Evaluation of self-sufficiency in post-acute stroke patients
Development and Testing of a New Tool for Evaluating Functional Self-sufficiency in Post-acute Stroke Patients
Palacky University · NCT06518460
This study is testing a new tool to see how well stroke patients can take care of themselves during their recovery.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 150 (estimated) |
| Ages | 18 Years to 80 Years |
| Sex | All |
| Sponsor | Palacky University (other) |
| Locations | 1 site (Olomouc, Czech) |
| Trial ID | NCT06518460 on ClinicalTrials.gov |
What this trial studies
This observational study aims to design and validate a new tool called the Functional Efficiency of Self-sufficiency Test (FEST) for assessing self-sufficiency in patients recovering from acute strokes. The study will evaluate various factors that influence changes in self-sufficiency during post-acute rehabilitation. Patients diagnosed with ischemic or hemorrhagic strokes will undergo assessments at the beginning and end of their rehabilitation, focusing on categories such as mobility, dressing, and communication. Statistical methods will be employed to analyze the data and validate the FEST tool.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 and older who have experienced an ischemic or hemorrhagic stroke and are in the post-acute rehabilitation stage.
Not a fit: Patients with severe sensory deficits or those who are not recommended for participation due to cognitive issues may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide a reliable assessment tool to improve rehabilitation strategies for stroke patients.
How similar studies have performed: While the approach of developing a specific assessment tool for stroke rehabilitation is not widely tested, similar studies have shown the importance of tailored assessments in improving patient outcomes.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * diagnosed with ischemic or haemorrhagic stroke in the post-acute stage; aged ≥18 years; stable vital functions; rehabilitation load of 4 hours per day; maintained swallowing functions. Exclusion Criteria: * tracheostomy; not recommended by psychotherapist due to cognitive deficit and unwillingness; severe sensory deficit (hearing, vision).
Where this trial is running
Olomouc, Czech
- Palacky University — Olomouc, Czech, Czechia (RECRUITING)
Study contacts
- Study coordinator: Jana Vyskotova
- Email: jana.vyskotova@upol.cz
- Phone: +420585632834
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Stroke/Brain Attack