Improving arm use after stroke with therapy and sensory techniques
Constraint-Induced Movement Therapy Plus Sensory Components for Adults With Mild-to-Severe Arm and Hand Impairment After Stroke
This study is testing if adding sensory techniques to a therapy for stroke patients can help them use their affected arm better after treatment.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 15 (estimated) |
| Ages | 18 Years to 89 Years |
| Sex | All |
| Sponsor | University of Alabama at Birmingham Academic / other |
| Locations | 1 site (Birmingham, Alabama) |
| Trial ID | NCT05515237 on ClinicalTrials.gov |
What this trial studies
This study investigates the feasibility of enhancing Constraint-Induced Movement Therapy (CI Therapy) by incorporating sensory components for stroke patients with varying levels of upper extremity impairment. The intervention involves intensive treatment over two to three weeks, focusing on improving the use and motor ability of the more-affected arm through behavioral strategies and motor training techniques. Participants will be assessed using specific measures to evaluate their arm use and motor capacity before and after the intervention. The goal is to determine if adding sensory components can further improve recovery outcomes for stroke survivors.
Who should consider this trial
Good fit: Ideal candidates are individuals who are at least six months post-stroke and can demonstrate minimal active movement in their affected upper extremity.
Not a fit: Patients with severe cognitive impairments or those unable to participate in the therapy due to physical limitations may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly enhance the functional use of the affected arm in daily activities for stroke patients.
How similar studies have performed: Previous studies have shown strong evidence supporting the effectiveness of CI Therapy in improving upper extremity function after stroke, indicating that this approach may build on established methods.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * At least 6 months post stroke * The ability to demonstrate the minimum UE active movement criteria of shoulder ≥ 30 toward flexion or abduction, initiate movement at the elbow for flexion and extension, and initiate movement at the wrist, fingers, or thumb. * Mean score of \<2.5 on the Motor Activity Log/ G4/5 Motor Activity Log indicating the participant's use of the more-affected UE. Exclusion Criteria: * Score\< 24 on the Mini Mental State Exam * Inability to answer the MAL/ G4/5 MAL questions and/or provide informed consent * The inability to come in to the laboratory setting for treatment.
Where this trial is running
Birmingham, Alabama
- University of Alabama at Birmingham — Birmingham, Alabama, United States (Recruiting)
Study contacts
- Study coordinator: Mary Bowman, BS OT
- Email: mbowman@uab.edu
- Phone: 2059340069
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.