Examining the Effects of Patient Information Forms, Exercise Forms and Video Recordings (NCT06229028) | Clinical Trial Compass
CompletedNot Applicable
Examining the Effects of Patient Information Forms, Exercise Forms and Video Recordings
Turkey (Türkiye)75 participantsStarted 2024-01-01
Plain-language summary
The investigators believe that these information forms, exercise forms and video recordings that provide patient education will contribute to the collaborative approach of the patient and the clinician, the patient's participation in the treatment, the expectation of treatment and results, and their autonomy. The contribution of patient information forms, exercise forms and video recordings, which have become very important in recent years, to different degrees of results will be questioned.
Who can participate
Age range
18 Years – 65 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:
* who have a hand or forearm injury as a result of a work-related injury
* who has undergone primary surgery/conservative treatment related to the injury
* who is literate
* who has and can use technological equipment to use visual and audio communication materials (video)
Exclusion Criteria:
* who miss the evaluations
* who wants to leave 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
Impact of Event Scale-Revised
Timeframe: The evaluation were completed in the first session when the patient applied to the hand rehabilitation unit, and it was also repeated at 3th months after the surgery or conservative treatment.
2
State-trait Anxiety Inventory
Timeframe: The evaluation were completed in the first session when the patient applied to the hand rehabilitation unit, and it was also repeated at 3th months after the surgery or conservative treatment.