[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100632994":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":26,"centralContacts":30,"locations":36,"responsibleParty":52,"collaborators":26,"id":56,"slug":57,"hasResults":58,"nctId":59,"briefTitle":60,"officialTitle":61,"acronym":62,"eligibilityCriteria":63,"healthyVolunteers":58,"sex":64,"minAge":65,"maxAge":26,"enrollmentInfo":66,"targetDuration":26,"studyType":69,"phases":70,"briefSummary":72,"conditions":73,"keywords":77,"overallStatus":39,"whyStopped":26,"lastUpdateSubmitDate":85,"lastUpdatePostDateStruct":86,"startDateStruct":89,"completionDateStruct":91,"leadSponsor":93,"locationsCount":94},{"fullName":5,"class":6},"Giresun University","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Mobile-Based Perioperative Education","EXPERIMENTAL","Participants will receive routine perioperative care in addition to a structured mobile application-based perioperative education program including video-assisted pelvic floor muscle training, perioperative education content, reminders, and follow-up support.",[13],"Behavioral: Mobile-Based Perioperative Education Program",{"label":15,"type":16,"description":17,"interventionNames":18},"Standard Perioperative Care","ACTIVE_COMPARATOR","Participants will receive routine perioperative care and standard patient education.",[19],"Other: Standard Perioperative Care",[21,27],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"BEHAVIORAL","Mobile-Based Perioperative Education Program","A structured mobile application-based perioperative education program including video-assisted pelvic floor muscle training, perioperative education content, reminder notifications, and follow-up support.",[9],null,{"type":6,"name":15,"description":28,"armGroupLabels":29,"otherNames":26},"Routine perioperative care and standard patient education provided according to institutional practice.",[15],[31],{"name":32,"role":33,"phone":34,"phoneExt":26,"email":35},"ALKAY KARA, PhD","CONTACT","+905394416497","alkay@outlook.com.tr",[37],{"facility":38,"status":39,"city":40,"state":40,"zip":41,"country":42,"countryCode":26,"cosmosGeoPoint":43,"geoPoint":48,"contacts":49},"Giresun Prof. Dr. A. İlhan Özdemir State Hospital","RECRUITING","Giresun","28000","Turkey (Türkiye)",{"type":44,"coordinates":45},"Point",[46,47],38.38741,40.91698,{"lat":47,"lon":46},[50],{"name":51,"role":33,"phone":26,"phoneExt":26,"email":35},"ALKAY KARA",{"type":53,"investigatorFullName":54,"investigatorTitle":55,"investigatorAffiliation":5,"oldNameTitle":26,"oldOrganization":26},"PRINCIPAL_INVESTIGATOR","Alkay Kara","Assistant Professor, PhD","100632994","the-effect-of-mobile-based-perioperative-education-on-urinary-incontinence-and-erectile-function-after-radical-prostatectomy-100632994",false,"NCT07520916","The Effect of Mobile-Based Perioperative Education on Urinary Incontinence and Erectile Function After Radical Prostatectomy","The Effect of Mobile-Based Perioperative Education on Urinary Incontinence and Erectile Function After Radical Prostatectomy: A Randomized Controlled Trial","MPE-RP","Inclusion Criteria:\n\n* Patients diagnosed with prostate cancer and scheduled for elective radical prostatectomy (open, laparoscopic, or robotic)\n* Aged 18 years or older\n* Planned to undergo surgery at the study center(s)\n* Able to use a smartphone and having sufficient digital literacy to operate the mobile application\n* Provided written informed consent after being informed about the study\n\nExclusion Criteria:\n\n* Pre-existing urinary incontinence or erectile dysfunction before surgery\n* Severe cognitive impairment or severe visual or hearing impairment\n* Previous pelvic radiotherapy or a history of major pelvic surgery\n* Presence of severe comorbidity or terminal illness that may interfere with adherence to the study protocol\n* Technological insufficiency preventing the use of the mobile application","MALE","18 Years",{"count":67,"type":68},78,"ESTIMATED","INTERVENTIONAL",[71],"NA","This prospective randomized controlled study aims to evaluate the effect of mobile-based perioperative education on postoperative urinary incontinence and erectile function in patients undergoing radical prostatectomy. Patients scheduled for radical prostatectomy will be assigned to either an intervention group or a control group. The intervention group will receive standard care plus a structured mobile application-based perioperative education program including video-assisted pelvic floor muscle training, perioperative education modules, reminders, and follow-up components. The control group will receive routine perioperative care and standard patient education. Data will be collected preoperatively, after urinary catheter removal, and at 1 month and 3 months after surgery. The primary outcomes are urinary incontinence and erectile function, assessed using the International Consultation on Incontinence Questionnaire-Short Form (ICIQ-SF), the International Index of Erectile Function-5 (IIEF-5), and a 24-hour pad assessment. Secondary outcomes include lower urinary tract symptoms and disease-specific quality of life assessed by the International Prostate Symptom Score (IPSS), psychological status assessed by the Depression Anxiety Stress Scale-21 (DASS-21), and system usability assessed by the Turkish version of the Computer System Usability Questionnaire-Short Version (T-CSUQ-SV)",[74,75,76],"Prostate Cancer (Post Prostatectomy)","Urinary Incontinence (UI)","Erectile Dysfunction Following Radical Prostatectomy",[78,79,80,81,82,83,84],"Radical Prostatectomy","Mobile Health","mHealth","Perioperative Education","Pelvic Floor Muscle Training","Urinary Incontinence","Erectile Function","2026-04-03",{"date":87,"type":88},"2026-04-09","ACTUAL",{"date":90,"type":88},"2026-04-02",{"date":92,"type":68},"2027-04-02",{"name":5,"class":6},1]