[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Artvin Coruh University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":257},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,9,0,[8,47,76,97,129,148,174,201,229],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":29,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":46},"100634793","fatigue-and-mental-well-being-in-ms-patientsmultiple-sclerosis-100634793",false,"NCT07544303","Fatigue and Mental Well-Being in MS Patients(Multiple Sclerosis)","Evaluation of the Effect of Quran Recitation on Fatigue and Mental Well-Being in MS Patients: A Randomized Controlled Trial","MS","Inclusion Criteria:\n\n1. Having been diagnosed with Multiple Sclerosis at least 6 months ago\n2. Being between the ages of 18-80\n3. Agreeing to participate in the research\n4. Not having any obstacles to wearing headphones\n5. Not having any hearing problems\n\nExclusion Criteria:\n\n1. Those with major psychiatric disorders\n2. Those with any obstacle to communication","ALL","18 Years","80 Years",{"count":21,"type":22},52,"ESTIMATED","INTERVENTIONAL",[25],"NA","This study will be conducted to evaluate the effects of Quran recital on fatigue and mental well-being in patients with multiple sclerosis.\n\nHypotheses:\n\n1. Quran recital reduces fatigue in MS patients.\n2. Quran recital increases mental well-being in MS patients. The patients will be called by the researcher to ask whether they continue this practice. The control group will continue their routine treatment and care and no additional intervention will be applied. The final test measurements will be made by meeting with the patients in the hospital at the end of the 4th week.",[28],"Multiple Sclerosis",[30,31,32,33],"multiple Sclerosis,","Quran,","fatigue,","mental well-being,","RECRUITING","2026-04-15",{"date":37,"type":38},"2026-04-22","ACTUAL",{"date":40,"type":38},"2025-09-09",{"date":42,"type":22},"2026-05-15",{"name":44,"class":45},"Artvin Coruh University","OTHER",1,{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":4,"eligibilityCriteria":53,"healthyVolunteers":11,"sex":54,"minAge":55,"maxAge":56,"enrollmentInfo":57,"targetDuration":4,"studyType":59,"phases":4,"briefSummary":60,"conditions":61,"keywords":62,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":68,"lastUpdatePostDateStruct":69,"startDateStruct":71,"completionDateStruct":73,"leadSponsor":75,"locationsCount":46},"100611138","identification-of-factors-related-to-ui-in-patients-with-ms-and-emg-assessment-of-pfm-activity-100611138","NCT07236684","Identification of Factors Related to UI in Patients With MS and EMG Assessment of PFM Activity","Identification of Factors Related to Urinary Incontinence in Patients With Multiple Sclerosis and Electromyographic Assessment of Pelvic Floor Muscle Activity: A Cross-Sectional Study","Inclusion Criteria:\n\n* having an MS diagnosis according to the 2017 revised McDonald criteria,\n* experiencing symptoms of UI as defined by the International Continence Society (ICS),\n* having an EDSS score below 6.5,\n* PwMS with no communication issues.\n\nExclusion Criteria:\n\n* PwMS who did not give consent to participate,\n* those with medication changes in the past 6 months,\n* pregnant PwMS,\n* recent vaginal or caesarean deliveries within 6 months,\n* pelvic organ prolapse,\n* urinary tract infection,\n* recent attack history in the past month.","FEMALE","30 Years","50 Years",{"count":58,"type":22},47,"OBSERVATIONAL","The study aimed to explore the link between urinary incontinence (UI) severity in patients with multiple sclerosis (PwMS), electromyography (EMG) findings, and other relevant factors.",[28],[63,64,65,66,67],"multiple sclerosis","electromyography","urinary incontinence","pelvic floor","fatigue","2026-03-19",{"date":70,"type":38},"2026-03-23",{"date":72,"type":38},"2026-03-09",{"date":74,"type":22},"2026-09-30",{"name":44,"class":45},{"id":77,"slug":78,"hasResults":11,"nctId":79,"briefTitle":80,"officialTitle":81,"acronym":4,"eligibilityCriteria":82,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":83,"targetDuration":4,"studyType":23,"phases":85,"briefSummary":86,"conditions":87,"keywords":4,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":89,"lastUpdatePostDateStruct":90,"startDateStruct":92,"completionDateStruct":94,"leadSponsor":96,"locationsCount":46},"100622462","stress-ball-use-during-chemotherapy-in-gastrointestinal-cancer-patients-100622462","NCT07383935","Stress