Clinical trial Recruiting at 1 site Observational Ages 18 to 99

Understanding how social factors affect cognitive function after stroke

Official title: Understanding Stroke Outcomes: Stroke Resilience, Infarct Burden, and Long-Term Cognition

Run by National Institutes of Health Clinical Center (CC) · NCT06615973 · Data updated 2026-11-12

This study looks at how social factors, like support from family and friends, affect how well people recover mentally after having a stroke.

Quick facts

Study typeObservational
Ages18 Years to 99 Years
SexAll
Enrollment450 (estimated)
SponsorNational Institutes of Health Clinical Center (CC)
NIH
Locations1 site (Bethesda, Maryland)
StatusRecruiting
StartedSeptember 14, 2026
Main results expectedFebruary 1, 2027
Study endsFebruary 1, 2027
Registry record updatedSeptember 29, 2026
Trial IDNCT06615973 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults aged 18 and older who have previously participated in the Natural History of Stroke study and have an interpretable MRI scan.

Probably not a fit

Patients who have a modified Rankin Scale score of 6, indicating death, will not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to explore the impact of social determinants of health (SDOH) on cognitive function in individuals who have experienced a stroke. Participants, aged 18 and older, will be recruited from a previous study and will engage in a 45-minute telephone interview to discuss their health and social factors since their stroke. The study will analyze how these social factors relate to the severity of brain damage as measured by MRI and their influence on post-stroke recovery outcomes. The goal is to identify characteristics that may enhance resilience and improve recovery after a stroke.

Why it matters

Potential benefit: If successful, this study could provide insights that help improve cognitive outcomes for stroke survivors by addressing social factors.

How similar studies have gone: While studies have explored the impact of social factors on health, this specific approach focusing on post-stroke cognitive function is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
* INCLUSION CRITERIA:

In order to be eligible to participate in this study, an individual must meet all of the following criteria:

* Stated willingness to comply with all study procedures and availability for the duration of the study.
* Adults aged 18 or older.
* Previous participant in the Natural History of Stroke with an interpretable baseline MRI scan, NIHSS measured at baseline or discharge, and admission diagnosis of ischemic stroke.
* Fluent in English or Spanish

EXCLUSION CRITERIA:

An individual who meets any of the following criteria will be excluded from participation in this

study:

-Modified Rankin Scale (mRS) = 6 at any follow-up (usually up to 90 days) in the Natural History of Stroke study (mRS = 6 indicates the participant is dead).

Where it's running

  • National Institutes of Health Clinical Center
    Bethesda, Maryland, United States
    Recruiting

Study contacts

  • Principal investigator: Rebecca F Gottesman, M.D. — National Institute of Neurological Disorders and Stroke (NINDS)
  • Study coordinator: Rebecca F Gottesman, M.D.
  • Email: rebecca.gottesman@nih.gov
  • Phone: (301) 435-9321

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Other studies for the same condition or treatment. Recruiting studies are listed first.

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  • Endovascular treatment for stroke beyond 24 hours

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.