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Feasibility Study on PoRi Device

NCT06842901 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 10

Last updated 2025-12-19

No results posted yet for this study

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.

Conditions

  • Hand Spasticity

Interventions

DEVICE

Portable Rehabilitation (PoRi) device

Once the calibration is complete, the device moves the fingers to close and open the hand for a total of 20 minutes.

Sponsors & Collaborators

  • Yale University

    lead OTHER

Principal Investigators

  • Necolle Morgado-Vega · Yale University

Study Design

Allocation
NA
Purpose
DEVICE_FEASIBILITY
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-04-07
Primary Completion
2025-07-15
Completion
2025-07-15

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06842901 on ClinicalTrials.gov