[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100627992":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":31,"centralContacts":43,"locations":51,"responsibleParty":66,"collaborators":24,"id":70,"slug":71,"hasResults":72,"nctId":73,"briefTitle":74,"officialTitle":75,"acronym":24,"eligibilityCriteria":76,"healthyVolunteers":72,"sex":77,"minAge":78,"maxAge":79,"enrollmentInfo":80,"targetDuration":24,"studyType":83,"phases":84,"briefSummary":86,"conditions":87,"keywords":24,"overallStatus":89,"whyStopped":24,"lastUpdateSubmitDate":90,"lastUpdatePostDateStruct":91,"startDateStruct":94,"completionDateStruct":96,"leadSponsor":98,"locationsCount":99},{"fullName":5,"class":6},"Cairo University","OTHER",[8,15],{"label":9,"type":10,"description":11,"interventionNames":12},"Pelvic floor muscle rehabilitation supported by an immersive VR + Medical treatment","EXPERIMENTAL","Participants in this group will practice pelvic floor muscle rehabilitation supported by an immersive virtual reality system designed to enhance engagement and real-time biofeedback during exercise sessions in addition to medical treatment for SUI. The Intervention will last for 8 weeks, with training sessions conducted three times per week under physiotherapist supervision.",[13,14],"Other: Pelvic floor muscle rehabilitation supported by an immersive VR","Drug: Medical treatment",{"label":16,"type":6,"description":17,"interventionNames":18},"Medical treatment","Participants in this group will receive medical treatment for SUI.",[14],[20,25],{"type":6,"name":21,"description":22,"armGroupLabels":23,"otherNames":24},"Pelvic floor muscle rehabilitation supported by an immersive VR","The VR intervention, known as the VR Personality Project, will be delivered using an adjustable virtual reality headset equipped with integrated audio through the head-mounted display. Each participant will use lightweight, wireless Bluetooth controllers to engage and interact with the virtual environment. The Intervention will last for 8 weeks, with training sessions conducted three times per week under physiotherapist supervision. All participants will undergo baseline assessment prior to randomization, followed by a post-intervention assessment at 8 weeks.",[9],null,{"type":26,"name":16,"description":27,"armGroupLabels":28,"otherNames":29},"DRUG","Duloxetine which is a serotonin-norepinephrine reuptake inhibitor (SNRI) that increases urethral sphincter tone will be used for both groups.",[16,9],[30],"Duloxetine",[32,36,40],{"name":33,"affiliation":34,"role":35},"Afaf Mohamed Mahmoud, PhD","Ass. Professor, Cairo University","STUDY_CHAIR",{"name":37,"affiliation":38,"role":39},"Elham Shahat Hassan, PhD","Lecturer, Cairo University","STUDY_DIRECTOR",{"name":41,"affiliation":42,"role":39},"Hossam Al Din Hussein Kamel, PhD","Professor, Al-Azhar University",[44,49],{"name":45,"role":46,"phone":47,"phoneExt":24,"email":48},"Esraa Adel Khamees, B.Sc","CONTACT","+20 10 96034815","ptesraa97@gmail.com",{"name":50,"role":46,"phone":24,"phoneExt":24,"email":24},"Asmaa Khalil Mohamed, PhD",[52],{"facility":53,"status":24,"city":54,"state":24,"zip":24,"country":55,"countryCode":56,"cosmosGeoPoint":57,"geoPoint":62,"contacts":63},"Faculty of Physical Therapy - Cairo University","Giza","Egypt","EG",{"type":58,"coordinates":59},"Point",[60,61],31.20861,30.00944,{"lat":61,"lon":60},[64,65],{"name":45,"role":46,"phone":47,"phoneExt":24,"email":48},{"name":50,"role":46,"phone":24,"phoneExt":24,"email":24},{"type":67,"investigatorFullName":68,"investigatorTitle":69,"investigatorAffiliation":5,"oldNameTitle":24,"oldOrganization":24},"PRINCIPAL_INVESTIGATOR","Esraa Adel Khamees","Principal investigator","100627992","impact-of-virtual-reality-pelvic-floor-training-on-postpartum-stress-urinary-incontinence-100627992",false,"NCT07455838","Impact of Virtual Reality Pelvic Floor Training on Postpartum Stress Urinary Incontinence","Impact of Virtual Reality Pelvic Floor Training on Postpartum Stress Urinary Incontinence: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Females, aged 22-35 years.\n* Postpartum period: between 3 and 6 months after vaginal delivery .\n* Able to perform basic pelvic floor contractions (Oxford Grade ≥ 2).\n* Women who are multiparous(2-3times) and have delivered vaginally.\n* Postpartum women with body mass index 18.5-30 kg\u002Fm²\n\nExclusion Criteria:\n\n* Females Diagnosed with neurological conditions affecting pelvic control (e.g., multiple sclerosis, spinal cord injury).\n* History of pelvic floor surgery within the past 12 months.\n* Known visual, vestibular, or cognitive impairments that interfere with VR use.\n* Susceptibility to motion sickness or vertigo, worsened by visual simulation.","FEMALE","22 Years","35 Years",{"count":81,"type":82},50,"ESTIMATED","INTERVENTIONAL",[85],"NA","This study will be conducted to determine the effect of virtual reality (VR) on pelvic floor training on postpartum stress urinary incontinence (SUI) .",[88],"Stress Urinary Incontinence","NOT_YET_RECRUITING","2026-03-03",{"date":92,"type":93},"2026-03-06","ACTUAL",{"date":95,"type":82},"2026-03-10",{"date":97,"type":82},"2026-05-31",{"name":5,"class":6},1]