Ball Use During Chemotherapy in Gastrointestinal Cancer Patients","The Effect of Stress Ball on Anxiety, Fear and Vital Signs in Patients With Gastrointestinal System Cancer","Inclusion Criteria:\n\n* Being aged 18 years or older\n* Having a diagnosis of gastrointestinal system cancer and receiving chemotherapy\n* Having no communication problems\n* Having no physical disability that would prevent squeezing a stress ball\n* Willingness to participate in the study\n\nExclusion Criteria:\n\n\\-",{"count":84,"type":22},60,[25],"This study will investigate whether using a stress ball during chemotherapy can reduce anxiety, fear, and changes in vital signs in patients with gastrointestinal system cancers.\n\nPatients receiving chemotherapy for gastrointestinal cancers often experience anxiety and fear, which may affect their heart rate, blood pressure, and breathing. A stress ball is a simple, low-cost, and safe method that may help patients relax during treatment.\n\nIn this randomized controlled study, 60 patients receiving chemotherapy will be assigned to either a stress ball group or a routine care group. Patients in the stress ball group will squeeze a stress ball for 15 minutes during their chemotherapy session. Anxiety, fear levels, and vital signs will be measured before and after chemotherapy in both groups.\n\nThe results of this study may help determine whether stress ball use is an effective non-drug method to improve emotional well-being and physiological stability in patients undergoing chemotherapy.",[88],"Gastrointestinal System Cancer","2026-02-08",{"date":91,"type":38},"2026-02-11",{"date":93,"type":38},"2026-02-03",{"date":95,"type":22},"2027-02-03",{"name":44,"class":45},{"id":98,"slug":99,"hasResults":11,"nctId":100,"briefTitle":101,"officialTitle":102,"acronym":4,"eligibilityCriteria":103,"healthyVolunteers":104,"sex":17,"minAge":105,"maxAge":106,"enrollmentInfo":107,"targetDuration":4,"studyType":23,"phases":109,"briefSummary":110,"conditions":111,"keywords":113,"overallStatus":121,"whyStopped":4,"lastUpdateSubmitDate":93,"lastUpdatePostDateStruct":122,"startDateStruct":124,"completionDateStruct":126,"leadSponsor":128,"locationsCount":4},"100623764","use-of-acupressure-aromatherapy-and-virtual-reality-for-children-in-during-blood-collection-procedures-100623764","NCT07400874","Use of Acupressure, Aromatherapy, and Virtual Reality for Children in During Blood Collection Procedures","The Effects of Acupressure, Aromatherapy, and Virtual Reality on Pain, Fear, and Anxiety in Children During Blood Sampling Procedures","Inclusion Criteria:\n\nBeing between 5-10 years old Being healthy (no chronic disease diagnosis) Both child and parent agree to participate in the study Being able to communicate in Turkish Taking a blood sample in a single session Having no visual, auditory, or speech impairments, Being open to communication Being accompanied by a parent\n\nExclusion Criteria:\n\nHaving an allergy to any substance Having a chronic illness (Type 1 diabetes, etc.) Having upper respiratory tract diseases such as asthma, rhinitis, pharyngitis Having an obstructive condition in the nasal passages for any reason Having vision or hearing loss Having any neuropathological problem Having complaints of vomiting, nausea, or pain Having recently used sedatives, anesthetics, or analgesics Having a chronic illness Having visual-auditory and speech impairments History of sedative, analgesic, or narcotic substance use within 24 hours prior to admission",true,"5 Years","10 Years",{"count":108,"type":22},120,[25],"This study aims to evaluate the effects of acupressure, music listening, and virtual reality applications, which appeal to the senses of touch, hearing, and sight during blood sampling, on pain, fear, and anxiety levels in