Active — Not RecruitingNot Applicable

A Biomarker for Personalized Care in Post-Stroke Spatial Neglect

United States45 participantsStarted 2021-09-01

Plain-language summary

More than 30,000 Veterans are hospitalized for stroke each year, and in the critical first months of recovery, at least half are disabled by abnormal 3-D spatial function (spatial neglect). Their self-care, mobility, and ability to return home are severely limited.

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Stroke survivors \>18 years * 1-8 months post-stroke * Can undergo testing and give informed consent Exclusion Criteria: * Other serious * Chronic neurological disorders * Evidence of other serious strokes * Inability to undergo testing or give informed consent

What they're measuring

Change in functional ability for daily life tasks assessed on the FONE-FIM at 3 months

Timeframe: baseline to 3 months

SN severity at baseline

Timeframe: baseline

Change in functional ability assessed by the Barthel Index at 3 months

Timeframe: baseline to 3 months

Change in functional ability for daily life tasks assessed on the FONE-FIM at 6 months

Timeframe: baseline to 6 months

SN severity at 3 months

Timeframe: 3 months post-baseline

SN severity at 6 months

Timeframe: 6 months post-baseline

Change in functional ability assessed by the Barthel Index at 6 months

Timeframe: baseline to 6 months

Trial details

NCT IDNCT05256563

SponsorVA Office of Research and Development

Sponsor typeFED

Study typeOBSERVATIONAL

Primary completion2026-07-31

View on ClinicalTrials.gov More Spatial Neglect trials