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Safety and Feasibility of an ExoNET for Supination Assistance for Stroke Survivors

NCT06655636 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2025-01-09

No results posted yet for this study

Summary

The purpose of this study is to evaluate the safety, feasibility, and efficacy of an exoskeletal network of passive, multi-joint springs for forearm supination. Also known as the forearm ExoNET, the device is a passive, robotic device that will properly assist forearm supination in the post-stroke adult population.

Conditions

  • Stroke
  • Cerebral Vascular Accident

Interventions

DEVICE

Device tuned to Assistance

The device spring components will be tuned to produce an assistive supination torque on the forearm.

DEVICE

Device tuned to Sham (Slack Springs)

The device spring components will be tuned to slack springs to serve as a placebo. The user will think they are receiving forces but in reality the device will not be providing any forces.

DEVICE

Device tuned to Anti-Assistance

The device spring components will be tuned to produce a resistive supination torque on the forearm.

Sponsors & Collaborators

  • Shirley Ryan AbilityLab

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
40 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-12-04
Primary Completion
2025-12-31
Completion
2025-12-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

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 NCT06655636 on ClinicalTrials.gov