[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Okan University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":305},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,11,0,[8,42,65,98,128,150,182,201,226,248,276],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":4},"100636939","the-effect-of-kinesio-taping-applied-to-the-gastrocnemius-muscle-on-muscle-oxygenation-pain-pressure-threshold-and-muscle-mechanical-properties-100636939",false,"NCT07572201","The Effect of Kinesio Taping Applied to the Gastrocnemius Muscle on Muscle Oxygenation, Pain Pressure Threshold, and Muscle Mechanical Properties","Investigation of the Effects of Kinesio Taping Applied to the Gastrocnemius Muscle on Muscle Oxygenation, Pain Pressure Threshold, and Muscle Mechanical Properties in Young Healthy Individuals","Inclusion Criteria:\n\n* Right lower extremity being dominant,\n* Not having suffered a musculoskeletal injury to the lower extremity in the last 3 months\n\nExclusion Criteria:\n\n* Having any orthopedic, neurological, circulatory, or psychiatric diagnosis,\n* Having a history of lower extremity surgery,\n* Having an allergy to KT or similar tapes,\n* Using muscle relaxants and non-steroidal anti-inflammatory drugs,\n* Having received physiotherapy and rehabilitation treatment within the last 3 months.",true,"MALE","18 Years","30 Years",{"count":21,"type":22},50,"ESTIMATED","INTERVENTIONAL",[25],"NA","The aim of this study is to investigate the effects of kinesio taping applied to the gastrocnemius muscle on muscle oxygenation, pain pressure threshold, and mechanical properties of the muscle in healthy young individuals.",[28,29],"Kinesio Taping","Muscle Oxygenation","NOT_YET_RECRUITING","2026-04-29",{"date":33,"type":34},"2026-05-07","ACTUAL",{"date":36,"type":22},"2026-05-15",{"date":38,"type":22},"2026-08-15",{"name":40,"class":41},"Okan University","OTHER",{"id":43,"slug":44,"hasResults":11,"nctId":45,"briefTitle":46,"officialTitle":47,"acronym":4,"eligibilityCriteria":48,"healthyVolunteers":11,"sex":49,"minAge":18,"maxAge":50,"enrollmentInfo":51,"targetDuration":4,"studyType":23,"phases":53,"briefSummary":54,"conditions":55,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":57,"lastUpdatePostDateStruct":58,"startDateStruct":60,"completionDateStruct":62,"leadSponsor":64,"locationsCount":4},"100636553","comparison-of-the-effects-of-different-massage-techniques-in-individuals-with-bruxism-100636553","NCT07567183","Comparison of the Effects of Different Massage Techniques in Individuals With Bruxism","Comparison of the Effects of Different Massage Techniques on Pain, Orofacial Muscle Characteristics, Disability, and Sleep Quality in Individuals With Bruxism","Inclusion Criteria:\n\n* Possible diagnosis of sleep bruxism,\n* Reporting jaw or chewing muscle pain within the last 3 months\n\nExclusion Criteria:\n\n* Having any orthopedic, neurological, or psychiatric diagnosis,\n* Having systemic and\u002For degenerative disorders,\n* Neurological or psychiatric disorders (excluding anxiety and depression),\n* Using medications that affect sleep or motor behavior,\n* Having arthrogenic or mixed temporomandibular disorders,\n* Using an intraoral prosthesis,\n* Having a history of direct trauma or previous surgery in the orofacial region,\n* Using muscle relaxants and non-steroidal anti-inflammatory drugs,\n* Using a removable prosthesis,\n* Receiving any treatment for bruxism within the last 4 weeks.","ALL","45 Years",{"count":52,"type":22},42,[25],"The aim of this study is to compare the effects of occlusal splint therapy and different massage techniques on pain intensity and orofacial muscle tone and stiffness in individuals with possible sleep bruxism. A secondary aim is to evaluate the effects of these interventions on oral parafunctional behaviors, disability, and sleep quality.",[56],"Bruxism","2026-04-28",{"date":59,"type":34},"2026-05-05",{"date":61,"type":22},"2026-05-01",{"date":63,"type":22},"2026-09-01",{"name":40,"class":41},{"id":66,"slug":67,"hasResults":11,"nctId":68,"briefTitle":69,"officialTitle":69,"acronym":70,"eligibilityCriteria":71,"healthyVolunteers":16,"sex":49,"minAge":18,"maxAge":72,"enrollmentInfo":73,"targetDuration":4,"studyType":23,"phases":75,"briefSummary":76,"conditions":77,"keywords":84,"overallStatus":90,"whyStopped":4,"lastUpdateSubmitDate":91,"lastUpdatePostDateStruct":92,"startDateStruct":93,"completionDateStruct":95,"leadSponsor":97,"locationsCount":74},"100614171","the-effect-of-the-cesarean-eras-protocol-on-mother-infant-and-father-infant-bonding-a-multicenter-randomized-controlled-clinical-trial-100614171","NCT07276126","The Effect of the Cesarean ERAS Protocol on Mother-Infant and Father-Infant Bonding: a Multicenter, Randomized Controlled Clinical Trial.","ERAS-CS-BOND-1","IInclusion Criteria:\n\nPregnant women aged 18-60 years.