[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Dokuz Eylul University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":596},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,21,0,[8,45,72,103,137,166,194,235,262,291,319,344,363,386,418,441,471,496,520,547,572],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":27,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100547551","effects-of-corrective-external-support-and-regional-vibration-applications-in-subacromial-pain-syndrome-100547551",false,"NCT06409442","Effects of Corrective External Support and Regional Vibration Applications in Subacromial Pain Syndrome","Effects of Corrective External Support and Regional Vibration Applications Added to the Rehabilitation Program in Subacromial Pain Syndrome: Randomized Controlled Study","Inclusion Criteria:\n\n* Volunteering to participate in the study,\n* Being over 18 years of age,\n* Having diagnosed with subacromial impingement syndrome,\n* SIS-related complaints have persisted for at least 3 months,\n* Not having received any treatment for shoulder problems in the last 6 months,\n* No history of shoulder injury other than subacromial impingement and\u002For shoulder symptoms requiring treatment for the last 1 year,\n* To be able to read and write Turkish in order to complete all evaluations and applications in the study and to carry out evaluations that require reading and writing.\n\nExclusion Criteria:\n\n* Having a history of fractures and surgery in the upper extremity and cervicothoracic region,\n* Having another neurological, orthopedic or rheumatic shoulder problem such as frozen shoulder or instability,\n* Having a systemic musculoskeletal disease,\n* Known chest deformity, scoliosis diagnosis and physical disability,\n* Presence of a skin problem or a condition that may be a contraindication to the application in the area where KT or LVT will be applied.","ALL","18 Years",{"count":19,"type":20},63,"ESTIMATED","INTERVENTIONAL",[23],"NA","Sixty three individuals with chronic subacromial pain syndrome will be included in our study. In the evaluations to be made to the participants; Pain intensity will be measured with the Visual Analogue Scale (VAS), joint movement and shoulder proprioception will be measured with the inclinometer, and shoulder muscle strength will be measured with the digital hand dynamometer. In addition, functionality and disability levels will be determined by SPADI and Short form-Questionnaire for Arm, Shoulder and Hand Problems (Q-DASH). Supraspinatus tendon thickness and acromiohumeral space measurements will be made by ultrasonographic imaging. Patient satisfaction will be evaluated with the Visual Analog Patient Satisfaction Scale survey and quality of life will be evaluated with the SF-12 survey (The 12-item Short Form Survey).\n\nParticipants will be randomly divided into 3 groups of 21 participants each. In addition to the standard physiotherapy program, taping around the shoulder will be applied to the kinesio taping group, and localized vibration therapy around the shoulder will be applied to the localized vibration therapy group, in addition to the standard physiotherapy program. The Control Group (CG) will receive the same physiotherapy program as the other groups and will attend the same number of sessions as the other groups, accompanied by a physiotherapist. Evaluations will be made and analyzed before treatment, after 3 weeks of treatment, after 6 weeks of treatment, at 12 weeks and at the end of 24 weeks.",[26],"Subacromial Pain Syndrome",[28,29,30,31],"shoulder impingement syndrome","pain","physical therapy and rehabilitation","ultrasonography","RECRUITING","2026-06-23",{"date":35,"type":36},"2026-06-26","ACTUAL",{"date":38,"type":36},"2024-06-24",{"date":40,"type":20},"2027-05-30",{"name":42,"class":43},"Dokuz Eylul University","OTHER",1,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":49,"acronym":4,"eligibilityCriteria":50,"healthyVolunteers":51,"sex":16,"minAge":52,"maxAge":4,"enrollmentInfo":53,"targetDuration":4,"studyType":21,"phases":55,"briefSummary":56,"conditions":57,"keywords":4,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":64,"lastUpdatePostDateStruct":65,"startDateStruct":67,"completionDateStruct":69,"leadSponsor":71,"locationsCount":44},"100640256","development-of-a-chatbot-supported-personalized-exercise-program-for-older-adults-and-evaluation-of-its-effects-on-cognitive-functions-100640256","NCT07596082","Development of a Chatbot-supported Personalized Exercise Program for Older Adults and Evaluation of Its Effects on Cognitive Functions","Inclusion Criteria:\n\n* Aged 65 years and older\n* Normal or mildly impaired cognitive status\n* Medical condition that does not prevent participation in physical activity\n* Ability to use a smartphone or tablet (for chatbot access)\n* Voluntary participation\n\nExclusion Criteria:\n\n* Moderate to severe dementia\n* Severe depression or serious psychiatric disorders\n* Acute cardiovascular risk\n* Communication difficulties due to significant hearing or visual impairment\n* Regular engagement in structured exercise within the past 6 months (participants in the maintenance phase of exercise behavior)",true,"65 Years",{"count":54,"type":20},90,[23],"The purpose of this study is to develop an artificial intelligence-based chatbot application to support exercise behavior in individuals aged 60 and over who do not regularly exercise, and to evaluate its effectiveness. In addition, the study aims to examine the effects of changes in exercise habits on the cognitive (mental) functions of older adults.\n\nIn this study, the impact of a chatbot-supported personalized exercise program on cognitive functions in older individuals will be evaluated. A total of 90 participants is planned for inclusion in this study.\n\nIf you agree to participate in this study, depending on the group you are assigned to, you may receive:\n\n* An artificial intelligence-based chatbot program, along with educational materials about the importance of exercise, or\n* Only educational materials (brochures) prepared by the researchers about the importance of exercise.\n\nAt the beginning of the study, you will be asked to complete a data collection form. The same form will also be administered at week 12 and week 24.