[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Kutahya Health Sciences University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":660},{"pageToken":4,"total":5,"offset":6,"count":7,"results":8},null,40,0,25,[9,42,73,101,128,155,189,217,243,272,296,319,347,373,391,415,438,461,493,513,539,563,587,605,632],{"id":10,"slug":11,"hasResults":12,"nctId":13,"briefTitle":14,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":12,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":27,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":41},"100631930","the-effect-of-internal--or-external-focused-exercise-training-administered-in-conjunction-with-a-cognitive-task-on-walking-balance-and-cognitive-functions-in-individuals-with-multiple-sclerosis-100631930",false,"NCT07507084","The Effect of Internal- or External-Focused Exercise Training, Administered in Conjunction With a Cognitive Task, on Walking, Balance, and Cognitive Functions in Individuals With Multiple Sclerosis","Inclusion Criteria:\n\n* Diagnosis of Multiple Sclerosis according to the revised McDonald criteria\n* Aged between 20 and 60 years\n* Ability to understand and follow simple instructions\n* Ability to stand and walk independently or with an assistive device\n* Ability to speak and understand Turkish\n* Score of ≥21 on the Montreal Cognitive Assessment (MoCA)\n* Willingness to participate in the study\n\nExclusion Criteria:\n\n* MS relapse within the last 30 days\n* Presence of any other neurological disease besides Multiple Sclerosis\n* Any musculoskeletal condition that may affect walking or balance\n* History of uncontrolled cardiorespiratory conditions within the last 3 months (e.g., hypertension, arrhythmia, tachycardia, or acute cardiopulmonary events)\n* Severe visual or hearing impairment","ALL","18 Years","65 Years",{"count":5,"type":20},"ESTIMATED","INTERVENTIONAL",[23],"NA","This interventional clinical trial aims to investigate the effects of internal and external focus-based exercise training combined with cognitive dual-task training in individuals diagnosed with multiple sclerosis. The primary objective is to determine whether these exercise approaches improve gait, balance, and cognitive functions.\n\nThe main research questions are:\n\nDoes dual-task training combined with internal focus-based exercises improve gait, balance, and cognitive performance? Does dual-task training combined with external focus-based exercises lead to greater improvements compared to internal focus strategies?\n\nParticipants will be divided into two groups, and the researchers will compare the effects of internal focus-based and external focus-based dual-task exercise training on functional outcomes.\n\nParticipants will:\n\nPerform structured exercise sessions under the supervision of a physiotherapist Engage in dual-task activities by combining motor exercises with simple cognitive tasks (e.g., backward counting, word generation) Participate in an 8-week training program, with sessions held twice a week lasting approximately 45-60 minutes Undergo assessments of gait, balance, and cognitive function before and after the intervention\n\nThis study does not involve invasive procedures or biological sample collection. The findings are expected to contribute to the development of more effective dual-task rehabilitation strategies for individuals with multiple sclerosis.",[26],"Multiple Sclerosis",[28],"multiple sclerosis, dual-task training, internal focus, external focus, gait, balance, cognitive function, exercise therapy","RECRUITING","2026-06-29",{"date":32,"type":33},"2026-07-01","ACTUAL",{"date":35,"type":33},"2026-03-15",{"date":37,"type":20},"2028-08-30",{"name":39,"class":40},"Kutahya Health Sciences University","OTHER",1,{"id":43,"slug":44,"hasResults":12,"nctId":45,"briefTitle":46,"officialTitle":47,"acronym":48,"eligibilityCriteria":49,"healthyVolunteers":12,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":50,"targetDuration":4,"studyType":21,"phases":52,"briefSummary":53,"conditions":54,"keywords":58,"overallStatus":64,"whyStopped":4,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":41},"100642152","mobile-health-application-for-family-caregivers-in-home-palliative-care-100642152","NCT07654998","Mobile Health Application for Family Caregivers in Home Palliative Care","Effectiveness of a Mobile Health Application for Family Caregivers of Patients Receiving Home Palliative Care: A Randomized Controlled Trial","CARE-Mobile","Inclusion Criteria:\n\n* Family caregiver of a patient receiving home palliative care services.\n* Aged 18 years or older.\n* Providing unpaid care to the patient for at least 3 months.\n* Able to read and understand Turkish.\n* Owns or has regular access to a smartphone compatible with the mobile application.\n* Willing to participate and provide written informed consent.\n\nExclusion Criteria:\n\n* Professional or paid caregivers.\n* Participation in another structured caregiver support program during the study period.\n* Cognitive, visual, or hearing impairments that would prevent effective use of the mobile application.\n* Inability to complete study assessments.\n* Withdrawal of consent at any stage of the study.",{"count":51,"type":20},120,[23],"Family caregivers play a central role in providing daily care for patients receiving home palliative care. However, caregiving responsibilities may lead to increased burden, stress, and difficulties in symptom management and care coordination. Mobile health (mHealth) interventions may provide accessible education, symptom monitoring, and decision-support resources to improve caregiver outcomes and patient care.\n\nThe aim of this randomized controlled trial is to evaluate the effectiveness of a mobile health application developed for family caregivers of patients receiving home palliative care. The primary outcome is caregiver competence. Secondary outcomes include caregiver burden, self-efficacy, patient symptom burden, emergency department visits, and hospitalizations.\n\nA total of 120 family caregivers will be randomly assigned to either the intervention group, which will use the mobile health application for 6 weeks in addition to usual care, or the control group, which will receive usual care alone. Outcomes will be assessed at baseline, post-intervention (Week 6), and follow-up (Week 18).",[55,56,57],"Palliative Care","Cancer","Caregiver",[59,60,61,62,63],"Mobile Health","Family Caregiver","Home Palliative Care","Caregiver Competence","Caregiver Burden","NOT_YET_RECRUITING","2026-06-23",{"date":67,"type":33},"2026-06-26",{"date":69,"type":20},"2026-06-10",{"date":71,"type":20},"2026-10-30",{"name":39,"class":40},{"id":74,"slug":75,"hasResults":12,"nctId":76,"briefTitle":77,"officialTitle":78,"acronym":4,"eligibilityCriteria":79,"healthyVolunteers":12,"sex":16,"minAge":18,"maxAge":4,"enrollmentInfo":80,"targetDuration":4,"studyType":21,"phases":82,"briefSummary":83,"conditions":84,"keywords":86,"overallStatus":64,"whyStopped":4,"lastUpdateSubmitDate":93,"lastUpdatePostDateStruct":94,"startDateStruct":96,"completionDateStruct":98,"leadSponsor":100,"locationsCount":41},"100642824","nurse-led-telehealth-frailty-management-in-older-adults-100642824","NCT07634406","Nurse-Led Telehealth Frailty Management in Older Adults","The Effect of a Nurse-Led Telehealth-Supported Multicomponent Frailty Management Program on Frailty and Functional Status in Older Adults Living at Home: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Aged 65 years or older\n* Living at home and not receiving institutional care\n* Frail or at risk of frailty\n* Having sufficient hearing and cognitive ability to communicate by telephone\n* Able to read, understand, and communicate in Turkish\n* Providing written informed consent\n\nExclusion Criteria:\n\n* Having advanced cognitive impairment such as dementia\n* Having hearing or speech problems that prevent communication\n* Being bedridden\n* Being in the terminal stage of illness\n* Participating in another intervention or education program at the same time\n* Having a serious physical or psychiatric condition that may prevent regular participation in the intervention",{"count":81,"type":20},100,[23],"Frailty is an important geriatric syndrome associated with reduced physiological reserve, functional decline, falls, hospitalization, and increased health care use among older adults. This randomized controlled trial aims to evaluate the effect of a nurse-led telehealth-supported multicomponent frailty management program on frailty level and functional status in older adults living at home.