\n\nSingleton, live fetus, and ≥37 weeks of gestation.\n\nUndergoing elective or medically indicated cesarean delivery.\n\nAbility to read and understand Turkish (for questionnaire validity).\n\nMothers and fathers willing and able to complete postpartum follow-up assessments (2 hours, 24 hours, day 4, day 7).\n\nProvision of written informed consent by mother and, if participating, by father\u002Fpartner.\n\nMaternal postpartum clinical stability (no condition precluding questionnaire completion).\n\n❌ Exclusion Criteria (Dışlanma Kriterleri)\n\nExclusion Criteria:\n\nPreterm birth (\\\u003C37 weeks) or multiple gestation (twins, triplets).\n\nStillbirth, early neonatal death, or major congenital anomaly.\n\nNewborn requiring prolonged NICU stay preventing bonding assessments.\n\nMaternal severe obstetric complications:\n\nMassive postpartum hemorrhage\n\nHysterectomy\n\nSevere preeclampsia or eclampsia\n\nSevere postpartum infection\n\nMaternal active psychiatric disorder or use of psychotropic medication.\n\nMaternal need for high-dose opioid analgesia or sedation interfering with bonding assessments.\n\nInability to read\u002Funderstand Turkish or cognitive impairment preventing questionnaire completion.\n\nFailure to complete follow-up visits (2 hours, 24 hours, day 4, day 7).\n\nWithdrawal of consent at any time.","60 Years",{"count":74,"type":22},1,[25],"This is a multicenter, 1:1 parallel-group, randomized controlled trial designed to compare the effect of the Enhanced Recovery After Cesarean (ERAS) protocol versus standard perioperative care on mother-infant and father-infant bonding in women undergoing cesarean delivery. The study will initially be conducted as a single-center trial at Istanbul Okan University Hospital. Once adequate site preparation is completed, additional centers will be added to expand the study to a multicenter setting.\n\nPrimary Outcome:\n\nThe primary outcome is the total score on the Postpartum Bonding Questionnaire (PBQ) assessed on postpartum day 7, reflecting mother-infant bonding.\n\nSecondary Outcomes:\n\nSecondary outcomes include:\n\nMaternal\u002FParental Postnatal Attachment Scale (MIBS) score at 2 hours postpartum (mother)\n\nPBQ score at 24 hours postpartum (mother)\n\nPBQ score at day 4 postpartum (mother)\n\nPBQ score at day 7 postpartum (father-infant bonding)\n\nEdinburgh Postnatal Depression Scale (EPDS) scores for mothers at 2 hours and 7 days postpartum\n\nTime to initiation of breastfeeding\n\nRequirement for neonatal intensive care unit (NICU) admission\n\nSample Size:\n\nThe total multicenter target sample size is n=300, with 150 participants in the ERAS group and 150 in the standard care group. The initial single-center phase at Okan University Hospital will enroll a target of n=100 participants (50 per group).\n\nRandomization:\n\nParticipants will be randomized using a block and stratified randomization approach based on parity (primiparous vs multiparous) and planned type of anesthesia.\n\nBlinding (Masking):\n\nDue to the nature of the intervention, care providers cannot be blinded to group assignment. However, outcome assessors and data analysts will remain blinded to treatment allocation to minimize bias.\n\nStudy Timeline and Visits:\n\nParticipants will be evaluated at multiple time points following cesarean delivery: 2 hours postpartum, 24 hours postpartum, day 4 postpartum, and day 7 postpartum. All primary and secondary outcomes will be collected at the specified time points.\n\nSignificance and Rationale:\n\nThe ERAS protocol for cesarean delivery is designed to optimize perioperative care, enhance recovery, and potentially improve early parent-infant bonding. While previous studies have focused on maternal recovery and clinical outcomes, evidence regarding the impact of ERAS on both mother-infant and father-infant bonding remains limited. This trial aims to provide high-quality evidence on whether ERAS implementation can improve early bonding experiences, maternal mental health, breastfeeding initiation, and neonatal outcomes compared with standard perioperative care. The findings may guide future clinical practice and contribute to optimizing family-centered care in cesarean deliveries.