Feasibility Study of Passive Robots for Stroke Rehabilitation
This study is exploring a new way to help people recover arm and hand movement after a stroke. It uses two devices, SepaRRo and NeuRRoFES, which are designed to assist or resist your arm movements during exercises. NeuRRoFES also provides neuromuscular stimulation (gentle electrical pulses to muscles) during these activities. The goal is to see if these low-cost, non-motorized devices are practical and effective for stroke rehabilitation, potentially for use at home. Researchers are looking for 4 participants, aged 18 to 75, who have had a stroke and do not have major sensation problems or severe joint limitations. The study will measure how well the devices work and how easy they are to use immediately after the intervention.
- Study design
- This is an interventional study with an unspecified phase, aiming to enroll 4 participants. It is designed to evaluate the feasibility of using passive devices for stroke rehabilitation.
- What's involved
- Participants will perform functional movements with their arms using the SepaRRo and NeuRRoFES devices. Biofeedback may be provided during training.
- Compensation
- Not stated in the trial record.
- Follow-up
- Feasibility will be measured immediately following the last session of intervention.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Passive Robots for Stroke Rehabilitation: A Feasibility Study
At a glance
Conditions
NCT07218276
Where you'd take part
This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
University of Michigan - NeuRRo Lab
Ann Arbor, Michiganstudy coordinator listed
Recruiting
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Study leadership
- Chandramouli Krishnan, PT, PhD · PRINCIPAL_INVESTIGATOR · University of Michigan
Who to contact
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Inclusion
Exclusion
What this trial measures
- Device Survey For FeasibilityPost-intervention (immediately following last session of intervention)
Subjective feedback regarding feasibility of the device for training