children.",[112],"Blood Collection",[112,114,115,116,117,118,119,120],"Fear","Pain","Anxiety","Acupressure","Virtual reality","listening music","child","NOT_YET_RECRUITING",{"date":123,"type":38},"2026-02-10",{"date":125,"type":22},"2026-03-01",{"date":127,"type":22},"2026-10-01",{"name":44,"class":45},{"id":130,"slug":131,"hasResults":11,"nctId":132,"briefTitle":133,"officialTitle":134,"acronym":4,"eligibilityCriteria":135,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":136,"targetDuration":4,"studyType":23,"phases":137,"briefSummary":138,"conditions":139,"keywords":4,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":141,"lastUpdatePostDateStruct":142,"startDateStruct":143,"completionDateStruct":145,"leadSponsor":147,"locationsCount":46},"100621180","effect-of-mandala-coloring-on-anxiety-distress-and-comfort-in-breast-cancer-patients-receiving-outpatient-chemotherapy-100621180","NCT07367269","Effect of Mandala Coloring on Anxiety, Distress, and Comfort in Breast Cancer Patients Receiving Outpatient Chemotherapy","The Effect of Mandala Coloring on Psychological Distress, Anxiety, and Comfort in Breast Cancer Patients Receiving Outpatient Chemotherapy","Inclusion Criteria:\n\n* Being 18 years of age or older\n* Having a diagnosis of breast cancer and receiving chemotherapy\n* Having no communication problems\n* Having no physical disability that would prevent mandala coloring\n* Being willing to participate in the study\n\nExclusion Criteria:\n\n* not meeting inclusion criteria",{"count":84,"type":22},[25],"Breast cancer patients receiving chemotherapy often experience psychological distress, anxiety, and discomfort during treatment. Non-drug supportive methods may help improve patients' well-being during chemotherapy.\n\nThis study aims to evaluate whether mandala coloring during outpatient chemotherapy can reduce psychological distress and anxiety and improve comfort in breast cancer patients. Participants will be randomly assigned to either a mandala coloring group or a routine care group. Patients in the intervention group will color mandala patterns for 30 minutes during their chemotherapy session, while the control group will receive routine care only.\n\nPsychological distress, anxiety, and comfort levels will be measured before and after the chemotherapy session in both groups. The results of this study may provide evidence for a simple and low-cost supportive intervention to improve the psychological well-being of breast cancer patients during chemotherapy.",[140],"Breast Cancer","2026-01-31",{"date":93,"type":38},{"date":144,"type":38},"2026-01-27",{"date":146,"type":22},"2027-01-20",{"name":44,"class":45},{"id":149,"slug":150,"hasResults":11,"nctId":151,"briefTitle":152,"officialTitle":153,"acronym":4,"eligibilityCriteria":154,"healthyVolunteers":11,"sex":17,"minAge":105,"maxAge":155,"enrollmentInfo":156,"targetDuration":4,"studyType":23,"phases":158,"briefSummary":159,"conditions":160,"keywords":162,"overallStatus":121,"whyStopped":4,"lastUpdateSubmitDate":166,"lastUpdatePostDateStruct":167,"startDateStruct":169,"completionDateStruct":171,"leadSponsor":173,"locationsCount":4},"100611616","clinically-important-or-just-statistically-significant-mcid-for-dviss-and-pin-q-in-children-with-ui-100611616","NCT07242898","Clinically Important or Just Statistically Significant? MCID for DVISS and PIN-Q in Children With UI","Clinically Important or Just Statistically Significant? Minimal Clinically Important Difference for DVISS and PIN-Q in Children With Urinary Incontinence","Inclusion Criteria:\n\n* diagnosis of UI according to the International Children's Continence Society (ICCS) Guideline,\n* children aged 5-13 years (when UI becomes more prevalent in children).