\n\nKey Features:\n\nMulticenter, randomized controlled design\n\nParallel 1:1 allocation\n\nStratified randomization by parity and anesthesia type\n\nBlinded outcome assessment and data analysis\n\nMultiple postpartum evaluation points\n\nFocus on psychosocial and clinical outcomes\n\nExpected Contributions:\n\nThis study will provide comprehensive data on the feasibility and effectiveness of ERAS protocols in cesarean deliveries and their potential benefits for both maternal and paternal bonding with the newborn. The inclusion of both mother-infant and father-infant outcomes, as well as maternal mental health and breastfeeding indicators, ensures a holistic assessment of early family-centered outcomes.",[78,79,80,81,82,83],"Bonding","ERAS","Cesarean Section","Maternal Care","Father - Child Relations","Mother-Infant Interaction",[85,86,87,88,89],"eras","erac","cesarean","maternal bonding","paternal bonding","RECRUITING","2026-04-27",{"date":57,"type":34},{"date":94,"type":34},"2025-12-13",{"date":96,"type":22},"2026-04-20",{"name":40,"class":41},{"id":99,"slug":100,"hasResults":11,"nctId":101,"briefTitle":102,"officialTitle":103,"acronym":4,"eligibilityCriteria":104,"healthyVolunteers":11,"sex":105,"minAge":18,"maxAge":106,"enrollmentInfo":107,"targetDuration":4,"studyType":23,"phases":109,"briefSummary":110,"conditions":111,"keywords":113,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":120,"lastUpdatePostDateStruct":121,"startDateStruct":123,"completionDateStruct":125,"leadSponsor":127,"locationsCount":74},"100634477","effects-of-clinical-pilates-on-pain-and-quality-of-life-in-women-with-dyspareunia-100634477","NCT07540195","Effects of Clinical Pilates on Pain and Quality of Life in Women With Dyspareunia","The Effects of Clinical Pilates Exercises on Pain, Self-Esteem, Body Image, Depression and Quality of Life in Women With Dyspareunia","Inclusion Criteria:\n\n* Female participants aged 18-55 years\n* Sexually active\n* Willing to participate in the study\n* No communication problems\n* Experiencing dyspareunia\n\nExclusion Criteria:\n\n* Having respiratory or neurological problems\n* Being pregnant\n* History of urogenital surgery","FEMALE","55 Years",{"count":108,"type":22},20,[25],"The aim of this study is to investigate the effects of clinical Pilates exercises on pain, self-esteem, body image, depression, and quality of life in women with dyspareunia. The study addresses dyspareunia as a multifaceted health problem with psychological, social as well as physical implications. it evaluates the effects of pelvic floor-focused clinical Pilates interventions on physiological symptoms and psychosocial well-being. it also demonstrates this approach as effective, safe, and evidence-based method in the treatment of dyspareunia among women in Turkish society.",[112],"Dyspareunia",[114,115,116,117,118,119],"Dyspareunia;","Female;","Sexual Dysfunction;","Exercise Therapy;","Quality of Life;","Depression","2026-04-24",{"date":122,"type":34},"2026-04-30",{"date":124,"type":22},"2026-04-06",{"date":126,"type":22},"2026-06-20",{"name":40,"class":41},{"id":129,"slug":130,"hasResults":11,"nctId":131,"briefTitle":132,"officialTitle":133,"acronym":4,"eligibilityCriteria":134,"healthyVolunteers":16,"sex":49,"minAge":18,"maxAge":135,"enrollmentInfo":136,"targetDuration":4,"studyType":23,"phases":138,"briefSummary":139,"conditions":140,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":142,"lastUpdatePostDateStruct":143,"startDateStruct":145,"completionDateStruct":147,"leadSponsor":149,"locationsCount":4},"100628530","effect-of-connective-tissue-massage-in-low-back-pain-100628530","NCT07462832","Effect of Connective Tissue Massage in Low Back Pain","Examining the Effectiveness of Connective Tissue Massage Applied in Addition to Exercise in Individuals With Chronic Low Back Pain: A Randomized Sham-Controlled Study","Inclusion Criteria:\n\nParticipants aged 18-65 who have had chronic low back pain in the past 6 months, have a VAS score above 3, do not have any disease that prevents them from working, and are volunteers will be included in the study.