[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Hasan Kalyoncu University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":672},{"pageToken":4,"total":5,"offset":6,"count":7,"results":8},null,26,0,25,[9,48,80,105,137,166,192,212,235,259,290,317,341,366,395,422,450,470,498,521,544,569,593,619,645],{"id":10,"slug":11,"hasResults":12,"nctId":13,"briefTitle":14,"officialTitle":15,"acronym":4,"eligibilityCriteria":16,"healthyVolunteers":12,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":29,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100641973","gluten-free-vs-mediterranean-diet-in-rheumatoid-arthritis-100641973",false,"NCT07646262","Gluten-Free vs Mediterranean Diet in Rheumatoid Arthritis","Investigation of the Effects of a Gluten-Free Diet and the Mediterranean Diet on the Inflammatory Index, Disease Activity, and Quality of Life in Patients With Rheumatoid Arthritis.","Inclusion Criteria:\n\nDiagnosis of rheumatoid arthritis according to ACR\u002FEULAR criteria Age between 19-65 years Stable medication regimen for at least 3 months prior to enrollment Willingness to comply with dietary interventions and study procedures Ability to provide informed consent\n\nExclusion Criteria:\n\nPregnancy or lactation Presence of other autoimmune or inflammatory diseases (e.g., SLE, IBD) Severe comorbidities (e.g., advanced cardiovascular, renal, or hepatic disease) Use of special diets (e.g., gluten-free diet) in the last 3 months Recent change in biologic or corticosteroid therapy (\\\u003C3 months) Food allergies or intolerances affecting dietary intervention adherence Inability to comply with dietary protocol or follow-up visits","ALL","19 Years","65 Years",{"count":21,"type":22},66,"ESTIMATED","INTERVENTIONAL",[25],"NA","This study aims to evaluate the effects of different dietary interventions, including gluten-free, Mediterranean, and control diets, on disease activity, quality of life, and dietary inflammatory index in patients with rheumatoid arthritis. Participants will be followed for 12 weeks, and changes in clinical and nutritional outcomes will be assessed.",[28],"Rheumatoid Arthritis (RA",[30,31,32,33,34],"Rheumatoid arthritis","Mediterranean diet","Gluten-free diet","Dietary inflammatory index (DII)","Disease activity (DAS28)","RECRUITING","2026-06-09",{"date":38,"type":39},"2026-06-12","ACTUAL",{"date":41,"type":39},"2025-10-29",{"date":43,"type":22},"2026-08-31",{"name":45,"class":46},"Hasan Kalyoncu University","OTHER",1,{"id":49,"slug":50,"hasResults":12,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":4,"eligibilityCriteria":54,"healthyVolunteers":12,"sex":17,"minAge":55,"maxAge":56,"enrollmentInfo":57,"targetDuration":59,"studyType":60,"phases":4,"briefSummary":61,"conditions":62,"keywords":66,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":47},"100634497","the-effect-of-different-acoustic-conditions-on-6-minute-walk-test-performance-and-recovery-100634497","NCT07540455","The Effect of Different Acoustic Conditions on 6-Minute Walk Test Performance and Recovery","An Investigation of the Effect of Different Auditory Conditions on 6-Minute Walk Performance and Recovery in Healthy Young Adults: A Randomised Cross-Over Study","Inclusion Criteria:\n\n* Aged between 18 and 35,\n* Able to walk unaided (without the use of a walking aid),\n* Participants who agree to take part in the study on a voluntary basis and sign the informed consent form\n\nExclusion Criteria:\n\n* A history of myocardial infarction or unstable angina within the last month,\n* Acute illness or pain during the test that would prevent walking,\n* A lower limb injury or surgery within the last 3 months,\n* Resting systolic blood pressure \\>180 mmHg or diastolic blood pressure \\>100 mmHg,\n* Resting heart rate exceeding 120 beats per minute,\n* Those with cardiovascular or pulmonary conditions that may limit exercise,\n* Those with neurological conditions (balance disorders, stroke, epilepsy, etc.),\n* Those with musculoskeletal problems (lower limb fracture, severe arthritis, acute injury, etc.),\n* Those with an acute infection, fever or severe fatigue that could prevent walking during the test,\n* Those with a body mass index of 35 or above (obesity),\n* Those with a history of active vertigo, Meniere's disease or vestibular system disorders,\n* Participants with a diagnosed hearing problem","18 Years","35 Years",{"count":58,"type":22},40,"1 Day","OBSERVATIONAL","Study Design: Randomized Cross-Over Study\n\nObjective:\n\nThis study aims to compare the acute effects of three different auditory conditions (metronome, binaural beats, and silent control) on 6-Minute Walk Test (6MWT) performance, post-exercise recovery physiology, and perceived exertion in healthy young adults.\n\nBackground:\n\nAuditory-motor coupling mechanisms suggest that rhythmic auditory stimuli can lower the excitation threshold of motor neurons, thereby enhancing walking efficiency. Rhythmic stimuli such as metronomes are known to improve walking speed and coordination. Binaural beats are an auditory stimulus type generated by presenting two tones of slightly different frequencies to each ear, triggering cortical neural entrainment. It has been reported that listening to binaural beats at theta frequency following exercise increases parasympathetic activation and accelerates recovery. This study aims to examine these two auditory stimuli in comparison with a control condition in healthy young adults.\n\nParticipants:\n\nHealthy young adults aged 18-35 who can walk independently and have no cardiovascular, pulmonary, neurological, or musculoskeletal conditions. Minimum sample size will be calculated using G\\*Power following a pilot study, with a 20% dropout margin added.\n\nRandomization:\n\nAll participants will be exposed to all three conditions on separate days. The order of application will be determined by computer-based simple randomization (randomizer.org). Six possible sequence combinations will be used to balance order effects. A washout period of at least 24 hours will be applied between sessions.\n\nInterventions:\n\nMetronome Condition: Each participant's natural walking cadence will be measured, and the metronome tempo will be set at 110% of this baseline value.\n\nBinaural Beats Condition: A carrier frequency of 120 Hz will be delivered to the right ear and 100 Hz to the left ear, generating a 20 Hz binaural beat in the Beta frequency band. Participants will listen for 6 minutes at rest immediately before the walking test.\n\nControl Condition: No auditory stimulus will be applied.\n\nThe 6MWT will be conducted in all conditions along a 30-meter flat corridor in accordance with ATS\u002FERS standards.\n\nMeasurement Time Points: Pre-test, immediately post-test, and at the 1st, 3rd, and 5th minutes of the recovery period.\n\nOutcome Measures:\n\nPrimary: Total distance covered during 6MWT (meters), walking cadence (steps\u002Fmin) Secondary: Heart rate, blood pressure, peripheral oxygen saturation (SpO₂), perceived dyspnea, general fatigue, and quadriceps femoris muscle fatigue assessed via the Modified Borg Scale\n\nStatistical Analysis:\n\nOne-Way Repeated Measures ANOVA for walking distance and cadence; Two-Way Repeated Measures ANOVA (condition × time) for physiological parameters; Friedman test for Borg scale data; Bonferroni-corrected post-hoc tests where significant differences are found. Significance level set at p\\\u003C0.05.\n\nStudy Duration: April - June 2026 (3 months)",[63,64,65],"Recovery","Fatigue Recovery","Healhty",[67,68,69,70],"6 minutes walk test","metronome","binaural","recovery","NOT_YET_RECRUITING","2026-04-14",{"date":74,"type":39},"2026-04-20",{"date":76,"type":22},"2026-04-15",{"date":78,"type":22},"2026-07-01",{"name":45,"class":46},{"id":81,"slug":82,"hasResults":12,"nctId":83,"briefTitle":84,"officialTitle":84,"acronym":85,"eligibilityCriteria":86,"healthyVolunteers":87,"sex":17,"minAge":55,"maxAge":4,"enrollmentInfo":88,"targetDuration":4,"studyType":60,"phases":4,"briefSummary":90,"conditions":91,"keywords":94,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":98,"lastUpdatePostDateStruct":99,"startDateStruct":101,"completionDateStruct":102,"leadSponsor":104,"locationsCount":47},"100613218","determining-the-consistency-between-nurses-and-artificial-intelligence-chatgpt-5-in-delivering-scenario-based-discharge-education-to-coronary-artery-bypass-graft-patients-a-methodological-study-100613218","NCT07263724","Determining the Consistency Between Nurses and Artificial Intelligence (ChatGPT-5) in Delivering Scenario-Based Discharge Education to Coronary Artery Bypass Graft Patients: A Methodological Study","CABG-AI-EDU","Inclusion Criteria:\n\n* Patient scenarios representing individuals who have undergone coronary artery bypass graft (CABG) surgery.