[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Istanbul Medeniyet University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":554},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,20,0,[8,54,84,112,141,165,198,225,245,270,293,320,347,370,396,423,446,476,503,530],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":31,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":42,"lastUpdatePostDateStruct":43,"startDateStruct":46,"completionDateStruct":48,"leadSponsor":50,"locationsCount":53},"100642634","self-help-plus-sh-for-stress-reduction-in-social-service-workers-a-pilot-rct-100642634",false,"NCT07644949","Self-Help Plus (SH+) for Stress Reduction in Social Service Workers: A Pilot RCT","Feasibility and Preliminary Effectiveness of WHO Self-Help Plus (SH+) for Stress Reduction Among Social Service Workers: A Pilot Randomized Controlled Trial","Inclusion Criteria:\n\n* Currently employed (permanent, contracted, or temporary staff) at an institution under the Istanbul Provincial Directorate of Family and Social Services\n* Able to read and write in Turkish\n* Willing to participate voluntarily\n* Provides written informed consent\n\nExclusion Criteria:\n\n* Imminent suicide risk, screened at baseline (T0) via PHQ-9 item 9; participants scoring 2 or higher are not enrolled and are immediately referred to a mental health professional\n* Active psychosis, severe substance use disorder, or severe intellectual disability\n* An acute medical condition that would preclude participation\n* Planned extended leave (e.g., maternity or unpaid leave) during the study period",true,"ALL","18 Years",{"count":20,"type":21},50,"ESTIMATED","INTERVENTIONAL",[24],"NA","This is a two-arm, stratified cluster-randomized controlled pilot trial evaluating the feasibility and preliminary effectiveness of the World Health Organization's Self-Help Plus (SH+) intervention for stress reduction among social service workers employed by the Istanbul Provincial Directorate of Family and Social Services (ASHP). Four institutions (clusters) are randomized 1:1, stratified by service type, to receive either SH+ plus Enhanced Care as Usual (ECAU) or ECAU only, with a target of 50 participants (25 per arm). The primary aim is to assess feasibility indicators (recruitment, session attendance, retention, and acceptability) to inform a future full-scale definitive trial. Preliminary effects on perceived stress and related mental health and well-being outcomes are examined as secondary outcomes.",[27,28,29,30],"Stress, Psychological, Occupational","Stress, Psychological","Psychological Distress","Burnout, Professional",[32,33,34,35,36,37,38,39,40],"Self-Help Plus","SH+","social service workers","universal prevention","cluster randomized trial","pilot study","Acceptance and Commitment Therapy","Turkey","social care workers","NOT_YET_RECRUITING","2026-06-09",{"date":44,"type":45},"2026-06-12","ACTUAL",{"date":47,"type":21},"2026-07",{"date":49,"type":21},"2026-11",{"name":51,"class":52},"Istanbul Medeniyet University","OTHER",1,{"id":55,"slug":56,"hasResults":11,"nctId":57,"briefTitle":58,"officialTitle":59,"acronym":4,"eligibilityCriteria":60,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":61,"enrollmentInfo":62,"targetDuration":64,"studyType":65,"phases":4,"briefSummary":66,"conditions":67,"keywords":71,"overallStatus":75,"whyStopped":4,"lastUpdateSubmitDate":76,"lastUpdatePostDateStruct":77,"startDateStruct":79,"completionDateStruct":81,"leadSponsor":83,"locationsCount":53},"100637960","smartphone-addiction-posture-and-breathing-control-in-university-students-100637960","NCT07615322","Smartphone Addiction, Posture and Breathing Control in University Students","Effects of Smartphone Addiction on Posture and Breathing Control in University Students: The Role of Physical Activity and Demographic Factors","Inclusion Criteria:\n\n* Age between 18 and 35 years\n* Smartphone user\n* Ability to stand independently\n* Ability to perform activities of daily living independently\n* Ability to understand assessment instructions\n* Voluntary participation with signed informed consent\n\nExclusion Criteria:\n\n* • History of fracture\n\n  * Cardiovascular disease\n  * Pulmonary disease\n  * Neurological or orthopedic disorders affecting posture or breathing\n  * Inability to understand instructions","35 Years",{"count":63,"type":21},300,"1 Month","OBSERVATIONAL","The aim of this study is to investigate the effects of smartphone addiction on postural problems and breathing control in healthy university students.\n\nExcessive smartphone use has been associated with forward head posture, thoracic postural changes, and musculoskeletal complaints. These postural alterations may negatively influence respiratory biomechanics and breathing control. However, the relationship between smartphone addiction, postural deterioration, and dysfunctional breathing symptoms has not been comprehensively investigated.\n\nParticipants will complete questionnaires assessing smartphone addiction and breathing control, and posture will be evaluated using the New York Posture Rating Chart. Binary logistic regression analysis will be performed to determine whether smartphone addiction independently predicts postural problems. Additionally, multiple linear regression analyses will be conducted to examine the association between smartphone addiction, posture, and breathing control.",[68,69,70],"Smartphone Addiction","Postural Disorders","Dysfunctional Breathing",[72,73,74],"smartphone addiction","posture","breathing control","RECRUITING","2026-05-22",{"date":78,"type":45},"2026-05-29",{"date":80,"type":45},"2026-04-05",{"date":82,"type":21},"2026-06-20",{"name":51,"class":52},{"id":85,"slug":86,"hasResults":11,"nctId":87,"briefTitle":88,"officialTitle":89,"acronym":4,"eligibilityCriteria":90,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":91,"targetDuration":4,"studyType":22,"phases":93,"briefSummary":94,"conditions":95,"keywords":100,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":104,"lastUpdatePostDateStruct":105,"startDateStruct":107,"completionDateStruct":109,"leadSponsor":111,"locationsCount":4},"100634797","a-mindfulness-based-stress-reduction-training-program-model-100634797","NCT07544355","A Mindfulness-Based Stress Reduction Training Program Model","A Mindfulness-Based Stress Reduction Training Program Model for Empowering Nursing Students","Inclusion Criteria:\n\n* Volunteering to participate in the study,\n* Being a nursing student,\n* Having completed the pre-test,\n* Not having a stress score within the normal range,\n* Not having received any prior training on this subject,\n* Not having a severe psychiatric illness (psychosis, schizophrenia, etc.) diagnosed by a physician and requiring medication.