Using a robot to help stroke patients recover upper limb movement
Efficacy and Acceptability of the Luna EMG Rehabilitation Robot on Motor Recovery of the Upper Limb in the Chronic Phase of Stroke, Experimental Study in Single Cases.
NA · University Hospital, Brest · NCT05902910
This study is testing if a robot can help people who have had a stroke improve their arm and shoulder movement during recovery.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 5 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University Hospital, Brest (other) |
| Locations | 1 site (Brest) |
| Trial ID | NCT05902910 on ClinicalTrials.gov |
What this trial studies
This pilot study investigates the effectiveness of the Luna EMG rehabilitation robot in improving upper limb motor recovery in chronic stroke patients. Participants will undergo a structured rehabilitation program that includes intensive training with the robot, focusing on elbow and shoulder movements. The study employs a single case experimental design with multiple baselines, assessing motor function and fluidity of movements through various evaluations. The treatment duration spans 6 to 7.5 weeks, with a combination of baseline measurements and robotic therapy sessions aimed at enhancing upper limb functionality.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 and older who have experienced hemiparesis from a first stroke more than one year ago.
Not a fit: Patients with severe spasticity or complete loss of upper limb proprioception may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly improve motor recovery and functional independence for stroke patients.
How similar studies have performed: Previous studies have shown that robotic rehabilitation can be effective, but this specific approach with the Luna EMG robot is novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age \>= 18 years * Hemiparesis after a first stroke with more than 1 year time interval * Functional upper limb: ability to do a pointing task at 90% of the hand-acromion distance (free trunk). * Spastic hypertonia of the elbow flexors 0-2/4 on the Modified Ashworth scale * Patient affiliated with social security * Patient having signed a consent to participate in the research Exclusion Criteria: * Inability to sign written consent * Flexed elbow \> 30° during passive mobilization of the upper limb * EVA\>3 in the upper limb at rest or during mobilization * Complete loss of upper limb proprioception * Neuro-orthopedic surgery of the upper limb for spasticity: neurotomy, tenotomy, transfer * Pregnant or breastfeeding woman
Where this trial is running
Brest
- CHU Brest — Brest, France (RECRUITING)
Study contacts
- Principal investigator: Olivier Remy-Neris, PU-PH — CHRU BREST
- Study coordinator: Olivier Remy-Neris, PU-PH
- Email: olivier.remyneris@chu-brest.fr
- Phone: +33 2 98 22 31 52
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.
Conditions: Stroke, Robot, Joint