Seconder Complication Awareness of Caregivers (NCT07106190) | Clinical Trial Compass
CompletedNot Applicable
Seconder Complication Awareness of Caregivers
Turkey (Türkiye)80 participantsStarted 2025-08-15
Plain-language summary
Stroke-related secondary complications increase the length of hospital stay, negatively affect the functional expectation in the rehabilitation process and increase repeated hospital admissions. For these reasons, complications secondary to stroke are associated with mortality and increased economic burden. Prevention of secondary complications is important. Increasing the level of knowledge and awareness of caregivers, who are constantly with the patient, about secondary complications is effective in preventing secondary complications. The aim of this study was to evaluate the level of awareness of caregivers about secondary complications related to stroke and the effect of rehabilitation process. There is no study or scale evaluating the level of awareness of secondary complications related to stroke in the literature.
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:
* Followed by ischaemic or haemorrhagic stroke
* No more than 1 year has passed since the date of the incident
* Followed with the same caregiver for at least 1 month
* Patients and carers over 18 years of age
Exclusion Criteria:
* Cognitive or psychological impairment of the caregiver
* Not volunteering to participate in the study
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
Test
Timeframe: first day of hospitalisation and 4th week of hospitalisation