A Biomarker for Personalized Care in Post-Stroke Spatial Neglect (NCT05256563) | Clinical Trial Compass
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 range
18 Years
Sex
ALL
See this in plain English?
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
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Change in functional ability for daily life tasks assessed on the FONE-FIM at 3 months
Timeframe: baseline to 3 months
2
SN severity at baseline
Timeframe: baseline
3
Change in functional ability assessed by the Barthel Index at 3 months
Timeframe: baseline to 3 months
4
Change in functional ability for daily life tasks assessed on the FONE-FIM at 6 months
Timeframe: baseline to 6 months
5
SN severity at 3 months
Timeframe: 3 months post-baseline
6
SN severity at 6 months
Timeframe: 6 months post-baseline
7
Change in functional ability assessed by the Barthel Index at 6 months