\n* Scenarios that include demographic, socioeconomic, clinical, and psychosocial information consistent with current literature and clinical guidelines.\n* Scenarios describing patients who underwent median sternotomy and on-pump CABG procedure.\n* Scenarios that include relevant postoperative complications (e.g., delirium, bleeding, wound infection, arrhythmia) and comorbidities (e.g., diabetes, hypertension, COPD).\n* Scenarios that enable both nurse and ChatGPT-5 to prepare discharge education materials under the same standardized framework.\n* Scenarios reviewed and validated by cardiovascular surgery experts and nurse academicians for content validity.\n\nExclusion Criteria:\n\n* Patient scenarios not related to coronary artery bypass graft (CABG) surgery.\n* Scenarios lacking sufficient demographic, clinical, or psychosocial information to prepare individualized discharge education.\n* Scenarios that do not follow the standardized structure of six main domains and twenty-four subtopics.\n* Scenarios with inconsistent or contradictory medical data (e.g., incompatible diagnosis and treatment details).\n* Scenarios not validated by the expert review panel for clinical accuracy and content validity.\n* Scenarios that do not allow comparison between nurse-generated and ChatGPT-5-generated discharge education materials.",true,{"count":89,"type":22},30,"This methodological study aims to determine the level of agreement between nurses and an artificial intelligence system (ChatGPT-4.0) in providing scenario-based discharge education for patients who have undergone coronary artery bypass graft (CABG) surgery. Thirty standardized patient scenarios representing different demographic, clinical, and psychosocial characteristics will be used. For each scenario, both expert nurses and ChatGPT-4.0 will prepare discharge education content based on six main domains and twenty-four subtopics identified from the literature and clinical guidelines. The educational materials will be independently evaluated by two blinded reviewers in terms of content accuracy, completeness, scientific consistency, and clarity of language. Agreement between nurses and AI-generated content will be analyzed using Cohen's Kappa coefficient and Fisher's Exact Test. The findings are expected to provide evidence for the reliability and applicability of AI-assisted discharge education systems in cardiac surgery nursing practice.",[92,93],"Coronary Artery Bypass Graft Surgery (CABG)","Patient Education",[95,96,97],"Coronary Artery Bypass Graft","Discharge Education","Artificial Intelligence","2026-04-01",{"date":100,"type":39},"2026-04-02",{"date":78,"type":22},{"date":103,"type":22},"2027-12-01",{"name":45,"class":46},{"id":106,"slug":107,"hasResults":12,"nctId":108,"briefTitle":109,"officialTitle":110,"acronym":111,"eligibilityCriteria":112,"healthyVolunteers":12,"sex":17,"minAge":55,"maxAge":4,"enrollmentInfo":113,"targetDuration":4,"studyType":23,"phases":115,"briefSummary":116,"conditions":117,"keywords":127,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":129,"lastUpdatePostDateStruct":130,"startDateStruct":132,"completionDateStruct":134,"leadSponsor":136,"locationsCount":4},"100631668","cabg-ai-supported-discharge-education-100631668","NCT07503678","CABG-AI-Supported Discharge Education","The Effect of Artificial Intelligence-Supported Individualized Discharge Education on Postoperative Pain, Anxiety, Stress Response, Recovery, and Discharge Education Satisfaction in Patients Undergoing Coronary Artery Bypass Graft Surgery: A Randomized Controlled Trial","AI-D-E-CABG","Inclusion Criteria:\n\n* Patients who have undergone coronary artery bypass graft (CABG) surgery.\n* Age 18 years or older.\n* Hemodynamically stable at the time of enrollment.\n* Able to understand and communicate in Turkish.\n* Able to use or have access to a mobile phone capable of viewing the educational video.\n* Able to provide informed consent.\n* Scheduled for routine postoperative follow-up at the study hospital.\n\nExclusion Criteria:\n\n* Patients undergoing emergency CABG surgery.\n* Presence of severe cognitive impairment that prevents understanding or following instructions.\n* Diagnosed psychiatric disorders (e.g., schizophrenia, severe depression) that interfere with study participation.\n* Severe vision or hearing impairment that prevents receiving the education.\n* Presence of postoperative complications requiring intensive care readmission.\n* Patients with endocrine disorders affecting stress biomarkers (e.g., Cushing's syndrome, Addison's disease).\n* Chronic use of corticosteroids or medications that significantly alter cortisol levels.\n* Patients who decline to participate or withdraw consent.\n* Patients who are unable to complete follow-up assessments.",{"count":114,"type":22},128,[25],"This randomized controlled trial will evaluate the effectiveness of artificial intelligence-supported individualized discharge education for patients undergoing coronary artery bypass graft (CABG) surgery. Participants will be assigned to either the intervention group, which will receive personalized AI-generated discharge education delivered through a nurse-avatar video in addition to standard verbal education, or the control group, which will receive standard discharge education only. The study will compare postoperative pain, anxiety, physiological stress response, recovery, and satisfaction with discharge education between the two groups. Outcomes will be measured during hospitalization and at the routine postoperative follow-up visit. The findings may help improve patient education methods and postoperative recovery in cardiac surgery patients.",[118,119,120,121,122,123,124,125,126,96],"Coronary Artery Disease","Postoperative Care","Patient Discharge","Recovery of Function","Anxiety","Pain","Stress, Physiological","Surgical Nursing","Nursing",[118,119,120,128,125],"discharge education","2026-03-25",{"date":131,"type":39},"2026-03-31",{"date":133,"type":22},"2026-06-01",{"date":135,"type":22},"2027-02-01",{"name":45,"class":46},{"id":138,"slug":139,"hasResults":12,"nctId":140,"briefTitle":141,"officialTitle":142,"acronym":4,"eligibilityCriteria":143,"healthyVolunteers":87,"sex":17,"minAge":55,"maxAge":144,"enrollmentInfo":145,"targetDuration":4,"studyType":23,"phases":147,"briefSummary":148,"conditions":149,"keywords":154,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":159,"lastUpdatePostDateStruct":160,"startDateStruct":161,"completionDateStruct":163,"leadSponsor":165,"locationsCount":47},"100630854","acute-effects-of-posterior-talar-glide-mobilization-100630854","NCT07493083","Acute Effects of Posterior Talar Glide Mobilization","The Acute Effect of Posterior Talar Glide Mobilization on Weight Bearing Dorsiflexion Range of Motion and Walking Speed : A Randomized Sham-Controlled Trial","Inclusion Criteria:\n\n* Participants aged between 18 and 45,\n* Participants who have agreed to take part in the study on a voluntary basis,\n* Participants with no history of lower limb surgery\n\nExclusion Criteria:\n\n* Those with acute ankle pain or inflammation,\n* Those with ankle instability,\n* Those with a history of lower limb surgery within the last 6 months,\n* Those with balance or vestibular disorders,\n* Those with chronic conditions,","45 Years",{"count":146,"type":22},60,[25],"The aim of this study is to evaluate the acute effects of posterior talar glide mobilisation on dorsiflexion range of motion wieght bearing (measured using the Weight-Bearing Lunge Test) and walking speed, using a randomised, sham-controlled study design.",[150,151,152,153],"Ankle Dorsiflexion","Mobilization","Walking