\n\nExclusion Criteria:\n\n* congenital anomalies of the uro-genital system,\n* only neurogenic bladder dysfunction.","13 Years",{"count":157,"type":22},100,[25],"The goal of this study was to determine the Minimal Clinically Important Difference (MCID) for the Dysfunctional Voiding and Incontinence Symptom Score (DVISS) and the Pediatric Incontinence Questionnaire (PIN-Q) in children with urinary incontinence (UI).",[161],"Urinary Incontinence",[163,65,164,165],"minimal clinically important difference","quality of life","ROC curve","2025-11-19",{"date":168,"type":38},"2025-11-21",{"date":170,"type":22},"2026-09-01",{"date":172,"type":22},"2026-12-01",{"name":44,"class":45},{"id":175,"slug":176,"hasResults":11,"nctId":177,"briefTitle":178,"officialTitle":179,"acronym":4,"eligibilityCriteria":180,"healthyVolunteers":11,"sex":17,"minAge":181,"maxAge":182,"enrollmentInfo":183,"targetDuration":4,"studyType":23,"phases":185,"briefSummary":186,"conditions":187,"keywords":188,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":194,"lastUpdatePostDateStruct":195,"startDateStruct":197,"completionDateStruct":198,"leadSponsor":200,"locationsCount":46},"100596381","use-of-hand-puppets-and-image-watching-and-coloring-books-for-children-in-during-blood-collection-procedures-100596381","NCT07044713","Use of Hand Puppets and Image Watching and Coloring Books for Children in During Blood Collection Procedures","A Comparison of the Use of Hand Puppets and Image Watching and Coloring Books for Children in Reducing Pain and Fear During Blood Collection Procedures","Inclusion Criteria:\n\n* Being between 3-6 years old\n* Taking blood samples at once\n* No visual-auditory and speech disorders\n* Being open to communication and\n* Being accompanied by a parent.\n\nExclusion Criteria:\n\n* Having a chronic disease\n* Having a visual-auditory and speech disorder\n* History of sedative, analgesic or narcotic substance use within 24 hours before admission\n* Children whose parents do not agree to participate in the study.","3 Years","6 Years",{"count":184,"type":22},90,[25],"The aim of this study was to compare a hand puppet with image viewing and a coloring book for children in reducing children's pain and fear during blood collection.",[112],[189,190,120,191,192,193],"blood collection","fear","pain","hand puppet","Tracing and Painting the Image","2025-06-24",{"date":196,"type":38},"2025-07-01",{"date":196,"type":22},{"date":199,"type":22},"2026-01-01",{"name":44,"class":45},{"id":202,"slug":203,"hasResults":11,"nctId":204,"briefTitle":205,"officialTitle":206,"acronym":4,"eligibilityCriteria":207,"healthyVolunteers":11,"sex":54,"minAge":4,"maxAge":4,"enrollmentInfo":208,"targetDuration":4,"studyType":23,"phases":210,"briefSummary":211,"conditions":212,"keywords":216,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":221,"lastUpdatePostDateStruct":222,"startDateStruct":224,"completionDateStruct":226,"leadSponsor":228,"locationsCount":46},"100593608","digital-parenting-education-impact-on-mothers-social-media-use-and-childrens-tech-attitudes-100593608","NCT07008651","Digital Parenting Education: Impact on Mothers' Social Media Use and Children's Tech Attitudes","The Effects of Digital Parenting Training Given to Mothers on Social Media Addiction and Their Children's Knowledge and Attitudes Towards Technology Use","Inclusion Criteria:\n\n* Having at least a primary school degree\n* Being a mother with a 3-6 year old child\n* Using at least one of the digital devices such as a smart phone\u002Ftablet\u002Fcomputer\n* Having a social media account (Facebook, Instagram, WhatsApp etc.)\n\nExclusion Criteria:\n\n* Diagnosis of acute\u002Fchronic disease by the child or mother during the data collection period\n* Wanting to leave the study",{"count":209,"type":22},152,[25],"The aim of the study was to evaluate the knowledge and attitudes of mothers regarding social media addiction and their children's technology use.\n\nThe research is a randomized controlled trial. The universe of the research consists of all family health center affiliated with the Artvin Provincial Health Directorate, and the sample consists of mothers with healthy preschool children (3-6 years old) registered in family health center No. 1, determined by drawing lots.