\n\nThis form will include:\n\n* Basic information such as your age and gender,\n* Questions about your exercise habits,\n* A brief test to assess your cognitive (mental) functions,\n* Questions evaluating your level of physical activity. The study duration is 24 weeks, including 12 weeks of intervention and 12 weeks of follow-up.",[58,59,60,61,62],"Aged","Exercise","Cognition","Artificial Intelligence (AI)","Health Behavior","NOT_YET_RECRUITING","2026-05-12",{"date":66,"type":36},"2026-05-19",{"date":68,"type":20},"2026-08-01",{"date":70,"type":20},"2026-10-30",{"name":42,"class":43},{"id":73,"slug":74,"hasResults":11,"nctId":75,"briefTitle":76,"officialTitle":77,"acronym":78,"eligibilityCriteria":79,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":80,"targetDuration":4,"studyType":21,"phases":82,"briefSummary":83,"conditions":84,"keywords":88,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":95,"lastUpdatePostDateStruct":96,"startDateStruct":98,"completionDateStruct":100,"leadSponsor":102,"locationsCount":44},"100628667","virtual-vs-physical-art-therapy-for-anxiety-psychological-well-being-and-sleep-quality-in-colorectal-cancer-patients-100628667","NCT07464626","Virtual vs Physical Art Therapy for Anxiety, Psychological Well-being, and Sleep Quality in Colorectal Cancer Patients","Effects of Virtual Art Therapy Delivered Through Virtual Reality Glasses and Physical Art Therapy on Anxiety, Psychological Well-being, and Sleep Quality in Patients With Colorectal Cancer: A Randomized Controlled Trial","PVART-CRC","Inclusion Criteria Age 18 years or older Diagnosed with colorectal cancer Receiving outpatient chemotherapy (FOLFOX or XELOX regimen) ECOG performance status between 0 and 2 Not receiving radiotherapy No hearing or speech impairments No severe psychiatric disorders (e.g., schizophrenia, major depression, bipolar disorder) Able to understand the study procedures and provide informed consent Willing to participate in the study Exclusion Criteria ECOG performance status of 3 or higher Patients who do not meet the inclusion criteria Patients unwilling to participate in the study",{"count":81,"type":20},78,[23],"This randomized controlled trial aims to evaluate the effects of virtual reality-based art therapy and physical art therapy on anxiety, psychological well-being, and sleep quality in patients with colorectal cancer receiving outpatient chemotherapy. A total of 78 patients will be randomly assigned to three groups: a virtual reality art therapy group, a physical art therapy group, and a control group. Participants in the intervention groups will receive art therapy sessions every two weeks for eight weeks (four sessions in total). Anxiety, psychological well-being, and sleep quality will be assessed using validated scales before the intervention and after the fourth session. The findings are expected to contribute to the development of non-pharmacological supportive care interventions for oncology patients.",[85,86,87],"Colorectal Cancer (Diagnosis)","Anxiety","Sleep Disturbance",[89,90,91,92,93,94],"Art Therapy","Virtual Reality Art Therapy","Psychological Well-being","Sleep Quality","Cancer Supportive Care","Non-pharmacological Intervention","2026-03-07",{"date":97,"type":36},"2026-03-11",{"date":99,"type":36},"2026-03-01",{"date":101,"type":20},"2027-12-30",{"name":42,"class":43},{"id":104,"slug":105,"hasResults":11,"nctId":106,"briefTitle":107,"officialTitle":108,"acronym":4,"eligibilityCriteria":109,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":52,"enrollmentInfo":110,"targetDuration":4,"studyType":21,"phases":112,"briefSummary":113,"conditions":114,"keywords":120,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":129,"lastUpdatePostDateStruct":130,"startDateStruct":132,"completionDateStruct":134,"leadSponsor":136,"locationsCount":44},"100626714","qigong-and-multicomponent-exercise-in-panic-disorder-100626714","NCT07439224","Qigong and Multicomponent Exercise in Panic Disorder","Investigation of the Effects of Qigong Exercise Training and Multicomponent Exercise Training on Physical and Mental Health in People With Panic Disorder","Inclusion Criteria:\n\n* Being between the ages of 18-65\n* Being diagnosed with \"panic disorder\" by a psychiatrist\n* Not having another psychiatric illness\n* Wanting to participate in the research voluntarily and signing the informed consent\n* Not having a history of communication or neuromusculoskeletal disease that would not allow the application of evaluation and treatment methods\n\nExclusion Criteria:\n\n* Having a vision and\u002For hearing problem that would prevent participation in the study\n* History of neurological, cardiopulmonary and musculoskeletal system disease that would negatively affect participation in evaluation and treatment",{"count":111,"type":20},60,[23],"Panic disorder is a psychiatric disease characterized by recurrent panic attacks that occur in expected or unexpected situations and create feelings of intense fear, restlessness and discomfort. Panic disorder often has a chronic course, its frequency and severity can be irregular, various physical, mental, and behavioral symptoms can develop, and the quality of life of individuals can decrease significantly. Evidence-based psychotherapy and pharmacotherapy are effective in reducing the symptoms of panic disorder and managing the disorder. However, both of these treatment methods have certain limitations, and approximately one-third of patients do not respond to therapy or the response is not sufficiently effective. Delaying treatment of the disease results in a poor prognosis and more established symptoms. Exercise can be viewed as a low-cost, supportive treatment for relieving symptoms with comparable efficacy to medication and other psychological interventions. Although exercise is recommended for patients with anxiety-panic disorder, there remains uncertainty about whether its effects are sustainable, the type and intensity of exercise required for effective treatment, and thus the effects of qigong and multicomponent exercise on multiple health outcomes in panic disorder. The aim of this study is to examine the effects of Qigong exercise training and multicomponent exercise training on anxiety-panic, balance, mobility, walking, functional strength, physical activity, sleep quality, fatigue, chronic musculoskeletal pain, quality of life and cognition.",[115,116,117,118,59,119],"Panic Disorder","Panic Disorder (With or Without Agoraphobia)","Panic Attacks and Disorders","Qigong","Anxiety Disorders",[121,122,123,124,125,126,127,118,128],"Anxiety disorders","Baduanjin","Exercise training","Physical health","Mental health","Multicomponent exercise","Panic disorder","Mind-body exercises","2026-02-23",{"date":131,"type":36},"2026-02-27",{"date":133,"type":36},"2024-12-01",{"date":135,"type":20},"2028-09-30",{"name":42,"class":43},{"id":138,"slug":139,"hasResults":11,"nctId":140,"briefTitle":141,"officialTitle":142,"acronym":143,"eligibilityCriteria":144,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":145,"enrollmentInfo":146,"targetDuration":4,"studyType":148,"phases":4,"briefSummary":149,"conditions":150,"keywords":152,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":159,"lastUpdatePostDateStruct":160,"startDateStruct":161,"completionDateStruct":163,"leadSponsor":165,"locationsCount":44},"100626641","nirs-and-bis-monitoring-during-cerebral-aneurysm-coiling-100626641","NCT07438275","NIRS and BIS Monitoring During Cerebral Aneurysm Coiling","Evaluation of Near-Infrared Spectroscopy and Bispectral Index Monitoring During Cerebral Aneurysm Coil Embolization","NIRSBIS-ANEUR","* Age ≥18 years\n* Patients scheduled for endovascular coil embolization for intracranial (cerebral) aneurysm\n* American Society of Anesthesiologists (ASA) physical status I-III\n* Undergoing the procedure under general anesthesia\n* Ability to provide written informed consent Criteria\n\nExclusion Criteria:\n\n* Refusal or inability to provide informed consent\n* History of severe cerebrovascular disease other than the target aneurysm\n* Severe cardiac, pulmonary, hepatic, or renal dysfunction\n* Pre-existing neurological deficits interfering with NIRS or BIS interpretation\n* Known scalp or skin conditions preventing proper placement of NIRS or BIS sensors\n* Emergency procedures\n* Pregnancy -","75 Years",{"count":147,"type":20},75,"OBSERVATIONAL","This prospective observational study aims to evaluate the effectiveness of Near-Infrared Spectroscopy (NIRS) and Bispectral Index (BIS) monitoring during endovascular coil embolization of cerebral aneurysms under general anesthesia. Changes in regional cerebral oxygen saturation (rSO₂) measured by NIRS will be assessed in relation to BIS values and hemodynamic parameters throughout the procedure.