Speed, Mesh id D000072797","Range of Motion",[155,156,157,158],"ankle mobility","talar mobilization","range of motion","walking speed","2026-03-19",{"date":129,"type":39},{"date":162,"type":22},"2026-03-30",{"date":164,"type":22},"2026-05-30",{"name":45,"class":46},{"id":167,"slug":168,"hasResults":12,"nctId":169,"briefTitle":170,"officialTitle":171,"acronym":4,"eligibilityCriteria":172,"healthyVolunteers":87,"sex":17,"minAge":55,"maxAge":144,"enrollmentInfo":173,"targetDuration":4,"studyType":60,"phases":4,"briefSummary":175,"conditions":176,"keywords":180,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":184,"lastUpdatePostDateStruct":185,"startDateStruct":187,"completionDateStruct":189,"leadSponsor":191,"locationsCount":47},"100628987","masseter-muscle-thickness-in-individuals-with-chronic-neck-pain-100628987","NCT07468786","Masseter Muscle Thickness in Individuals With Chronic Neck Pain","Comparison of Masseter Muscle Thickness Measured by Ultrasonography in Individuals With Chronic Neck Pain Compared to Healthy Individuals","Inclusion Criteria:\n\n* Be between the ages of 18 and 45\n* Have neck pain that has persisted for at least 3 months\n* Agree to participate in the study voluntarily and provide written informed consent\n\nExclusion Criteria:\n\n* History of cervical spine surgery or severe trauma\n* Diagnosis of cervical radiculopathy, myelopathy, or neurological disease\n* Rheumatic, inflammatory, or systemic musculoskeletal diseases\n* Diagnosed temporomandibular joint disorder (TMD)\n* Diagnosis of bruxism or a pronounced habit of teeth clenching\u002Fgrinding\n* History of manual therapy, injection, or surgical intervention in the face, jaw, or neck region within the last 6 months\n* Currently undergoing orthodontic treatment or history of orthodontic treatment within the last 6 months\n* Cognitive impairment or conditions that prevent understanding and responding to questionnaires",{"count":174,"type":22},90,"The primary objective of our study is to compare the thickness of the masseter muscle, measured by ultrasound, in individuals with chronic neck pain to that of healthy individuals. The secondary objective of the study is to examine the relationships between masseter muscle thickness and pain intensity, neck disability level, pain catastrophizing level, and clinical diagnostic criteria in individuals with chronic neck pain.",[177,178,179],"Masseter Muscle","Ultrasonographic","Chronic Neck Pain",[181,182,183],"chronic neck pain","Ultrasonographic measurement","Masseter muscle","2026-03-09",{"date":186,"type":39},"2026-03-13",{"date":188,"type":22},"2026-03-20",{"date":190,"type":22},"2026-05-20",{"name":45,"class":46},{"id":193,"slug":194,"hasResults":12,"nctId":195,"briefTitle":196,"officialTitle":197,"acronym":198,"eligibilityCriteria":199,"healthyVolunteers":87,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":200,"targetDuration":4,"studyType":60,"phases":4,"briefSummary":202,"conditions":203,"keywords":4,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":205,"lastUpdatePostDateStruct":206,"startDateStruct":208,"completionDateStruct":209,"leadSponsor":211,"locationsCount":4},"100625934","the-clinical-decision-making-skills-of-operating-room-nurses-regarding-knowledge-of-inadvertent-perioperative-hypothermia-100625934","NCT07429084","The Clinical Decision-Making Skills of Operating Room Nurses Regarding Knowledge of Inadvertent Perioperative Hypothermia","THE EFFECT OF OPERATING ROOM NURSES' KNOWLEDGE LEVELS OF INADVENTENT PERIOPERATIVE HYPERTHERMIA ON THEIR CLINICAL DECISION-MAKING SKILLS: A SCENARIO-BASED MULTICENTRE-CROSS-SECTIONAL STUDY","Hypothermia","Inclusion Criteria:\n\n* Nurses who have worked as operating room nurses for the past year,\n* and who volunteer to participate in the study will be included.\n\nExclusion Criteria:\n\n• Data from nurses who volunteered to participate in the study but wished to withdraw at any stage will not be included in the study.",{"count":201,"type":22},165,"This research is planned to examine the effect of operating room nurses' knowledge levels regarding inadvertent perioperative hypothermia (IPH) on their clinical decision-making skills. IPH is a preventable patient safety issue that can lead to serious complications such as cardiac arrhythmias, blood loss, infection, and prolonged hospital stay. The literature indicates that nurses' knowledge levels regarding IPH are generally insufficient, and this negatively impacts their clinical decision-making processes.\n\nThis research is a cross-sectional study to be conducted in the operating room of Kahramanmaraş Sütçü İmam University Health Practice and Research Hospital between March 2026 and May 2026. The sample size was determined to be at least 165 nurses using power analysis.\n\nData will be collected using a Demographic Information Form, the Inadvertent Perioperative Hypothermia Knowledge Test (IPH-BT), and a 15-item Clinical Decision-Making Scenarios Form developed by the researchers. Data will be analyzed using SPSS software; group comparisons, correlation, and multiple linear regression analyses will be performed.\n\nThis study will test whether nurses' knowledge levels differ according to demographic characteristics, their relationship with clinical decision-making skills, and whether knowledge level predicts decision-making skills.\n\nThis research is expected to contribute to identifying the training needs of operating room nurses regarding IPD management and strengthening their evidence-based clinical decision-making skills.",[204],"THE EFFECT OF KNOWLEDGE LEVELS OF INADVERTET PERIOPERATIVE HYPOTHERMIA ON CLINICAL DECISION-MAKING SKILLS","2026-02-23",{"date":207,"type":39},"2026-02-24",{"date":162,"type":22},{"date":210,"type":22},"2026-06-30",{"name":45,"class":46},{"id":213,"slug":214,"hasResults":12,"nctId":215,"briefTitle":216,"officialTitle":217,"acronym":4,"eligibilityCriteria":218,"healthyVolunteers":87,"sex":17,"minAge":55,"maxAge":19,"enrollmentInfo":219,"targetDuration":4,"studyType":60,"phases":4,"briefSummary":220,"conditions":221,"keywords":224,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":227,"lastUpdatePostDateStruct":228,"startDateStruct":230,"completionDateStruct":232,"leadSponsor":234,"locationsCount":47},"100625646","ultrasound-examination-of-the-vmo-in-patellofemoral-pain-syndrome-100625646","NCT07425340","Ultrasound Examination of the VMO in Patellofemoral Pain Syndrome","Ultrasonography Examination of the Vastus Medialis Obliquus and Vastus Medialis Longus Muscles in Patellofemoral Pain Syndrome","Inclusion Criteria:\n\n* Between the ages of 18 and 65\n* Have had localized pain in the front of the knee for at least the past 3 months\n* Experience pain during activities that require stair climbing, squatting, prolonged sitting, or knee flexion\n* Have been diagnosed with patellofemoral pain syndrome based on clinical evaluation\n* Volunteer to participate in the study and sign the informed consent form\n\nExclusion Criteria:\n\n* History of previous surgery on the knee joint\n* History of significant trauma to the knee region within the last 6 months\n* Diagnosis of meniscus, ligament injuries, knee osteoarthritis, or inflammatory rheumatic disease\n* Neurological diseases or systemic diseases affecting the musculoskeletal system\n* Presence of other lower extremity pathologies causing pain at a level that could affect measurements",{"count":58,"type":22},"The aim of this study is to examine in detail the ultrasonographic characteristics of the vastus medialis obliquus and vastus medialis longus muscles in individuals with patellofemoral pain syndrome and to compare these findings with those of healthy individuals. It is anticipated that the results obtained will contribute to a better understanding of the muscle-based mechanisms of PFAS and provide a scientific basis for the development of muscle-specific assessment and intervention strategies in physical therapy and rehabilitation practices.",[222,178,223],"Vastus Medialis","Patello Femoral Pain Syndrome",[225,226,182],"Patellofemoral Pain","Vastus Medialis