[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"intestinal-stoma\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:intestinal-stoma":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":30,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":4},"100612973","effect-of-a-mobile-application-on-stoma-adaptation-and-quality-of-life-100612973",false,"NCT07260539","Effect of a Mobile Application on Stoma Adaptation and Quality of Life","The Effect of Education, Counseling, and Monitoring Provided to Individuals With Stoma Via a Mobile Application on Adaptation to Stoma and Quality of Lif","STOMATERAPİ-M","Inclusion Criteria:\n\nAge ≥18 years Able to read and write Turkish Undergoing ostomy surgery for the first time Permanent ostomy or expected to remain for at least 6 months No major mental, physical, or communication impairment Owns an iOS\u002FAndroid smartphone with active internet access Able to use mobile applications Uses WhatsApp for digital form submission during follow-up\n\nExclusion Criteria:\n\nReceiving stoma-related education or counseling from another institution or professional during the study period","ALL","18 Years",{"count":20,"type":21},66,"ESTIMATED","INTERVENTIONAL",[24],"NA","This single-blind, parallel-group randomized controlled trial aims to evaluate the effects of a mobile app-based education, counseling, and follow-up program on stoma adaptation and quality of life in adults with a newly ostomy. The study will be conducted at the Stomatherapy Unit of Gazi University Health Research and Application Center (Ankara, Turkey). Participants meeting the inclusion criteria (n=66) will be assigned to intervention (mobile app support + standard care) and control (standard care only) groups in a 1:1 ratio via block randomization; participants will be kept unaware of their group assignment. Participants in the intervention group will download the \"Stomatherapy-M\" app on the day of discharge and will access structured educational content, receive nurse counseling (messaging and scheduled video calls), and share scheduled follow-up records regularly for six months. Follow-up frequency will be weekly in the first month, biweekly in the second month, and monthly in the following months. Primary outcomes; Adaptation to the stoma (Ostomy Adjustment Inventory) and stoma-related quality of life (Quality of Life Adaptation Scale) assessed at 15 days and 1, 3, and 6 months after discharge. App usability (MAUS) will be measured at 6 months only in the intervention group.",[27,28,29],"Intestinal Stoma","Ileostomy","Colostomy - Stoma",[31,32,33,34],"Mobile application","ostomy","adaptation","quality of life","NOT_YET_RECRUITING","2025-11-21",{"date":38,"type":39},"2025-12-03","ACTUAL",{"date":41,"type":21},"2026-01-01",{"date":43,"type":21},"2026-12-30",{"name":45,"class":46},"Gazi University","OTHER"]