\n\nExclusion Criteria:\n\n* Not volunteering to participate in the study,\n* Not being a nursing student,\n* Not completing the pre-test,\n* Having a stress score within the normal range in the pre-test results,\n* Not having received any prior training on this subject,\n* Having a psychiatric illness (psychosis, schizophrenia, etc.) diagnosed by a physician and requiring medication.",{"count":92,"type":21},93,[24],"Mindfulness-based practices are used to regulate mood, alleviate or completely eliminate symptoms that cause stress and depression, and positively influence well-being. The Mindfulness-Based Stress Reduction Program is a mindfulness approach applied to individuals with physical and psychological complaints and aims to reduce stress levels (Kral et al., 2022).\n\nThe Mindfulness-Based Stress Reduction Program is a widely used meditation practice that includes individual or group practices aimed at creating awareness in individuals, such as breath awareness meditation, body scan, walking meditation, and yoga, taught by a practitioner. Each of the practices involves focusing attention on the experience of the present moment (Kral et al., 2022). However, it aims for individuals under stress to respond consciously to situations instead of automatically reacting (Gotink et al., 2016). Unlike traditional meditation, the Mindfulness-Based Stress Reduction Program is based on focused attention, the individual's clear observation of themselves and events, and breath meditation. The aim is for individuals to recognize their automatic responses to events and to transform their existing responses without judgment (Gotink et al., 2016).\n\nThe main objective of this study is to determine the effect of a mindfulness-based stress reduction training program on emotion regulation and stress levels of nursing students, thereby enabling them to gain competence in this area.",[96,97,98,99],"Depression","Anxiety","Stress","Well-Being, Psychological",[101,102,103],"Mindfulness","Nursing Students","Mindful Awareness","2026-04-15",{"date":106,"type":45},"2026-04-22",{"date":108,"type":21},"2026-04-20",{"date":110,"type":21},"2027-01-30",{"name":51,"class":52},{"id":113,"slug":114,"hasResults":11,"nctId":115,"briefTitle":116,"officialTitle":117,"acronym":4,"eligibilityCriteria":118,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":119,"enrollmentInfo":120,"targetDuration":4,"studyType":65,"phases":4,"briefSummary":122,"conditions":123,"keywords":127,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":135,"lastUpdatePostDateStruct":136,"startDateStruct":137,"completionDateStruct":138,"leadSponsor":140,"locationsCount":53},"100634314","validation-of-web-based-star-cancellation-and-line-bisection-tests-in-hemiplegic-stroke-100634314","NCT07538076","Validation of Web-Based Star Cancellation and Line Bisection Tests in Hemiplegic Stroke","Development and Validity of Web Based Star Cancellation Test and Line Bisection Test in the Assessment of Visuospatial Neglect in Hemiplegic Stroke Patients","Inclusion Criteria:\n\n* Age 18 to 80 years\n* First-ever ischemic or hemorrhagic stroke\n* Hemiplegia secondary to stroke\n* Stroke in the subacute or chronic phase, defined as 1 to 24 months after stroke onset\n* Ability to provide written informed consent\n\nExclusion Criteria:\n\n* History of neurological or severe psychiatric disease before stroke that could significantly affect cognitive function or attention, such as brain tumor, traumatic brain injury, vasculitis, multiple sclerosis, or schizophrenia\n* Severe visual field defect not attributable to visuospatial neglect, such as isolated homonymous hemianopia\n* Severe upper extremity motor impairment or apraxia preventing interaction with the tablet or stylus pen\n* Inability to understand test instructions, cooperate with the assessment, or complete the evaluation process","80 Years",{"count":121,"type":21},105,"The goal of this observational study is to evaluate the clinical usability and diagnostic performance of newly developed web-based Star Cancellation and Line Bisection tests in assessing visuospatial neglect in hemiplegic stroke patients. It will also compare these digital tests with conventional paper-and-pencil assessments.\n\nThe main questions it aims to answer are:\n\nCan the web-based Star Cancellation and Line Bisection tests accurately distinguish between stroke patients with and without visuospatial neglect? Do digital test parameters (such as completion time, search speed, and search patterns) provide additional clinical information beyond conventional test scores? Researchers will compare the results of the web-based tests with standard paper-and-pencil tests to evaluate their diagnostic accuracy and clinical validity.\n\nParticipants will:\n\nComplete conventional paper-and-pencil Star Cancellation and Line Bisection tests Perform web-based (digital) versions of the same tests using a tablet and stylus Undergo routine clinical and cognitive assessments as part of standard care Provide demographic and clinical information",[124,125,126],"Stroke","Spatial Neglect","Spatial Neglect After Stroke",[128,125,129,130,131,132,133,134],"Visuospatial Neglect","Stroke Rehabilitation","Digital Assessment","Web-Based Assessment","Star Cancellation Test","Line Bisection Test","Neuropsychological Testing","2026-04-12",{"date":108,"type":45},{"date":104,"type":21},{"date":139,"type":21},"2026-12-01",{"name":51,"class":52},{"id":142,"slug":143,"hasResults":11,"nctId":144,"briefTitle":145,"officialTitle":146,"acronym":4,"eligibilityCriteria":147,"healthyVolunteers":11,"sex":17,"minAge":64,"maxAge":18,"enrollmentInfo":148,"targetDuration":4,"studyType":65,"phases":4,"briefSummary":149,"conditions":150,"keywords":152,"overallStatus":75,"whyStopped":4,"lastUpdateSubmitDate":157,"lastUpdatePostDateStruct":158,"startDateStruct":160,"completionDateStruct":162,"leadSponsor":164,"locationsCount":53},"100629723","transcutaneous-po-monitoring-in-picu-100629723","NCT07478380","Transcutaneous pO₂ Monitoring in PICU","COMPARISON OF TRANSCUTANEOUS PCO₂ AND PO₂ MEASUREMENTS WITH ARTERIAL BLOOD GAS ANALYSIS IN PEDIATRIC INTENSIVE CARE PATIENTS: IS TRANSCUTANEOUS pO₂ A RELIABLE ALTERNATIVE?","Eligibility Criteria\n\nInclusion Criteria:\n\n* Age between 1 month and 18 years\n* Admission to the Pediatric Intensive Care Unit (PICU)\n* Presence of an arterial catheter allowing arterial blood gas (ABG) sampling\n* Simultaneous or paired transcutaneous pCO₂ and pO₂ monitoring