Obliqus","2026-02-13",{"date":229,"type":39},"2026-02-20",{"date":231,"type":22},"2026-02-25",{"date":233,"type":22},"2026-06-25",{"name":45,"class":46},{"id":236,"slug":237,"hasResults":12,"nctId":238,"briefTitle":239,"officialTitle":240,"acronym":4,"eligibilityCriteria":241,"healthyVolunteers":87,"sex":242,"minAge":243,"maxAge":55,"enrollmentInfo":244,"targetDuration":4,"studyType":60,"phases":4,"briefSummary":246,"conditions":247,"keywords":251,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":227,"lastUpdatePostDateStruct":255,"startDateStruct":256,"completionDateStruct":257,"leadSponsor":258,"locationsCount":47},"100625645","validity-and-reliability-of-the-two-minute-step-test-in-hemophilia-100625645","NCT07425327","Validity and Reliability of the Two-minute Step Test in Hemophilia","Investigating the Validity and Reliability of the Two-minute Step Test in Patients With Hemophilia","Inclusion Criteria:\n\n* Diagnosed with Hemophilia (A-B) by a physician,\n* Aged 6-18 years,\n* Receiving regular prophylactic treatment,\n* Inhibitor positive or negative,\n* No history of lower extremity joint bleeding within the last month,\n* Individuals who are willing to participate in the study,\n\nExclusion Criteria:\n\n* Patients who have undergone surgery on the lower extremities for any reason within the last 6 months,\n* Patients with neurological sequelae following a history of intracranial hemorrhage,\n* Patients experiencing cognitive impairment to the extent that they cannot understand the tests,\n* Patients who indicate they will be unable to participate in follow-up measurements.","MALE","6 Years",{"count":245,"type":22},35,"The aim of our study was to evaluate the psychometric properties of the 2-minute step test in hemophilia patients, assess its intra-rater and inter-rater reliability, and evaluate its convergent validity and construct validity supported by measurements of gait, balance, and functionality.",[248,249,250],"Hemophilia","Step","Reliability and Validity",[252,253,254],"Hemophilia A","Hemophilia B","Two minute step test",{"date":229,"type":39},{"date":231,"type":22},{"date":233,"type":22},{"name":45,"class":46},{"id":260,"slug":261,"hasResults":12,"nctId":262,"briefTitle":263,"officialTitle":264,"acronym":4,"eligibilityCriteria":265,"healthyVolunteers":12,"sex":17,"minAge":55,"maxAge":266,"enrollmentInfo":267,"targetDuration":4,"studyType":23,"phases":269,"briefSummary":270,"conditions":271,"keywords":276,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":282,"lastUpdatePostDateStruct":283,"startDateStruct":285,"completionDateStruct":287,"leadSponsor":289,"locationsCount":47},"100617770","effects-of-exercise-with-visual-feedback-in-parkinsons-disease-100617770","NCT07322939","Effects of Exercise With Visual Feedback in Parkinson's Disease","Effects of Visual Indicator Exercises for the Trunk and Lower Extremities on Activity and Participation in Parkinson's Disease","Inclusion Criteria\n\n* Individuals diagnosed with idiopathic Parkinson's disease\n* Disease severity classified as stage 1 to 3 according to the Modified Hoehn and Yahr Scale\n* Patients receiving oral antiparkinsonian treatment only\n\nExclusion Critera\n\n* Presence of musculoskeletal, cardiovascular, or vestibular disorders that may interfere with the completion of the assessments or treatment protocol\n* Presence of additional neurological or psychiatric disorders other than Parkinson's disease\n* Presence of visual impairment insufficient to perceive visual feedback","85 Years",{"count":268,"type":22},32,[25],"Patients with Parkinson's disease who apply to the Hasan Kalyoncu University Application and Research Center and meet the inclusion criteria will be included in the study. The included participants will be randomly assigned into either the intervention group or the control group using a sealed-envelope method. Both groups will undergo a standard exercise program, consisting of posture, strengthening, and balance training, under the supervision of a physiotherapist for 8 weeks, 3 days per week. In addition to this, the intervention group will receive an additional exercise program incorporating visual feedback using a laser pointer, targeting the trunk and lower extremities, also under the supervision of a physiotherapist for 8 weeks, 3 days per week.",[272,273,274,275],"Parkinson Disease","Balance Impairment","Exercise Training","Postural Control",[277,278,279,280,281],"parkinson disease","balance","postural control","visual feedback","exercise","2026-01-24",{"date":284,"type":39},"2026-01-27",{"date":286,"type":39},"2025-12-01",{"date":288,"type":22},"2026-05-05",{"name":45,"class":46},{"id":291,"slug":292,"hasResults":12,"nctId":293,"briefTitle":294,"officialTitle":295,"acronym":296,"eligibilityCriteria":297,"healthyVolunteers":87,"sex":17,"minAge":55,"maxAge":298,"enrollmentInfo":299,"targetDuration":4,"studyType":23,"phases":301,"briefSummary":302,"conditions":303,"keywords":307,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":309,"lastUpdatePostDateStruct":310,"startDateStruct":312,"completionDateStruct":314,"leadSponsor":316,"locationsCount":4},"100618419","eft-and-resilience-in-nursing-students-100618419","NCT07331376","EFT and Resilience in Nursing Students","Improving Perceived Stress, Anxiety, and Sleep Quality Among Nursing Students: Enhancing Resilience Through Emotional Freedom Techniques","Emotional","Inclusion Criteria:\n\n* Currently enrolled in the Nursing Department at Muş Alparslan University,\n* Be 18 years of age or older,\n* Agree to participate in the study voluntarily,\n* Have no psychiatric diagnosis or regular use of psychotropic medication.\n\nExclusion Criteria:\n\nStudents who do not regularly participate in the application process,\n\n* Students who do not complete the data collection forms in full,\n* Students who report physical or psychological discomfort during the EFT application process.","24 Years",{"count":300,"type":22},105,[25],"The purpose of this study is to determine the effect of Emotional Freedom Technique (EFT) application on stress, anxiety, and sleep quality in nursing students.\n\nThe nursing education process can cause high levels of psychological and physiological stress in students due to many factors such as a heavy theoretical knowledge load, clinical practice stress, exam anxiety, and shift work. This situation results in increased anxiety and impaired sleep quality, thereby negatively affecting students' academic performance, clinical skills, and overall well-being.\n\nIn this context, the study aims to evaluate whether EFT, as a complementary method, is effective in reducing stress and anxiety levels in nursing students, as well as improving sleep quality.\n\nIt is believed that the results of this research will contribute to the development of alternative approaches that support psychological well-being in nursing education and will provide evidence-based data on the integration of EFT into educational programs.",[304,305,306],"Emotional Well-being","Sleep Quality","Nursing Students",[306,305,308],"Emotional Freedom Techniques (EFT)","2025-12-30",{"date":311,"type":39},"2026-01-09",{"date":313,"type":22},"2025-12-22",{"date":315,"type":22},"2026-06-20",{"name":45,"class":46},{"id":318,"slug":319,"hasResults":12,"nctId":320,"briefTitle":321,"officialTitle":322,"acronym":4,"eligibilityCriteria":323,"healthyVolunteers":12,"sex":17,"minAge":55,"maxAge":4,"enrollmentInfo":324,"targetDuration":4,"studyType":60,"phases":4,"briefSummary":326,"conditions":327,"keywords":331,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":334,"lastUpdatePostDateStruct":335,"startDateStruct":337,"completionDateStruct":338,"leadSponsor":340,"locationsCount":47},"100614175","reliability-of-the-scoliosis-caregiver-response-and-emotional-scale-scares-questionnaire-100614175","NCT07276178","Reliability of the Scoliosis Caregiver Response and Emotional Scale (SCaRES) Questionnaire","Reliability of the Turkish Version of the Scoliosis Caregiver Response and Emotional Scale (SCaRES) Questionnaire","Inclusion Criteria:\n\n* Individuals who are an adult (parent or primary caregiver) responsible for the care of an individual diagnosed with scoliosis between the ages of 10 and 18.\n* Individuals who are able to read and understand Turkish.