Using pressure splints to improve movement in stroke patients with hemiplegia
Effect of Pressure Splints on Lower Extremity Functions in Hemiplegic Stroke Patients
This study tests if using special pressure splints during rehab exercises can help stroke patients with hemiplegia move better and recover more effectively.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 30 (estimated) |
| Ages | 50 Years to 80 Years |
| Sex | All |
| Sponsor | Istinye University Academic / other |
| Locations | 1 site (Jounieh, Keserwan) |
| Trial ID | NCT06965894 on ClinicalTrials.gov |
What this trial studies
This study investigates the effects of lower extremity pressure splints on movement and function in individuals with hemiplegia resulting from a stroke. Participants will be randomly assigned to either a Splint Group, which will use the pressure splints during rehabilitation exercises, or a Control Group, which will perform the same exercises without splints. The intervention will last for six weeks, during which all participants will receive neurodevelopmental therapy. The goal is to determine if the splints can enhance muscle function and improve recovery outcomes.
Who should consider this trial
Good fit: Ideal candidates are individuals aged 50-80 who have experienced a stroke within the last month to year and have hemiplegia.
Not a fit: Patients with severe cognitive impairment, other neurological disorders, or contraindications to exercise may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly improve mobility and quality of life for stroke patients with hemiplegia.
How similar studies have performed: While similar approaches have been explored, the specific use of pressure splints in this context is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Having hemiplegia because of stroke * Time since stroke: 1 month to 1 year * Ability to Participate (a score of \>24 on the Mini-Mental State Examination). * Being voluntary * Age between 50-80 Exclusion Criteria: Severe Cognitive Impairment Other Neurological Disorders Severe Comorbidities or Spasticity on Lower Extremity Contraindications to Exercise Recurrent Stroke
Where this trial is running
Jounieh, Keserwan
- Monseigneur Cortbawi Hospital — Jounieh, Keserwan, Lebanon (Recruiting)
Study contacts
- Study coordinator: Çiçek Günday, Asst. Prof.
- Email: cicek.gunday@istinye.edu.tr
- Phone: 0090 850 283 60 00
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.