available\n* Hemodynamically stable at the time of measurement\n\nExclusion Criteria:\n\n* Severe skin disease, burns, or local skin infection at the transcutaneous sensor site\n* Severe peripheral perfusion impairment (e.g., refractory shock or high-dose vasopressor support)\n* Congenital or acquired conditions interfering with accurate transcutaneous measurements\n* Technical failure or inability to obtain reliable transcutaneous readings\n* Missing or incomplete paired ABG-transcutaneous measurement data",{"count":20,"type":21},"Arterial blood gas analysis is commonly used in pediatric intensive care units (PICUs) to assess oxygen and carbon dioxide levels in critically ill children. However, arterial blood sampling is invasive, can be painful, and may need to be repeated frequently. Transcutaneous monitoring provides a noninvasive method to continuously measure oxygen (pO₂) and carbon dioxide (pCO₂) levels through the skin, but its accuracy in critically ill pediatric patients requires further evaluation.\n\nThe purpose of this observational study is to compare transcutaneous pO₂ and pCO₂ measurements with arterial blood gas values in pediatric intensive care unit patients. By analyzing paired measurements obtained simultaneously during routine clinical care, this study aims to evaluate the agreement between transcutaneous and arterial measurements, with a particular focus on whether transcutaneous pO₂ can serve as a reliable alternative to arterial sampling.\n\nThe results of this study may help clarify the role of transcutaneous monitoring in pediatric intensive care and may contribute to reducing the need for invasive blood sampling in selected patients.",[151],"Pediatric Critical Illness",[153,154,155,156],"Pediatric Intensive Care Unit","Transcutaneous Monitoring","Arterial Blood Gas","Noninvasive Monitoring","2026-03-13",{"date":159,"type":45},"2026-03-17",{"date":161,"type":45},"2026-03-10",{"date":163,"type":21},"2026-10-10",{"name":51,"class":52},{"id":166,"slug":167,"hasResults":11,"nctId":168,"briefTitle":169,"officialTitle":170,"acronym":171,"eligibilityCriteria":172,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":173,"enrollmentInfo":174,"targetDuration":4,"studyType":22,"phases":176,"briefSummary":177,"conditions":178,"keywords":182,"overallStatus":75,"whyStopped":4,"lastUpdateSubmitDate":190,"lastUpdatePostDateStruct":191,"startDateStruct":193,"completionDateStruct":195,"leadSponsor":197,"locationsCount":53},"100625735","osteopathic-manual-therapy-vs-ganglion-impar-block-for-chronic-coccydynia-100625735","NCT07426497","Osteopathic Manual Therapy vs Ganglion Impar Block for Chronic Coccydynia","Comparison of Osteopathic Manual Therapy and Ganglion Impar Block in Patients With Chronic Coccydynia","COCCY-OMT-GIB","Inclusion Criteria:\n\n* Age 18-75 years\n* Chronic coccygodynia ≥3 months\n* Baseline NRS ≥4\n* ODI ≥20\n* Failure of prior conservative treatment\n* Imaging excludes fracture, infection, or malignancy\n* Ability to provide written informed consent\n\nExclusion Criteria:\n\n* Acute coccygodynia\n* Prior spinal or coccygeal surgery\n* Malignancy\n* Pelvic fracture\n* Pregnancy\n* Coagulation disorder\n* Severe psychiatric disease\n* Prior osteopathic manual therapy or ganglion impar block","75 Years",{"count":175,"type":21},100,[24],"Chronic coccydynia is a condition characterized by persistent pain in the coccyx region that can significantly impair sitting tolerance, daily activities, and quality of life. Various conservative and interventional treatment options have been described, including manual therapy techniques and ganglion impar block. However, the comparative effectiveness of these approaches remains unclear.\n\nThe aim of this randomized controlled study is to compare the effects of osteopathic manual therapy and ganglion impar block on pain intensity and functional disability in patients with chronic coccydynia. Participants will be randomly assigned to one of the two treatment groups. Pain severity will be assessed using the Numeric Rating Scale (NRS), and functional status will be evaluated with the Oswestry Disability Index (ODI) at baseline, week 3, and month 3.\n\nThe results of this study are expected to provide evidence regarding the relative effectiveness of these two commonly used treatment methods and to guide clinicians in selecting appropriate management strategies for patients with chronic coccydynia.",[179,180,181],"Coccydynia","Chronic Pain","Coccygodynia",[183,184,185,186,187,188,189],"Chronic coccydynia","Ganglion impar block","Osteopathic manual therapy","Coccyx pain","Manual therapy","Interventional pain","Numeric Rating Scale","2026-02-22",{"date":192,"type":45},"2026-02-24",{"date":194,"type":45},"2025-08-28",{"date":196,"type":21},"2026-02-16",{"name":51,"class":52},{"id":199,"slug":200,"hasResults":11,"nctId":201,"briefTitle":202,"officialTitle":202,"acronym":4,"eligibilityCriteria":203,"healthyVolunteers":11,"sex":17,"minAge":204,"maxAge":4,"enrollmentInfo":205,"targetDuration":64,"studyType":65,"phases":4,"briefSummary":207,"conditions":208,"keywords":210,"overallStatus":75,"whyStopped":4,"lastUpdateSubmitDate":217,"lastUpdatePostDateStruct":218,"startDateStruct":220,"completionDateStruct":222,"leadSponsor":224,"locationsCount":53},"100621255","turkish-translation-and-content-validity-of-the-nottwil-environmental-factors-inventory-nefi-in-persons-with-spinal-cord-injury-100621255","NCT07368244","Turkish Translation and Content Validity of the Nottwil Environmental Factors Inventory (NEFI) in Persons With Spinal Cord Injury","Inclusion Criteria:\n\n* Adults (\\>=16 years) with a diagnosis\u002Fhistory of spinal cord injury (traumatic or non-traumatic)\n* Living in Turkey\n* Able to read\u002Funderstand Turkish and provide informed consent\n* Clinically stable to complete questionnaires\n\nExclusion Criteria:\n\n* Fully recovered from SCI \u002F no longer living with SCI-related functional consequences (as defined by your protocol)\n* Severe cognitive\u002Fcommunication limitations preventing valid completion\n* Any condition judged by investigators to preclude participation","16 Years",{"count":206,"type":21},405,"This observational methodology study will produce a Turkish version of the Nottwil Environmental Factors Inventory (NEFI-TR) within one month using a standardized translation and cultural adaptation process. Content validity will be assessed using an expert panel (and, if applicable, cognitive debriefing with adults with spinal cord injury) to ensure relevance, clarity, and comprehensibility of each item in the Turkish context.",[209],"Spinal Cord