Study of the Participation of People With Aphasia Post Stroke and Their Caregivers in Valladolid … (NCT06948721) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Study of the Participation of People With Aphasia Post Stroke and Their Caregivers in Valladolid Region (Spain)
50 participantsStarted 2025-05-06
Plain-language summary
The objective of this study is to determine the level of community participation of people with post-stroke aphasia and their caregivers, as well as the factors that facilitate or interfere with this participation in the Valladolid region (Spain).
The main questions that this study aims to answer are:
1. What is the retained activities of the people with aphasia post-stroke?
2. What is the retained activities of the caregivers of people with aphasia post-stroke?
3. What factors influence the community participation of people with aphasia post-stroke and their caregivers?
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:
* Chronic Stroke (stroke onset above six months).
* Aphasia post stroke.
* Residents in Valladolid Region.
* Age over 18 years.
* Ability to walk equal to or greater than 3 according to the Functional Ambulation Category (FAC).
* Informed consent acceptance.
Exclusion Criteria:
* Stroke onset below of Six months
* Age under 18 years
* Both in the case of the person with aphasia and their caregiver, presence of other pathologies that affect functional independence
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.