\n\nThe frequency, duration, and severity of cerebral desaturation episodes detected by NIRS, as well as their association with anesthetic depth and hemodynamic fluctuations, will be analyzed. The study does not involve any additional intervention beyond routine clinical monitoring.",[151],"Cerebral Aneurysm",[153,154,155,156,157,158],"Near-Infrared Spectroscopy","Bispectral Index","Cerebral Oxygenation","Neuroanesthesia","Endovascular Treatment","Coil Embolization","2026-02-22",{"date":131,"type":36},{"date":162,"type":20},"2026-03",{"date":164,"type":20},"2026-10",{"name":42,"class":43},{"id":167,"slug":168,"hasResults":11,"nctId":169,"briefTitle":170,"officialTitle":170,"acronym":4,"eligibilityCriteria":171,"healthyVolunteers":51,"sex":16,"minAge":172,"maxAge":173,"enrollmentInfo":174,"targetDuration":4,"studyType":21,"phases":176,"briefSummary":177,"conditions":178,"keywords":182,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":186,"lastUpdatePostDateStruct":187,"startDateStruct":189,"completionDateStruct":191,"leadSponsor":193,"locationsCount":4},"100615934","the-effect-of-a-guessing-game-on-fear-pain-and-emotional-state-during-blood-collection-in-children-aged-6-12-100615934","NCT07299058","The Effect of a Guessing Game on Fear, Pain, and Emotional State During Blood Collection in Children Aged 6-12","Inclusion Criteria:\n\n* Being between 6 and 12 years of age\n* Not having a previous diagnosis of a serious hematological\u002Fpsychiatric disease\n* The child and parent must be willing to participate in the study\n* Being able to speak and understand Turkish\n\nExclusion Criteria:\n\n* Having received sedation, analgesics, or anxiolytic medication during the procedure\n* Having a visual\u002Fhearing impairment\n* Having previously undergone an invasive procedure on the same day","6 Years","12 Years",{"count":175,"type":20},70,[23],"The aim of this study is to evaluate the effects of a guessing game on fear, pain and emotional state during blood collection in children aged 6-12 years.",[179,180,181],"Pain","Blood Sampling Procedure","Fear Anxiety",[29,183,184,185],"fear","emotional state","children","2025-12-09",{"date":188,"type":36},"2025-12-23",{"date":190,"type":20},"2025-12-20",{"date":192,"type":20},"2026-12-31",{"name":42,"class":43},{"id":195,"slug":196,"hasResults":11,"nctId":197,"briefTitle":198,"officialTitle":199,"acronym":4,"eligibilityCriteria":200,"healthyVolunteers":11,"sex":201,"minAge":17,"maxAge":52,"enrollmentInfo":202,"targetDuration":4,"studyType":21,"phases":204,"briefSummary":205,"conditions":206,"keywords":216,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":227,"lastUpdatePostDateStruct":228,"startDateStruct":230,"completionDateStruct":232,"leadSponsor":234,"locationsCount":44},"100603856","yoga-in-women-with-surgical-menopause-after-gynecological-cancer-100603856","NCT07141953","Yoga in Women With Surgical Menopause After Gynecological Cancer","The Effect of Yoga on Quality of Life, Sleep Quality, and Spiritual Well-Being in Women Who Undergo Surgical Menopause Following Gynecological Cancer Surgery: A Randomized Controlled Trial","Inclusion Criteria:\n\nAge between 18-65 years Diagnosis of primary gynecological cancer (ovarian, endometrial, cervical, vaginal, or vulvar) (Stage I-III) Ability to read, understand, and speak Turkish Completion of all adjuvant treatments (surgery, chemotherapy, and\u002For radiotherapy) at least 6 months prior Access to the internet Having a computer\u002Ftablet\u002Fphone with a camera Willingness and ability to attend at least 80% of the yoga sessions Voluntary participation in the study\n\nExclusion Criteria:\n\nAny condition that prevents communication Cognitive, sensory, or physical impairment that prevents yoga practice Diagnosis of metastatic gynecological cancer Regular yoga practice within the last 6 months (at least once a week for 8 consecutive weeks)","FEMALE",{"count":203,"type":20},46,[23],"This randomized controlled trial investigates the effects of yoga on quality of life, sleep quality, and spiritual well-being in women who have entered surgical menopause after gynecological cancer surgery. Yoga is expected to be a supportive intervention for symptom management and to improve overall well-being in this patient population.",[207,208,209,210,211,212,92,213,214,215],"Gynecological Oncology","Gynecology","Oncology","Surgical Menopause","Symptom Management","Quality of Life","Well-being","Yoga","Yoga for Cancer",[217,218,219,220,221,222,223,224,225,226],"gynecological oncology","gynecology","oncology","surgical menopause","symptom management","quality of life","sleep quality","well-being","yoga","yoga for cancer","2025-08-19",{"date":229,"type":36},"2025-08-26",{"date":231,"type":20},"2025-09-01",{"date":233,"type":20},"2026-06-01",{"name":42,"class":43},{"id":236,"slug":237,"hasResults":11,"nctId":238,"briefTitle":239,"officialTitle":240,"acronym":4,"eligibilityCriteria":241,"healthyVolunteers":51,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":242,"targetDuration":4,"studyType":21,"phases":243,"briefSummary":244,"conditions":245,"keywords":249,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":255,"lastUpdatePostDateStruct":256,"startDateStruct":258,"completionDateStruct":260,"leadSponsor":261,"locationsCount":4},"100601984","virtual-reality-in-nursing-students-communication-skills-100601984","NCT07117604","Virtual Reality in Nursing Students' Communication Skills","Effects of Virtual Reality Application on Nursing Students' Skills in Breaking Bad News and Approaching Crying Patients","Inclusion Criteria:\n\n* being ≥18 years old\n* being a nursing student,\n* taking a communication course for the first time\n* volunteering to participate in the study\n\nExclusion Criteria:\n\n* having a condition preventing the student from using the VR tool\n* having problems such as nausea and vomiting due to the use of VR headsets\n* having been participated in any training given on breaking bad news",{"count":111,"type":20},[23],"The purpose of this clinical trial is to determine the effect of a virtual reality application on nursing students' skills in breaking bad news and approaching crying patients at a nursing faculty in western Turkey.