\n\nExclusion Criteria:\n\n* pregnant women,\n* individuals with fibromyalgia and chronic fatigue syndrome,\n* individuals with uncontrolled hypertension,\n* cancer, and diabetes,\n* individuals with lumbar spine fractures and those who have undergone surgical interventions in the back region,\n* and individuals who are unwilling or uncooperative.","65 Years",{"count":137,"type":22},40,[25],"Connective tissue massage (CTM) is a manual therapy method that aims to modulate the autonomic response using special stroking techniques performed on connective tissue, and its analgesic effects are described in the literature. However, studies examining the effects of CTM on multidimensional parameters such as mobility, flexibility, endurance, balance, proprioception, emotional state, and quality of life, in addition to pain and disability in chronic low back pain, are limited.\n\nThis study is designed as a randomized controlled trial to evaluate the multifaceted effects of KDM applied in addition to exercise and sham massage in individuals with chronic low back pain. The study will include a total of 40 participants aged 18-65 years who have experienced low back pain for at least six months. The eight-week interventions will be conducted twice weekly; all assessments will be performed before and after treatment. The study will assess pain (VAS), functional status (RMDQ), quality of life (NHP), fatigue (FSS), sleep quality (PUKİ), lumbar mobility, flexibility, balance, core endurance, and autonomic functions.",[141],"Chronic Low-back Pain","2026-03-08",{"date":144,"type":34},"2026-03-10",{"date":146,"type":22},"2026-02-09",{"date":148,"type":22},"2026-07-30",{"name":40,"class":41},{"id":151,"slug":152,"hasResults":11,"nctId":153,"briefTitle":154,"officialTitle":155,"acronym":156,"eligibilityCriteria":157,"healthyVolunteers":11,"sex":49,"minAge":18,"maxAge":135,"enrollmentInfo":158,"targetDuration":4,"studyType":23,"phases":160,"briefSummary":161,"conditions":162,"keywords":165,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":174,"lastUpdatePostDateStruct":175,"startDateStruct":177,"completionDateStruct":179,"leadSponsor":181,"locationsCount":4},"100628084","digital-follow-up-and-nursing-education-in-bariatric-surgery-patients-100628084","NCT07457034","Digital Follow-Up and Nursing Education in Bariatric Surgery Patients","The Effect of the Use of a PHP-MySQL Database-Based Follow-Up System and Nursing Education on Quality of Life in Patients Undergoing Bariatric Surgery","DigiBarQoL","Inclusion Criteria:\n\n* Adults aged 18-65 years Undergoing bariatric surgery Eligible for physical activity participation according to the International Physical Activity Questionnaire (IPAQ) Able to use the PHP-MySQL based digital follow-up system Willing to participate and provide written informed consent\n\nExclusion Criteria:\n\n* Severe cardiopulmonary disease or any medical condition that contraindicates exercise Uncontrolled hypertension or uncontrolled diabetes Severe musculoskeletal limitations preventing participation in the exercise program Severe psychiatric disorder impairing compliance or follow-up Participation in another interventional study during the study period Refusal or inability to provide informed consent",{"count":159,"type":22},52,[25],"This randomized controlled experimental study aims to evaluate the effect of a PHP-MySQL database-based digital follow-up system combined with structured nursing education on quality of life, body mass index (BMI), and exercise habits in patients undergoing bariatric surgery. Although bariatric surgery is an effective treatment for morbid obesity, long-term success depends largely on adherence to lifestyle modifications, including regular physical activity and sustained behavioral change.