New program aims to help young stroke survivors rebuild their lives
NCT ID NCT04560140
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests a program that combines storytelling and practical skills training to help young adults (ages 18-64) who have had a stroke feel more connected and capable in their communities. Over six months, 208 participants will attend eight one-on-one sessions with a facilitator. The goal is to see if this approach improves community reintegration and reduces depressive symptoms.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Narrative and Skills-building Intervention (behavioural program)
- What this could lead to
- If it works, this could offer a practical, non-drug way to help young stroke survivors feel more connected and capable in daily life.
- What could go wrong
- This is a relatively small, early-stage trial testing a behavioural program, so results may not apply broadly. The intervention requires significant time and commitment from participants.
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.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 208 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Sep 2021
- Expected to finish
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Dec 2028
An estimate. End dates often move.
- Lead sponsor
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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.
- Ages
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18 to 64 years
- Sex
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Anyone
- Healthy volunteers
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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 Hide 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: * (1) are 18-64 years of age, * (2) have a clinical diagnosis of first-ever or recurrent ischaemic or haemorrhagic stroke, * (3) are living at home after discharge from hospital, * (4) have a Montreal Cognitive Assessment score \>20, * (5) have a modified Rankin Scale score ≥3, * (6) can communicate in Cantonese, and * (7) are able to attend all intervention sessions. Exclusion Criteria: * 1\) transient ischaemic attack, subdural or epidural haemorrhage, * 2\) experienced cerebrovascular events due to tumours or head trauma, * 3\) mental condition such as depression, schizophrenia, bipolar or personality disorder, * 4\) incomprehensible speech or difficulty in comprehending conversations, or * 5\) have received a self-management programme in the past.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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
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Suzanne Lo
RECRUITINGHong Kong, Hong Kong
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