Clinical Trials Directory

Trials / Completed

CompletedNCT06842901

Feasibility Study on PoRi Device

Feasibility Study on Portable Rehabilitation (PoRi) Device in Hand Spasticity

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
10 (actual)
Sponsor
Yale University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study is a feasibility study of a new device that moves the hand of patients with spasticity to reduce hand muscle tone. The device's ability to improve spasticity before and after a 20-minute session with the device at Yale New Haven Hospital's outpatient clinic of Physical Medicine \& Rehabilitation, or the Inpatient Rehabilitation Unit.

Detailed description

Each patient will participate in a single 20 minute session, during which the device will extend and flex finger muscles. Each participant's duration will be approximately 1 hour during clinic, including time to address any further questions, to calibrate the device, and to measure the Modified Ashworth Score (MAS) before and after the intervention.

Conditions

Interventions

TypeNameDescription
DEVICEPortable Rehabilitation (PoRi) deviceOnce the calibration is complete, the device moves the fingers to close and open the hand for a total of 20 minutes.

Timeline

Start date
2025-04-07
Primary completion
2025-07-15
Completion
2025-07-15
First posted
2025-02-24
Last updated
2025-12-19

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT06842901. Inclusion in this directory is not an endorsement.