\n\nParticipants will be randomly assigned to either an intervention group or a control group. The intervention group will receive structured nursing education along with an 8-week digitally monitored exercise program starting at postoperative month four. The control group will receive standard postoperative care. Outcomes will be assessed using the Moorehead-Ardelt Quality of Life Questionnaire II (MA-II), BMI measurements, and the International Physical Activity Questionnaire (IPAQ). The study aims to provide evidence for integrating digital health technologies and structured nursing interventions into postoperative bariatric care.",[163,164],"Obesity (BMI > 35)","Bariatric Surgery",[166,167,168,169,170,171,172,173],"bariatric surgery","obesity","nursing education","digital health","exercise program","Quality of Life","Physical Activity","Randomized Controlled Trial","2026-03-03",{"date":176,"type":34},"2026-03-09",{"date":178,"type":22},"2026-03-07",{"date":180,"type":22},"2026-12-31",{"name":40,"class":41},{"id":183,"slug":184,"hasResults":11,"nctId":185,"briefTitle":186,"officialTitle":186,"acronym":4,"eligibilityCriteria":187,"healthyVolunteers":11,"sex":49,"minAge":18,"maxAge":4,"enrollmentInfo":188,"targetDuration":190,"studyType":191,"phases":4,"briefSummary":192,"conditions":193,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":174,"lastUpdatePostDateStruct":195,"startDateStruct":196,"completionDateStruct":198,"leadSponsor":200,"locationsCount":74},"100628151","the-relationship-between-pain-anxiety-and-post-operative-pain-in-patients-undergoing-cholecystectomy-surgery-100628151","NCT07457905","THE RELATIONSHIP BETWEEN PAIN ANXIETY AND POST-OPERATIVE PAIN IN PATIENTS UNDERGOING CHOLECYSTECTOMY SURGERY","Inclusion Criteria:\n\n* Adults aged 18 years and older Scheduled for elective cholecystectomy Able to speak and understand Turkish Conscious and able to complete questionnaires independently Voluntarily agree to participate in the study\n\nExclusion Criteria:\n\n* Use of anxiolytic medication Diagnosed psychiatric disorder that may affect pain perception Cognitive impairment preventing completion of study forms Emergency cholecystectomy Development of major postoperative complications requiring intensive care",{"count":189,"type":22},106,"106 Years","OBSERVATIONAL","This descriptive observational study aims to examine the relationship between preoperative fear of postoperative pain and postoperative pain intensity in patients undergoing cholecystectomy.\n\nPostoperative pain is one of the most common and significant clinical problems following surgical procedures. Psychological factors such as anxiety and fear of pain are known to influence pain perception and recovery outcomes. Preoperative fear related to postoperative pain may increase perceived pain intensity and negatively affect the postoperative recovery process.\n\nThe study will be conducted in the general surgery clinics of a tertiary care hospital. A total of 106 adult patients scheduled for cholecystectomy will be included. Preoperative fear of postoperative pain will be assessed one day before surgery using the Postoperative Pain Fear Scale. Postoperative pain intensity will be evaluated using the Numeric Rating Scale at the 4th, 12th, and 24th hours after surgery.\n\nThe findings of this study are expected to contribute to a better understanding of the relationship between preoperative pain-related fear and postoperative pain severity, and to provide evidence to improve perioperative nursing care and pain management strategies.",[194],"Cholecystectomy, Laparoscopic",{"date":176,"type":34},{"date":197,"type":22},"2026-02-15",{"date":199,"type":22},"2026-12-30",{"name":40,"class":41},{"id":202,"slug":203,"hasResults":11,"nctId":204,"briefTitle":205,"officialTitle":206,"acronym":4,"eligibilityCriteria":207,"healthyVolunteers":16,"sex":49,"minAge":18,"maxAge":72,"enrollmentInfo":208,"targetDuration":4,"studyType":23,"phases":210,"briefSummary":211,"conditions":212,"keywords":214,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":219,"lastUpdatePostDateStruct":220,"startDateStruct":222,"completionDateStruct":223,"leadSponsor":225,"locationsCount":4},"100624343","exercise-program-combined-with-ergonomic-training-in-textile-workers-100624343","NCT07408401","Exercise Program Combined With Ergonomic Training in Textile Workers","Examining the Effectiveness of an Exercise Program Combined With Ergonomic Training for Textile Workers: A Randomized Controlled Trial","Inclusion Criteria:\n\nVolunteers aged 18-60 who have been working in the textile industry for at least 6 months will be included in the study.