Injuries (SCI)",[211,212,213,214,215,216],"InSCI","Nottwil Environmental Factors Inventory","NEFI","Turkish","cultural adaptation","content validity","2026-01-18",{"date":219,"type":45},"2026-01-26",{"date":221,"type":45},"2026-01-01",{"date":223,"type":21},"2026-02-05",{"name":51,"class":52},{"id":226,"slug":227,"hasResults":11,"nctId":228,"briefTitle":229,"officialTitle":229,"acronym":4,"eligibilityCriteria":230,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":231,"targetDuration":232,"studyType":65,"phases":4,"briefSummary":233,"conditions":234,"keywords":4,"overallStatus":75,"whyStopped":4,"lastUpdateSubmitDate":237,"lastUpdatePostDateStruct":238,"startDateStruct":240,"completionDateStruct":242,"leadSponsor":244,"locationsCount":53},"100614987","ultrasound-assesment-of-radial-nerve-in-humeral-shaft-fracture-patients-with-radial-palsy-100614987","NCT07286734","Ultrasound Assesment Of Radial Nerve In Humeral Shaft Fracture Patients With Radial Palsy","Inclusion Criteria:\n\n* Adult patients aged 18 years or older.\n* Diagnosed with traumatic humeral shaft fracture.\n* Admitted and followed according to the local clinical protocol with a confirmed diagnosis.\n* Underwent required investigations, including high-resolution ultrasonography and\u002For electromyography (EMG).\n* Provided written informed consent to participate in the study.\n\nExclusion Criteria:\n\n* Pathological fractures due to malignancy or metabolic disorder.\n* History of previous humeral fracture or pre-traumatic radial nerve deficit.\n* Clinically detected vascular injury or major soft tissue loss accompanying the fracture.\n* Incomplete diagnostic workup (absence of ultrasound or EMG examination).\n* Declined participation or were lost to follow-up.\n* Persons under 18 years of age.",{"count":5,"type":21},"12 Months","This study investigates how well ultrasound imaging can identify damage to the radial nerve in patients with a broken upper arm bone (humeral shaft fracture). Some of these patients also have weakness or paralysis in their hand and wrist due to injury to the radial nerve. The study compares patients with and without radial nerve problems to see if early ultrasound scans can accurately detect nerve damage before surgery.\n\nAll patients will receive standard care, including surgery to fix the fracture. Those with nerve problems will also have the nerve explored during surgery. The results of the ultrasound will be compared to what is found during the operation. Patients will be followed closely over 12 months to monitor nerve recovery, healing of the bone, and any complications.\n\nThe goal is to improve the early diagnosis and management of nerve injuries in arm fractures, using a safe, non-invasive ultrasound scan that could help guide treatment decisions.",[235,236],"Humerus Shaft Fracture","Radial Nerve Palsy","2025-12-03",{"date":239,"type":45},"2025-12-16",{"date":241,"type":45},"2024-01-01",{"date":243,"type":21},"2026-02",{"name":51,"class":52},{"id":246,"slug":247,"hasResults":11,"nctId":248,"briefTitle":249,"officialTitle":250,"acronym":4,"eligibilityCriteria":251,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":252,"enrollmentInfo":253,"targetDuration":4,"studyType":22,"phases":255,"briefSummary":256,"conditions":257,"keywords":260,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":262,"lastUpdatePostDateStruct":263,"startDateStruct":265,"completionDateStruct":267,"leadSponsor":269,"locationsCount":4},"100611027","the-effect-of-digital-games-on-ethical-sensitivity-and-decision-making-in-nursing-students-100611027","NCT07235241","The Effect of Digital Games on Ethical Sensitivity and Decision Making in Nursing Students","The Effect of Digital Game-Based Teaching Methods on the Development of Ethical Sensitivity and Ethical Decision-Making Processes in Nursing Students","Inclusion Criteria:\n\nStudents must:\n\n* Have taken and successfully completed the Nursing Ethics course,\n* Be a fourth-year nursing student who has successfully completed all professional courses and is undertaking the 'Professional Training in the Workplace' placement.\n\nExclusion Criteria:\n\n* Students who have not taken the Nursing Ethics course or have failed the course before taking the Professional Training in the Workplace course.\n* Having a conditional grade point average (CGPA \\\u003C2.00) up to the period when the data was collected.","40 Years",{"count":254,"type":21},60,[24],"The study was planned using a randomised controlled experimental design to determine the effectiveness of digital game-based teaching in the development of ethical sensitivity and ethical decision-making processes among nursing students.",[258,259],"Decision Making","Ethics",[259,258,261,102],"Digital Game","2025-11-17",{"date":264,"type":45},"2025-11-19",{"date":266,"type":21},"2026-03",{"date":268,"type":21},"2026-06",{"name":51,"class":52},{"id":271,"slug":272,"hasResults":11,"nctId":273,"briefTitle":274,"officialTitle":274,"acronym":4,"eligibilityCriteria":275,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":119,"enrollmentInfo":276,"targetDuration":4,"studyType":22,"phases":277,"briefSummary":278,"conditions":279,"keywords":282,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":285,"lastUpdatePostDateStruct":286,"startDateStruct":288,"completionDateStruct":290,"leadSponsor":292,"locationsCount":4},"100606759","comparison-of-the-effects-of-external-oblique-intercostal-plane-block-subcostal-transverse-abdominis-plane-block-and-their-combination-in-the-management-of-postoperative-pain-in-laparoscopic-cholecystectomy-surgery-100606759","NCT07179731","Comparison of the Effects of External Oblique Intercostal Plane Block, Subcostal Transverse Abdominis Plane Block, and Their Combination in the Management of Postoperative Pain in Laparoscopic Cholecystectomy Surgery","Inclusion Criteria:\n\n* Patients scheduled for laparoscopic cholecystectomy surgery\n* Patients aged between 18 to 80 years\n* Having an anesthesiology risk assessment of ASA I, II, or III\n\nExclusion Criteria:\n\n* Patients who do not give written and oral consent\n* Patients with coagulopathy\n* History of allergic reaction or intoxication by local anesthetics\n* Severe organ failure\n* Mental retardation or illiteracy\n* Presence of infection on the injection site\n* Pregnancy\n* Patients whom the procedure is extended to open cholecystectomy",{"count":121,"type":21},[24],"This study aims to compare the efficacy of Subcostal Transversus Abdominis Plan Block, External Oblique Intercostal Plan Block and the combination of these two blocks, which are used in anesthesiology practice