\n* Individuals who are actively involved in the child's treatment process (e.g., use of a brace, exercise program, follow-up appointments).\n* Individuals who volunteer to participate in the study.\n\nExclusion Criteria:\n\n* Participants whose children have a history of other comorbidities (neurological, etc.),\n* Children whose children have a history of spinal surgery,\n* Individuals who do not have an active role in the care process (e.g., parents who only provide financial support),\n* Caregivers with intellectual disabilities, serious psychiatric diagnoses, or cognitive impairments that limit communication,\n* Participants with incomplete or invalid survey forms.",{"count":325,"type":22},23,"The aim of this study is to examine the psychometric properties of the Turkish version of the Scoliosis Caregiver Response and Emotional Scale (SCaRES) questionnaire; to evaluate the reliability of the Turkish form and to ensure its usability in clinical and research fields.",[328,329,330],"Scoliosis Idiopathic","Scoliosis Idiopathic Adolescent","Caregiver Anxiety",[329,332,333],"Reliability","Caregiver","2025-11-28",{"date":336,"type":39},"2025-12-10",{"date":336,"type":22},{"date":339,"type":22},"2026-03-10",{"name":45,"class":46},{"id":342,"slug":343,"hasResults":12,"nctId":344,"briefTitle":345,"officialTitle":346,"acronym":4,"eligibilityCriteria":347,"healthyVolunteers":12,"sex":348,"minAge":349,"maxAge":55,"enrollmentInfo":350,"targetDuration":4,"studyType":60,"phases":4,"briefSummary":352,"conditions":353,"keywords":356,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":334,"lastUpdatePostDateStruct":360,"startDateStruct":361,"completionDateStruct":363,"leadSponsor":365,"locationsCount":47},"100614174","reliability-and-validity-of-the-adolescent-idiopathic-scoliosis---truncal-anterior-asymmetry-scoliosis-questionnaire-taasq-100614174","NCT07276165","Reliability and Validity of the Adolescent Idiopathic Scoliosis - Truncal Anterior Asymmetry Scoliosis Questionnaire (TAASQ)","Reliability and Validity of the Turkish Version of the Adolescent Idiopathic Scoliosis-Truncal Anterior Asymmetry Scoliosis Questionnaire (TAASQ)","Inclusion Criteria:\n\n* Adolescent idiopathic diagnosis\n\nExclusion Criteria:\n\n* Individuals who did not agree to participate in the study","FEMALE","10 Years",{"count":351,"type":22},29,"The survey examines how individuals with scoliosis define themselves and their physical appearance. Our aim in this study was to translate this survey into Turkish and demonstrate its reliability and validity.",[329,354,355],"Scoliosis Define Themselves","Physical Perception of Their Bodies",[357,358,359],"Scoliosis","Body appearance","Female",{"date":336,"type":39},{"date":362,"type":22},"2025-12-15",{"date":364,"type":22},"2026-03-15",{"name":45,"class":46},{"id":367,"slug":368,"hasResults":12,"nctId":369,"briefTitle":370,"officialTitle":371,"acronym":4,"eligibilityCriteria":372,"healthyVolunteers":87,"sex":17,"minAge":55,"maxAge":19,"enrollmentInfo":373,"targetDuration":4,"studyType":23,"phases":375,"briefSummary":376,"conditions":377,"keywords":381,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":388,"lastUpdatePostDateStruct":389,"startDateStruct":391,"completionDateStruct":393,"leadSponsor":394,"locationsCount":47},"100610883","effect-of-myofascial-release-on-pain-grip-strength-manual-dexterity-and-quality-of-life-in-late-term-rehabilitation-of-hand-flexor-tendon-repairs-100610883","NCT07233369","Effect of Myofascial Release on Pain, Grip Strength, Manual Dexterity, and Quality of Life in Late-Term Rehabilitation of Hand Flexor Tendon Repairs","Myofascial Release","Inclusion Criteria:\n\n* Being between the ages of 18 and 65,\n* Having a hand flexor tendon injury and subsequent surgery,\n* Not having a symptom of deterioration in the extremity being cared for,\n* Having adequate communication skills,\n* Voluntarily participating in the study.\n\nExclusion Criteria:\n\n* Having had previous hand surgery for any reason other than this injury,\n* Having a comorbid mental, physical, or neurological chronic illness,\n* Having cognitive problems that prevent communication,\n* Having any problem that prevents cooperation.",{"count":374,"type":22},42,[25],"The aim of this study was to investigate the effectiveness of myofascial release exercises performed in the late period compared to classical physiotherapy training in individuals with hand flexor tendon repair.",[378,379,380],"Hand Flexor Tendon","Facial Mobilization","Exercise",[382,383,380,384,385,386,387],"hand flexor tendon","facial mobilization","pain","grip strenght","hand skills","quality of life","2025-11-14",{"date":390,"type":39},"2025-11-18",{"date":392,"type":22},"2025-11-30",{"date":98,"type":22},{"name":45,"class":46},{"id":396,"slug":397,"hasResults":12,"nctId":398,"briefTitle":399,"officialTitle":400,"acronym":4,"eligibilityCriteria":401,"healthyVolunteers":12,"sex":242,"minAge":402,"maxAge":55,"enrollmentInfo":403,"targetDuration":405,"studyType":60,"phases":4,"briefSummary":406,"conditions":407,"keywords":410,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":414,"lastUpdatePostDateStruct":415,"startDateStruct":417,"completionDateStruct":419,"leadSponsor":421,"locationsCount":47},"100607558","effects-of-emicizumab-treatment-in-patients-with-hemophilia-a-100607558","NCT07190118","Effects of Emicizumab Treatment in Patients With Hemophilia A","Effects of Emicizumab Treatment on the Musculoskeletal System in Children With Hemophilia A: A Prospective Study","Inclusion Criteria:\n\n* Children who are under 18 years of age,\n* Have been diagnosed with Hemophilia A by a physician,\n* Have a factor level of 1% (IU) or less,\n* Have inhibitors positive or negative,\n* Have no obstacles to starting subcutaneous (emicizumab) treatment,\n* Willing to participate in the study\n\nExclusion Criteria:\n\n\\- Children with a history of cerebrovascular bleeding who present any neurological findings that would prevent participation in the study","1 Year",{"count":404,"type":22},20,"6 Months","The aim of our study is to investigate the effects of emicizumab treatment on the musculoskeletal system in children with hemophilia A.",[252,408,409],"Musculoskeletal Assessment","Musculoskeletal Abnormalities",[252,411,412,413],"Emicizumab","Musculoskeletal system","Measurement","2025-09-23",{"date":416,"type":39},"2025-09-24",{"date":418,"type":22},"2025-09-30",{"date":420,"type":22},"2026-02-10",{"name":45,"class":46},{"id":423,"slug":424,"hasResults":12,"nctId":425,"briefTitle":426,"officialTitle":427,"acronym":4,"eligibilityCriteria":428,"healthyVolunteers":12,"sex":17,"minAge":56,"maxAge":19,"enrollmentInfo":429,"targetDuration":4,"studyType":23,"phases":431,"briefSummary":432,"conditions":433,"keywords":438,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":442,"lastUpdatePostDateStruct":443,"startDateStruct":445,"completionDateStruct":447,"leadSponsor":449,"locationsCount":47},"100605543","the-effect-of-fascial-treatment-in-patients-with-adhesive-capsulitis-100605543","NCT07163884","The Effect of Fascial Treatment in Patients With Adhesive Capsulitis","Adheziv kapsülit tanılı Hastalarda Fasyal Tedavinin ağrı, Normal Eklem Hareket açıklığı, Propriosepsiyon ve Fasya Mimarisine Etkisinin araştırılması","Inclusion Criteria:\n\n* Patients diagnosed with adhesive capsulitis by a specialist,\n* Patients between the ages of 35 and 60,\n* Those not diagnosed with cervical disc herniation that could cause other shoulder pathologies,\n* Those who have not participated in an upper extremity-related physiotherapy program within the last 6 months,\n* Individuals who volunteer to participate in the study,\n\nExclusion Criteria:\n\n* Individuals who have undergone shoulder surgery consistent with any pathology,\n* Individuals with a neurological history,\n* Individuals diagnosed with diabetes mellitus (DM)",{"count":430,"type":22},36,[25],"Our study is unique in that it utilizes a self-designed fascial mobilization protocol and ultrasonographic evaluation for adhesive capsulitis. Therefore, the aim of our study is to investigate the effects of fascial therapy on pain, normal joint range of motion, proprioception, and fascial architecture in patients diagnosed with adhesive