\n\nExclusion Criteria:\n\n* Individuals with orthopedic or neurological conditions that prevent exercise,\n* those with chronic pulmonary disease, those with psychological disorders, and\n* those who have undergone surgery that prevents exercise will not be included in the study.",{"count":209,"type":22},60,[25],"Most studies in the literature focus on musculoskeletal disorders and pain levels in occupational groups with repetitive workloads, such as textile workers. However, due to the nature of the work environment, decreased respiratory function and postural disorders are also frequently observed in these individuals. There is no comprehensive study in the literature that combines respiratory exercises, posture training, and ergonomics training for textile workers. Therefore, this study will examine the effects of a regular exercise program implemented alongside ergonomics training provided to textile workers on respiratory parameters, musculoskeletal disorders, posture, functionality, pain levels, and fatigue intensity.",[213],"Textile Worker",[215,216,217,218],"breathing exercise","posture exercise","textile workers","ergonomics","2026-02-10",{"date":221,"type":34},"2026-02-13",{"date":146,"type":22},{"date":224,"type":22},"2026-06-30",{"name":40,"class":41},{"id":227,"slug":228,"hasResults":11,"nctId":229,"briefTitle":230,"officialTitle":231,"acronym":4,"eligibilityCriteria":232,"healthyVolunteers":16,"sex":49,"minAge":18,"maxAge":233,"enrollmentInfo":234,"targetDuration":4,"studyType":191,"phases":4,"briefSummary":236,"conditions":237,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":240,"lastUpdatePostDateStruct":241,"startDateStruct":243,"completionDateStruct":245,"leadSponsor":247,"locationsCount":4},"100582314","blood-flow-technique-effect-on-the-muscle-mechanics-100582314","NCT06861699","Blood Flow Technique Effect on the Muscle Mechanics","Kan Akımı Kısıtlayıcı Egzersizin Kas Mekanikleri Üzerine Akur Etkisi","Inclusion Criteria:\n\n* Being a healthy male or female volunteer between 18 and 35 (who has not participated in any resistance training program for at least 6 months).\n* Being right-hand dominant according to the results of the Edinburgh Handedness Inventory.\n\nExclusion Criteria:\n\n* Having a history of biceps musculoskeletal injury.\n* Having any condition that prevents participation in resistance exercise.\n* Having cardiovascular disease.\n* Using medication for blood pressure control.","25 Years",{"count":235,"type":22},57,"This study will be a study in which we take measurements with the myotonPRO device to determine whether the resistant exercises performed without the blood flow restrictive technique and with the blood flow restrictive technique affect the biceps muscle of the participants, who were divided into groups by randomization method after determining the 1 max repetition you can lift.",[238,239],"Biceps","Muscle Rigidity","2025-03-01",{"date":242,"type":34},"2025-03-06",{"date":244,"type":22},"2025-03-03",{"date":246,"type":22},"2025-05-01",{"name":40,"class":41},{"id":249,"slug":250,"hasResults":11,"nctId":251,"briefTitle":252,"officialTitle":253,"acronym":4,"eligibilityCriteria":254,"healthyVolunteers":16,"sex":49,"minAge":233,"maxAge":50,"enrollmentInfo":255,"targetDuration":4,"studyType":23,"phases":256,"briefSummary":257,"conditions":258,"keywords":260,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":268,"lastUpdatePostDateStruct":269,"startDateStruct":271,"completionDateStruct":273,"leadSponsor":275,"locationsCount":74},"100564875","comparison-of-the-effects-of-intermittent-pneumatic-compression-graston-technique-and-percussive-therapy-100564875","NCT06634862","Comparison of the Effects of Intermittent Pneumatic Compression, Graston Technique and Percussive Therapy","Comparison of the Effects of Intermittent Pneumatic Compression, Graston Technique and Percussive Therapy on Muscle Pain, Muscle Tone and Balance After Quadriceps Fatigue Protocol","Inclusion Criteria:\n\n* To be between 25-45 years old.\n* Not having any chronic disease.\n* Not doing active sports for at least 6 months.\n* Not having any previously diagnosed lower extremity pathology.\n* Not having a chronic lower extremity problem and not having a major trauma (fracture, anterior cruciate ligament injury, etc.).\n* Not having any cognitive problem that prevents them from following and adapting to a specific exercise programme.\n* No visual, vestibular and neurological disorders.\n\nExclusion Criteria:\n\n* Having a chronic disease.\n* Any musculoskeletal problem in the lower extremities.\n* Use of sedative medication due to chronic disease (rheumatism, lung and\u002For heart etc.)