for postoperative pain in laparoscopy cholecystectomy surgery.",[280,281],"External Oblique Intercostal Plane Block","Subcostal Transverse Abdominis Plane Block",[283,284],"external oblique intercostal block","subcostal transverse abdominis block","2025-09-17",{"date":287,"type":45},"2025-09-18",{"date":289,"type":21},"2025-09-23",{"date":291,"type":21},"2025-12-31",{"name":51,"class":52},{"id":294,"slug":295,"hasResults":11,"nctId":296,"briefTitle":297,"officialTitle":298,"acronym":299,"eligibilityCriteria":300,"healthyVolunteers":11,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":301,"targetDuration":64,"studyType":65,"phases":4,"briefSummary":303,"conditions":304,"keywords":306,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":312,"lastUpdatePostDateStruct":313,"startDateStruct":315,"completionDateStruct":317,"leadSponsor":319,"locationsCount":53},"100596294","trichoscopic-predictors-of-treatment-response-in-tinea-capitis-a-prospective-study-100596294","NCT07043582","Trichoscopic Predictors of Treatment Response in Tinea Capitis: A Prospective Study","Tinea Capitis Patients: The Predictive Value of Trichoscopic Findings for Treatment Response - A Prospective Observational Study","TCTREP","Inclusion Criteria:\n\n* Age between 0 and 18 years\n\nClinical and trichoscopic findings compatible with tinea capitis\n\nLaboratory confirmation of tinea capitis (positive potassium hydroxide \\[KOH\\] smear and\u002For fungal culture)\n\nEligible for systemic antifungal treatment with terbinafine\n\nWritten informed consent obtained from a parent or legal guardian\n\nExclusion Criteria:\n\n* Age over 18 years\n\nNegative KOH smear and negative culture\n\nCurrent use of immunosuppressive therapy or presence of severe systemic illness (e.g., malignancy, HIV, organ transplant)\n\nContraindication to terbinafine treatment\n\nPoor compliance or unwillingness to attend follow-up visits\n\nCoexisting dermatologic conditions in the affected scalp area (e.g., seborrheic dermatitis, alopecia areata, lichen planus)",{"count":302,"type":21},150,"Brief Summary (Plain Language Version)\n\nThe goal of this observational study is to learn how well changes seen under a special microscope called a trichoscope (used to look at hair and scalp) match the success of treatment in children and adolescents with a scalp fungal infection called tinea capitis. The main questions it aims to answer are:\n\nDo changes in trichoscopic findings show when the fungal infection is cured?\n\nDoes having more severe trichoscopic findings at the start mean that treatment will take longer or be less successful?\n\nDo different fungus types respond differently to the same treatment?\n\nParticipants will:\n\nBe between the ages of 0 and 18 with confirmed tinea capitis based on lab tests (microscopy and\u002For culture)\n\nReceive an oral antifungal medicine called terbinafine for 4 weeks (dosing based on weight)\n\nAttend regular checkups every 4 weeks until both scalp appearance and lab tests show the infection is gone\n\nAt each visit, participants will:\n\nHave their scalp examined using a trichoscope\n\nProvide scalp samples for fungal testing\n\nBe assessed for symptoms like itching, redness, and scaling\n\nThe study will also look at how fast different signs on the scalp go away, and which of these signs are best at predicting whether the fungus is still present.",[305],"Tinea Capitis",[307,308,309,310,311],"tinea capitis","dermotoscopy","trichoscopy","wood lamp","mycology","2025-06-27",{"date":314,"type":45},"2025-06-29",{"date":316,"type":21},"2025-07-24",{"date":318,"type":21},"2025-10-10",{"name":51,"class":52},{"id":321,"slug":322,"hasResults":11,"nctId":323,"briefTitle":324,"officialTitle":325,"acronym":4,"eligibilityCriteria":326,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":61,"enrollmentInfo":327,"targetDuration":4,"studyType":65,"phases":4,"briefSummary":329,"conditions":330,"keywords":333,"overallStatus":75,"whyStopped":4,"lastUpdateSubmitDate":338,"lastUpdatePostDateStruct":339,"startDateStruct":341,"completionDateStruct":343,"leadSponsor":345,"locationsCount":346},"100591304","the-validity-and-reliability-of-the-turkish-version-of-the-bbaq-100591304","NCT06978686","The Validity and Reliability of the Turkish Version of the BBAQ","The Validity and Reliability of the Turkish Version of the Barriers to Being Active Quiz","Inclusion Criteria:\n\n* Aged 18 years or older\n* Ability to read and write in Turkish\n* No visual or hearing impairments that would interfere with participation\n* Ability to follow simple instructions\n* Willingness to participate in the study\n\nExclusion Criteria:\n\n* Diagnosis of rheumatological conditions that may limit physical activity and are characterized by chronic inflammation and\u002For joint deformities (e.g., rheumatoid arthritis, ankylosing spondylitis, systemic lupus erythematosus, psoriatic arthritis)\n* Physical limitations due to neurological or orthopedic conditions (e.g., stroke, cerebral palsy, multiple sclerosis, limb amputation, or orthopedic surgery within the past six months)\n* History of psychiatric disorders that may impair cognitive functioning (e.g., schizophrenia, bipolar disorder, severe depression, attention deficit hyperactivity disorder)\n* Presence of any cognitive impairment",{"count":328,"type":21},210,"The Barriers to Being Active Quiz (BBAQ) was originally developed in English to identify barriers to physical activity. This study aims to translate and cross-culturally adapt the BBAQ into Turkish (BBAQ-T) and evaluate its psychometric properties.",[331,332],"Health Knowledge, Attitudes, Practice","Physical Inactivity",[334,335,336,337],"exercise","questionnaires","physical activity","validation study","2025-06-15",{"date":340,"type":45},"2025-06-18",{"date":342,"type":45},"2025-05-20",{"date":344,"type":21},"2025-08-20",{"name":51,"class":52},2,{"id":348,"slug":349,"hasResults":11,"nctId":350,"briefTitle":351,"officialTitle":351,"acronym":4,"eligibilityCriteria":352,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":353,"enrollmentInfo":354,"targetDuration":4,"studyType":65,"phases":4,"briefSummary":356,"conditions":357,"keywords":360,"overallStatus":75,"whyStopped":4,"lastUpdateSubmitDate":338,"lastUpdatePostDateStruct":363,"startDateStruct":365,"completionDateStruct":367,"leadSponsor":369,"locationsCount":53},"100583406","reliability-and-validity-of-the-turkish-version-of-general-sleep-disturbance-scale-gsds-t-in-multiple-sclerosis-100583406","NCT06875908","Reliability and Validity of the Turkish Version of General Sleep Disturbance Scale (GSDS-T) in Multiple Sclerosis","Inclusion Criteria:\n\n* Individuals over the age of 18 who have been diagnosed with Multiple Sclerosis for at least two years,\n* Those with an EDSS score \\>2.