The Effects of Blood Flow Restriction Rope Training on Athletic Performance, Muscle Strength, and Hypertrophy in Male Volleyball Players","8wBFR_rope","Inclusion Criteria:\n\n* Being healthy\n* Male volleyball athletes\n* Willing to maintain the intervention for all sessions\n\nExclusion Criteria:\n\n* Being under 18 years old\n* Having a chronic disease\n* Contraindications for exercise","MALE","25 Years",{"count":330,"type":22},26,[25],"The study will be conducted during the preparatory period of the volleyball players and will span eight weeks. Throughout this period, athletes will continue their regular volleyball training four days per week, while the experimental group (n = 10) will perform rope training with blood flow restriction (BFR) twice per week, and the control group (n = 10) will perform the same rope training without BFR. Assessments will be carried out at the beginning of the 8-week period (pre-test) and at the end of the intervention (post-test). For both groups, all exercises will target the upper-extremity muscle groups. During the study, participants will be instructed to avoid consuming any medications, engaging in additional strenuous physical activities, and using any techniques or ergogenic aids that might influence the results. In both testing sessions, a standardized warm-up protocol will be implemented, consisting of a 5-minute treadmill run at 9 km\u002Fh on a Sprint Runner device (Hoggan Health Industries, Draper, UT), followed by 3 minutes of light full-body stretching. This warm-up procedure will be applied consistently across both groups to ensure standardization.",[334,335,336],"Volleyball","Performance","Power",[338,339,340,341],"blood flow restriction","rope","volleyball","hypertrophy","2025-12-26",{"date":344,"type":40},"2026-01-08",{"date":346,"type":22},"2025-12-11",{"date":348,"type":22},"2026-03-05",{"name":46,"class":47},{"id":351,"slug":352,"hasResults":11,"nctId":353,"briefTitle":354,"officialTitle":355,"acronym":4,"eligibilityCriteria":356,"healthyVolunteers":16,"sex":17,"minAge":56,"maxAge":57,"enrollmentInfo":357,"targetDuration":4,"studyType":23,"phases":359,"briefSummary":360,"conditions":361,"keywords":4,"overallStatus":137,"whyStopped":4,"lastUpdateSubmitDate":346,"lastUpdatePostDateStruct":363,"startDateStruct":365,"completionDateStruct":366,"leadSponsor":368,"locationsCount":48},"100615861","diaphragmatic-release-for-low-back-pain-100615861","NCT07298109","Diaphragmatic Release for Low Back Pain","Investigating the Effectiveness of Diaphragmatic Release in Patients With Low Back Pain.","Inclusion Criteria:\n\n* Being between 18-65 years of age\n* Having been diagnosed with chronic non-specific lower back pain (pain between the gluteal folds and the 12th ribs lasting at least 12 weeks and without a known pathoanatomical cause)\n* Being willing to participate in the study\n\nExclusion Criteria:\n\n* Psychological disorders, mental disorders, cancer, and severe depression\n* History of primary or metastatic spinal malignancy or spinal fracture\n* Neurological disease (Hemiplegia, Multiple Sclerosis, Parkinson's, etc.)\n* Having been diagnosed with advanced osteoporosis\n* Having undergone previous surgery or had an acute infection in the lumbar region",{"count":358,"type":22},42,[25],"Low back pain is one of the most common musculoskeletal disorders, significantly affecting the quality of life of individuals. In non-specific low back pain, a lack of stabilization in the core region negatively impacts the performance of activities. The diaphragm forms the framework of the core region, and its dysfunction can contribute to both respiratory problems and low back pain. This study will investigate the effects of diaphragm relaxation, added to spinal stabilization exercises, on pain, disability, quality of life, central sensitization, and trunk muscle endurance.",[225,362],"Diaphragm; Relaxation",{"date":364,"type":40},"2025-12-23",{"date":346,"type":40},{"date":367,"type":22},"2026-12-15",{"name":46,"class":47},{"id":370,"slug":371,"hasResults":11,"nctId":372,"briefTitle":373,"officialTitle":374,"acronym":4,"eligibilityCriteria":375,"healthyVolunteers":16,"sex":17,"minAge":376,"maxAge":4,"enrollmentInfo":377,"targetDuration":4,"studyType":60,"phases":4,"briefSummary":378,"conditions":379,"keywords":4,"overallStatus":137,"whyStopped":4,"lastUpdateSubmitDate":381,"lastUpdatePostDateStruct":382,"startDateStruct":384,"completionDateStruct":386,"leadSponsor":388,"locationsCount":48},"100612129","comparison-of-patients-with-copd-and-prism-100612129","NCT07249567","Comparison of Patients With COPD and PRISM","Comparison of Respiratory and Peripheral Muscle Strength, Exercise Capacity, and Muscle Oxygenation in Individuals With COPD and PRISM","Inclusion Criteria:\n\nFor the COPD group:\n\n* Being \\>40 years old,\n* Being diagnosed with COPD,\n* Being clinically stable,\n* Volunteering to participate in the study.