Robot-assisted online rehabilitation for stroke recovery
Feasibility of a Kinect-Based Citizen Science Telerehabilitation Platform
This study tests if using a robot-assisted online program can help stroke patients recover their arm movement better while they interact with others or work alone.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 40 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | Johns Hopkins University Academic / other |
| Locations | 1 site (Baltimore, Maryland) |
| Trial ID | NCT03096262 on ClinicalTrials.gov |
What this trial studies
This study aims to enhance upper limb rehabilitation for stroke patients through a combination of robot-mediated therapy and citizen science participation. Participants will engage in various tasks using a low-cost haptic device while interacting on an online platform, either competing, cooperating, or working in isolation. The effectiveness of these different social interaction modes will be evaluated based on rehabilitation performance, motivation to contribute, and other metrics. The study seeks to empower patients by involving them actively in their rehabilitation process.
Who should consider this trial
Good fit: Ideal candidates include individuals with post-stroke hemiparesis for more than three months who can stand or sit independently and possess sufficient cognitive skills.
Not a fit: Patients with visual deficits or other neurological conditions may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly improve rehabilitation outcomes for stroke patients by leveraging technology and social interaction.
How similar studies have performed: Other studies have shown promise in using technology for rehabilitation, but this specific approach combining citizen science and robot-mediated therapy is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: For treatment group: * post-stroke hemiparesis \>3 months * ability to stand or sit independently * sufficient cognitive skills to perform the exercises as demonstrated * full passive range of motion in the affected arm but limited active movement as determined by a upper extremity Fugl-Meyer score of \<50/66 * technical savvy and interest to use an internet platform For control group: (ii) no history of learning disabilities (iii) technical savvy and interest to use an internet platform Exclusion Criteria: For treatment group: * visual deficit such as deficit in visual acuity, eye movements, visual field cut, or neglect * medical comorbidity such as other neurological conditions (e.g. Parkinson's disease, brain tumor, epilepsy), or previous injury to the upper limb * pain in the upper limbs that prevents full passive range of motion to perform the exercises. For control group: * visual deficit such as deficit in visual acuity, eye movements, visual field cut, or neglect * any previous injury or medical condition that prevents full passive range of motion to perform the exercises.
Where this trial is running
Baltimore, Maryland
- Matthew Bird — Baltimore, Maryland, United States (Recruiting)
Study contacts
- Principal investigator: Preeti Raghavan, MD — Johns Hopkins University
- Study coordinator: Matthew Bird, MA
- Email: mbird6@jhmi.edu
- Phone: 410-955-1347
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.