Your daily environment may shape stroke recovery
NCT ID NCT07504692
First seen Jun 26, 2026 · Last updated Aug 14, 2026 · Updated 2 times
Summary
This completed study looked at how a person's total daily-life exposure—called the 'exposome'—affects health after a stroke. Researchers tracked 150 stroke survivors, measuring biological, environmental, social, and lifestyle factors alongside motor and cognitive tests. The goal was to understand which factors help or hinder recovery, without testing any new treatment.
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 research could help identify which environmental, social, and lifestyle factors most influence recovery after a stroke, guiding future rehabilitation strategies.
- What could go wrong
- This is an observational study, not a treatment trial. It cannot prove cause and effect, and results may not apply to all stroke survivors.
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
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150 people
The number who actually took part.
- Started
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Mar 2025
- Finished
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Nov 2025
- 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.
Who is studied
post-stroke patients
- Ages
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5 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: * Subjects with Cerebral Stroke, both ischemic and hemorrhagic, in either pediatric or adult age; * Age \> 5 years * Absence of ongoing clinical acute conditions * Able to provide written informed consent to participate in the study if of legal age, or consent from a legal representative if a minor * Absence of major psychiatric disorders associated with the disability condition Exclusion Criteria: * Inability to provide informed consent * Presence of other neurological conditions (e.g. Multiple Sclerosis, Parkinson's Disease…) * Presence of ongoing clinical acute conditions * Presence of major psychiatric disorders associated with the disability condition
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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.
Contacts and locations
Locations
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IRCCS Fondazione Don Carlo Gnocchi
Milan, Milano, 20148, Italy
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IRCCS Scientific Institute E. Medea
Bosisio Parini, Lecco, 23842, Italy
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Villa Beretta Rehabilitation Center
Costa Masnaga, Lecco, 23845, Italy
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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