capsulitis.",[434,435,436,437],"Adhesive Capsulitis","Ultrasonography","Fascia","Treatment (ProudMe)",[439,384,157,440,441],"adhezsiv capsulitis","proprioception","fascia architecture","2025-09-01",{"date":444,"type":39},"2025-09-09",{"date":446,"type":22},"2025-09-15",{"date":448,"type":22},"2025-11-15",{"name":45,"class":46},{"id":451,"slug":452,"hasResults":12,"nctId":453,"briefTitle":454,"officialTitle":455,"acronym":4,"eligibilityCriteria":456,"healthyVolunteers":12,"sex":17,"minAge":56,"maxAge":19,"enrollmentInfo":457,"targetDuration":4,"studyType":23,"phases":458,"briefSummary":459,"conditions":460,"keywords":461,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":464,"lastUpdatePostDateStruct":465,"startDateStruct":467,"completionDateStruct":468,"leadSponsor":469,"locationsCount":47},"100605110","effects-of-exercise-on-adhesive-capsulitis-100605110","NCT07158255","Effects of Exercise on Adhesive Capsulitis","Effect of Exercise Training on Pain, Range of Motion, Functionality and Shoulder Architecture in Patients With Adhesive Capsulitis","Inclusion Criteria:\n\n* Diagnosed with adhesive capsulitis by a physician,\n* Between the ages of 35-60,\n* Not diagnosed with cervical disc herniation that could cause other shoulder pathologies,\n* Not participating in an upper extremity-related physiotherapy program within the last 6 months,\n* Volunteering individuals to participate in the study\n\nExclusion Criteria:\n\n* Individuals who have undergone shoulder surgery consistent with any pathology,\n* Individuals with a neurological history,\n* Individuals diagnosed with diabetes mellitus (DM)",{"count":268,"type":22},[25],"Our study aims to investigate the effects of exercise training on pain, range of motion, functionality and shoulder architecture in patients with adhesive capsulitis.",[434,380,435],[439,384,157,462,463,281],"functionality","shoulder architecture","2025-08-28",{"date":466,"type":39},"2025-09-05",{"date":466,"type":22},{"date":448,"type":22},{"name":45,"class":46},{"id":471,"slug":472,"hasResults":12,"nctId":473,"briefTitle":474,"officialTitle":475,"acronym":476,"eligibilityCriteria":477,"healthyVolunteers":12,"sex":17,"minAge":349,"maxAge":55,"enrollmentInfo":478,"targetDuration":4,"studyType":23,"phases":480,"briefSummary":481,"conditions":482,"keywords":484,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":490,"lastUpdatePostDateStruct":491,"startDateStruct":493,"completionDateStruct":495,"leadSponsor":497,"locationsCount":47},"100598102","augmented-reality-assisted-physiotherapy-for-adolescents-with-idiopathic-scoliosis-a-qualitative-study-100598102","NCT07067125","Augmented Reality-Assisted Physiotherapy for Adolescents With Idiopathic Scoliosis: A Qualitative Study","A Qualitative Evaluation of the Effects of Augmented Reality-Supported Training Methods on Body Awareness and Exercise Adherence in Adolescents With Idiopathic Scoliosis","AR-AIS","Inclusion Criteria:\n\n* Aged between 10 and 18 years\n* Diagnosed with adolescent idiopathic scoliosis (AIS)\n* Completed at least 4 weeks of AR-based physiotherapy\n* Sufficient Turkish language proficiency to participate in interviews\n* Provided written informed consent (adolescent and guardian)\n\nExclusion Criteria:\n\n* Presence of neurological or cognitive conditions interfering with communication\n* Withdrew before completing the intervention program\n* Declined audio recording of interviews",{"count":479,"type":22},15,[25],"This study aims to explore the effects of augmented reality (AR)-supported physiotherapy on body awareness, motivation, and exercise adherence in adolescents diagnosed with Adolescent Idiopathic Scoliosis (AIS). Using a qualitative phenomenological approach, the study will involve semi-structured interviews with adolescents who have completed at least four weeks of AR-based physiotherapeutic scoliosis-specific exercises. The goal is to understand participants' lived experiences with AR-enhanced rehabilitation and to inform the development of adolescent-centered, technology-integrated physiotherapy strategies in conservative scoliosis care.",[329,483],"Scoliosis Idiopathic Adolescent Treatment",[485,486,487,488,489],"Adolescent idiopathic scoliosis","augmented reality","qualitative research","psychosocial adjustment","physiotherapy","2025-07-04",{"date":492,"type":39},"2025-07-16",{"date":494,"type":39},"2025-06-01",{"date":496,"type":22},"2025-07-31",{"name":45,"class":46},{"id":499,"slug":500,"hasResults":12,"nctId":501,"briefTitle":502,"officialTitle":502,"acronym":4,"eligibilityCriteria":503,"healthyVolunteers":87,"sex":348,"minAge":4,"maxAge":4,"enrollmentInfo":504,"targetDuration":4,"studyType":23,"phases":506,"briefSummary":507,"conditions":508,"keywords":512,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":514,"lastUpdatePostDateStruct":515,"startDateStruct":517,"completionDateStruct":519,"leadSponsor":520,"locationsCount":47},"100588896","the-effects-of-education-given-to-primiparous-pregnant-women-who-have-fear-of-childbirth-according-to-joyce-travelbees-human-to-human-relationship-model-on-fear-of-childbirth-readiness-for-childbirth-and-acceptance-of-the-maternal-role-100588896","NCT06947369","The Effects of Education Given to Primiparous Pregnant Women Who Have Fear of Childbirth According to Joyce Travelbee's Human-to-Human Relationship Model on Fear of Childbirth, Readiness for Childbirth and Acceptance of the Maternal Role","Inclusion Criteria:1. The pregnant woman's first pregnancy. 2. A mid-level or above score on the Wijma Childbirth Expectation\u002FExperience Scale Version A.\n\n3\\. The pregnant woman is between 28-40 weeks of gestation (third trimester). 4. The pregnant woman does not have a chronic health problem. 5. The pregnant woman has a single fetus. 6. The pregnant woman has not received infertility treatment. 7. The pregnant woman has not received a psychiatric diagnosis. 8. The pregnant woman does not have a high-risk pregnancy. 9. The pregnant woman's acceptance to participate in the study.\n\nExclusion Criteria:1. Not willing to participate in the study 2. Not speaking Turkish 3. Illiterate, having communication difficulties 4. Not meeting the study criteria\n\n\\-",{"count":505,"type":22},70,[25],"The research is planned as a randomised controlled experimental study. Research data will be collected between March-July 2025. The population of the study will consist of all pregnant women who come to Kilis Prof.Dr.Alaeddin Yavaşca State Hospital Gynaecology and Obstetrics Polyclinics. The sample of the study will consist of primiparous pregnant women who meet the research criteria and accept to participate in the study among the pregnant women who come to Kilis Prof.Dr.Alaeddin Yavaşca State Hospital Gynaecology and Obstetrics Polyclinics.\n\nData will be collected from primiparous pregnant women who meet the inclusion criteria and accept the study after being informed about the study by meeting the pregnant women who come to Kilis Prof.Dr.Alaeddin Yavaşca State Hospital Gynaecology and Obstetrics Outpatient Clinic before or after their outpatient examinations.