[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100612973":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":18,"centralContacts":25,"locations":18,"responsibleParty":31,"collaborators":18,"id":35,"slug":36,"hasResults":37,"nctId":38,"briefTitle":39,"officialTitle":40,"acronym":41,"eligibilityCriteria":42,"healthyVolunteers":37,"sex":43,"minAge":44,"maxAge":18,"enrollmentInfo":45,"targetDuration":18,"studyType":48,"phases":49,"briefSummary":51,"conditions":52,"keywords":56,"overallStatus":61,"whyStopped":18,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":70,"locationsCount":18},{"fullName":5,"class":6},"Gazi University","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Experimental","EXPERIMENTAL","Participants will install the \"Stomaterapi-M\" mobile application on discharge day and will receive structured education (texts\u002Fvideos), nurse counseling via in-app messaging and scheduled video calls, and planned monitoring for 6 months (weekly in month 1, bi-weekly in month 2, monthly in months 3-6) in addition to standard care.",[13],"Behavioral: Stomaterapi-M Mobile Application Support",{"label":15,"type":16,"description":17,"interventionNames":18},"Standard Care","NO_INTERVENTION","Participants will receive routine stomatherapy education, counseling, and follow-up provided by the clinic. Outcome assessments will be completed digitally at the same time points as the intervention group, without access to the mobile application.",null,[20],{"type":21,"name":22,"description":23,"armGroupLabels":24,"otherNames":18},"BEHAVIORAL","Stomaterapi-M Mobile Application Support","Participants will use the \"Stomaterapi-M\" mobile application for 6 months starting on discharge day. The app provides structured stoma education (texts and videos), nurse counseling via in-app messaging and scheduled video calls, and a planned monitoring module. Monitoring frequency is weekly during month 1, bi-weekly during month 2, and monthly during months 3-6, with reminder notifications before each planned entry.",[9],[26],{"name":27,"role":28,"phone":29,"phoneExt":18,"email":30},"FERZAN KALAYCI EMEK, RESEARCH Asistan","CONTACT","+905436540498","ferzan.kalayciemek@ksbu.edu.tr",{"type":32,"investigatorFullName":33,"investigatorTitle":34,"investigatorAffiliation":5,"oldNameTitle":18,"oldOrganization":18},"PRINCIPAL_INVESTIGATOR","Ferzan Kalaycı Emek","RESEARCH ASSISTANT","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":46,"type":47},66,"ESTIMATED","INTERVENTIONAL",[50],"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.",[53,54,55],"Intestinal Stoma","Ileostomy","Colostomy - Stoma",[57,58,59,60],"Mobile application","ostomy","adaptation","quality of life","NOT_YET_RECRUITING","2025-11-21",{"date":64,"type":65},"2025-12-03","ACTUAL",{"date":67,"type":47},"2026-01-01",{"date":69,"type":47},"2026-12-30",{"name":5,"class":6}]