\n\nThe study will be conducted as a single-center, two-arm, parallel-group randomized controlled trial. A total of 100 older adults aged 65 years and older who are living at home and are frail or at risk of frailty will be randomly assigned to either the intervention group or the control group in a 1:1 ratio.\n\nParticipants in the intervention group will receive an 6-week nurse-led telehealth-supported frailty management program, including weekly telephone counseling and individualized follow-up. Participants in the control group will continue usual care. Data will be collected at baseline, at 6 weeks, and at 18 weeks. The primary outcome is frailty level measured using the FRAIL Scale. Secondary outcomes include functional status, depressive symptoms, number of falls, emergency department visits, and hospitalizations.",[85],"Frailty",[87,88,89,90,91,92],"Older adults","Telehealth","Nursing intervention","Frailty management","Functional status","Home care","2026-06-12",{"date":95,"type":33},"2026-06-16",{"date":97,"type":20},"2026-06-05",{"date":99,"type":20},"2026-10-15",{"name":39,"class":40},{"id":102,"slug":103,"hasResults":12,"nctId":104,"briefTitle":105,"officialTitle":106,"acronym":107,"eligibilityCriteria":108,"healthyVolunteers":12,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":109,"targetDuration":4,"studyType":110,"phases":4,"briefSummary":111,"conditions":112,"keywords":114,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":121,"lastUpdatePostDateStruct":122,"startDateStruct":124,"completionDateStruct":125,"leadSponsor":127,"locationsCount":41},"100643702","early-prediction-of-icu-hypotension-using-machine-learning-100643702","NCT07627607","Early Prediction of ICU Hypotension Using Machine Learning","A Prospective Observational Machine Learning Study for the Early Prediction of Hypotension in Adult Intensive Care Unit Patients","ICU-HypoAI","Inclusion Criteria:\n\n* Age 18 years or older\n* Admission to the adult intensive care unit during the study period\n* Length of stay in the intensive care unit of at least 24 hours\n* Availability of routine intensive care unit monitoring data\n* Availability of non-invasive blood pressure and heart rate measurements recorded during ICU monitoring\n* Availability of medication-dose and\u002For fluid-balance records during ICU monitoring\n\nExclusion Criteria:\n\n* Age younger than 18 years\n* Length of stay in the intensive care unit of less than 24 hours\n* Absence of usable blood pressure monitoring data\n* Records with irrecoverable timestamp inconsistencies\n* Insufficient monitoring duration for feature construction and future outcome labeling",{"count":81,"type":20},"OBSERVATIONAL","This prospective observational study aims to develop and internally validate a machine learning model for the early prediction of hypotension in adult intensive care unit patients. The model will use routinely collected non-invasive vital signs, heart rate, medication-dose records, and fluid-balance data recorded during standard ICU care. No intervention will be assigned by the study, and patient management will not be changed according to the model output. The primary aim is to predict hypotension 30 minutes before its occurrence; shorter 5- and 15-minute prediction horizons will also be evaluated.",[113],"Hypotension",[115,116,117,118,119,120],"Intensive Care Unit","Machine Learning","Artificial Intelligence","Non-Invasive Blood Pressure","Hemodynamic Monitoring","Prediction Model","2026-06-04",{"date":123,"type":33},"2026-06-08",{"date":35,"type":33},{"date":126,"type":20},"2026-07-15",{"name":39,"class":40},{"id":129,"slug":130,"hasResults":12,"nctId":131,"briefTitle":132,"officialTitle":133,"acronym":134,"eligibilityCriteria":135,"healthyVolunteers":12,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":136,"targetDuration":4,"studyType":21,"phases":138,"briefSummary":139,"conditions":140,"keywords":142,"overallStatus":64,"whyStopped":4,"lastUpdateSubmitDate":121,"lastUpdatePostDateStruct":149,"startDateStruct":150,"completionDateStruct":152,"leadSponsor":154,"locationsCount":41},"100643619","nurse-led-caregiver-support-program-in-home-palliative-care-100643619","NCT07593729","Nurse-Led Caregiver Support Program in Home Palliative Care","Effect of a Nurse-Led Caregiver Support Program on Caregiver Competency and Healthcare Utilization Among Family Caregivers in Home Palliative Care: A Randomized Controlled Trial","CARE-PAL","Inclusion Criteria:\n\n* Adult family caregivers of patients receiving home palliative care services\n* Age 18 years or older\n* Being the primary caregiver responsible for the patient's daily care\n* Ability to communicate in Turkish\n* Willingness to participate in the study\n\nExclusion Criteria:\n\n* Professional or paid caregivers\n* Caregivers with severe cognitive impairment or severe psychiatric disorders\n* Inability to participate in follow-up assessments",{"count":137,"type":20},150,[23],"This randomized controlled trial aims to evaluate the effect of a nurse-led caregiver support program on caregiver competency and healthcare utilization among family caregivers of patients receiving home palliative care. Family caregivers in the intervention group will receive a structured 6-week nurse-led support program including face-to-face education, weekly telephone coaching, caregiver guidance materials, and decision support for symptom management and healthcare utilization. The control group will continue to receive routine home palliative care services. Primary outcome is caregiver competency. Secondary outcomes include caregiver burden, self-efficacy, patient symptom burden, emergency department visits, and hospitalizations.",[55,63,141],"Home Care",[143,144,145,92,146,147,148],"Nurse-led intervention","Family caregiver","Caregiver competency","Randomized controlled trial","Palliative care","Healthcare utilization",{"date":123,"type":33},{"date":151,"type":20},"2026-05-12",{"date":153,"type":20},"2026-09-30",{"name":39,"class":40},{"id":156,"slug":157,"hasResults":12,"nctId":158,"briefTitle":159,"officialTitle":160,"acronym":161,"eligibilityCriteria":162,"healthyVolunteers":12,"sex":16,"minAge":163,"maxAge":164,"enrollmentInfo":165,"targetDuration":4,"studyType":21,"phases":167,"briefSummary":168,"conditions":169,"keywords":173,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":181,"lastUpdatePostDateStruct":182,"startDateStruct":184,"completionDateStruct":186,"leadSponsor":188,"locationsCount":41},"100622832","espb-vs-spsip-for-postoperative-analgesia-after-cabg-100622832","NCT07388745","ESPB vs SPSIP for Postoperative Analgesia After CABG","A Randomized Trial Comparing Erector Spinae Plane Block Versus Serratus Posterior Superior Intercostal Plane Block for Postoperative Analgesic Efficacy in Patients Undergoing Coronary Artery Bypass Graft Surgery","ESP-SPSIP-CABG","Inclusion Criteria:\n\n* Age 45-85 years\n* Scheduled for elective coronary artery bypass graft (CABG) surgery\n* American Society of Anesthesiologists (ASA) I-II-III\n* Patients who provide written informed consent and agree to participate in the study\n\nExclusion Criteria:\n\n* Emergency cases\n* ASA IV-V\n* Known allergy to local anesthetics\n* Coagulopathy (platelet count \\\u003C100,000\u002Fmm³, INR \\>1.5, aPTT \\>1.5× normal)\n* Infection at the block injection site\n* Pregnancy\n* Patients who do not provide written informed consent or decline to participate after being informed","45 Years","85 Years",{"count":166,"type":20},64,[23],"This prospective, randomized, active-controlled, double-blind, parallel-group study compares the postoperative analgesic efficacy and safety of ultrasound-guided bilateral Erector Spinae Plane Block (ESPB) versus bilateral Serratus Posterior Superior Intercostal Plane Block (SPSIPB) in adult patients (45-85 years, ASA I-III) undergoing elective coronary artery bypass graft surgery. The primary outcome is postoperative pain intensity assessed by Numeric Rating Scale (NRS) at 2, 4, 8, 16, 24, and 48 hours after surgery. Secondary outcomes include intraoperative fentanyl\u002Fremifentanil consumption, postoperative morphine consumption, patient-controlled analgesia (PCA) demand\u002Fdelivery parameters (if PCA is used), need for rescue analgesics, extubation and mobilization