PoRI Clinical Trial
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorYale University
About this trial
This randomized clinical trial compares the Portable Rehabilitation Interface (PoRI) device for rehabilitation of hand motor function in post-stroke patients with conventional hand therapy.
Eligibility criteria
Qualifiers
Between 2 days and a maximum of 2 months have passed since the stroke event
0-3/5 muscle strength
Participants with paralysis or sensorimotor function problems of the fingers of one or both hands.
Participants must be able to fit their hand comfortably into the device.
Disqualifiers
Less than 2 days or greater than 2 months have passed since the stroke event
4-5/5 muscle strength
Vulnerable populations.
Inability of fingers and wrist to stretch to neutral during passive range of motion
Trial design
Treatments tested in this trial
- Portable Rehabilitation Interface (PoRI)
Treatment groups
12 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov