[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100621340":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":12,"centralContacts":24,"locations":12,"responsibleParty":30,"collaborators":12,"id":34,"slug":35,"hasResults":36,"nctId":37,"briefTitle":38,"officialTitle":39,"acronym":40,"eligibilityCriteria":41,"healthyVolunteers":42,"sex":43,"minAge":44,"maxAge":45,"enrollmentInfo":46,"targetDuration":12,"studyType":49,"phases":50,"briefSummary":52,"conditions":53,"keywords":56,"overallStatus":60,"whyStopped":12,"lastUpdateSubmitDate":61,"lastUpdatePostDateStruct":62,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":12},{"fullName":5,"class":6},"Saglik Bilimleri Universitesi","OTHER",[8,13],{"label":9,"type":10,"description":11,"interventionNames":12},"Control Group","NO_INTERVENTION","The control group consisted of participants who only received the hospital's routine NBD education. No additional intervention was provided. The NBD education was delivered by clinical nurses. At the end of the 4th and 12th weeks, the links for the post-tests were sent to the participants in the control group via WhatsApp messages to their phones. After the completion of the study, a link to the mobile application was also provided to the control group via WhatsApp along with an explanatory note.",null,{"label":14,"type":15,"description":16,"interventionNames":17},"intervention group","EXPERIMENTAL","İndividuals in the intervention group will receive the same routine education as the control group. In addition to the routine education, on the day of discharge, a link will be sent to their phones through which the mobile application will be downloaded. Participants will create an account in the mobile application by entering their name, surname, and password. The purpose of installing the mobile application on the day of discharge is to prevent individuals in the control group from becoming aware of the mobile application. After discharge, participants will be followed up during the 4th and 12th weeks.",[18],"Other: Mobil Application",[20],{"type":6,"name":21,"description":22,"armGroupLabels":23,"otherNames":12},"Mobil Application","After discharge, the documents to be completed will be delivered to the intervention group participants via the mobile application and to the control group participants via WhatsApp. At the end of the study, after the final assessment is completed, participants will be informed of their group allocation, and those in the control group will be provided with access to the mobile application via a WhatsApp link.",[14],[25],{"name":26,"role":27,"phone":28,"phoneExt":12,"email":29},"Zuhal Associate Professor","CONTACT","+90 505 253 86 29","zuhalozisler@gmail.com",{"type":31,"investigatorFullName":32,"investigatorTitle":33,"investigatorAffiliation":5,"oldNameTitle":12,"oldOrganization":12},"SPONSOR_INVESTIGATOR","Senem Duman","Lecturer","100621340","artificial-int-neurogenic-bowel-education-in-spinal-cord-injury-patients-100621340",false,"NCT07369349","Artificial Int: Neurogenic Bowel Education in Spinal Cord Injury Patients","Artificial Intelligence Application of Neurogenic Bowel Training in Patients With Spinal Cord Injury","ArtInt","Inclusion Criteria:\n\n* Volunteers who consent to participate.\n* Age over 18 years.\n* Diagnosed with spinal cord injury (SCI).\n* Diagnosed with neurogenic bowel dysfunction (NBD).\n* Not in spinal shock (return of the bulbocavernosus reflex).\n* Having received routine NBD education at the study center within the last month.\n\nExclusion Criteria:\n\n* Individuals with mental retardation.\n* Individuals with visual and\u002For hearing impairments.\n* Individuals with communication problems.\n* Individuals with a history of additional injuries other than SCI (e.g., head trauma, pelvic injury, pelvic surgery).\n* Individuals diagnosed with neurological disorders such as stroke, Parkinson's disease, polyneuropathy, or multiple sclerosis.\n* Individuals with irritable bowel syndrome (IBS) or inflammatory bowel disease (IBD).\n* Individuals diagnosed with gastrointestinal malignancy.",true,"ALL","18 Years","65 Years",{"count":47,"type":48},34,"ESTIMATED","INTERVENTIONAL",[51],"NA","The aim of this study is to evaluate the effectiveness of patient education delivered through an artificial intelligence (AI)-based mobile application in the management of neurogenic bowel dysfunction in individuals with spinal cord injury. Within the scope of the study, it will be examined whether the mobile application reduces neurogenic bowel scores, contributes to maintaining stool scores within the normal range, and improves the quality of life of individuals. Accordingly, the AI-based education model to be developed is expected to facilitate the integration of bowel management practices into daily life, prevent complications, and enhance social participation.\n\n\\-",[54,55],"Spinal Cord Injury","Neurogenic Bowel Dysfunction",[57,58,59],"spinal cord injury","neurogenic bowel dysfunction","Artificial Intelligence","NOT_YET_RECRUITING","2026-01-17",{"date":63,"type":64},"2026-01-27","ACTUAL",{"date":66,"type":48},"2026-02-20",{"date":68,"type":48},"2026-11-01",{"name":32,"class":6}]