\n\nThe primary questions to be addressed are:\n\nIs there a significant difference in breaking bad news skills between students receiving the virtual reality intervention and those receiving the standard curriculum? Is there a significant difference in skills related to approaching crying patients between students receiving the virtual reality intervention and those receiving the standard curriculum? Comparison group: The researchers will compare the intervention group, which receives the virtual reality application, with the control group, which follows the standard curriculum, to assess differences in skill development.\n\nParticipants:\n\nNursing students aged 18 years or older, who are taking a communication course for the first time and voluntarily participating.\n\nParticipants will be randomly assigned to the intervention or control groups.\n\nParticipants in the intervention group will:\n\nAttend an orientation session for the virtual reality application, Engage in a virtual reality scenario based on the SPIKES protocol involving breaking bad news and approaching a crying patient, Participate in a debriefing session to discuss their experiences. Participants in the control group will receive the standard curriculum course.",[246,247,248],"Nursing Students","Virtual Reality","Breaking Bad News Skills",[250,251,252,253,254],"Virtual reality","cancer","breaking bad news","nursing","communication","2025-08-11",{"date":257,"type":36},"2025-08-12",{"date":259,"type":20},"2025-08",{"date":259,"type":20},{"name":42,"class":43},{"id":263,"slug":264,"hasResults":11,"nctId":265,"briefTitle":266,"officialTitle":267,"acronym":4,"eligibilityCriteria":268,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":269,"targetDuration":4,"studyType":148,"phases":4,"briefSummary":271,"conditions":272,"keywords":277,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":283,"lastUpdatePostDateStruct":284,"startDateStruct":286,"completionDateStruct":288,"leadSponsor":290,"locationsCount":44},"100596138","cardiovascular-risk-factors-and-physical-activity-in-chronic-kidney-patients-on-peritoneal-dialysis-100596138","NCT07041554","Cardiovascular Risk Factors and Physical Activity in Chronic Kidney Patients on Peritoneal Dialysis","Examination of Cardiovascular Risk Factors and Physical Activity in Chronic Kidney Patients Treated With Peritoneal Dialysis","Inclusion Criteria:\n\n* Diagnosed with chronic kidney disease\n* Peritoneal dialysis treatment for at least three months\n* Age ≥ 18\n\nExclusion Criteria:\n\n* Mini Mental Test Score \\\u003C 24\n* Serious cardiovascular, pulmonary, or neurological conditions that make it impossible to wear an accelerometer\n* Inability to walk independently\n* Conditions affecting participation in daily life due to lower limb injury or surgery",{"count":270,"type":20},23,"The objective of this study was to examine the association between cardiovascular risk factors and physical activity parameters in patients with chronic kidney disease who are treated with peritoneal dialysis.",[273,274,275,276],"Chronic Kidney Diseases","Cardiovascular Risk Factors","Arterial Stiffness","Physical Activity",[278,279,280,281,282],"cardiovascular risk factors","physical activity","arterial stiffness","accelerometer","peritoneal dialysis","2025-06-18",{"date":285,"type":36},"2025-06-27",{"date":287,"type":20},"2025-06-23",{"date":289,"type":20},"2025-12-31",{"name":42,"class":43},{"id":292,"slug":293,"hasResults":11,"nctId":294,"briefTitle":295,"officialTitle":296,"acronym":4,"eligibilityCriteria":297,"healthyVolunteers":11,"sex":201,"minAge":17,"maxAge":145,"enrollmentInfo":298,"targetDuration":4,"studyType":21,"phases":300,"briefSummary":301,"conditions":302,"keywords":307,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":283,"lastUpdatePostDateStruct":312,"startDateStruct":313,"completionDateStruct":315,"leadSponsor":317,"locationsCount":318},"100596069","comparison-of-two-position-and-four-position-cervical-injection-techniques-for-sentinel-lymph-node-mapping-in-endometrial-cancer-using-methylene-blue-100596069","NCT07040657","Comparison of Two-Position and Four-Position Cervical Injection Techniques for Sentinel Lymph Node Mapping in Endometrial Cancer Using Methylene Blue","Comparison of Two-Point and Four-Point Cervical Injection Techniques Using Methylene Blue for Sentinel Lymph Node Mapping in Endometrial Cancer","Inclusion Criteria:\n\n* Individuals diagnosed with stage I endometrial cancer based on CT and PET-CT imaging.\n* Individuals with a pathologically confirmed diagnosis of stage I endometrial cancer.\n\nExclusion Criteria:\n\nMedical Conditions\n\n* Individuals diagnosed with dementia.\n* Individuals with allergies to methylene blue or iodine.\n* Individuals who have received active treatment for another malignancy within the past five years.\n* Inability to successfully perform PLD (pelvic lymphadenectomy) or history of prior PLD.\n* Women with multiple and confluent lymph nodes identified as positive on FDG-PET\u002FCT (such cases are not considered stage I).\n\nCancer-Related Conditions\n\n* Individuals with clinically or radiologically identified positive lymph nodes or metastatic disease.\n* Individuals with a history of pelvic dissection and\u002For radiation therapy.\n* Individuals with advanced cervical or uterine cancer.\n* Individuals with T3\u002FT4 lesions.\n* Individuals with cervical tumors larger than 2 cm.\n\nOrgan Dysfunction\n\n• Individuals with hepatic dysfunction and a MELD score ≥ 10 and creatinine ≥ 2·0 mg\u002Fdl patients.",{"count":299,"type":20},100,[23],"This clinical trial evaluates lymph node mapping in newly diagnosed endometrial cancer patients undergoing surgery. The standard technique uses a 2-point methylene blue cervical injection. The study aims to determine if increasing injection points improves mapping success.",[303,304,305,306],"Endometrial Neoplasms","Endometrial Cancer Stage I","Sentinel Lymph Node","Metastasis",[308,309,310,311],"endometrial neoplasm","methylene blue","metastasis","cervix",{"date":285,"type":36},{"date":314,"type":36},"2025-05-01",{"date":316,"type":20},"2026-11-01",{"name":42,"class":43},2,{"id":320,"slug":321,"hasResults":11,"nctId":322,"briefTitle":323,"officialTitle":323,"acronym":4,"eligibilityCriteria":324,"healthyVolunteers":51,"sex":201,"minAge":52,"maxAge":325,"enrollmentInfo":326,"targetDuration":4,"studyType":21,"phases":328,"briefSummary":329,"conditions":330,"keywords":332,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":336,"lastUpdatePostDateStruct":337,"startDateStruct":339,"completionDateStruct":341,"leadSponsor":343,"locationsCount":44},"100594178","acute-effects-of-motor-imagery-and-action-observation-in-the-elderly-single-blind-randomized-controlled-trial-100594178","NCT07016061","Acute Effects of Motor Imagery and Action Observation in the Elderly: Single-Blind Randomized Controlled Trial","Inclusion Criteria:\n\n* Being aged 65 years or older, Female gender, Literate in Turkish, Scoring 21 or above on the Montreal Cognitive Assessment (MoCA) Version 7.1, No health conditions that would prevent participation in exercise\n\nExclusion Criteria:\n\n* Presence of serious health problems