\n\nThe sample size was determined as 152 participants, with 76 assigned to the experimental group and 76 to the control group. The digital parenting training to be given to mothers consists of 8 sessions of 20 minutes each. The digital parenting training content, presentation and brochure were prepared according to the Ministry of Family and Social Services' \"Parental Guide for Protecting Children from Digital Risks\", the Ministry of Health's \"Technology Addiction Parental Guide\" and the Presidency's Directorate of Communications' \"Social Media Usage Guide\". Opinions of 10 experts were received for the prepared training presentation and brochure. As a result of the evaluation, descriptive statistics; number (N) and percentage (%) for variables between groups, mean, standard deviation (SD), minimum (min), maximum (max) values for numerical data and significance level will be stated as p\\\u003C0.05.",[213,214,215],"Parenting","Social Media Addiction","Internet Addiction",[217,218,219,220],"digital parent","mother","social media","technology","2025-05-29",{"date":223,"type":38},"2025-06-06",{"date":225,"type":38},"2025-03-27",{"date":227,"type":22},"2025-12-19",{"name":44,"class":45},{"id":230,"slug":231,"hasResults":11,"nctId":232,"briefTitle":233,"officialTitle":234,"acronym":4,"eligibilityCriteria":235,"healthyVolunteers":104,"sex":17,"minAge":236,"maxAge":4,"enrollmentInfo":237,"targetDuration":4,"studyType":23,"phases":238,"briefSummary":239,"conditions":240,"keywords":242,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":249,"lastUpdatePostDateStruct":250,"startDateStruct":252,"completionDateStruct":254,"leadSponsor":256,"locationsCount":46},"100568784","laughter-yoga-is-role-in-enhancing-sleep-and-well-being-in-the-elderly-100568784","NCT06685731","Laughter Yoga is Role in Enhancing Sleep and Well-being in the Elderly","The Effects of Laughter Yoga on Sleep Quality, Vitality, Active Aging, and Quality of Life in Elderly Individuals","Inclusion Criteria:\n\n* Reside in Şavşat,\n* Aged 60 or over,\n* No issues with vision, hearing, or perception,\n* Scored 24 or higher on the Mini-Mental State Examination,\n* Not undergoing psychiatric treatment,\n* No physical limitations that would impede participation in laughter yoga (e.g., fractures, open wounds, or muscle weakness in the hands, wrists, or arms),\n* Literate,\n* Open to communication,\n* Willing to participate in the study.\n\nExclusion Criteria:\n\n* Scored below 24 on the Mini-Mental State Examination,\n* Severe hearing or perceptual impairments that hinder communication,\n* Major psychiatric disorders,\n* Underwent surgery within the last three months,\n* Medical conditions that could cause physical strain or increase abdominal pressure during laughter yoga (e.g., bleeding hemorrhoids, any type of hernia, persistent cough, severe back pain, heart disease, hypertension, urinary incontinence, epilepsy), and individuals with oncological conditions will be excluded from the study.","60 Years",{"count":84,"type":22},[25],"Objective:\n\nThe study aims to evaluate the effects of Laughter Yoga on sleep quality, vitality, active aging, and quality of life in individuals aged 60 and over.\n\nMethod:\n\nThis randomized controlled experimental study will be conducted between 01.09.2024 and 31.12.2024 with elderly individuals aged 60 and over who are registered at Şavşat Family Health Center No. 1. The study population consists of 6,797 individuals. Participants will be randomly assigned to an experimental group (30) and a control group (30) using a simple randomization method. Data will be collected using a Personal Information Form, Mini-Mental State Examination, Active Aging Scale, Pittsburgh Sleep Quality Index, Subjective Vitality Scale, and Quality of Life Scale for the Elderly. The experimental group will participate in 12 Laughter Yoga sessions, conducted twice a week for 6 weeks, with each session lasting 40 minutes. No intervention will be applied to the control group. At the end of the 6th week, final measurements will be taken from both groups at the family health center.",[241],"ELDERLY PEOPLE",[243,244,245,246,247,248],"elderly","Laughter Yoga","Sleep Quality","Vitality","Active Aging","Elderly Quality of Life","2024-11-11",{"date":251,"type":38},"2024-11-12",{"date":253,"type":38},"2024-09-05",{"date":255,"type":22},"2024-12-31",{"name":44,"class":45},""]