times, peak inspiratory flow measured by incentive spirometry at predefined time points, ICU and hospital length of stay, recovery quality (QoR-15 at 0, 24, and 48 hours), mortality, and block-related adverse events.",[170,171,172],"Coronary Arterial Disease","Coronary Artery Bypass Grafting (CABG) Surgery","Postoperative Pain Management",[174,175,176,177,178,179,180],"Coronary Artery Bypass Grafting","Erector Spinae Plane Block","Serratus Posterior Superior Intercostal Plane Block","Regional Anesthesia","Ultrasound-Guided Nerve Block","Postoperative Pain","Numeric Rating Scale","2026-05-10",{"date":183,"type":33},"2026-05-13",{"date":185,"type":33},"2026-03-01",{"date":187,"type":20},"2026-08-31",{"name":39,"class":40},{"id":190,"slug":191,"hasResults":12,"nctId":192,"briefTitle":193,"officialTitle":194,"acronym":4,"eligibilityCriteria":195,"healthyVolunteers":12,"sex":16,"minAge":17,"maxAge":196,"enrollmentInfo":197,"targetDuration":199,"studyType":110,"phases":4,"briefSummary":200,"conditions":201,"keywords":203,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":209,"lastUpdatePostDateStruct":210,"startDateStruct":212,"completionDateStruct":214,"leadSponsor":216,"locationsCount":41},"100635924","effects-of-hemiplegic-shoulder-pain-on-upper-extremity-motor-function-trunk-control-fear-of-falling-mobility-and-indepence-in-activities-of-daily-living-in-patients-with-stroke-100635924","NCT07559006","Effects of Hemiplegic Shoulder Pain on Upper Extremity Motor Function, Trunk Control, Fear of Falling, Mobility and Indepence in Activities of Daily Living in Patients With Stroke","Effects of Hemiplegic Shoulder Pain on Body Structure and Activity in Patients With Stroke","Inclusion Criteria:\n\n* Having a diagnosis of stroke\n* Aged ≥ 18 years old\n* Mini Mental State Test score ≥ 24 points\n* Having a shoulder VAS score of 3 points or higher\n\nExclusion Criteria:\n\n* Having another neurological disease (except for stroke\n* Having communication deficits or neglect\n* Having a surgery upper or lower extremity in the last 6 months","80 Years",{"count":198,"type":20},62,"1 Day","This study aimed to examine the effects of hemiplegic shoulder pain on upper extremity motor assessment, trunk control, fear of falling, mobility, and functional indepedence patients with stroke.",[202],"Stroke",[204,205,206,207,208],"stroke","hemiplegic shoulder pain","trunk control","upper extremity","mobility","2026-04-26",{"date":211,"type":33},"2026-04-30",{"date":213,"type":33},"2026-03-20",{"date":215,"type":20},"2026-09-15",{"name":39,"class":40},{"id":218,"slug":219,"hasResults":12,"nctId":220,"briefTitle":221,"officialTitle":222,"acronym":4,"eligibilityCriteria":223,"healthyVolunteers":12,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":224,"targetDuration":4,"studyType":110,"phases":4,"briefSummary":226,"conditions":227,"keywords":229,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":235,"lastUpdatePostDateStruct":236,"startDateStruct":238,"completionDateStruct":240,"leadSponsor":242,"locationsCount":41},"100634778","predictors-of-functional-status-in-chronic-neck-pain-100634778","NCT07544108","Predictors of Functional Status in Chronic Neck Pain","Predictors of Functional Status in Chronic Non-Spesific Neck Pain","Inclusion Criteria:\n\n* patients aged 18-65\n* patients have experienced non-specific neck pain for at least 3 months, patients who are literate, and no cognitive impairment.\n\nExclusion Criteria:\n\n* patients with serious and secondary musculoskeletal diseases (inflammatory, neuropathic and malignancy)\n* patiens who have undergone spinal and abdominal surgery and trauma\n* patients who smoke\n* patients if any lung disease that will affect respiration,\n* patients with a body mass index greater than 40\n* patients who cannot operate.",{"count":225,"type":20},80,"Although it has been reported that these problems seen together with neck pain are related to functional limitations and disability, there is still insufficient evidence regarding the relationship between factors affecting functional status and chronic neck pain symptoms in individuals with chronic neck pain. Furthermore, a mixed methodology approach has not been used to comprehensively investigate this relationship. Identifying factors affecting functional status in CNP will help guide the prevention, treatment, and management of neck pain. Therefore, the aim of this study is to investigate the relationships between functional status and psychosocial and bodily functions in CNP.",[228],"Neck Pain",[230,231,232,233,234],"Chronic neck pain","neck disability","maximum inspiratory pressure","maximum expiratory pressure","anxiety","2026-04-22",{"date":237,"type":33},"2026-04-27",{"date":239,"type":33},"2025-10-20",{"date":241,"type":20},"2026-06-20",{"name":39,"class":40},{"id":244,"slug":245,"hasResults":12,"nctId":246,"briefTitle":247,"officialTitle":248,"acronym":4,"eligibilityCriteria":249,"healthyVolunteers":12,"sex":16,"minAge":250,"maxAge":251,"enrollmentInfo":252,"targetDuration":4,"studyType":21,"phases":253,"briefSummary":254,"conditions":255,"keywords":259,"overallStatus":64,"whyStopped":4,"lastUpdateSubmitDate":265,"lastUpdatePostDateStruct":266,"startDateStruct":268,"completionDateStruct":269,"leadSponsor":271,"locationsCount":4},"100635550","the-effect-of-body-percussion-training-on-neuromotor-performance-attention-and-functionality-in-adolescents-with-mild-intellectual-disability-100635550","NCT07554144","The Effect of Body Percussion Training on Neuromotor Performance, Attention, and Functionality in Adolescents With Mild Intellectual Disability","The Effect of Body Percussion Training on Neuromotor Performance, Attention, and Functionality in Adolescents With Mild Intellectual Disability: A Randomized Controlled Study","Inclusion Criteria:\n\n* Being an adolescent aged 14-19 attending high school (e.g., special education high school)\n* Having been diagnosed with mild intellectual disability (IQ range according to relevant psychological assessment)\n* Having communication skills sufficient to understand simple commands and adapt to work\n* Being able to perform basic daily living activities (toilet hygiene and management, bladder\u002Fbowel management, eating, bathing, personal hygiene, dressing, functional mobility, etc.) independently or with minimal support, regardless of the level of disability\n* Signing an informed consent form with family consent and\u002For legal guardian consent\n\nExclusion Criteria:\n\n* Painful musculoskeletal\u002Forthopedic (rheumatic, etc.) problems that may prevent physical participation in rhythm-based body percussion training, restrict movement during training, and cause pain\n* Cardiovascular problems (arrhythmia, hypertension, etc.) that may prevent participants from attending training during the study period\n* Diagnosis of moderate or severe intellectual disability\n* Presence of additional diagnoses such as autism spectrum disorder, cerebral palsy, or developmental coordination disorder\n* Participation in a systematic physical therapy program other than rhythm or motor training\n* Conditions affecting motor performance due to medical or surgical treatment (within the last 6 months)\n* Severe auditory and visual deficits that hinder communication and the ability to imitate movements\n* Individuals who cannot attend regularly during the study period due to personal or family reasons\n* The family\u002Fadolescent's desire to withdraw from the study of their own accord","14 Years","19 Years",{"count":7,"type":20},[23],"The aim of this randomized controlled trial is to investigate the effects of group-based rhythm-based body percussion training on neuromotor performance, attention, and functionality in adolescents with mild intellectual disability.\n\nThe study will be conducted in individuals aged 14-18 years with mild intellectual disability using a two-arm, parallel-group, evaluator-blind design. Participants will be assigned to experimental and control groups using a simple randomization method.\n\nThe experimental group will receive structured body percussion training twice a week for 45 minutes over 8 weeks. This training consists of rhythmic patterns including clapping, knee tapping, chest tapping, finger snapping, and foot tapping, and will be presented as a progressively advancing program with metronome accompaniment.\n\nThe control group will receive passive music listening without intervention for the same duration and frequency.