that would prevent participation in the study (e.g., trauma, cancer, surgery, severe cardiac or musculoskeletal disorders)\n\nParticipation in other intervention trials or observational studies during the intervention period, or initiation of a physical exercise program within 2 weeks following the intervention period\n\nAny medical condition or chronic medication use that may jeopardize safety or affect cognitive functions (e.g., neuroleptics)","85 Years",{"count":327,"type":20},50,[23],"The aim of this study is to investigate the effects of acute action observation, motor imagery, exercise, and combined exercise training on parameters such as balance, reaction time, flexibility, fear of falling, cognitive status, attention, and memory in older adults.",[331],"Elderly (People Aged 65 or More)",[333,334,335],"imagery","Mirror Neurons","exercise","2025-06-03",{"date":338,"type":36},"2025-06-11",{"date":340,"type":20},"2025-06-15",{"date":342,"type":20},"2025-08-20",{"name":42,"class":43},{"id":345,"slug":346,"hasResults":11,"nctId":347,"briefTitle":348,"officialTitle":349,"acronym":4,"eligibilityCriteria":350,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":351,"targetDuration":4,"studyType":21,"phases":352,"briefSummary":353,"conditions":354,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":356,"lastUpdatePostDateStruct":357,"startDateStruct":359,"completionDateStruct":360,"leadSponsor":362,"locationsCount":44},"100588419","gamified-combined-cognitive-bias-modification-in-adults-diagnosed-with-ocd-randomized-controlled-trial-100588419","NCT06941155","Gamified Combined Cognitive Bias Modification in Adults Diagnosed With OCD: Randomized Controlled Trial","A Randomized Controlled Trial on the Effects of Mobile-Based Gamified Combined Cognitive Bias Modification on OCD Symptoms, Obsessive Beliefs, Cognitive Biases, Depressive Symptoms and Distress in Adults Diagnosed With OCD","Inclusion Criteria:\n\n* Age 18 years or older\n* Primary diagnosis of obsessive-compulsive disorder (OCD), confirmed by a licensed clinician using the Structured Clinical Interview for DSM-5 (SCID-5)\n* No current suicidal ideation or psychotic symptoms\n* Access to the internet and a mobile phone\n* Stable psychiatric medication use for at least one month prior to enrollment, with no changes in dosage during the 4-week intervention period\n* No current neurological or medical condition that would interfere with participation\n* Ability to perceive colored visual stimuli (e.g., no color blindness)\n* Not currently enrolled in another intervention-based study\n* Not receiving any other form of psychological treatment at the time of participation\n\nExclusion Criteria:\n\n* Presence of active suicidal ideation or psychotic symptoms\n* Unstable psychiatric medication use (e.g., recent dose change within the past month or expected change during the intervention period)\n* Significant neurological or medical illness that may interfere with participation\n* Visual impairments that would prevent accurate perception of colored stimuli (e.g., color blindness)\n* Current participation in another clinical trial involving psychological intervention\n* Receiving concurrent psychotherapy or other psychological treatments outside of the study",{"count":54,"type":20},[23],"This randomized controlled trial examines the effects of a mobile-based gamified combined cognitive bias modification (CBM-C) intervention on obsessive-compulsive symptoms, obsessive beliefs, attentional and interpretation biases, depressive symptoms, and psychological distress. The gamified CBM-C condition is compared to a standard mobile-based CBM-C and a placebo control condition. All interventions are delivered via a mobile application. Assessments are conducted at baseline, post-intervention (week 4), and 3-month follow-up.",[355],"Obsessive Compulsive Disorder (OCD)","2025-05-14",{"date":358,"type":36},"2025-05-15",{"date":356,"type":36},{"date":361,"type":20},"2027-04-02",{"name":42,"class":43},{"id":364,"slug":365,"hasResults":11,"nctId":366,"briefTitle":367,"officialTitle":368,"acronym":4,"eligibilityCriteria":369,"healthyVolunteers":51,"sex":201,"minAge":17,"maxAge":325,"enrollmentInfo":370,"targetDuration":4,"studyType":148,"phases":4,"briefSummary":372,"conditions":373,"keywords":377,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":378,"lastUpdatePostDateStruct":379,"startDateStruct":381,"completionDateStruct":383,"leadSponsor":385,"locationsCount":44},"100496059","sarcopenia-and-related-factors-in-lipedema-100496059","NCT05739279","Sarcopenia and Related Factors in Lipedema","Evaluation of Sarcopenia and Associated Factors in Patients with Lipedema","Inclusion Criteria:\n\n* between the ages of 18-85\n* with a diagnosis of lipoedema\n* who agreed to participate in the study\n* having a sociocultural level suitable for participation in the study\n* healthy volunteers in a similar age group for the control group\n\nExclusion Criteria:\n\n* with chronic venous insufficiency and\u002For lymphedema\n* with Parkinson's disease, previous stroke, cerebellar diseases, multiple sclerosis, major depression, neuromuscular diseases, history of major orthopedic surgery, severe hip\u002Fknee osteoarthritis, rheumatological diseases, malignancies, advanced heart\u002Fliver\u002Frenal failure, visual impairment, and vestibular diseases, and those who use any assistive device to walk\n* who are illiterate and have cognitive impairment that will prevent them from giving written consent will not be included in the study",{"count":371,"type":20},102,"Lipedema is a common disease of subcutaneous adipose tissue. The most common complaint of patients with swelling in the affected extremity is pain. In addition, patients with lipedema may experience conditions that can greatly affect the health and quality of life of the individual, such as loss of muscle strength and exercise capacity, and deterioration in activity levels of daily living. It is still unknown whether the decrease in muscle strength in patients with lipedema is part of this condition or whether decreased activity levels lead to decreased muscle strength.\n\nSarcopenia is an important health problem characterized by age-related loss of muscle mass and muscle function. The relationship between muscle weakness and sarcopenia in patients with lipedema has not been investigated before. Early recognition of possible sarcopenia and functional limitations in these patients may be important to increase the ability of patients to participate in physical activity as part of their conservative management.