\n\nData Collection Tools Personal Information Form, Wijma Birth Anticipation \u002F Experience Scale A Version scale and Prenatal Self-Assessment Scale Dependent variables of the study: Wijma Birth Expectancy \u002F Experience Questionnaire (W-DEQ) A Version and Prenatal Self-Assessment Scale subscales of acceptance of maternal role and readiness for childbirth scales. Independent variables of the study: Socio-demographic and obstetric characteristics of primiparous pregnant women",[509,510,511],"Fear of Childbirth, Pregnant Woman","Healthy Pregnant Woman","Healt",[513],"Primiparous pregnant, fear of childbirth,role of motherhood, Joyce Travelbee, childbirth readiness","2025-04-25",{"date":516,"type":39},"2025-04-27",{"date":518,"type":39},"2025-03-03",{"date":496,"type":22},{"name":45,"class":46},{"id":522,"slug":523,"hasResults":12,"nctId":524,"briefTitle":525,"officialTitle":526,"acronym":527,"eligibilityCriteria":528,"healthyVolunteers":12,"sex":17,"minAge":55,"maxAge":4,"enrollmentInfo":529,"targetDuration":4,"studyType":60,"phases":4,"briefSummary":531,"conditions":532,"keywords":533,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":537,"lastUpdatePostDateStruct":538,"startDateStruct":539,"completionDateStruct":541,"leadSponsor":543,"locationsCount":47},"100588573","self-efficacy-and-medication-adherence-in-patients-with-coronary-artery-disease-a-descriptive-study-100588573","NCT06943157","Self-Efficacy and Medication Adherence in Patients With Coronary Artery Disease: A Descriptive Study","Investigation of the Relationship Between Self-Efficacy and Adherence to Medication in Individuals With Coronary Artery Disease: A Descriptive and Correlational Study","SEMACAD","Inclusion Criteria:\n\n* Being 18 years of age or older\n\nHaving been diagnosed with Coronary Artery Disease (angina pectoris, unstable angina, myocardial infarction) at least 1 year ago\n\nBeing followed\n\nBeing able to communicate in Turkish\n\nVoluntarily agreeing to participate in the study\n\nHaving no diagnosed mental disorder\n\nExclusion Criteria:\n\n* Having a primary diagnosis other than Coronary Artery Disease\n\nBeing unable to complete the questionnaires due to mental health problems\n\nProviding incomplete data or withdrawing from the study",{"count":530,"type":22},135,"This descriptive study aims to examine the relationship between self-efficacy and medication adherence in individuals with coronary artery disease (CAD). The study will be conducted between March and October 2025 at Adıyaman University Training and Research Hospital with a planned sample size of 135 participants. Data will be collected using a Descriptive Information Form, the Self-Efficacy for Managing Chronic Disease Scale, and the Medication Adherence Report Scale (MARS).",[118],[534,118,535,536],"Nurse","Self-Efficacy","Medication Adherence","2025-04-24",{"date":516,"type":39},{"date":540,"type":39},"2025-03-01",{"date":542,"type":22},"2025-10-01",{"name":45,"class":46},{"id":545,"slug":546,"hasResults":12,"nctId":547,"briefTitle":548,"officialTitle":549,"acronym":4,"eligibilityCriteria":550,"healthyVolunteers":87,"sex":17,"minAge":551,"maxAge":552,"enrollmentInfo":553,"targetDuration":4,"studyType":23,"phases":555,"briefSummary":556,"conditions":557,"keywords":559,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":561,"lastUpdatePostDateStruct":562,"startDateStruct":564,"completionDateStruct":566,"leadSponsor":568,"locationsCount":47},"100580073","the-effect-of-surgical-incision-drep-use-in-endotracheal-tube-fixation-100580073","NCT06832553","The Effect of Surgical Incision Drep Use in Endotracheal Tube Fixation","The Effect of Surgical Incision Drep Use in Endotracheal Tube Fixation in Neonatal Preterm Infants: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Preterm infants between 28-34 weeks of gestation hospitalized in neonatal intensive care unit,\n* Intubated infants on invasive mechanical ventilators,\n* Babies who were orally intubated were included in the study.\n\nExclusion Criteria:\n\n* Congenital skin condition,\n* With circulatory problems,\n* Congenital anomalies and metabolic disorders,\n* Small for gestational age (SGA) and large for gestational age (LGA),\n* Unplanned extubation taking place,\n* Babies intubated for less than 24 hours will be excluded from the study.","28 Weeks","34 Weeks",{"count":554,"type":22},110,[25],"It is aimed to minimise both unplanned extubation and skin damage with the surgical incision drep that we will use to fix the endotracheal tube in neonatal preterm infants and to reduce the complications that may develop due to these events. In addition, it is aimed to evaluate the relationship between these parameters by using devices measuring skin moisture, skin pH and Neonatal Skin Condition Assessment Scale in experimental and control groups.",[558],"Preterm",[560],"preterm","2025-03-11",{"date":563,"type":39},"2025-03-14",{"date":565,"type":39},"2024-10-15",{"date":567,"type":22},"2025-07-15",{"name":45,"class":46},{"id":570,"slug":571,"hasResults":12,"nctId":572,"briefTitle":573,"officialTitle":574,"acronym":4,"eligibilityCriteria":575,"healthyVolunteers":12,"sex":348,"minAge":55,"maxAge":576,"enrollmentInfo":577,"targetDuration":4,"studyType":23,"phases":578,"briefSummary":579,"conditions":580,"keywords":582,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":585,"lastUpdatePostDateStruct":586,"startDateStruct":588,"completionDateStruct":590,"leadSponsor":592,"locationsCount":47},"100582203","different-exercise-training-programs-in-university-students-with-primary-dysmenorrhea-100582203","NCT06860256","Different Exercise Training Programs in University Students with Primary Dysmenorrhea","Comparison of the Effects of Different Exercise Training Programs on Dysmenorrhea Symptoms, Sleep and Quality of Life in University Students with Primary Dysmenorrhea","Inclusion Criteria:\n\n* Nulliparous female university students aged 18-25 years who volunteered to participate in the study, met the criteria specified in the PD Consensus Guidelines and were diagnosed with PD by a gynecologist\n* Individuals with a body mass index (BMI) between 18-35\n* Individuals with a regular menstrual cycle (28 ± 7 days)\n* Individuals with menstrual pain Visual Analog Scale (VAS) score of 4 cm or higher for the last 6 months\n\nExclusion Criteria:\n\n* Gastrointestinal, urogynecologic, autoimmune, psychiatric, neurological diseases or other chronic pain syndromes\n* Having given birth and\u002For being pregnant\n* Intrauterine device users\n* Pelvic surgery patients\n* Taking oral contraceptives or medication, including antidepressants, for at least 6 months before the study\n* Those with a pathological history or ultrasonography result indicating secondary dysmenorrhea\n* Those who use alternative treatment methods and exercise regularly\n* Serious traumatic life events that occurred in the three months prior to the start of the study\n* Communication problems that may interfere with the implementation of assessments and\u002For treatment program","25 Years",{"count":174,"type":22},[25],"Dysmenorrhea is severe lower abdominal pain in women during menstruation. The pain is usually cramping and can radiate to the thighs or lower spine. Lower abdominal pain may be accompanied by vomiting, headache, back pain, diarrhea, fatigue, etc. Depending on the pathophysiology, dysmenorrhea is classified into two types: primary and secondary. Primary dysmenorrhea (PD) is menstrual pain associated with normal ovulatory cycles in the absence of pelvic pathology and a clear physiologic etiology and is most commonly seen in adolescents and young adults. There are numerous studies on PD in the literature, but there is still a lack of studies on which of the non-pharmacologically recommended exercise and other methods is more effective on dysmenorrhea symptoms, sleep and quality of life for individuals with this problem. Different exercise intensities may affect PD symptoms through different mechanisms. Moderate to high intensity exercise may reduce pain by increasing anti-inflammatory cytokines, whereas less intense exercise, such as yoga, affects pain levels by decreasing cortisol levels. The lack of research on which exercise training is more effective in PD individuals was considered as a limitation. In the light of this information, the aim of the investigators study is to compare the effects of different training techniques on dysmenorrhea symptoms, sleep and quality of life in PD treatment and to present the preferability of these techniques based on evidence.",[380,581],"Primary Dysmenorrhea",[583,584],"primary dysmenorrhea","exercises","2025-02-28",{"date":587,"type":39},"2025-03-06",{"date":589,"type":22},"2025-02-25",{"date":591,"type":22},"2025-10-25",{"name":45,"class":46},{"id":594,"slug":595,"hasResults":12,"nctId":596,"briefTitle":597,"officialTitle":597,"acronym":598,"eligibilityCriteria":599,"healthyVolunteers":87,"sex":17,"minAge":55,"maxAge":576,"enrollmentInfo":600,"targetDuration":4,"studyType":23,"phases":602,"briefSummary":603,"conditions":604,"keywords":608,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":611,"lastUpdatePostDateStruct":612,"startDateStruct":614,"completionDateStruct":616,"leadSponsor":618,"locationsCount":4},"100579072","the-effect-of-mindfulness-based-stress-reduction-programme-on-smartphone-addiction-stress-and-quality-of-life-in-university-students-100579072","NCT06819540","The