[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100576535":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":18,"centralContacts":25,"locations":18,"responsibleParty":35,"collaborators":18,"id":39,"slug":40,"hasResults":41,"nctId":42,"briefTitle":43,"officialTitle":44,"acronym":18,"eligibilityCriteria":45,"healthyVolunteers":41,"sex":46,"minAge":47,"maxAge":18,"enrollmentInfo":48,"targetDuration":18,"studyType":51,"phases":52,"briefSummary":54,"conditions":55,"keywords":58,"overallStatus":64,"whyStopped":18,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"locationsCount":18},{"fullName":5,"class":6},"Hiroshima University","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Assistive Device Intervention","EXPERIMENTAL","Patients and caregivers will be trained in self-care with stroke disabilities (e.g. eating, grooming, bathing, dressing, toileting), physical exercise, lifestyle modification, prevention of complications after stroke through researcher developed \"Health booklet\". Based on their disabilities some adjustive and exercise devices will be provided to them for improving functional independence.",[13],"Behavioral: Assistive Device and health Education",{"label":15,"type":16,"description":17,"interventionNames":18},"Control Group","NO_INTERVENTION","No \"Education booklet\" or adjustive device are provided to them. The patients with family caregivers in control group will receive the usual care.",null,[20],{"type":21,"name":22,"description":23,"armGroupLabels":24,"otherNames":18},"BEHAVIORAL","Assistive Device and health Education","After discharge they will be assessed and followed by RA nurses through home visit and tele services for 2 months. The nurses will contact the patients periodically over telephone, and follow up their regular self-care activities, adjustment to devices, exercise and adaptive behavior.",[9],[26,31],{"name":27,"role":28,"phone":29,"phoneExt":18,"email":30},"Salma Akhter, PhD","CONTACT","07037923841","dncsalma@gmail.com",{"name":32,"role":28,"phone":33,"phoneExt":18,"email":34},"Dr. Mahmudul Islam, MD","+88 01822496267","drmahmudul@yahoo.com",{"type":36,"investigatorFullName":37,"investigatorTitle":38,"investigatorAffiliation":5,"oldNameTitle":18,"oldOrganization":18},"PRINCIPAL_INVESTIGATOR","Salma Akhter","Doctoral Researcher","100576535","nurse-led-rehabilitation-to-improve-self-care-among-stroke-patients-in-bangladesh-100576535",false,"NCT06786559","Nurse-led Rehabilitation to Improve Self-care Among Stroke Patients in Bangladesh","Post Discharge Nurse-led Rehabilitation to Improve Self-care Among Stroke Patients in Bangladesh: A Pilot Randomized Controlled Trial","Inclusion Criteria:\n\n* For Patient\n\n  1. who is 18 years old and above, both males \\& females,\n  2. is irrespective of type of stroke and time of stroke,\n  3. is within 5 days to 2 weeks of onset of the current stroke\n  4. Physician advice rehabilitation, and who needs assistive devices for ADL,\n  5. has family caregivers,\n  6. lives in the study area, and\n  7. who will provide written consent \\& willing to participate in the study.\n\nFor family care giver\n\n1. Primary caregivers irrespective of sex and aged 18 years old and above, living with the patient who take care of an above patient and who meets all the inclusion criteria.\n2. Who will provide written consent \\& willing to participate in the study\n\nExclusion Criteria:\n\n* For patient\n\n  1. Participation in other clinical trials,\n  2. not having a smartphone at home, For family care giver No exclusion criteria","ALL","18 Years",{"count":49,"type":50},64,"ESTIMATED","INTERVENTIONAL",[53],"NA","Stroke causes various levels of disability, which decreases physical function for a prolonged period. The purpose of this study is to test the feasibility and efficacy of a nurse-led rehabilitation program focused on improving the activity of daily living (ADL) among post-stroke patients in Bangladesh. A feasibility study, including descriptive and randomized controlled trial (RCT), will be conducted at the National Institute of Neuroscience \\& Hospital (NINS\\&H) in Dhaka, Bangladesh, from March 2025 to August 2025. Participants will be the post-stroke patients who got discharged from NINS\\&H from 5th days to 2 weeks after the onset of stroke and the family caregivers of the patients and meet the inclusion criteria. The sample size will be calculated based on G-Power analysis with a medium effect size and will be 64. The intervention will be designed to provide the 3-month nurse-led rehabilitation program regarding self-care and the use of assistive devices. Assessment for rehabilitation will be performed by the multidisciplinary team with research nurses (RA nurses), physiotherapists (PT), and occupational therapists (OT). The control group will receive the usual care. The Functional Independence Measure (FIM) measures the primary outcome as improved self-care. The secondary outcomes are self-efficacy and participation in social activities for patients and the care burden of family caregivers. We also qualitatively describe changes and improvements of cognitive, emotional, and behavioral aspects among patients and their families. The endpoints will be compared at baseline and the 3rd month. Rehabilitation with proper assistive devices may improve self-dependence, ADL, and social participation. The caregiver's burden will decrease through the implementation of self-care education and assistive devices for daily life adjustment.",[56,57],"Stroke","Disability Physical",[56,59,60,61,62,63],"Disability","Rehabilitation","Assistive device","Self-Care","Care Burden","NOT_YET_RECRUITING","2025-01-15",{"date":67,"type":68},"2025-01-22","ACTUAL",{"date":70,"type":50},"2025-03-01",{"date":72,"type":50},"2025-08-30",{"name":5,"class":6}]