\n\nThere is no study in the literature investigating sarcopenia in patients with a diagnosis of lipedema. The aim of this study is to evaluate patients with a diagnosis of lipedema in terms of sarcopenia. In addition, the relationship between sarcopenia and age, body mass index, exercise frequency, lipedema type, and stage will be investigated in patients diagnosed with lipedema.",[374,375,376],"Lipedema","Sarcopenia","Musculoskeletal Diseases",[374,375,376],"2025-03-09",{"date":380,"type":36},"2025-03-12",{"date":382,"type":36},"2023-01-01",{"date":384,"type":20},"2025-12",{"name":42,"class":43},{"id":387,"slug":388,"hasResults":11,"nctId":389,"briefTitle":390,"officialTitle":391,"acronym":4,"eligibilityCriteria":392,"healthyVolunteers":51,"sex":201,"minAge":4,"maxAge":4,"enrollmentInfo":393,"targetDuration":4,"studyType":21,"phases":395,"briefSummary":396,"conditions":397,"keywords":400,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":410,"lastUpdatePostDateStruct":411,"startDateStruct":413,"completionDateStruct":415,"leadSponsor":417,"locationsCount":4},"100579436","online-and-mobile-support-program-and-fertility-100579436","NCT06824272","Online and Mobile Support Program and Fertility","The Effect of a Hybrid Support Program Based on the Hypnofertility and Health Improvement Model on Infertile Women's Fertility Readiness, Self-Efficacy, Lifestyle, and Pregnancy Outcomes","Inclusion Criteria:\n\n* Having been diagnosed with primary infertility,\n\n  * Having been diagnosed with female, male factor and unexplained infertility,\n  * Cycles where fresh embryos will be applied\n  * Having In Vitro Fertilization (IVF) treatment,\n  * Knowing how to read and write Turkish,\n  * Being able to use a computer, internet and mobile phone\n  * Having a smart phone,\n  * Being able to use a smart phone,\n  * Having internet access,\n  * Agreeing to participate in the study\n\nExclusion Criteria:\n\n* Cycles to be performed with frozen embryos\n\n  * Having any psychiatric disorder,\n  * Attending less than 80% of the trainings (not attending more than 2 classes) in this case women will be excluded from the study and in order to reach a sufficient sample, institutions will be visited again and cases that meet the sample criteria will be found. Re-randomization will be done among women who meet the criteria\n  * Having any chronic disease for which they are receiving treatment.",{"count":394,"type":20},128,[23],"Our study is designed as a randomized controlled experimental study with a pre-test and post-test control group to determine the effects of online fertility preparation classes and fertility mobile application support, based on the Philosophy of Hypnofertility and Pender's Health Promotion Model, on infertile women's fertility readiness, fertility self-efficacy, lifestyle, and pregnancy outcomes.",[398,399],"Infertility","Stress",[401,402,403,404,405,406,407,408,409],"Hypnofertility","Fertility Preparedness","Self-efficacy","Lifestyle","Pregnancy Outcome","Mobile Application","Online Education","infertility","pender","2025-02-12",{"date":412,"type":36},"2025-02-13",{"date":414,"type":20},"2025-03-30",{"date":416,"type":20},"2025-12-01",{"name":42,"class":43},{"id":419,"slug":420,"hasResults":11,"nctId":421,"briefTitle":422,"officialTitle":423,"acronym":4,"eligibilityCriteria":424,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":425,"targetDuration":427,"studyType":148,"phases":4,"briefSummary":428,"conditions":429,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":433,"lastUpdatePostDateStruct":434,"startDateStruct":436,"completionDateStruct":438,"leadSponsor":440,"locationsCount":44},"100573546","association-between-sleep-quality-and-self-care-in-heart-failure-patients-100573546","NCT06747689","Association Between Sleep Quality and Self-Care in Heart Failure Patients","Effect of Sleep Quality on Self-Care in Patients with Heart Failure: a Longitudinal Analysis","The study will include patients who:\n\n* Are diagnosed with heart failure according to international guidelines,\n* Are aged 18 years or older,\n* Can communicate via phone, and\n* Are willing to participate in the study.\n\nExclusion Criteria:\n\nThe study will exclude patients who:\n\n* Have been hospitalized within one month prior to inclusion,\n* Have experienced major psychological trauma or stress in the last three months,\n* Have serious comorbidities or malignant cancers,\n* Have advanced hearing impairment,\n* Are using prescription drugs for insomnia or psychiatric conditions,\n* Work night shifts, or\n* Reside in nursing homes.",{"count":426,"type":20},207,"6 Months","The research will be conducted as a prospective and relational study to longitudinally investigate the effect of sleep quality on self-care in patients with heart failure (HF) and to evaluate the relationship between self-care, sleep quality, and cognitive functions. The sample size was calculated using the multiple linear regression model with the G\\*Power Version 3.1 program. Based on a medium effect size of 0.15, an alpha of 0.05, a power of 0.95, and 18 predictors, the sample size was determined to be 188. Considering a potential dropout rate of 10%, it was decided to complete the study with a minimum of 207 participants.\n\nData will be collected from patients who apply to the Dokuz Eylül University Cardiology Outpatient Clinic and meet the inclusion criteria. After signing the informed consent form, participants will be followed up at baseline, the 1st month, the 3rd month, and the 6th month by telephone. The Statistical Package for Social Sciences (SPSS) 24.0 will be used to analyze the numerical data of the research. Descriptive statistics, including number, percentage, mean, and standard deviation, as well as inferential statistics such as the χ2 test, t-test for independent groups, and multiple linear regression, will be employed in the data analysis.",[430,92,431,432],"Heart Failure","Self Care","Cognitive Function","2025-02-05",{"date":435,"type":36},"2025-02-06",{"date":437,"type":36},"2024-12-20",{"date":439,"type":20},"2026-01-20",{"name":42,"class":43},{"id":442,"slug":443,"hasResults":11,"nctId":444,"briefTitle":445,"officialTitle":446,"acronym":4,"eligibilityCriteria":447,"healthyVolunteers":51,"sex":16,"minAge":448,"maxAge":449,"enrollmentInfo":450,"targetDuration":4,"studyType":21,"phases":452,"briefSummary":453,"conditions":454,"keywords":457,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":464,"lastUpdatePostDateStruct":465,"startDateStruct":466,"completionDateStruct":468,"leadSponsor":470,"locationsCount":318},"100517410","effects-of-myofascial-release-technique-on-mobility-sensorimotor-function-and-performance-in-volleyball-players-100517410","NCT06017180","Effects of Myofascial Release Technique on Mobility, Sensorimotor Function and Performance in Volleyball Players","Investigation of the Effects of Myofascial Release Techniques on Shoulder-Elbow Mobility, Sensorimotor Function and Performance in Volleyball Players","Inclusion criteria:\n\n* Being playing volleyball\n* Training at least two hours a week Being between the ages of 13-40\n* Full active movement of the shoulder and elbow in all directions\n* To have at least 3 years of overhead sports activity (volleyball) (Kurt, 2022)\n* Active participation in training and competitions\n* Absence of shoulder pain\n* To be able to complete all the evaluations and applications to be made in the study\n\nExclusion criteria:\n\n* Not wanting to participate in the study and not being able to fulfill its requirements\n* History of upper extremity injury in the last 1 year\n* Any history of surgery or fracture in the upper extremity\n* The