\n\nFor the PRISm group:\n\n* Being \\>40 years old,\n* Being diagnosed with PRISm,\n* Volunteering to participate in the study.\n\nFor the healthy control group:\n\n* Being \\>40 years old,\n* Volunteering to participate in the study.\n\nExclusion Criteria:\n\nFor the COPD group:\n\n* Having severe orthopedic, neurological, or cardiac diseases,\n* Being in a COPD exacerbation,\n* Having a comorbid lung disease,\n* Being on clinically unstable medication,\n* Voluntarily not participating in the study.\n\nFor the PRISm group:\n\n* Being diagnosed with COPD,\n* Having severe orthopedic, neurological, or cardiac diseases,\n* Having a comorbid lung disease,\n* Voluntarily not participating in the study.\n\nFor the healthy control group:\n\n* Having a known chronic disease,\n* Voluntarily not participating in the study.","40 Years",{"count":192,"type":22},"COPD is a preventable and treatable lung disease characterized by persistent and progressive airflow limitation. PRISm, on the other hand, is a spirometry pattern that does not meet COPD diagnostic criteria despite symptoms and functional impairments, but requires maintenance. PRISm can predispose to the development of COPD and exacerbations, and can reduce exercise capacity by reducing respiratory function and oxygen consumption. There are no studies in the literature comparing respiratory muscle strength, peripheral muscle strength, and oxygenation in PRISm, COPD, and healthy individuals. Therefore, this study aimed to evaluate these parameters and compare them with healthy individuals.",[380],"COPD","2025-11-18",{"date":383,"type":40},"2025-11-25",{"date":385,"type":40},"2025-10-05",{"date":387,"type":22},"2026-11-30",{"name":46,"class":47},{"id":390,"slug":391,"hasResults":11,"nctId":392,"briefTitle":393,"officialTitle":394,"acronym":4,"eligibilityCriteria":395,"healthyVolunteers":16,"sex":17,"minAge":396,"maxAge":170,"enrollmentInfo":397,"targetDuration":4,"studyType":23,"phases":398,"briefSummary":399,"conditions":400,"keywords":404,"overallStatus":137,"whyStopped":4,"lastUpdateSubmitDate":410,"lastUpdatePostDateStruct":411,"startDateStruct":413,"completionDateStruct":415,"leadSponsor":417,"locationsCount":48},"100593097","the-effects-of-scapular-stabilization-exercises-in-traditional-archery-athletes-100593097","NCT07002008","The Effects of Scapular Stabilization Exercises in Traditional Archery Athletes","The Effects of Scapular Stabilization Exercises on Shooting Accuracy and Upper Extremity Performance in Traditional Archery Athletes: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Aged 15 to 35 years\n\nLicensed traditional archers with at least 2 years of experience\n\nRegular participation in training programs\n\nWillingness to participate and provide informed consent\n\nExclusion Criteria:\n\n* History of upper extremity orthopedic surgery in the past year\n\nExisting musculoskeletal disorders in the upper extremity\n\nPresence of any neurological disease","15 Years",{"count":108,"type":22},[25],"This randomized controlled trial aims to investigate the effects of an 8-week scapular stabilization exercise program on shooting accuracy and upper extremity performance in athletes engaged in traditional archery. Thirty licensed archers aged between 15 and 35, with at least 2 years of experience, will be randomly assigned to an intervention group or a control group. The intervention group will receive scapular stabilization exercises in addition to their regular training, while the control group will continue their usual training routine. Pre- and post-intervention evaluations will assess upper extremity strength, stability, proprioception, and shooting performance.",[401,402,403],"Athletes","Exercise","Archery",[405,406,407,408,35,409,34],"traditional archery","scapular stabilization","shooting performance","strength","endurance","2025-07-04",{"date":412,"type":40},"2025-07-10",{"date":414,"type":40},"2025-05-01",{"date":416,"type":22},"2025-07",{"name":46,"class":47},{"id":419,"slug":420,"hasResults":11,"nctId":421,"briefTitle":422,"officialTitle":423,"acronym":4,"eligibilityCriteria":424,"healthyVolunteers":16,"sex":327,"minAge":56,"maxAge":170,"enrollmentInfo":425,"targetDuration":4,"studyType":23,"phases":426,"briefSummary":427,"conditions":428,"keywords":4,"overallStatus":137,"whyStopped":4,"lastUpdateSubmitDate":430,"lastUpdatePostDateStruct":431,"startDateStruct":433,"completionDateStruct":435,"leadSponsor":437,"locationsCount":48},"100589820","myofascial-release-techniques-in-football-players-100589820","NCT06959381","Myofascial Release Techniques in Football Players","Investigation of Acute Effects of Myofascial Release Techniques on Jumping Performance, Balance, and Proprioception in Football Players","Inclusion Criteria:\n\n* Being between the ages of 18-35\n* Being able to communicate in Turkish\n* Being willing to participate in the study.\n* Being a licensed football player\n\nExclusion Criteria:\n\n* Those with a body mass index of 30 kg\u002Fm² or higher\n* Those with a history of lower extremity surgery in the last 6 months\n* Those with cardiac, musculoskeletal, vestibular, and neurological problems\n* Those with mental, perceptual problems (Mini-mental test score \\\u003C24)",{"count":244,"type":22},[25],"Fascial tissue ensures optimal function and mobility by providing gliding and force transfer during movement. However, fascial order can be disrupted in cases such as overuse and trauma. Therefore, treatment of fascial tissue is important. Therefore, this study aimed to investigate the effects of different myofascial release techniques on jumping performance, flexibility, balance, and proprioception in amateur football players.",[429],"Fasciae (Anatomy)--Inflammation","2025-06-11",{"date":432,"type":40},"2025-06-15",{"date":434,"type":40},"2025-04-28",{"date":436,"type":22},"2025-12-31",{"name":46,"class":47},{"id":439,"slug":440,"hasResults":11,"nctId":441,"briefTitle":442,"officialTitle":443,"acronym":4,"eligibilityCriteria":444,"healthyVolunteers":11,"sex":17,"minAge":56,"maxAge":376,"enrollmentInfo":445,"targetDuration":4,"studyType":23,"phases":446,"briefSummary":447,"conditions":448,"keywords":451,"overallStatus":137,"whyStopped":4,"lastUpdateSubmitDate":454,"lastUpdatePostDateStruct":455,"startDateStruct":457,"completionDateStruct":459,"leadSponsor":461,"locationsCount":48},"100592281","acute-effects-of-myofascial-release-in-individuals-with-text-neck-syndrome-100592281","NCT06991387","Acute Effects of Myofascial Release in Individuals With Text Neck Syndrome","Exploring the Short-Term Effects of Myofascial Release in Text Neck Syndrome","Inclusion Criteria:\n\n* Aged between 18 and 40 years (inclusive)\n* Uses a mobile device for ≥3 hours\u002Fday\n* Reports at least 3 out of the following 6 symptoms associated with Text Neck Syndrome (TNS):\n\nNeck pain Shoulder pain Back pain Headache Insomnia Numbness\u002Ftingling in hands\n\n-Voluntarily agrees to participate and provides informed consent\n\nExclusion Criteria:\n\n* History of congenital, traumatic, or surgical pathology affecting the cervical -------spine or shoulder region\n* Neurological disorders that cause headaches (e.g., migraines due to underlying neurological conditions)\n* Presence of inflammatory, infectious spinal diseases, or diagnosed spinal deformities\n* Received trigger point injections in the cervical region within the past 6 months",{"count":5,"type":22},[25],"This study aims to investigate the acute effects of myofascial release therapy on neck pain, functional status, and cervical range of motion in individuals diagnosed with Text Neck Syndrome (TNS). Text Neck Syndrome is increasingly prevalent due to excessive use of smartphones and other digital devices, particularly among young adults. The intervention will consist of a single session of standardized myofascial release techniques applied to the cervical and thoracic regions. The primary outcome will be neck pain intensity measured using the Numeric Rating Scale (NRS-11), while secondary outcomes will include cervical range of motion and the modified Neck Disability Index (NDI). Assessments will be performed immediately before and after the intervention. The study will be conducted with volunteer participants between the ages of 18 and 40, who use mobile devices for more than 3 hours per day and meet the diagnostic criteria for TNS",[449,28,450],"Text Neck Posture","Myofascial Release Technique",[452,28,453],"Text Neck Syndrome","Myofascial Release","2025-06-03",{"date":456,"type":40},"2025-06-05",{"date":458,"type":40},"2025-05-10",{"date":460,"type":22},"2025-08",{"name":46,"class":47},{"id":463,"slug":464,"hasResults":11,"nctId":465,"briefTitle":466,"officialTitle":467,"acronym":4,"eligibilityCriteria":468,"healthyVolunteers":11,"sex":17,"minAge":56,"maxAge":469,"enrollmentInfo":470,"targetDuration":4,"studyType":23,"phases":471,"briefSummary":472,"conditions":473,"keywords":477,"overallStatus":137,"whyStopped":4,"lastUpdateSubmitDate":482,"lastUpdatePostDateStruct":483,"startDateStruct":485,"completionDateStruct":487,"leadSponsor":489,"locationsCount":48},"100564336","effectiveness-of-the-fascial-distortion-model-in-temporomandibular-disorders-a-randomized-sham-controlled-trial-100564336","NCT06627855","Effectiveness of the Fascial Distortion Model in Temporomandibular Disorders: A Randomized Sham-controlled Trial","Investigation of the Effectiveness of Manual Therapy Based on Fascial Distortion Model in Individuals With Temporomandibular Disorder: A Randomized Sham-controlled Trial","Inclusion Criteria:\n\n* Having temporomandibular joint complaints and being diagnosed with temporomandibular disorder according to the Diagnostic Criteria for Temporomandibular Disorders Axis I\n* Understand and be willing to answer assessment questions\n* A temporomandibular joint complaint for the last three months\n* Pain in the jaw, face or neck\n\nExclusion Criteria:\n\n* Has a systemic disease (neurological, rheumatologic, oncologic, etc.) that may affect the temporomandibular joint, cervical spine and\u002For assessment\n* Any history of trauma that may have affected the cranio-cervico-facial region\n* Having undergone any surgical intervention in the cranio-cervico-facial region within the last six months\n* Receiving surgical treatment, medical treatment, splint therapy or physiotherapy for temporomandibular disorder in the last month\n* Radiotherapy in the head and neck region\n* Pregnancy or breastfeeding\n* Exercise therapy for craniocervical posture for the last month","64 Years",{"count":108,"type":22},[25],"The aim of the study was to investigate the effectiveness of Manual Therapy Based on the Fascial Distortion Model in individuals with temporomandibular disorders compared to sham control. Individuals diagnosed with temporomandibular disorder will be randomly assigned to groups as Group 1 (Manual Therapy Based on Fascial Distortion Model) and Group 2 (Sham Control). Head posture, cervical and temporomandibular joint range of motion, cervical muscle performance, pain intensity, pressure pain thresholds, temporomandibular disorder severity, disability, dysfunction, health-related quality of life, kinesiophobia, and central sensitization will be assessed.",[474,475,476],"Temporomandibular Disorders (TMD)","Manual Therapy","Fascial Distortion",[478,479,480,481],"manual therapy","fascial distortion model","temporomandibular disorders","head posture","2025-03-11",{"date":484,"type":40},"2025-03-12",{"date":486,"type":40},"2024-10-03",{"date":488,"type":22},"2025-12",{"name":46,"class":47},{"id":491,"slug":492,"hasResults":11,"nctId":493,"briefTitle":494,"officialTitle":495,"acronym":4,"eligibilityCriteria":496,"healthyVolunteers":16,"sex":81,"minAge":56,"maxAge":328,"enrollmentInfo":497,"targetDuration":4,"studyType":23,"phases":499,"briefSummary":500,"conditions":501,"keywords":505,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":510,"lastUpdatePostDateStruct":511,"startDateStruct":513,"completionDateStruct":514,"leadSponsor":516,"locationsCount":48},"100575858","model-supported-breast-examination-training-for-midwifery-students-100575858","NCT06777745","Model Supported Breast Examination Training for Midwifery Students","Improvement of Breast Examination Skills of Midwifery Students: Model Supported Education Study","Inclusion Criteria:\n\n* Being a 2nd, 3rd or 4th year midwifery student at Karabük University Faculty of Health Sciences\n* Being between the ages of 18-25\n* Voluntarily agreeing to participate in the study\n* Being a citizen of the Republic of Turkey\n\nExclusion Criteria:\n\n* Leave whenever you want without working.",{"count":498,"type":22},64,[25],"Breast cancer is the most common cancer among women worldwide and early detection significantly improves treatment success. Screening methods used for early detection include breast self-examination (BSE), clinical breast examination (CBE) and mammography. It is critical for midwifery students to learn CCM and teach this method to women. CPM allows women to recognise early signs through breast self-examination. This method is simple and inexpensive and can be applied without requiring much time and labour. Practical training of midwifery students helps them to ensure the effectiveness and correct application of this method. The use of breast examination models during the training process gives students practical experience in detecting signs of breast cancer, such as nipple depression, discharge, asymmetry of the breasts and the appearance of orange peel. In addition, midwifery students can develop their clinical skills by having the opportunity to make mistakes and gain hands-on experience in a safe environment. This process can contribute to increasing early diagnosis rates and improving treatment processes.The sample of this pre-test, post-test, follow-up randomised controlled study consisted of 64 midwifery students (experimental=32, and control=32). Data will be collected with Personal Information Form (PIF), Breast Examination Skills Assessment Form (BESAF), Self-Confidence Scale (SC) and Student Satisfaction and Confidence in Learning Scale (SCSLS). After obtaining the consent of the students in the experimental group, pre-test data will be obtained by filling out the 'Personal Information Form', 'Self-Confidence Scale' and 'Student Satisfaction and Confidence in Learning Scale'. Then, theoretical information will be given and the examination stages such as determining the area to be examined, manual examination of the area, examination method, nipple examination and detection of malignant formations in the breast will be explained practically in the breast examination model in the laboratory environment. Students will be taken in groups of 10, and after the application is explained, each student will perform the breast examination and evaluation individually. Approximately 15 minutes will be allocated for each student. Two weeks after the breast model application, the same students will be taken to the laboratory and asked to perform all the examination steps again. While the students are performing the examination steps, the researcher will mark the complete and incomplete applications on the 'Breast Examination Skill Evaluation Form' and the missing steps will be explained to the students and they will be asked to complete them. At the same time, 'Self-confidence Scale' and 'Student Satisfaction and Confidence in Learning Scale' will be filled out for the post-test. Then, two weeks later, the 'Self-Confidence Scale' and 'Student Satisfaction and Confidence in Learning Scale' will be filled out again for the final post-test. After obtaining the consent of the students in the control group, pre-test data will be collected by applying 'Personal Information Form', 'Self-Confidence Scale' and 'Student Satisfaction and Confidence in Learning Scale' to the students. Then, the students will be given theoretical information and a video will be shown to them, which includes examination stages such as determining the area to be examined, manual examination of the area, examination method, nipple examination and detection of malignant formations in the breast.\n\nTwo weeks later, the students will be taken to the laboratory environment and will be asked to perform the application steps in line with the theoretical course they have taken. While the students are performing the examination steps, the researcher will mark the complete and incomplete applications on the 'Breast Examination Skill Evaluation Form', then the missing steps will be explained to the students and they will be asked to complete them. In the post-test phase, the 'Self-Confidence Scale' and the 'Student Satisfaction and Confidence in Learning Scale' will be administered to the students again. Two weeks after this process, the same scales will be filled in again for the final post-test.",[502,503,198,504],"Breast Self-Examination","Midwifery Students Education","Self-Confidence",[506,507,508,509],"Midwife","student","breast examination","model","2025-01-15",{"date":512,"type":40},"2025-01-16",{"date":510,"type":22},{"date":515,"type":22},"2025-08-15",{"name":46,"class":47},""]