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Can nurse support after stroke improve recovery? new study in tanzania aims to find out

NCT ID NCT07319312

Knowledge-focused Sponsor: Shandong University Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looks at whether a nurse-led transitional care program helps stroke survivors and their caregivers after leaving the hospital. About 130 stroke survivors, their caregivers, and healthcare workers in Tanzania will take part. The program includes face-to-face sessions and phone calls to improve discharge readiness, self-management, and quality of life over six months.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If successful, this program could improve how stroke patients transition from hospital to home, leading to better self-care and quality of life.
What could go wrong
This is an observational study with only 130 participants, so results may not apply broadly. It measures outcomes like self-efficacy and quality of life, not survival or cure.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

About 130 people

The number the study aims to enrol. It can still change while the study runs.

Started

Aug 2025

Expected to finish

Mar 2026

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

The study will include nurses, doctors, stroke survivors and caregivers who are directly involved in hospital-to-home transition.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

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 family caregivers * Stroke survivors who can't read/write * Stroke survivors who have no mobile phones. * Family caregivers without mobile phone that is accessible

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Conditions

The condition(s) this trial relates to.

stroke disorder transient ischemic attack

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Stroke (CVA) or transient ischemic attack Stroke, acute

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Muhimbili University of Health and Allied Sciences

    RECRUITING

    Dar es Salaam, 65001, Tanzania

More trials for these conditions

Other studies related to the condition(s) this trial covers.