occurrence of pain during evaluations and applications\n* Having a diagnosed disease related to the neck and shoulder\n* Having any diagnosed systemic (rheumatological) musculoskeletal disease\n* Have a lower extremity injury (acute and\u002For active) in the last six months\n* Having acne and similar skin problems, open wounds that may prevent the application of rounded myofascial relaxation\n* Previous application of similar rounded myofascial relaxation\n* Diagnosis of diabetes mellitus and peripheral neuropathy\n* Having been diagnosed with osteoporosis\n* Having a diagnosis of vertigo\n* Having a cardiovascular disease\n* Being pregnant","13 Years","40 Years",{"count":451,"type":20},54,[23],"Sports that require overhead activities (volleyball, tennis, basketball) include components such as rapid displacement, strength and movement control.Volleyball is also called as an overhead sport in terms of the way it is played. In the realization of these sports; Sub-parameters such as proprioceptive sense, strength, throwing rate, flexibility play a role. During these activities, the shoulder and elbow joints are overloaded. To meet this load, the joint must provide the necessary mobility and stability. Proprioceptive sense in increasing the quality and width of movement as well as providing dynamic joint stability in overhead sports; Increasing the range of motion of the joint, reducing muscle stiffness and thus increasing flexibility are effective in providing mobility. That's why it's important to develop them. Likewise, muscle strength should be increased in order to maintain movement performance and prevent injuries. The use of myofascial release techniques as an exercise method has increased in recent years. Application; The effects on parameters such as strength, performance and flexibility were investigated. Studies have focused more on the lower extremities and acute effects. There is no study on the subject examining proprioceptive sensation in volleyball players in the upper extremity. Therefore, our aim is to examine the chronic effects of the application on shoulder and elbow joint mobility, sensorimotor function and performance.",[455,456],"Athletes","Volleyball",[458,459,460,461,462,463],"foam rolling","volleyball","proprioception","upper extremity","strength","performance","2025-02-04",{"date":435,"type":36},{"date":467,"type":36},"2023-09-30",{"date":469,"type":20},"2026-12-30",{"name":42,"class":43},{"id":472,"slug":473,"hasResults":11,"nctId":474,"briefTitle":475,"officialTitle":476,"acronym":4,"eligibilityCriteria":477,"healthyVolunteers":11,"sex":201,"minAge":17,"maxAge":478,"enrollmentInfo":479,"targetDuration":4,"studyType":21,"phases":481,"briefSummary":482,"conditions":483,"keywords":486,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":489,"lastUpdatePostDateStruct":490,"startDateStruct":492,"completionDateStruct":493,"leadSponsor":495,"locationsCount":318},"100577531","the-effect-of-mindfulness-based-lifestyle-support-program-on-infertile-women-100577531","NCT06799507","The Effect of Mindfulness-Based Lifestyle Support Program on Infertile Women","The Effect of Mindfulness-Based Lifestyle Support Program on Quality of Life, Lifestyle, Mindfulness Level and Treatment Outcomes in Infertile Women","Inclusion Criteria:\n\n* Primary infertility,\n* Going to undergo IVF treatment,\n* Under 45 years of age,\n* Having a smart phone or computer\n\nExclusion Criteria:\n\n* Participate in any program related to mindfulness\n* Prior mindfulness training\n* Knowing\u002Fdoing mindfulness practices beforehand\n* Having any psychiatric disorder\n* Having any chronic disease\n* Disability (hearing\u002Fvision etc.)\n* Attending less than 80% of the trainings (missing more than 2 Mindfulness trainings)\n* Conception during research","45 Years",{"count":480,"type":20},92,[23],"This randomized controlled trial aimed to determine whether a mindfulness-based lifestyle support program would improve quality of life, lifestyle, mindfulness, attention and meditation level and treatment outcomes in women undergoing IVF treatment.",[484,485],"Fertility Disorders","Infertility (IVF Patients)",[398,487,212,488],"Mindfulness","Life Style","2025-01-31",{"date":491,"type":36},"2025-02-03",{"date":489,"type":36},{"date":494,"type":20},"2026-06-15",{"name":42,"class":43},{"id":497,"slug":498,"hasResults":11,"nctId":499,"briefTitle":500,"officialTitle":501,"acronym":59,"eligibilityCriteria":502,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":52,"enrollmentInfo":503,"targetDuration":4,"studyType":21,"phases":505,"briefSummary":506,"conditions":507,"keywords":509,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":513,"lastUpdatePostDateStruct":514,"startDateStruct":516,"completionDateStruct":518,"leadSponsor":519,"locationsCount":44},"100572778","effects-of-aerobic-and-resistance-exercise-training-in-individuals-with-cancer-cachexia-100572778","NCT06737692","Effects of Aerobic and Resistance Exercise Training in Individuals with Cancer Cachexia","Investigation of the Effects of Aerobic and Resistance Exercise Training in Individuals with Gastrointestinal Cancer and Cachexia: Randomized Controlled Single-Blind Study","Inclusion Criteria:\n\n* Stage III-IV gastrointestinal cancer diagnosis\n* Age 18-65\n* Receiving systemic treatment (chemotherapy and\u002For targeted therapy and\u002For immunotherapy), at least 6 weeks after surgery,\n* Karnofsky performance score 80 and above,\n* Diagnosis of cachexia according to diagnostic criteria and Glasgow Prognostic Score (5,30) (\\>5% weight loss in the last 6 months or \\>2% weight loss in patients with BMI less than 20 kg\u002Fm2 or \\>2% weight loss in sarcopenic individuals)\n\nExclusion Criteria:\n\n* Musculoskeletal disorder\n* Neurological disorder\n* Severely impaired hematological capacity\n* History of cardiac disease\n* Uncontrolled hypertension\n* Severe renal insufficiency\n* Advanced osteoporosis\n* Decreased ability to stand or walk",{"count":504,"type":20},40,[23],"This study aims to evaluate the effects of a 12-week aerobic and resistance exercise program in cancer patients with cachexia compared to standard care.\n\nA total of 40 participants aged 18 to 65, diagnosed with gastrointestinal cancer and cachexia, will be included in the study. Participants will be randomly assigned to the exercise group (aerobic and resistance training) or the control group (standard care), with 20 individuals in each group.\n\nBefore the 12-week intervention, both the exercise and control groups will undergo evaluations. Demographic and clinical data will be recorded. The following assessments will be conducted:\n\nBody Composition: Bioelectrical impedance analysis Sarcopenia Assessment: SARC-F questionnaire Functional Exercise Capacity: 6-minute walk test Gait Parameters: 8-meter walk test Mobility and Balance: Timed Up and Go test Muscle Strength: Knee extensor and hand grip strength measured with dynamometers 30-second sit-to-stand test Additionally, participants will complete several questionnaires, including the Edmonton Symptom Assessment Scale, Karnofsky Performance Status scale, FRAIL scale, Fatigue Severity Scale, and EORTC-QLQ30.