\n* Those without symptoms of insomnia according to the Diagnostic and Statistical Manual of Mental Disorders-5 (DSM-5) diagnostic criteria\n* Individuals whose native language is Turkish and who have the ability to speak and understand.\n\nExclusion Criteria:\n\n* Those with severe spasticity,\n* Those with vision and hearing problems,\n* Those with a known mental illness (major depression, schizophrenia, psychosis, etc.),\n* Those in an acute relapse phase,\n* Those using dietary supplements,\n* Those using tranquilizers or immunosuppressants.","65 Years",{"count":355,"type":21},126,"The GSDS-T was developed by Lee KA to assess difficulty falling asleep, waking up during sleep, sleep quality, and daytime alertnes. The Turkish validity and reliability of the scale have been conducted on stroke patients but not on multiple sclerosis patients. The aim of this study is to investigate the validity and reliability of the Turkish version of general sleep disturbance scale (GSDS-T) in patients with multiple sclerosis",[358,359],"Multiple Sclerosis","Sleep Disturbance",[361,362],"Multiple sclerosis","Sleep disturbances",{"date":364,"type":45},"2025-06-17",{"date":366,"type":45},"2025-04-15",{"date":368,"type":21},"2025-08-10",{"name":51,"class":52},{"id":371,"slug":372,"hasResults":11,"nctId":373,"briefTitle":374,"officialTitle":375,"acronym":4,"eligibilityCriteria":376,"healthyVolunteers":11,"sex":17,"minAge":377,"maxAge":18,"enrollmentInfo":378,"targetDuration":4,"studyType":22,"phases":379,"briefSummary":380,"conditions":381,"keywords":383,"overallStatus":75,"whyStopped":4,"lastUpdateSubmitDate":388,"lastUpdatePostDateStruct":389,"startDateStruct":391,"completionDateStruct":393,"leadSponsor":395,"locationsCount":53},"100554094","effects-of-botulinum-toxin-injection-combined-with-reswt-in-lower-extremity-spasticity-in-children-with-cerebral-palsy-100554094","NCT06494618","Effects of Botulinum Toxin Injection Combined with RESWT in Lower Extremity Spasticity in Children with Cerebral Palsy","The Effects of Botulinum Toxin Type a Injection Combined with RESWT in Lower Extremity Spasticity in Children with Cerebral Palsy","Inclusion Criteria:\n\n* Diagnosed with cerebral palsy.\n* Spasticity in at least one of the lower extremity muscle groups.\n* No contraindications to shockwave therapy.\n* Applied Botulinum Toxin Type A injection for at least one spastic muscle of lower extremity.\n* Agreed to participate to study (patient\u002Fprimary caregiver)\n\nExclusion Criteria:\n\n* Surgery history within the last year of the muscle to be injected and treated\n* Having uncontrolled epilepsy.\n* Having infection\n* Coagulopathy","2 Years",{"count":5,"type":21},[24],"This study aimed to check and compare the effects of botulinum toxin injection combined with shock wave therapy versus botulinum toxin injection only for lower extremity spasticity in children with cerebral palsy",[382],"Cerebral Palsy, Spastic",[384,385,386,387],"cerebral palsy","spasticity","botulinum toxin injection","extracorporeal shockwave therapy","2025-03-08",{"date":390,"type":45},"2025-03-11",{"date":392,"type":21},"2025-03",{"date":394,"type":21},"2025-06",{"name":51,"class":52},{"id":397,"slug":398,"hasResults":11,"nctId":399,"briefTitle":400,"officialTitle":401,"acronym":4,"eligibilityCriteria":402,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":403,"targetDuration":4,"studyType":22,"phases":405,"briefSummary":406,"conditions":407,"keywords":411,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":415,"lastUpdatePostDateStruct":416,"startDateStruct":418,"completionDateStruct":420,"leadSponsor":422,"locationsCount":4},"100579438","effect-of-tens-on-bladder-tenesmus-related-pain-and-patient-comfort-after-urinary-surgery-100579438","NCT06824298","Effect of TENS on Bladder Tenesmus-related Pain and Patient Comfort After Urinary Surgery","Effect of TENS on Bladder Tenesmus-related Pain and Patient Comfort in the Early Postoperative Period After Urinary Surgery","Inclusion Criteria:\n\n* Being 18 years or older\n* To undergo endoscopic urological surgery (Transurethral prostate resection\u002Fbladder surgery)\n* Having an ASA score of 1-2\n* Inserting a urinary catheter during surgery\n* To be willing to participate in the study\n\nExclusion Criteria:\n\n* To undergo emergency surgery\n* Being under the age of 18\n* Having an ASA score of 3 and above\n* Having a urinary catheter inserted before surgery\n* Not agreeing to participate in the study",{"count":404,"type":21},80,[24],"Bladder tenesmu is defined as the need to urinate despite the person urinating and is associated with various causes such as bladder spasm, infection, stones, catheters. Catheters used in urinary surgeries can cause various complications, especially pain and discomfort. There is no sufficient study in the literature on bladder tenesmus caused by mechanical interactions related to urinary catheters, and this situation negatively affects patient comfort. Transcutaneous Electrical Nerve Stimulation (TENS) is an effective method of reducing pain with low-voltage electrical current. However, there are no studies on the application of TENS in the management of symptoms associated with bladder tenesmus after urinary surgery. This study aims to investigate the effect of TENS application on bladder tenesmus-related pain and patient comfort in the early postoperative period after urinary surgery.",[408,409,410],"Urinary Surgery","Pain, Postoperative","Comfort",[412,413,410,414],"Bladder tenesmus","Pain","Nursing care","2025-02-12",{"date":417,"type":45},"2025-02-13",{"date":419,"type":21},"2025-03-03",{"date":421,"type":21},"2026-09-03",{"name":51,"class":52},{"id":424,"slug":425,"hasResults":11,"nctId":426,"briefTitle":427,"officialTitle":427,"acronym":4,"eligibilityCriteria":428,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":429,"targetDuration":4,"studyType":22,"phases":431,"briefSummary":432,"conditions":433,"keywords":435,"overallStatus":75,"whyStopped":4,"lastUpdateSubmitDate":438,"lastUpdatePostDateStruct":439,"startDateStruct":441,"completionDateStruct":443,"leadSponsor":445,"locationsCount":53},"100458723","the-effect-of-progressive-muscle-relaxation-exercises-on-pain-and-disability-after-spinal-surgery-100458723","NCT05253326","The Effect of Progressive Muscle Relaxation Exercises on Pain and Disability After Spinal Surgery","Inclusion Criteria:\n\n* Having undergone spinal surgery (such as Discectomy, Laminectomy, Spinal fusion, Foraminatomy),\n* 18 years of age or older\n* Agreeing to apply progressive relaxation exercises and willing and willing to participate in the study,\n* Having no medically diagnosed health problems (neurological, psychiatric, orthopedic) that will prevent learning and practicing progressive muscle relaxation exercises,\n* Patients who do not know and practice progressive relaxation exercises before will be included in the study.