\n* Regular use of painkillers, muscle relaxants or anti-inflammatory drugs.\n* Any history of surgery on the lower extremity.\n* Any history of pain in the lower extremity during the fatigue protocol.\n* Pregnancy.",{"count":209,"type":22},[25],"The aim of this study was to compare the effects of intermittent pneumatic pressure, percussive therapy and graston after a fatigue protocol applied to the leg muscles.",[259],"Recovery Method",[261,262,263,264,265,266,267],"Recovery","Quadriceps Fatigue Protocol","Intermittent pneumatic pressure","Soft Tissue Mobilization Technique","Percussive therapy","Muscle Fatigue","Muscle Tone","2024-10-10",{"date":270,"type":34},"2024-10-15",{"date":272,"type":22},"2024-12-02",{"date":274,"type":22},"2025-05-18",{"name":40,"class":41},{"id":277,"slug":278,"hasResults":11,"nctId":279,"briefTitle":280,"officialTitle":281,"acronym":4,"eligibilityCriteria":282,"healthyVolunteers":16,"sex":49,"minAge":283,"maxAge":284,"enrollmentInfo":285,"targetDuration":4,"studyType":23,"phases":286,"briefSummary":287,"conditions":288,"keywords":290,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":297,"lastUpdatePostDateStruct":298,"startDateStruct":300,"completionDateStruct":302,"leadSponsor":304,"locationsCount":74},"100557250","the-effect-of-kamishibai-diabetes-education-on-knowledge-hba1c-and-quality-of-life-in-children-100557250","NCT06535672","The Effect of Kamishibai Diabetes Education on Knowledge, HbA1c, and Quality of Life in Children","The Effect of Diabetes Education Given to Children Diagnosed With Type 1 Diabetes Mellitus Using the Kamishibai Method on Patients' Knowledge Level, HbA1c Parameter, and Quality of Life: A Randomized Controlled Trial","Inclusion Criteria:\n\n* The child is 8-12 years old.\n* Diagnosed with Type 1 Diabetes Mellitus (T1DM) for at least 1 year.\n* Followed up on an outpatient basis.\n* The child is using insulin.\n* The child can understand and speak Turkish.\n\nExclusion Criteria:\n\n* Presence of another chronic disease other than T1DM that may affect glycemic control.\n* Using an insulin pump.\n* Having vision and\u002For hearing problems.\n* Having a mental and\u002For neurological problem.\n* Having a diagnosis of a psychiatric disease.","8 Years","12 Years",{"count":209,"type":22},[25],"Children diagnosed with Type 1 Diabetes Mellitus (T1DM) initially receive intensive education with their families. Studies indicate that over time, this initial education becomes routine, reducing its effectiveness and failing to adequately address developmental stages, thus requiring repetition. Current methods involve long and intensive educational sessions in hospitals using the Childhood Diabetes Education Guide. These extended, non-interactive sessions often lead to a loss of motivation, decreased learning efficiency, and negative attitudes among patients and their families.\n\nThis study aims to develop an educational tool utilizing the Kamishibai method specifically for children with T1DM aged 8-12. The Kamishibai method is designed to align with their cognitive and sensory development, promoting effective and engaging learning experiences for diabetic patients. By incorporating interactive and visually stimulating elements, Kamishibai seeks to enhance motivation and retention of diabetes education.\n\nHypothesis 1: Children diagnosed with Type 1 DM have higher knowledge levels in the group educated with the Kamishibai method compared to those receiving routine education.\n\nHypothesis 2: The Hemoglobin A1c parameter is lower in the Kamishibai-educated group.\n\nHypothesis 3: The quality of life is higher in the Kamishibai-educated group.\n\nThis study will assess the effectiveness of the Kamishibai method by comparing it to routine educational approaches. The detailed protocol includes technical aspects of the intervention, measurement tools, data collection methods, and statistical analysis plans to ensure a comprehensive evaluation of the method's impact on knowledge levels, HbA1c parameters, and quality of life.",[289],"DIABETES EDUCATION",[291,292,293,294,295,296],"Type 1 Diabetes Mellitus (Type 1 DM)","Kamishibai method","Hemoglobin A1c (HbA1c)","Pediatric diabetes education","Quality of life in children","Randomized controlled tria","2024-07-30",{"date":299,"type":34},"2024-08-02",{"date":301,"type":22},"2024-08-10",{"date":303,"type":22},"2025-07-15",{"name":40,"class":41},""]