\n\nParticipants will be evaluated at two time points: before and after the intervention. Evaluation tools include: The tests cover neuromotor performance with the Minnesota Hand Skills Test and the Four Square Step Test, rhythm coordination with the Metronome Synchronization Test, attention with the Stroop Test, and functionality with the World Health Organization Disability Assessment Chart 2.0.",[256,257,258],"Mild Cognitive Impairment","Attention Impaired","Adolescent Development",[256,260,261,262,263,264],"attention","neuromotor performance","functionality","adolescents","body percussion training","2026-04-21",{"date":267,"type":33},"2026-04-28",{"date":211,"type":20},{"date":270,"type":20},"2026-07-03",{"name":39,"class":40},{"id":273,"slug":274,"hasResults":12,"nctId":275,"briefTitle":276,"officialTitle":277,"acronym":4,"eligibilityCriteria":278,"healthyVolunteers":12,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":279,"targetDuration":4,"studyType":21,"phases":280,"briefSummary":281,"conditions":282,"keywords":284,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":288,"lastUpdatePostDateStruct":289,"startDateStruct":291,"completionDateStruct":293,"leadSponsor":295,"locationsCount":41},"100583405","effect-of-motor-imagery-training-on-pain-functionality-proprioception-and-kinesiophobia-in-partial-rotator-cuff-tear-100583405","NCT06875895","Effect of Motor Imagery Training on Pain, Functionality, Proprioception and Kinesiophobia in Partial Rotator Cuff Tear","Effect of Motor Imagery Training on Pain, Functionality, Proprioception and Kinesiophobia in Patients With Partial Rotator Cuff Tears","Inclusion Criteria:\n\n* Partial rotator cuff tear diagnosis.\n* Between the ages of 18-65\n* Patients experiencing pain for at least 4 weeks.\n* Having a valid score on the Mini Mental Test (\\>24)\n* Those without a history of any neurological or serious psychological illness.\n* Those who have not participated in a previous study on motor imagery training\n\nExclusion Criteria:\n\n* Complete rotator cuff tear or conditions requiring surgical intervention,\n* Participants who have received treatment with corticosteroids by any means in the previous 6 months,\n* Participants who have a rotator cuff tear due to acute traumatic conditions (proximal humerus fracture).",{"count":225,"type":20},[23],"The aim of this study is to investigate the effects of motor imagery training on pain, functionality, proprioception and kinesiophobia in patients with partial rotator cuff tears. Participants will be randomly assigned to traditional physiotherapy and motor imagery groups. Interventions will be performed with a physiotherapist for a total of 20 sessions for 4 weeks, 5 days a week. The intervention program will be determined by the Specialist Physical Therapy Physician. Data will be collected before the study, at the end of the training in the 4th week and at the 8th week (follow-up evaluation). Motor imagery ability will be assessed with the Movement Imagery Questionnaire (MIQ-R), pain will be assessed with the Numerical Assessment Scale for functionality with the DASH, proprioception will be assessed with the inclinometer and kinesiophobia will be assessed with the Tampa Kinesiophobia Scale.",[283],"Rotator Cuff Tears",[285,286,287],"Rotator Cuff","Exercise therapy","Imagery","2026-04-20",{"date":290,"type":33},"2026-04-23",{"date":292,"type":33},"2025-01-16",{"date":294,"type":20},"2026-05-03",{"name":39,"class":40},{"id":297,"slug":298,"hasResults":12,"nctId":299,"briefTitle":300,"officialTitle":300,"acronym":301,"eligibilityCriteria":302,"healthyVolunteers":12,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":303,"targetDuration":199,"studyType":110,"phases":4,"briefSummary":305,"conditions":306,"keywords":308,"overallStatus":64,"whyStopped":4,"lastUpdateSubmitDate":313,"lastUpdatePostDateStruct":314,"startDateStruct":315,"completionDateStruct":317,"leadSponsor":318,"locationsCount":41},"100634806","validity-and-reliability-of-the-turkish-version-of-the-breathing-vigilance-questionnaire-100634806","NCT07544472","Validity and Reliability of the Turkish Version of the 'Breathing Vigilance Questionnaire'","Breathe-VQ","Inclusion Criteria:\n\n* individuals without a self-reported diagnosis of respiratory and\u002For cardiac problems\n* individuals without a COVID-19 diagnosis and\u002For chronic COVID syndrome (\"long COVID\") within the last 3 months (primary respiratory dysfunction is excluded as we are dealing with this)\n* individuals who can read and write in Turkish\n\nExclusion Criteria:\n\n* Individuals with symptomatic heart disease, a history of lung surgery, neurological disorders, and malignancies that may affect exercise performance, and those with severe cognitive impairment who have difficulty understanding and completing the questionnaire items will be excluded from the study.",{"count":304,"type":20},60,"In the literature, assessment questionnaires related to dyspnea measure beliefs about breathing-related symptoms but do not directly measure breath awareness. For this purpose, the Breath Vigilance Questionnaire (BVQ) is a subjective questionnaire developed from the Pain Awareness Questionnaire that directly measures breath-specific awareness and includes questions evaluating the interaction between conscious monitoring and control of breathing and anxiety. The questionnaire, consisting of 6 questions, was developed on healthy individuals and its validity and reliability were established. It uses a 5-point Likert scale from 1 (never) to 5 (always), with scores ranging from 6 to 30, and higher scores indicate higher breath awareness .\n\nThe reliability and validity of the Turkish version of the Breath Vigilance Questionnaire will assist researchers in assessing dysfunctional breathing and developing treatment strategies by evaluating breath awareness. Therefore, the study aimed to investigate the validity and reliability of the Turkish version.",[307],"Healthy Adult Participants",[309,310,311,312],"breathing","Awareness","respiration","vigilance","2026-04-15",{"date":235,"type":33},{"date":316,"type":20},"2026-04-10",{"date":69,"type":20},{"name":39,"class":40},{"id":320,"slug":321,"hasResults":12,"nctId":322,"briefTitle":323,"officialTitle":324,"acronym":4,"eligibilityCriteria":325,"healthyVolunteers":12,"sex":16,"minAge":17,"maxAge":326,"enrollmentInfo":327,"targetDuration":4,"studyType":110,"phases":4,"briefSummary":329,"conditions":330,"keywords":334,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":339,"lastUpdatePostDateStruct":340,"startDateStruct":342,"completionDateStruct":344,"leadSponsor":346,"locationsCount":41},"100621827","hba1c-levels-and-gastric-emptying-assessed-by-gastric-ultrasound-100621827","NCT07375680","HbA1c Levels and Gastric Emptying Assessed by Gastric Ultrasound","Evaluation of the Effect of Hemoglobin A1c Levels on Gastric Emptying Assessed by Gastric Ultrasound","Inclusion Criteria:\n\nAdults aged 18 to 70 years. ASA physical status I-III. Scheduled for elective surgery under general anesthesia. Ability to provide written informed consent.\n\nExclusion Criteria:\n\nScheduled for emergency surgery. Refusal or inability to provide informed consent. Pregnancy. Age \\\u003C18 years or \\>70 years. History of gastric surgery. Neuromuscular disease. Current use of opioid or anticholinergic medications.","70 Years",{"count":328,"type":20},134,"Delayed gastric emptying increases the risk of pulmonary aspiration during general anesthesia. Diabetes mellitus and poor long-term glycemic control have been associated with impaired gastric motility. Hemoglobin A1c (HbA1c) is a marker of long-term glycemic control; however, its relationship with gastric emptying in surgical patients is not fully understood.\n\nThis prospective observational study aims to evaluate the association between HbA1c levels and gastric emptying using preoperative bedside gastric ultrasonography. Adult patients scheduled for elective surgery under general anesthesia will undergo gastric ultrasound examination after standard fasting. Gastric antral cross-sectional area and estimated gastric volume will be assessed and compared according to HbA1c levels.\n\nThe findings of this study may help improve preoperative risk stratification for aspiration and support individualized anesthetic management in patients with impaired glycemic control.",[331,332,333],"Delayed Gastric Emptying","Diabetes Mellitus","Pulmonary Aspiration",[335,336,337,338],"Hemoglobin A1c","Gastric Ultrasonography","General Anesthesia","Preoperative Assessment","2026-04-06",{"date":341,"type":33},"2026-04-08",{"date":343,"type":33},"2026-02-15",{"date":345,"type":20},"2026-09",{"name":39,"class":40},{"id":348,"slug":349,"hasResults":12,"nctId":350,"briefTitle":351,"officialTitle":352,"acronym":4,"eligibilityCriteria":353,"healthyVolunteers":12,"sex":16,"minAge":354,"maxAge":326,"enrollmentInfo":355,"targetDuration":4,"studyType":21,"phases":356,"briefSummary":357,"conditions":358,"keywords":361,"overallStatus":64,"whyStopped":4,"lastUpdateSubmitDate":366,"lastUpdatePostDateStruct":367,"startDateStruct":369,"completionDateStruct":370,"leadSponsor":372,"locationsCount":41},"100631761","effects-of-aerobic-exercise-in-rheumatoid-arthritis-100631761","NCT07504887","Effects of Aerobic Exercise in Rheumatoid Arthritis","Evaluation of the Effects of Aerobic Exercise Therapy on Quality of Life, Functional Capacity, Mood, Fatigue, and Inflammatory Markers in Patients With Rheumatoid Arthritis","Inclusion Criteria:\n\n* Diagnosed with RA according to ACR\u002FEULAR 2010 criteria\n* Female patients aged 30-70 years\n* Low disease activity (DAS-28 \\\u003C 3.2)\n* Voluntary participation\n\nExclusion Criteria:\n\n* Cardiovascular diseases (CAD, heart failure, etc.)\n* Respiratory diseases\n* Neurological disorders\n* BMI \\> 35\n* Malignancy\n* Pregnancy or breastfeeding\n* Recent medication change (last 3 months)\n* Musculoskeletal conditions preventing exercise","30 Years",{"count":166,"type":20},[23],"This study aims to evaluate the effects of aerobic exercise therapy on quality of life, functional capacity, mood, and fatigue in patients with rheumatoid arthritis. Additionally, the study investigates the impact of aerobic exercise on inflammatory markers, pain, and disease activity.",[359,360],"Rheumatic Diseases","Rheumatic Disorder",[362,363,364,365],"RHEUMATIC DISEASE","RHEUMATIC ARTRIT","PAIN","PHYSICAL MEDICINE AND REHABILITATION","2026-03-26",{"date":368,"type":33},"2026-04-01",{"date":368,"type":20},{"date":371,"type":20},"2027-01-30",{"name":39,"class":40},{"id":374,"slug":375,"hasResults":12,"nctId":376,"briefTitle":377,"officialTitle":378,"acronym":4,"eligibilityCriteria":379,"healthyVolunteers":12,"sex":16,"minAge":354,"maxAge":380,"enrollmentInfo":381,"targetDuration":4,"studyType":21,"phases":382,"briefSummary":383,"conditions":384,"keywords":4,"overallStatus":64,"whyStopped":4,"lastUpdateSubmitDate":366,"lastUpdatePostDateStruct":386,"startDateStruct":388,"completionDateStruct":389,"leadSponsor":390,"locationsCount":41},"100631494","high-intensity-laser-therapy-in-hemiplegic-shoulder-pain-100631494","NCT07501416","High-Intensity Laser Therapy in Hemiplegic Shoulder Pain","Effectiveness of High-Intensity Laser Therapy Combined With Exercise on Clinical and Ultrasonographic Outcomes in Patients With Hemiplegic Shoulder Pain","Inclusion Criteria:\n\n* Age 30-75 years\n* Hemiplegic shoulder pain after stroke\n* Stroke within last 6 months\n* VAS ≥ 3 for pain\n* Medically stable\n\nExclusion Criteria:\n\n* Neurological disorders (MS, Parkinson, etc.)\n* Recent shoulder surgery\u002Finjection\n* Botulinum toxin (last 6 months)\n* Malignancy\n* Pregnancy\n* Epilepsy or photosensitivity\n* Cognitive impairment","75 Years",{"count":304,"type":20},[23],"This randomized, sham-controlled clinical trial aims to evaluate the effectiveness of high-intensity laser therapy (HILT) combined with exercise on pain, functional status, disability, and ultrasonographic findings in patients with hemiplegic shoulder pain following stroke.",[385],"Hemiplegia and\u002For Hemiparesis Following Stroke",{"date":387,"type":33},"2026-03-30",{"date":368,"type":20},{"date":371,"type":20},{"name":39,"class":40},{"id":392,"slug":393,"hasResults":12,"nctId":394,"briefTitle":395,"officialTitle":396,"acronym":4,"eligibilityCriteria":397,"healthyVolunteers":12,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":398,"targetDuration":4,"studyType":110,"phases":4,"briefSummary":399,"conditions":400,"keywords":402,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":407,"lastUpdatePostDateStruct":408,"startDateStruct":410,"completionDateStruct":412,"leadSponsor":414,"locationsCount":41},"100560511","executive-function-in-obese-100560511","NCT06578091","Executive Function in Obese","Effects of Executive Dysfunction on Physical Performance and General Well-Being in Obese Individuals","Inclusion Criteria:\n\nFor the study group;\n\n* Individuals volunteering for the study with BMI ≥30 kg\u002Fm2\n* Individuals between the ages of 18-65 who volunteer to work\n* Individuals who scored 21 points and above in the cognitive assessment\n\nFor the control group;\n\n* Individuals volunteering for the study with BMI ≥30 kg\u002Fm2\n* Individuals between the ages of 18 and 65 who are willing to work\n* Scoring less than 21 points on the cognitive assessment\n\nExclusion Criteria:\n\n* Being at a mental level that cannot understand and answer the questions posed\n* Having a diagnosed neurological disease\n* Having had cancer within the last 2 years\n* Having major organ dysfunction\n* Having uncontrolled type 2 diabetes\n* Loss of vision, hearing",{"count":81,"type":20},"This study was planned to examine the effect of executive function problems on physical performance and general well-being in obese individuals.",[401],"Obesity",[403,404,405,406],"obesity","executive functions","physical performance","well-being","2026-03-09",{"date":409,"type":33},"2026-03-10",{"date":411,"type":33},"2025-01-30",{"date":413,"type":20},"2026-12-01",{"name":39,"class":40},{"id":416,"slug":417,"hasResults":12,"nctId":418,"briefTitle":419,"officialTitle":420,"acronym":4,"eligibilityCriteria":421,"healthyVolunteers":12,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":422,"targetDuration":4,"studyType":110,"phases":4,"briefSummary":423,"conditions":424,"keywords":428,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":407,"lastUpdatePostDateStruct":432,"startDateStruct":433,"completionDateStruct":435,"leadSponsor":437,"locationsCount":41},"100561340","investigation-of-motor-imagery-ability-body-awareness-and-cognitive-functions-in-type-2-diabetes-mellitus-100561340","NCT06588894","Investigation of Motor Imagery Ability, Body Awareness and Cognitive Functions in Type 2 Diabetes Mellitus","Relationship Between Motor Imagery Ability, Body Awareness and Cognitive Functions in Individuals With Type 2 Diabetes Mellitus","Inclusion Criteria:\n\n* Being a type 2 DM patient between the ages of 18-65 for at least 5 years,\n* Being willing to participate in the study,\n* Not having any vision, hearing or speech problems that would prevent the tests from being performed.\n\nExclusion Criteria:\n\n* Having previous experience with Motor Imagery techniques or training,\n* Having any orthopedic problems that prevent walking,\n* Having a history of neurological disease,\n* People who are receiving any medication that affects the central nervous system will not be included in the study.",{"count":81,"type":20},"The aim of this study is to examine the relationship between motor imagery skills, body awareness and cognitive functions in individuals with Type 2 Diabetes mellitus.",[425,426,427],"Type 2 Diabetes Mellitus (T2DM)","Cognitive Function","Motor İmagery Ability",[429,430,431],"cognitive functions","motor imagery ability","type 2 diabetes mellitus",{"date":409,"type":33},{"date":434,"type":33},"2024-10-14",{"date":436,"type":20},"2026-12-10",{"name":39,"class":40},{"id":439,"slug":440,"hasResults":12,"nctId":441,"briefTitle":442,"officialTitle":443,"acronym":4,"eligibilityCriteria":444,"healthyVolunteers":12,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":445,"targetDuration":4,"studyType":110,"phases":4,"briefSummary":447,"conditions":448,"keywords":453,"overallStatus":64,"whyStopped":4,"lastUpdateSubmitDate":456,"lastUpdatePostDateStruct":457,"startDateStruct":458,"completionDateStruct":459,"leadSponsor":460,"locationsCount":41},"100628327","cbct-and-audiological-analysis-of-the-tmj-tinnitus-relationship-100628327","NCT07460193","CBCT and Audiological Analysis of the TMJ-Tinnitus Relationship","Investigation of the Interaction Between Temporomandibular Joint and Tinnitus Using CBCT and Audiological Methods: A Prospective Cross-Sectional Study","Inclusion Criteria:\n\n* Patients aged 18 years and older.\n* Patients presenting with otological symptoms such as tinnitus and ear pain.\n* Patients diagnosed with Temporomandibular Disorders (TMD) based on clinical and radiographic examination.\n* Patients who have been referred for CBCT imaging as part of their routine diagnostic process for TMD.\n* Willingness to provide written informed consent to participate in the study.\n\nExclusion Criteria:\n\n* Presence of objective tinnitus (e.g., vascular or muscular origin).\n* History of chronic otitis media or other middle ear pathologies that could cause hearing loss or tinnitus.\n* Previous history of temporomandibular joint surgery or major maxillofacial trauma.\n* Presence of systemic metabolic bone diseases or inflammatory rheumatic diseases (e.g., Rheumatoid Arthritis).\n* History of malignancy in the head and neck region.\n* Pregnancy (due to CBCT imaging contraindication).\n* Neurological or psychological disorders that would prevent cooperation during clinical and audiological examinations.",{"count":446,"type":20},50,"The aim of this study is to investigate the relationship between Temporomandibular Disorders (TMD) and subjective tinnitus at both morphological and functional levels. Current literature suggests that somatosensory inputs from the temporomandibular joint (TMJ) and masticatory muscles can modulate auditory pathways, a phenomenon known as Somatosensory Tinnitus. However, the specific role of TMJ bone morphology and critical neighboring structures, such as the Petrotympanic Fissure (PTF), in this interaction remains unclear.\n\nIn this clinical study, patients with tinnitus will undergo a comprehensive evaluation including Cone Beam Computed Tomography (CBCT) to quantitatively analyze condylar morphology and osteoarthritic changes. Additionally, audiological tests will be performed to assess the functional state of the auditory system. This multidisciplinary approach aims to clarify the biological link between TMD and tinnitus, potentially improving diagnostic protocols and highlighting the importance of TMJ stabilization in tinnitus management.",[449,450,451,452],"Tinnitus","Temporomandibular Joint Disorders","Somatosensory Tinnitus","Osteoarthritis, Temporomandibular Joint",[449,450,454,455],"Cone-Beam Computed Tomography","Audiometry","2026-03-04",{"date":409,"type":33},{"date":368,"type":20},{"date":32,"type":20},{"name":39,"class":40},{"id":462,"slug":463,"hasResults":12,"nctId":464,"briefTitle":465,"officialTitle":466,"acronym":467,"eligibilityCriteria":468,"healthyVolunteers":12,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":469,"targetDuration":471,"studyType":110,"phases":4,"briefSummary":472,"conditions":473,"keywords":479,"overallStatus":64,"whyStopped":4,"lastUpdateSubmitDate":485,"lastUpdatePostDateStruct":486,"startDateStruct":488,"completionDateStruct":490,"leadSponsor":492,"locationsCount":4},"100625961","morphometric-and-morphological-analysis-of-cervical-vertebrae-in-disc-displacement-100625961","NCT07429435","Morphometric and Morphological Analysis of Cervical Vertebrae in Disc Displacement","Imaging-Based Morphometric and Morphological Analysis of Cervical Vertebrae in Patients With TMJ Disc Displacement","TMJ","Inclusion Criteria:\n\n* Presence of TMJ symptoms on at least one side, including pain, abnormal mandibular movements, or joint noises.\n* Parafunctional habits such as bruxism or clenching.\n* Patients with disc displacement of TMJ.\n\nExclusion Criteria:\n\n* Presence of malformations affecting the craniofacial region.\n* History of trauma of the maxillofacial region.\n* History of cervical surgery or any procedure involving the cervical region.\n* Patients with tumors, cysts, hypoplasia, or hyperplasia in the TMJ region.\n* Any condition related to a congenital anomaly or syndrome.\n* Presence of contraindications to magnetic resonance imaging.\n* Pregnancy.\n* Women in the breastfeeding period.",{"count":470,"type":20},115,"1 Week","Temporomandibular disorders (TMDs) are multifactorial clinical conditions affecting the masticatory muscles, the temporomandibular joint (TMJ), and the surrounding structures. The most common subtype is disc displacement, which is characterized by an abnormal position of the articular disc. Magnetic resonance imaging (MRI) is considered the gold standard for the diagnosis of disc displacement because it provides excellent soft tissue contrast, allows direct visualization of the disc, and enables dynamic evaluation. The parallel nature of mandibular and head-neck movements reflects the functional relationship between the temporomandibular and cervical neuromuscular systems. In addition, various craniofacial skeletal anomalies have been reported to be associated with disorders of the cervical vertebrae. TMD restricts mandibular movements and causes pain in the surrounding muscles, which may lead to referred pain in the neck, shoulder, and cervical muscles, thereby affecting head posture. Head and neck postural abnormalities are closely associated with cervical pain and dysfunction related to TMD. This relationship is thought to be bidirectional and can be explained through biomechanical, neurological, and pathophysiological mechanisms. In particular, upper cervical vertebral dysfunctions and changes in head position may influence the severity of TMD symptoms. For this purpose, lateral cephalometric radiography is frequently used to evaluate the hyoid position and the cervical spine in relation to the TMJ. Upper cervical vertebral anomalies and craniofacial morphological characteristics can be analyzed using these images.",[474,475,476,477,478],"Temporomandibular Disorder (TMD)","Cervical Vertebrae","Disc Displacement","Dentistry","Cephalometric Analysis",[480,481,482,483,484],"temporomandibular disorder","cervical vertebrae","disc displacement","dentistry","cephalometric analysis","2026-02-20",{"date":487,"type":33},"2026-02-24",{"date":489,"type":20},"2026-02-28",{"date":491,"type":20},"2026-07-31",{"name":39,"class":40},{"id":494,"slug":495,"hasResults":12,"nctId":496,"briefTitle":497,"officialTitle":498,"acronym":4,"eligibilityCriteria":499,"healthyVolunteers":500,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":501,"targetDuration":4,"studyType":110,"phases":4,"briefSummary":503,"conditions":504,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":507,"lastUpdatePostDateStruct":508,"startDateStruct":510,"completionDateStruct":511,"leadSponsor":512,"locationsCount":41},"100623914","mobbing-exposure-and-job-satisfaction-among-physiotherapists-100623914","NCT07402824","Mobbing Exposure and Job Satisfaction Among Physiotherapists","Investigation of Mobbing Exposure and Job Satisfaction Levels Among Physiotherapists","Inclusion Criteria:\n\n* Currently working or having previously worked as a physiotherapist in Turkey.\n* Graduation from a minimum 4-year Physiotherapy and Rehabilitation degree program.\n* Voluntary participation.\n\nExclusion Criteria:\n\n* Forms with incorrect answers to dummy questions (trap questions).\n* Forms with missing data.",true,{"count":502,"type":20},200,"Physiotherapists, who hold a significant place in the healthcare sector, are at risk for mobbing and low levels of job satisfaction due to both demanding physical working conditions and emotional stress. This study was designed to investigate the mobbing exposure and job satisfaction levels of physiotherapists.",[505,506],"Job Satisfaction","Bullying, Workplace","2026-02-04",{"date":509,"type":33},"2026-02-11",{"date":507,"type":33},{"date":187,"type":20},{"name":39,"class":40},{"id":514,"slug":515,"hasResults":12,"nctId":516,"briefTitle":517,"officialTitle":518,"acronym":4,"eligibilityCriteria":519,"healthyVolunteers":12,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":520,"targetDuration":4,"studyType":21,"phases":522,"briefSummary":523,"conditions":524,"keywords":526,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":532,"lastUpdatePostDateStruct":533,"startDateStruct":535,"completionDateStruct":537,"leadSponsor":538,"locationsCount":41},"100622017","clay-therapy-in-schizophrenia-patients-100622017","NCT07378150","Clay Therapy in Schizophrenia Patients","The Effect of Clay Therapy on Functional Improvement and Individual and Social Performance in Schizophrenic Patients","Inclusion Criteria:\n\n* Having been diagnosed with schizophrenia,\n* Being aged 18 or over,\n* Having completed at least primary school education,\n* Having achieved treatment compliance,\n* Currently undergoing pharmacological treatment,\n* Being in remission,\n* Having attended the Community Mental Health Centre regularly over the past year,\n* Having agreed to participate in the study\n* Scoring 20 points or higher on the Mini Mental State Examination\n\nExclusion Criteria:\n\n* Being under 18 years of age,\n* Not having an education,\n* Not having a diagnosis of schizophrenia,\n* Not adhering to treatment,\n* Not taking pharmacological treatment regularly,\n* Being in an acute attack\u002Factive phase,\n* Lacking insight",{"count":521,"type":20},17,[23],"In recent years, art therapies have been discussed for their positive effects on mental disorders. One such therapy, clay therapy, is being studied to examine its effect on the functional recovery and individual and social performance of schizophrenia patients undergoing pharmacological treatment.",[525],"Schizophrenia and Related Disorders",[527,528,529,530,531],"schizophrenia","clay therapy","Functional Recovery","Individual and Social Performance","art therapy","2026-01-29",{"date":534,"type":33},"2026-01-30",{"date":536,"type":33},"2025-12-01",{"date":485,"type":20},{"name":39,"class":40},{"id":540,"slug":541,"hasResults":12,"nctId":542,"briefTitle":543,"officialTitle":544,"acronym":4,"eligibilityCriteria":545,"healthyVolunteers":12,"sex":16,"minAge":546,"maxAge":547,"enrollmentInfo":548,"targetDuration":4,"studyType":21,"phases":549,"briefSummary":550,"conditions":551,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":555,"lastUpdatePostDateStruct":556,"startDateStruct":558,"completionDateStruct":560,"leadSponsor":562,"locationsCount":41},"100618718","effects-of-swaddling-and-nesting-on-pain-and-stress-in-newborns-100618718","NCT07335263","Effects of Swaddling and Nesting on Pain and Stress in Newborns","The Effect of Swaddling and Nesting Methods on Pain and Stress Levels in Newborns Undergoing Noninvasive Mechanical Ventilation","Inclusion Criteria:\n\n* Birth week greater than 35 weeks and birth weight greater than 2000 grams\n* Requirement for nasal CPAP\u002Fnoninvasive mechanical ventilation\n* Legal guardians' consent to participate in the study\n* Postnatal diagnosis of transient tachypnea of the newborn\n\nExclusion Criteria:\n\nMother:\n\n* Taking cortisol-containing medication during the antenatal period\n* Taking narcotics during the antenatal period\n* Having chorioamnionitis\n* Having a metabolic disorder (adrenal insufficiency, etc.)\n\nNewborn:\n\n* Amniotic fluid stained with meconium\n* Being intubated\n* Having an Apgar score below 6\n* Receiving analgesic or narcotic drugs for sedation\n* The newborn receiving cortisol-containing medication\n* Being unable to obtain a saliva sample or the sample being contaminated with blood\n* Signs of nasal injury during noninvasive mechanical ventilation\n* Congenital defects (spina bifida, gastroschisis, etc.) that prevent positioning using the swaddling or cradling methods\n* Resuscitation\n* Cerebral hypoxia-ischemia\n* Non-respiratory causes (congenital pneumonia, respiratory distress syndrome, congenital heart disease, hypocalcemia, persistent hypoglycemia, development of sepsis)\n* Hypocalcemia (low calcium level detected in blood gas sample taken while establishing an intravenous line prior to nCPAP)","0 Days","28 Days",{"count":81,"type":20},[23],"This study aims to investigate the effects of swaddling and cradling methods on pain and stress levels in newborn infants receiving respiratory support.\n\nInfants receiving respiratory support in the neonatal intensive care unit may experience stress and discomfort during treatment. In this study, two different care methods that help infants feel more comfortable and secure will be scientifically compared. Only one of the Swaddling or Nesting methods will be applied to the newborns participating in the study. These methods are comfort-enhancing care practices routinely used in neonatal intensive care that do not harm the baby. The newborn's heart rate, respiratory rate, oxygen level, pain and stress symptoms will be closely and safely monitored by the healthcare team. A pain-free saliva sample will be collected to assess the newborn's stress level. It does not involve needles, does not hurt, and takes approximately 2 minutes. Pain and stress levels will be assessed in a multifaceted manner using clinical observation, physiological parameters, and saliva cortisol levels. The study aims to contribute to the strengthening of evidence-based non-pharmacological care practices in neonatal intensive care.",[552,553,554],"Stress","Non Pharmacological Intervention","Newborn Diseases","2026-01-23",{"date":557,"type":33},"2026-01-26",{"date":559,"type":33},"2025-02-17",{"date":561,"type":20},"2026-03-13",{"name":39,"class":40},{"id":564,"slug":565,"hasResults":12,"nctId":566,"briefTitle":567,"officialTitle":568,"acronym":4,"eligibilityCriteria":569,"healthyVolunteers":12,"sex":16,"minAge":570,"maxAge":571,"enrollmentInfo":572,"targetDuration":4,"studyType":21,"phases":574,"briefSummary":575,"conditions":576,"keywords":4,"overallStatus":64,"whyStopped":4,"lastUpdateSubmitDate":579,"lastUpdatePostDateStruct":580,"startDateStruct":582,"completionDateStruct":584,"leadSponsor":586,"locationsCount":41},"100620565","effects-of-neurodynamic-and-carpal-bone-mobilization-in-mild-to-moderate-carpal-tunnel-syndrome-100620565","NCT07359274","Effects of Neurodynamic and Carpal Bone Mobilization in Mild-to-Moderate Carpal Tunnel Syndrome","Clinical and Morphological Effects of Neurodynamic Mobilization and Carpal Bone Mobilization Techniques in Patients With Mild-to-Moderate Carpal Tunnel Syndrome","Inclusion Criteria:\n\n* Diagnosis of mild-to-moderate carpal tunnel syndrome confirmed by electrodiagnostic testing\n* CTS symptoms for at least 3 months\n* Ability to provide informed consent\n\nExclusion Criteria:\n\n* Previous carpal tunnel surgery\n* Diabetes mellitus or polyneuropathy\n* Cervical radiculopathy\n* Pregnancy or breastfeeding\n* Central nervous system disorders","20 Years","55 Years",{"count":573,"type":20},93,[23],"Carpal tunnel syndrome (CTS) is the most common entrapment neuropathy caused by compression of the median nerve at the wrist. Conservative interventions such as splinting and manual therapy are frequently used in individuals with mild-to-moderate CTS. Neurodynamic mobilization and carpal bone mobilization aim to improve neural and soft tissue mobility; however, their comparative effects on clinical outcomes and median nerve morphology are not fully understood.\n\nThis interventional, non-randomized clinical study aims to compare the clinical and ultrasonographic effects of neurodynamic mobilization plus splinting, carpal bone mobilization plus splinting, and splinting alone in patients with mild-to-moderate CTS. Ninety-three participants diagnosed with mild-to-moderate carpal tunnel syndrome based on electrodiagnostic criteria will be included. Participants will be allocated into three parallel groups without randomization. All participants will receive a neutral-position wrist splint as standard conservative care.\n\nTwo intervention groups will additionally receive either neurodynamic mobilization exercises or carpal bone mobilization techniques administered by a physiotherapist for four weeks. Clinical outcomes and median nerve morphology will be evaluated at baseline and immediately after the intervention period.\n\nThe primary outcome is the change in the Boston Carpal Tunnel Questionnaire score. Secondary outcomes include pain intensity, neuropathic pain, functional disability, muscle strength, pressure pain threshold, and ultrasonographic measurements of the median nerve.",[577,578],"Carpal Tunnel Syndrome","Splints","2026-01-13",{"date":581,"type":33},"2026-01-22",{"date":583,"type":20},"2026-01-15",{"date":585,"type":20},"2027-03-15",{"name":39,"class":40},{"id":588,"slug":589,"hasResults":12,"nctId":590,"briefTitle":591,"officialTitle":592,"acronym":4,"eligibilityCriteria":593,"healthyVolunteers":500,"sex":16,"minAge":17,"maxAge":594,"enrollmentInfo":595,"targetDuration":4,"studyType":110,"phases":4,"briefSummary":597,"conditions":598,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":579,"lastUpdatePostDateStruct":600,"startDateStruct":601,"completionDateStruct":602,"leadSponsor":604,"locationsCount":41},"100618683","test-retest-reliability-of-grip-force-sense-for-proprioception-assessment-100618683","NCT07334808","Test-Retest Reliability of Grip Force Sense for Proprioception Assessment","Test-Retest Reliability of Grip Force Sense for Proprioception Assessment in Healthy Participants","Inclusion Criteria:\n\n* Age 18-24 years\n* Volunteering to participate\n\nExclusion Criteria:\n\n* Having a history of hand surgery\n* Having any active pathology or pain complaints in the hand","24 Years",{"count":596,"type":20},55,"The aim of this study is to investigate the test-retest reliability of the grip force sense, a component of proprioception, using a dynamometer that is easily accessible and usable in a clinical setting. This provides an accessible assessment method for research in the field of proprioception.",[599],"Healthy Volunteers",{"date":583,"type":33},{"date":579,"type":33},{"date":603,"type":20},"2026-12-19",{"name":39,"class":40},{"id":606,"slug":607,"hasResults":12,"nctId":608,"briefTitle":609,"officialTitle":609,"acronym":4,"eligibilityCriteria":610,"healthyVolunteers":500,"sex":611,"minAge":17,"maxAge":163,"enrollmentInfo":612,"targetDuration":4,"studyType":21,"phases":613,"briefSummary":614,"conditions":615,"keywords":617,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":624,"lastUpdatePostDateStruct":625,"startDateStruct":627,"completionDateStruct":629,"leadSponsor":631,"locationsCount":41},"100601550","investigation-of-the-effects-of-early-skin-to-skin-contact-on-mother-and-baby-in-cesarean-births-100601550","NCT07111949","Investigation of the Effects of Early Skin-to-Skin Contact on Mother and Baby in Cesarean Births","Inclusion Criteria:\n\nMothers;\n\n* Planning a cesarean section with spinal anesthesia\n* Being between the ages of 18-45\n* Having a singleton pregnancy\n* Being between the gestational age of 37-40 weeks\n* Not having any known health problems (diabetes, gestational diabetes, hypertension, preeclampsia, renal failure, cardiac problems, psychiatric disorders, etc.)\n* Agreeing to participate in the study\n* Having stable general conditions and vital signs before the skin-to-skin contact procedure\n* Residing in Kütahya\n\nNewborns (0-28 days)\n\n* Having a gestational age between 37-40 weeks\n* Having a birth weight between 2500-4500 grams\n* 1-5. Apgar score ≥ 7 per minute\n* No health problems, anomalies or congenital diseases\n* No conditions that prevent sucking such as frenulum (tongue tie) or palate problems\n\nExclusion Criteria:\n\n* Caesarean births performed with general anesthesia\n* Normal births","FEMALE",{"count":51,"type":20},[23],"The rate of cesarean birth continues to increase in the world and in our country. As with all surgeries, the risks of cesarean birth include the possibility of bleeding and infection, prolonged recovery time after birth, delays in initiating breastfeeding and skin-to-skin contact (SSC), and increased likelihood of complications in future pregnancies.\n\nWhile many hospitals apply SSC after normal births, it is known that the number of hospitals that apply SSC in the operating room after cesarean birth is very few. Factors that prevent the initiation of SSC after cesarean birth include the effect of the current operating room culture, the physiological evaluation process of the baby after birth, the presence of procedures such as measuring body weight, aspiration, and Apgar score evaluation.\n\nSince the mother and baby are separated after cesarean birth, the mother's initiation of breastfeeding in the first hour of life may be delayed, and the duration of exclusive breastfeeding may be shortened. The 90-minute uninterrupted skin-to-skin contact during which the baby is dried and placed directly on the mother's bare chest after birth maximizes the chance that babies are physically ready to breastfeed.\n\nAlthough there are studies showing the benefits of SSC application in the operating room such as breastfeeding rates, maintaining the body temperature of the newborn, reducing maternal stress levels, and increasing oxytocin levels, a limited number of studies have been reached in the literature using SSC application guidelines developed to ensure the sustainability of SSC application in the operating room, post-op care unit, and obstetrics clinic. The first contribution of this planned study to the literature will be to standardize SSC application with SSC checklists prepared for use in the cesarean operation room, post-op care unit, and obstetrics ward based on SSC application guidelines. As a second contribution, considering the conditions of the health institution where the study will be conducted, the effects of starting SSC as early as possible and applying it in the cesarean operation room, post-op care unit, and obstetrics ward on the stress level of newborns, sucking success, and pain and salivary cortisol (stress) levels of mothers will be evaluated.",[616],"Skin-to-skin Contact",[618,619,620,621,622,623],"skin-to-skin contact","newborn","mother","stress","cesarean delivery","pain","2026-01-12",{"date":626,"type":33},"2026-01-14",{"date":628,"type":33},"2025-03-19",{"date":630,"type":20},"2026-01-31",{"name":39,"class":40},{"id":633,"slug":634,"hasResults":12,"nctId":635,"briefTitle":636,"officialTitle":637,"acronym":638,"eligibilityCriteria":639,"healthyVolunteers":12,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":640,"targetDuration":642,"studyType":110,"phases":4,"briefSummary":643,"conditions":644,"keywords":646,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":652,"lastUpdatePostDateStruct":653,"startDateStruct":654,"completionDateStruct":656,"leadSponsor":658,"locationsCount":659},"100586455","drug-coated-coronary-balloons-in-different-clinical-scenarios-100586455","NCT06915597","Drug-Coated Coronary Balloons in Different Clinical Scenarios","Procedural Success and Short- and Long-Term Outcomes of Drug-Coated Coronary Balloons Used in Different Clinical Scenarios","DCB-DCS","Inclusion Criteria:\n\nAge ≥18 years. Patients with coronary artery disease undergoing percutaneous coronary intervention (PCI) in whom a drug-coated balloon (DCB) is used as the intended treatment strategy for at least one target lesion.\n\nDCB use in any clinical presentation, including stable coronary artery disease and acute coronary syndromes.\n\nDCB treatment for different lesion subsets, including de novo lesions, in-stent restenosis, bifurcation lesions, small and large vessels, and chronic total occlusions.\n\nSuccessful lesion preparation allowing DCB angioplasty (residual stenosis ≤30% and absence of flow-limiting dissection before DCB inflation, according to operator judgment).\n\nAvailability of baseline clinical, angiographic, and procedural data. Ability to provide informed consent for prospective enrollment or availability of data according to local regulations for retrospective inclusion.\n\nPlanned clinical follow-up.\n\nExclusion Criteria:\n\nPrimary treatment strategy without the use of a drug-coated balloon (e.g., exclusive drug-eluting stent implantation without DCB).\n\nCardiogenic shock at the time of index procedure. Life expectancy less than 1 year due to non-cardiac comorbidities. Contraindication to antiplatelet therapy. Known severe allergy to contrast media not amenable to premedication. Pregnancy. Inability to comply with clinical follow-up. Participation in another interventional clinical trial that could confound outcome assessment.",{"count":641,"type":20},1500,"1 Year","Coronary stents are the best treatment method ever accepted in the treatment of coronary artery stenoses. Due to some limitations and complications of stent use, the operators tried to find new solutions. Drug Coated Balloons (DCBs) have been accepted as a new method in the treatment of in-stent restenosis and small vessel disease. Furthermore, they have been used in the treatment of de novo coronary lesions, chronic total occlusions and bifucation lesions. But data is limited in the short and long term success of DCBs in all these clinical scenarios. In our study we aimed to investigate the procedural success and short and long term outcomes of DCB use in different clinical scenarios.",[645],"Coronary Arterial Disease (CAD)",[647,648,649,650,651],"drug coted balloons","coronary artery disease","chronic total occlusions","de novo lesions","small vessel disease","2026-01-11",{"date":579,"type":33},{"date":655,"type":33},"2025-05-31",{"date":657,"type":20},"2026-05-31",{"name":39,"class":40},5,""]