\n\nExclusion Criteria:\n\n* Patients who will undergo emergency surgery,\n* Do not want to apply progressive relaxation exercises,\n* Do not apply them as desired during the working process,\n* Those have health problems (neurological, psychiatric, orthopedic) that may affect their ability to do the exercises",{"count":430,"type":21},70,[24],"This study was planned as a randomized controlled experimental study to determine the effect of progressive muscle relaxation exercises on pain and disability in patients undergoing spinal surgery.",[434],"Spinal Stenosis Lumbar",[436,437,413],"Lumbar Surgery","Progressive muscle relaxation","2024-11-16",{"date":440,"type":45},"2024-11-19",{"date":442,"type":45},"2022-05-01",{"date":444,"type":21},"2025-05-01",{"name":51,"class":52},{"id":447,"slug":448,"hasResults":11,"nctId":449,"briefTitle":450,"officialTitle":451,"acronym":4,"eligibilityCriteria":452,"healthyVolunteers":11,"sex":17,"minAge":453,"maxAge":18,"enrollmentInfo":454,"targetDuration":4,"studyType":22,"phases":456,"briefSummary":457,"conditions":458,"keywords":462,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":469,"lastUpdatePostDateStruct":470,"startDateStruct":472,"completionDateStruct":474,"leadSponsor":475,"locationsCount":53},"100564921","motivational-interviewing-and-whatsapp-based-monitoring-for-metabolic-control-and-self-efficacy-in-adolescents-with-t1dm-100564921","NCT06635460","Motivational Interviewing and WhatsApp-Based Monitoring for Metabolic Control and Self-Efficacy in Adolescents With T1DM","The Impact of Motivational Interviewing and Social Media-Based Patient Monitoring on Metabolic Control and Self-Efficacy in Adolescents With Type 1 Diabetes: A Randomized Controlled Trial","Inclusion criteria:\n\n* 13-18 years old,\n* Diagnosed with type 1 DM at least 6 months ago,\n* HbA1C level \\>7.0,\n* 3-monthly outpatient visits,\n* Completed basic type 1 DM education and scored high (≥15 points) on the Type 1 Diabetes Knowledge Assessment Form,\n* A WhatsApp user with a smart phone and internet access,\n* Adolescents who can speak and understand Turkish.\n\nExclusion criteria:\n\n* Using an insulin pump,\n* Having a chronic disease other than diabetes,\n* Cognitive, intellectual, hearing, vision, or speech disabilities","13 Years",{"count":455,"type":21},56,[24],"This clinical study aims to determine the effects of motivational interviewing and social media-based patient monitoring on metabolic control and self-efficacy in adolescents with Type 1 diabetes. Additionally, the study will assess the adolescents\\' attitudes toward their disease, quality of life, and perceived levels of social support. The primary research questions are as follows:\n\nFor adolescents with Type 1 diabetes who receive motivational interviewing and social media-based monitoring:\n\nHow do their attitudes toward their disease compare to those in the control group? How do their perceived levels of social support compare to those in the control group? How do their self-efficacy levels compare to those in the control group? How does their quality of life compare to that of the control group? How do their HbA1c levels compare to those in the control group?",[459,460,461],"Type 1 Diabetes Mellitus (T1DM)","Motivational Interviewing","Metabolic Control",[463,464,465,466,467,468],"Type 1 diabetes mellitus","adolescent","motivational interviewing","social media-based monitoring","metabolic control","Self efficacy","2024-10-08",{"date":471,"type":45},"2024-10-10",{"date":473,"type":21},"2024-10-15",{"date":366,"type":21},{"name":51,"class":52},{"id":477,"slug":478,"hasResults":11,"nctId":479,"briefTitle":480,"officialTitle":481,"acronym":4,"eligibilityCriteria":482,"healthyVolunteers":11,"sex":483,"minAge":484,"maxAge":485,"enrollmentInfo":486,"targetDuration":4,"studyType":22,"phases":488,"briefSummary":489,"conditions":490,"keywords":492,"overallStatus":75,"whyStopped":4,"lastUpdateSubmitDate":495,"lastUpdatePostDateStruct":496,"startDateStruct":498,"completionDateStruct":500,"leadSponsor":502,"locationsCount":53},"100555153","the-effect-of-perception-of-improvement-in-patients-with-fibromyalgia-100555153","NCT06508385","The Effect of Perception of Improvement in Patients With Fibromyalgia","The Effect of Perception of Improvement Provided Virtual Reality Environment on Symptom Presence and Severity in Patients With Fibromyalgia","Inclusion Criteria:\n\nDiagnosed with Fibromyalgia at least 1 year ago according to ACR criteria\n\nAge range 25-55\n\nFemale\n\nScored at least 24 on the Mini-Mental State Assessment Test\n\nReported weekly pain intensity of at least 40 mm on the Visual Analog Scale\n\nBe on a stable dose of medication for at least 6 months (serotonin norepinephrine reuptake inhibitors \\[e.g., duloxetine, milnacipran\\]; alpha 2-delta receptor ligand \\[e.g., pregabalin\\]; gabapentinoids)\n\nExclusion Criteria:\n\nHaving inflammatory rheumatic disease, malignancy, neurological disease, connective tissue disease, severe anemia, uncontrolled endocrine diseases\n\nBody Mass Index (BMI) ≥ 30 Kg\u002Fm2\n\nBeing pregnant\n\nHaving inability to understand, read and speak Turkish\n\nHaving difficulty in hearing and seeing\n\nHaving any metallic or electronic device in the body that will create incompatibility with the magnetic field in the fMRI scan Having any disease diagnosis (serious psychotic disorder, delirium, mental retardation, epilepsy, heart disease, lung diseases, etc.) that may prevent participation in the evaluation and training to be conducted within the scope of the research","FEMALE","25 Years","55 Years",{"count":487,"type":21},39,[24],"Fibromyalgia (FM) is a chronic pain syndrome characterized by impaired perception, transmission, and processing of nociceptive stimuli and causing widespread pain. Pain in FM is the disease itself and is characterized by nociplastic pain that may occur independently of any peripheral nociceptor activity or be felt without disease or damage to the somatosensory system. It is thought that the pain processing process is disrupted due to the changing neurotransmitter release activity and this situation causes pain to be felt more in FM. Chronic pain is the result of perception alteration associated with nociceptive afferent information affecting the cortex; underlying this change are limbic emotional learning mechanisms. Numerous factors, including emotional state, attention, and past painful experiences, modulate nociceptive inputs with the activation of multiple brain regions, resulting in a personalized pain experience. The chronic pain management program should target the central nervous system rather than the peripheral tissues because pain originates in the sensitized nervous system. For this reason, it is important to include plasticity-oriented approaches, cortical disinhibition methods, and strategies for improving perception and behavior change, which aim to replace negative beliefs with positive beliefs, into clinical practice. Our project aims to investigate the effectiveness of the therapeutic intervention, which consists of patient education supported Neuro-Linguistic Programming (NLP), visual feedback and metaphor-assisted breathing therapy designed to provide a perception of improvement and presented in a virtual reality environment, on pain processing, pain intensity, pain-pressure threshold, psychosomatic reflections (biomechanical and viscoelastic properties of tissue, sleep quality, pain catastrophizing behavior, anxiety and depression), disease impact and quality of life in FM patients.",[491],"Fibromyalgia",[493,413,494],"functional brain activity","Tissue properties","2024-09-02",{"date":497,"type":45},"2024-09-19",{"date":499,"type":45},"2024-08-13",{"date":501,"type":21},"2026-08-15",{"name":51,"class":52},{"id":504,"slug":505,"hasResults":11,"nctId":506,"briefTitle":507,"officialTitle":508,"acronym":4,"eligibilityCriteria":509,"healthyVolunteers":11,"sex":483,"minAge":510,"maxAge":511,"enrollmentInfo":512,"targetDuration":4,"studyType":22,"phases":514,"briefSummary":515,"conditions":516,"keywords":518,"overallStatus":75,"whyStopped":4,"lastUpdateSubmitDate":522,"lastUpdatePostDateStruct":523,"startDateStruct":525,"completionDateStruct":527,"leadSponsor":529,"locationsCount":53},"100468964","the-effect-of-myofascial-chain-release-techniques-on-shoulder-joint-range-of-motion-in-breast-cancer-survivors-100468964","NCT05386628","The Effect of Myofascial Chain Release Techniques on Shoulder Joint Range of Motion in Breast Cancer Survivors","The Effect of Myofascial Chain Release Techniques on Shoulder Joint Range of Motion Following Mastectomy Surgery in Breast Cancer Survivors","Inclusion Criteria:\n\n* Women between the ages of 30-60\n* Having breast surgery within 2 years\n* Not have received conservative treatment for shoulder rehabilitation in the last 6 months\n* Having limitation of movement of the shoulder joint due to breast surgery\n\nExclusion Criteria:\n\n* Not having agreed to participate in the study\n* Having undergone radical mastectomy surgery\n* Having connective tissue disease\n* Presence of brachial plexus paresis\u002Fplegia\n* Presence of radiogenic fibrosis\n* Presence of additional orthopedic (scoliosis, etc.), neurological (multiple sclerosis, stroke, etc.) and rheumatological diseases (ankylosing spondylitis, rheumatoid arthritis, etc.) that will affect upper extremity functions\n* Presence of active metastases\n* Having undergone reconstruction surgery\n* Continuation of radiotherapy (must have ended at least 3 months ago) or chemotherapy applications\n* Having had a bilateral mastectomy\n* To develop lymphedema in the arm-trunk\n* Use of muscle relaxants\n* Patients with severe chemotherapy side effects (hyperesthesia, nausea, skin changes, weakness, etc.)","30 Years","60 Years",{"count":513,"type":21},48,[24],"In breast cancer patients, limitation of shoulder joint movement occurs following mastectomy surgery. Studies have reported that damage to the fascia on the pectoralis major muscle during mastectomy surgery contributes to the development of the limitation. The aim of this study is to investigate the effect of release techniques applied to the fascia on the pectoralis major muscle and the fascial chain on the incerasing of shoulder joint range of motion.",[517],"Breast Cancer Survivors",[519,520,521],"breast cancer","range of motion","lymphatic drainage","2024-07-12",{"date":524,"type":45},"2024-07-15",{"date":526,"type":45},"2022-08-15",{"date":528,"type":21},"2025-07-15",{"name":51,"class":52},{"id":531,"slug":532,"hasResults":11,"nctId":533,"briefTitle":534,"officialTitle":535,"acronym":4,"eligibilityCriteria":536,"healthyVolunteers":11,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":537,"targetDuration":4,"studyType":65,"phases":4,"briefSummary":538,"conditions":539,"keywords":542,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":546,"lastUpdatePostDateStruct":547,"startDateStruct":549,"completionDateStruct":551,"leadSponsor":553,"locationsCount":53},"100548475","using-machine-learning-to-detect-risky-behavior-in-psychiatric-clinics-100548475","NCT06421480","Using Machine Learning to Detect Risky Behavior in Psychiatric Clinics","Detecting Risky Behaviors and Providing a Safe Environment in Patients Receiving Inpatient Treatment in a Psychiatric Clinic Using Machine Learning Model","Inclusion Criteria:\n\n* It is suitable for all adult patients receiving inpatient treatment in psychiatric clinics. It is designed for the room where patients sleep.\n\nExclusion Criteria:\n\n* People under the age of 18 will be excluded from the study",{"count":53,"type":21},"The aim of this study is to ensure the safety of patients in a psychiatric clinic and to detect risky behaviors by using machine learning method. Risky behaviors are defined as behaviors that are personally, socially and developmentally undesirable and endanger life and health.Patient safety and maintaining a safe environment are among the primary duties of healthcare professionals. Suicide is the most important evidence-based risk factor, especially among individuals with psychiatric illnesses, and is one of the most important factors that threaten patient safety. At the end of this study, it is aimed to detect risky behaviors of patients before they harm themselves and to enable healthcare professionals to make early intervention for these behaviors, thus supporting a safe treatment environment, with the computer system that has been trained with the machine learning model installed in the clinics.",[540,541],"Machine Learning","Dangerous Behavior",[543,544,545],"psychiatric clinic","machine learning","risky behavior","2024-06-09",{"date":548,"type":45},"2024-06-11",{"date":550,"type":21},"2024-06-20",{"date":552,"type":21},"2024-09-20",{"name":51,"class":52},""]