Nurse chat before discharge may boost stroke recovery adherence
NCT ID NCT07524036
First seen Jun 24, 2026 · Last updated Aug 19, 2026 · Updated 3 times
Summary
This study tests whether a one-on-one nursing education session just before a stroke patient goes home can improve how well they follow their medication and care plan. Researchers will enroll 300 stroke survivors who are returning home and randomly assign half to receive the extra nurse consultation. Four months later, they will compare medication adherence between the two groups using a standard questionnaire.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- nursing educational consultation
- What this could lead to
- If it works, this could show that a simple nurse-led chat before leaving hospital helps stroke patients follow their medication and recovery plan better.
- What could go wrong
- This is a small, early-stage study that only measures self-reported adherence, not actual health outcomes. Results may not apply to all stroke patients.
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 300 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2026
- Expected to finish
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Jun 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 years and older
- 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: * Patients admitted to the Neurovascular Unit (UNV) of CHCB for ischemic stroke and/or hemorrhagic stroke confirmed by brain imaging and/or TIA with an ABCD2 score \>5, * Patients whose discharge orientation is a return home * Age ≥ 18 years * NIHSS \< 15 * Montreal Cognitive Assessment (MoCa) \> 21/30 * Free and informed consent signed by the patient. * Person affiliated with or a beneficiary of a social security scheme Exclusion Criteria: * Patients admitted for mechanical thrombectomy, outside the Basque Coast Hospital (CHCB) * Rankin score estimated at discharge ≥ 4 * Patients requiring assistance from a third party at home for the management of their medication or with stroke follow-up at Prado * Patients placed under protection measures
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Genom att skicka in godkänner du våra Användarvillkor
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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Centre Hospitalier de la Côte Basque
RECRUITINGBayonne, 64100, France
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