Digital peer support may ease long-term stroke recovery for younger survivors
NCT ID NCT07725666
First seen Jul 24, 2026 · Last updated Jul 24, 2026
Summary
Stroke survivors often face unmet needs long after the initial event, especially younger adults who must balance rehabilitation with work and family. This trial tests a 12-month digital education and peer support program, co-designed with patients and delivered through LINE communities and Google platforms, against usual care. Researchers will measure whether the program reduces unmet needs and improves self-efficacy, mood, quality of life, and return-to-work status in 148 survivors aged 31–64.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- a 12-month digital education and peer support program delivered through LINE communities and Google platforms
- What this could lead to
- If effective, this program could offer a scalable way to address persistent unmet needs and improve recovery for younger stroke survivors balancing rehabilitation with work and family.
- What could go wrong
- This is a relatively small trial (148 participants) testing a behavioral intervention, so results may not generalize widely. The program relies on digital engagement, which may not suit everyone.
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 148 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Aug 2026
An estimate. Start dates often move.
- Expected to finish
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Jul 2029
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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31 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: * Aged 31 to 64 years. * Diagnosis of stroke confirmed by computed tomography (CT) or magnetic resonance imaging (MRI) and physician diagnosis. * Received treatment at the Stroke Center of Linkou Chang Gung Memorial Hospital. * Conscious and able to communicate, including individuals with mild aphasia. * Willing and able to provide informed consent. Exclusion Criteria: * End-stage cancer. * Severe aphasia resulting in inability to communicate. * Dependent in basic activities of daily living before the index stroke (Barthel Index \<100), regardless of the underlying cause.
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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 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.
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Brazilian version of a behavior change intervention to support healthy lifestyle adoption after stroke - iVIDAVC: protocol for a pilot randomized study
- Determination of efficacy of sustained motor contraction generated using StimWave peripheral nerve stimulator
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