Intensified occupational therapy for stroke recovery
Effect of Intensified Occupational Therapy on Basic Activities of Daily Living: a Randomized Controlled Trial
This study tests whether extra occupational therapy can help people who have had a stroke become more independent in their daily activities.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 20 (estimated) |
| Ages | 18 Years to 75 Years |
| Sex | All |
| Sponsor | University of Aarhus Academic / other |
| Locations | 1 site (Hammel, Midtjylland) |
| Trial ID | NCT05638607 on ClinicalTrials.gov |
What this trial studies
This study investigates the impact of intensified occupational therapy on improving independence in basic activities of daily living (ADL) for individuals who have experienced a first-time stroke. Participants will receive tailored therapy aimed at enhancing their ability to perform daily tasks. The intervention focuses on practical skills and rehabilitation techniques to foster greater autonomy in everyday life. The study aims to measure the effectiveness of this approach in a clinical setting.
Who should consider this trial
Good fit: Ideal candidates are individuals who have experienced a first-time stroke and score 4 or lower on four of the six Functional Independence Measure (FIM) basic ADL items.
Not a fit: Patients who are unable to understand Danish will not benefit from this study due to communication barriers.
Why it matters
Potential benefit: If successful, this intervention could significantly enhance the quality of life for stroke survivors by improving their independence in daily activities.
How similar studies have performed: While similar approaches have been explored in occupational therapy, the specific intensified intervention for stroke recovery is relatively novel and may provide new insights into rehabilitation effectiveness.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * First-time stroke * \<=4 on four of six Functional Independence Measure (FIM) basic ADL items Exclusion Criteria: * Not able to understand danish
Where this trial is running
Hammel, Midtjylland
- Hammel Neurorehabilitation Centre and University Research Clinic — Hammel, Midtjylland, Denmark (Recruiting)
Study contacts
- Principal investigator: Jesper Fabricius, PhD — Hammel Neurorehabilitation Centre and University Research Clinic
- Study coordinator: Jesper Fabricius, PhD
- Email: Jesper.Fabricius@rm.dk
- Phone: +4578419051
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.