Effect of Mindfulness-Based Stress Reduction Programme on Smartphone Addiction, Stress and Quality of Life in University Students","Mindfulness","Inclusion Criteria:\n\n* Individuals over 18 years of age,\n* From the highest on the smartphone addiction scale students from the beginning until the sample size is reached\n* No diagnosed psychiatric illness or medication not to use it,\n* Volunteering to participate in the study\n* Muş Alparslan University at the time of the research Continuing education in the Department of Nursing\n\nExclusion Criteria:\n\n* Students who did not participate in at least two group programs and",{"count":601,"type":22},120,[25],"The aim of this observational study was to examine the effect of Mindfulness-Based Stress Reduction Program on Smartphone Addiction, Stress and Quality of Life in Nursing Students. The main question it aims to answer is:\n\nIs there a significant relationship between smartphone addiction, quality of life and stress in nursing students? Smartphone addiction scale will be applied and students with risky scores will be determined and pre-test will be applied to the students in the experimental group according to randomization. During an 8-week intervention period, in addition to mindfulness practices and experiential studies, experiential practices will be carried out on stress, stress management and how mindfulness is applied in daily life and interpersonal communication through the sharing of the participants.",[605,606,607],"Smartphone Addiction","Mindfulness Based Stress Reduction","Quality of Life",[598,609,610],"University Students","Stress","2025-02-10",{"date":613,"type":39},"2025-02-11",{"date":615,"type":22},"2025-02-22",{"date":617,"type":22},"2025-12-20",{"name":45,"class":46},{"id":620,"slug":621,"hasResults":12,"nctId":622,"briefTitle":623,"officialTitle":623,"acronym":624,"eligibilityCriteria":625,"healthyVolunteers":87,"sex":17,"minAge":19,"maxAge":626,"enrollmentInfo":627,"targetDuration":4,"studyType":23,"phases":629,"briefSummary":630,"conditions":631,"keywords":634,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":638,"lastUpdatePostDateStruct":639,"startDateStruct":640,"completionDateStruct":642,"leadSponsor":644,"locationsCount":4},"100578940","the-effect-of-su-jok-therapy-applied-to-the-elderly-on-constipation-symptoms-and-quality-of-life-100578940","NCT06817824","The Effect of Su-Jok Therapy Applied to the Elderly on Constipation Symptoms and Quality of Life","Su-Jok Therapy","Inclusion Criteria:\n\n* Young individuals aged 65-74 years, middle-aged individuals aged 75-84 years and hospitalised individuals aged 85 years and over who agreed to participate in the study,\n* Scores of 24 and above on the Mini Mental Test,\n* Those who score 3 points and above on the Visual Comparison Scale,\n* Those who meet the Rome IV Criteria,\n* Elderly people aged 65 years and over who do not have any lesion, infection, etc. that would prevent the application of Su Jok treatment on the hands and feet, who do not have acute diarrhoea, who do not have significant intestinal pathology such as incontinence and faecal impaction, who do not have inflammatory bowel disease, who have not had bowel surgery before, who do not use laxatives during the application will be included in the study.\n\nExclusion Criteria:\n\n* Those who do not fulfil the inclusion criteria,\n* Patients with cognitive impairment such as dementia and Alzheimer's,\n* Patients with hearing problems or using hearing aids,\n* Older people who did not want to participate in the study.","100 Years",{"count":628,"type":22},80,[25],"This article discusses the prevalence and health implications of constipation in the elderly population. Health problems increase with age and negatively affect quality of life. Constipation is a common problem in the elderly that severely reduces quality of life and is associated with many factors. Pharmacologic and non-pharmacologic methods are used for the management of constipation, but long-term use of pharmacologic treatments may lead to adverse effects. Therefore, non-pharmacologic approaches are gaining more importance.\n\nIn this context, Su Jok therapy, as an oriental medicine method, is a treatment method that aims to affect various organs of the body by using reflection points on the hands and feet. It is argued that Su Jok therapy can be beneficial in terms of symptom management and improving quality of life, especially in fields such as nursing and midwifery. In Turkey, there are no studies examining the effect of Su Jok therapy on constipation symptoms. This project aims to determine the effect of Su Jok therapy on constipation symptoms and quality of life, and the results are expected to contribute to the development of health services and treatment methods",[632,607,633],"Elderly (people Aged 65 or More)","Constipation",[635,636,637],"elderly","constipation","sujok therapy","2025-02-04",{"date":611,"type":39},{"date":641,"type":22},"2025-02-01",{"date":643,"type":22},"2025-10-20",{"name":45,"class":46},{"id":646,"slug":647,"hasResults":12,"nctId":648,"briefTitle":649,"officialTitle":650,"acronym":4,"eligibilityCriteria":651,"healthyVolunteers":12,"sex":17,"minAge":652,"maxAge":55,"enrollmentInfo":653,"targetDuration":4,"studyType":23,"phases":655,"briefSummary":656,"conditions":657,"keywords":659,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":664,"lastUpdatePostDateStruct":665,"startDateStruct":667,"completionDateStruct":669,"leadSponsor":671,"locationsCount":4},"100563608","effectiveness-of-biofeedback-training-in-children-with-neurogenic-bladder-and-bowel-disorder-wth-spina-bifida-100563608","NCT06618378","Effectiveness of Biofeedback Training in Children with Neurogenic Bladder and Bowel Disorder Wıth Spina Bifida","Effectiveness of Biofeedback Training in Children with Neurogenic Bladder and Bowel Disorder with Spina Bifida","Inclusion Criteria:\n\n* Diagnosed with meningomyelocele type spina bifida\n* Individuals between the ages of 5-18.\n\nExclusion Criteria:\n\n* Presence of lower urinary tract infection\n* Presence of abdominal surgery in the last 3 months.","5 Years",{"count":654,"type":22},24,[25],"The aim of this study is to examine and compare the bladder and bowel functions, activation of pelvic floor and abdominal muscle groups and quality of life of children diagnosed with spina bifida who did not receive any treatment due to bladder-intestinal dysfunction, received only urotherapy training and received biofeedback training combined with breathing.\n\nThe type of study is clinical trial. Question 1: Does biofeedback training combined with breathing have an effect on bladder and bowel functions, activation of pelvic floor and abdominal muscle groups and quality of life in spina bifida patients with neurogenic bladder and bowel disorders? Question 2: Does urotherapy training have an effect on bladder and bowel functions, activation of pelvic floor and abdominal muscle groups and quality of life in spina bifida patients with neurogenic bladder and bowel disorders? Group 1: control group Group 2: urotherapy training group Group 3: Biofeedback exercise training group combined with breathing There will be no extra treatment to group 1. Urotherapy Training: Standard urotherapy is a combined method that includes clinical assessment (recording voiding frequencies, voiding volumes and incontinence episodes in a bladder diary), voiding habit training, behavior modification instructions, lifestyle recommendations regarding fluid intake and supporting children and their parents through the process.\n\nExercise Training: Urotherapy training will be given at the beginning of the treatment process. Contraction and relaxation will be applied around the external sphincter in combination with diaphragmatic breathing by visual imagery with EMG biofeedback application.\n\nGroup 1, group 2 and group 3 will be compared.",[658],"Spina Bifida",[660,661,662,663],"spina bifida","biofeedback","urotherapy","neurogenicbladder","2024-09-26",{"date":666,"type":39},"2024-10-01",{"date":668,"type":22},"2024-10-21",{"date":670,"type":22},"2026-07-21",{"name":45,"class":46},""]