\n\nThe exercise group will participate in a supervised and home-based exercise program consisting of aerobic and resistance exercises over 12 weeks.\n\nThe intensity will be progressively adjusted based on the individual's perceived exertion.",[508],"Cancer Cachexia (CC)",[335,251,510,511,512],"cachexia","aerobic","resistance","2024-12-16",{"date":515,"type":36},"2024-12-17",{"date":517,"type":20},"2025-01-01",{"date":289,"type":20},{"name":42,"class":43},{"id":521,"slug":522,"hasResults":11,"nctId":523,"briefTitle":524,"officialTitle":525,"acronym":526,"eligibilityCriteria":527,"healthyVolunteers":11,"sex":16,"minAge":528,"maxAge":529,"enrollmentInfo":530,"targetDuration":4,"studyType":21,"phases":531,"briefSummary":532,"conditions":533,"keywords":535,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":540,"lastUpdatePostDateStruct":541,"startDateStruct":543,"completionDateStruct":545,"leadSponsor":546,"locationsCount":44},"100571423","care-bundle-containing-chlorhexidine-dressing-on-port-catheter-and-central-venous-catheters-100571423","NCT06720064","Care Bundle Containing Chlorhexidine Dressing on Port Catheter and Central Venous Catheters","Care Bundle Containing Chlorhexidine Dressing on Port Catheter and Central Venous Catheter-Related Bloodstream Infections in Pediatric Cancer Patients","CHG-port","Inclusion Criteria:\n\n* The child is receiving inpatient treatment at the Hematology and Oncology unit and hematopoietic stem cell transplantation unit\n* The child has a diagnosis of hematological or oncological cancer\n* The child's age range is between 1 and 17\n* Having a port catheter inserted and no early complications have occurred\n* The child agrees to participate in the study voluntarily\n* The parent agrees to participate in the study voluntarily\n* Obtaining the consent form from the child and parent\n* He has been in the hospital for more than 48 hours\n\nExclusion Criteria:\n\n* Have a systemic infection.","1 Year","17 Years",{"count":504,"type":20},[23],"In order to provide treatment in pediatric hematology-oncology patients, in some cases a central venous catheter is required in children. The most important situation to pay attention to when using a central venous catheter is \"Central line-associated bloodstream infections\".\n\nThese infections are infections that develop after admission to the hospital and are not in the incubation period at the time of admission, or although they usually develop in the hospital 48-72 hours after hospitalization, they can sometimes appear after discharge. Central line-associated bloodstream infections significantly increase morbidity and mortality. In this context, the effect of using a care bundle containing chlorhexidine dressing on port catheter and central venous catheter-related bloodstream infections in pediatric cancer patients was examined.",[534],"Pediatric Cancer",[536,537,538,251,539],"Care bundle","chlorhexidine","pediatric","catheter-related bloodstream infections","2024-12-05",{"date":542,"type":36},"2024-12-06",{"date":544,"type":36},"2024-05-07",{"date":384,"type":20},{"name":42,"class":43},{"id":548,"slug":549,"hasResults":11,"nctId":550,"briefTitle":551,"officialTitle":552,"acronym":4,"eligibilityCriteria":553,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":52,"enrollmentInfo":554,"targetDuration":4,"studyType":21,"phases":556,"briefSummary":557,"conditions":558,"keywords":560,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":564,"lastUpdatePostDateStruct":565,"startDateStruct":567,"completionDateStruct":569,"leadSponsor":571,"locationsCount":44},"100563589","effects-of-virtual-reality-exercises-on-individuals-with-peripheral-artery-disease-100563589","NCT06618131","Effects of Virtual Reality Exercises on Individuals With Peripheral Artery Disease","Examination of the Effects of Virtual Reality Exercises on Lower Extremity Skin Temperature, Arterial Stiffness, Gait Parameters and Enjoyment of Exercise in Individuals With Peripheral Arterial Disease","Inclusion Criteria:\n\n* Being diagnosed with PAD\n* Being between 18-65 years of age\n* Ankle-brachial index less than 0.9\n* Not having a lower extremity injury or surgery that would prevent participation in the exercise program\n\nExclusion Criteria:\n\n* History of cardiovascular events less than 3 months before the start of the study\n* Uncontrolled severe hypertension (systolic blood pressure ≥ 180 mmHg or diastolic blood pressure ≥ 110 mmHg)\n* Uncontrolled diabetes mellitus (glycemic index ≥ 290)\n* Critical Limb Ischemia\n* Balance Problems\n* Vertigo\n* History of epilepsy\n* Dementia\n* Chronic diseases that may be contraindications for exercise",{"count":555,"type":20},24,[23],"The aim of this study is to investigate the effects of virtual reality exercises on lower extremity skin temperature, arterial stiffness, gait parameters and enjoyment of exercise in individuals with peripheral arterial disease.",[559],"Peripheral Arterial Disease(PAD)",[561,335,280,562,563],"virtual reality","gait analysis","skin temperature","2024-09-26",{"date":566,"type":36},"2024-10-01",{"date":568,"type":20},"2024-10",{"date":570,"type":20},"2025-03",{"name":42,"class":43},{"id":573,"slug":574,"hasResults":11,"nctId":575,"briefTitle":576,"officialTitle":577,"acronym":578,"eligibilityCriteria":579,"healthyVolunteers":11,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":580,"targetDuration":4,"studyType":148,"phases":4,"briefSummary":582,"conditions":583,"keywords":585,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":588,"lastUpdatePostDateStruct":589,"startDateStruct":591,"completionDateStruct":593,"leadSponsor":595,"locationsCount":44},"100276897","cardiopulmonary-resuscitation-in-operating-room-100276897","NCT02884271","Cardiopulmonary Resuscitation in Operating Room","Intraoperative Cardiac Arrest: Incidence and Outcome","CPR","Inclusion Criteria:\n\n* All patients who develop cardiac arrest in the operating room\n\nExclusion Criteria:\n\n* Absence of informed consent\n* Patients arriving into the operating room with ongoing CPR",{"count":581,"type":20},7,"In the last ten years patient safety during routine surgical interventions has increased; however as there is an increase in the number of specialized surgical interventions and high risk patients like elderly and emergency patients, the incidence of perioperative cardiac arrest has not reduced but remains fixed. The incidence of perioperative cardiac arrest varies from 4.3-34.6 for each 10,000 procedures. However as in a lot of other countries exact data are lacking also for Turkey. With this study the investigators want to start collecting data about intraoperative cardiac arrest in Turkey, starting at their institution The aim is to evaluate the incidence and outcome in the study. Secondary aim is to assess the causes of cardiac arrest in the operating room.",[584],"Intraoperative Cardiac Arrest",[578,586,587],"cardiac arrest","operating room","2024-02-16",{"date":590,"type":36},"2024-02-20",{"date":592,"type":36},"2016-03",{"date":594,"type":20},"2027-05",{"name":42,"class":43},""]