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Hand Assistive Rehabilitation Orthotic Device Effectiveness Study

NCT04565639 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 3

Last updated 2020-09-25

No results posted yet for this study

Summary

The primary objective of this study is to evaluate pinch strength improvements and improvements in coordination and functional ability. Pinch strength measurements are made on subjects both with and without the device to evaluate the potential improvements. Also, coordination and functional testing is performed both with and without the device to compare performance under both conditions and evaluate potential improvement.

Conditions

  • Orthoses
  • Prostheses

Interventions

DEVICE

Powered Hand Orthosis

A prototype powered hand orthosis system designed to improve grip strength and improve ability to perform tasks of daily living.

Sponsors & Collaborators

  • Liberating Technologies, Inc.

    lead INDUSTRY

Principal Investigators

  • Kevin Keough · Liberating Technologies, Inc.

Study Design

Allocation
RANDOMIZED
Purpose
DEVICE_FEASIBILITY
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
89 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-08-14
Primary Completion
2019-11-07
Completion
2019-11-07
FDA Device
Yes

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 NCT04565639 on ClinicalTrials.gov