Evaluating the Effect of Nurse-Led Stroke Transitional Care in Tanzania (NCT07319312) | Clinical Trial Compass
RecruitingNot Applicable
Evaluating the Effect of Nurse-Led Stroke Transitional Care in Tanzania
Tanzania130 participantsStarted 2025-08-01
Plain-language summary
The goal of this observational study is to assess the effects of nurse-led stroke transitional care in stroke survivors, caregivers and healthcare providers who participate in nurse-led stroke transitional care program to improve discharge preparedness, disease self-management and quality of life among stroke survivors. The main question it aims to answer is: does nurse-led stroke transitional care program improve discharge preparedness, disease self-management and quality of life among stroke survivors? Participants are currently participating in nurse-led stroke transitional care program as part of their medical care. Stroke survivors and their caregivers will be followed for six months period to assess their transitional care quality and clinical outcome measures.
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion criteria
* Clinical nurses and physicians with six months of working experience in stroke care
* Clinical nurses and physicians with a minimum of diploma in their professions.
* Stroke survivors with 18 years old and above
* Stroke survivors admitted in the stroke units
* Stroke survivors with primary diagnosis of stroke confirmed by brain CT/MRI
* Stroke survivors who undergo usual discharge process
* Stroke survivors who live with their family caregivers
* Stroke survivors who have mobile phones
* Stroke survivors who can read and write
* Stroke survivors who are able to communicate
* Stroke survivors with National Institutes of Health Stroke Scale (NIHSS) \< 6
* Stroke survivors with Modified Barthel Index (MBI) \> 9
* Stroke survivors with Modified Rankin Scale (mRS) \< 5
* Stroke survivors with Montreal Cognitive Assessment Test (MoCA) \> 14
* Stroke survivors who are expected to stay in the ward for 3-5 days,
* Stroke survivors who are expected to survive for 3 months
* Family caregivers with mobile phones
* Family caregivers who can read and write
* Family caregivers who are able to communicate
* Family caregivers who live with the patient after stroke
Exclusion criteria
* Healthcare providers who will be on leave during the study period.
* Stroke survivors with previous stroke who are not admitted in stroke units
* Stroke survivors who are discharged against medical advice
* Stroke survivors who have end-stage organ failure
* Stroke survivors who have fam…
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Self-efficacy among stroke survivors
Timeframe: 6 months after discharge
2
Quality of life among stroke survivors
Timeframe: 6 months after discharge
3
Discharge preparedness among survivors
Timeframe: within 1 month after discharge
4
Discharge preparedness among health care providers
Timeframe: within 1 month after discharge
5
Resilience among caregivers
Timeframe: 6 months after discharge
6
Quality of transition care among survivors and caregivers