NCT07887776Completed
Physical Performance and Cognitive Functions in Patients With Chronic Stroke
The Effect of Cognitive Impairment on Upper Extremity Physical Performance and Cognitive Functions in Patients With Chronic Stroke
Source: ClinicalTrials.gov · Last updated 21 Oct 2026
Brief summary (registry, in English)
This study aims to investigate the impact of cognitive impairment on upper extremity physical performance, cognitive skills, and functional independence in individuals with chronic stroke. A total of 66 chronic stroke survivors will be enrolled and categorized into two groups based on their Montreal Cognitive Assessment (MoCA) scores: the Cognitive Impairment Group (n=33) and the Control Group (n=33). Upper extremity performance, cognitive functions, and functional independence will be comprehensively evaluated using standardized clinical outcome measures.
- Status (registry)
- Completed
- Study type
- Observational
- Enrollment
- 66 (actual)
- First submitted
- 15 Oct 2026
- Start date
- 1 Jan 2025
- Primary completion date
- 30 Jun 2026
- Lead sponsor
- Kutahya Health Sciences University
- Diseases
- Stroke
- NCT number
- NCT07887776
What you commit to
- Study type: Observational
- Participants enrolled: 66
- From 1 Jan 2025 to the primary completion date, 30 Jun 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Presence of any other concurrent orthopedic or neurological disease affecting physical or cognitive performance
Other illness
- Having a chronic and severe medical condition (e.g., epilepsy, cerebral palsy)
- History of recent surgery
- History of any pre-existing condition affecting cognitive status (e.g., dementia, neurodegenerative diseases)
Other
- Complete loss of vision or hearing
Who the study is looking for
- History of ischemic or hemorrhagic stroke diagnosed at least 6 months prior to the study,
- First-ever stroke
- Absence of communication or language disorders that would prevent understanding and cooperation
- Ability to read and write
- Not currently receiving psychotropic medication treatment
- Willingness to participate and provision of signed informed consent
Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Doç. Dr. Mustafa Kalemli Tavsanli State Hospital Coordinator of this site? Confirm its status | Kütahya | Turkey (Türkiye) | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.