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Assessing Force Feedback With the SoftHand Pro

NCT03412656 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 27

Last updated 2020-11-20

No results posted yet for this study

Summary

The trial is designed to test the effectiveness of a force-feedback cuff in combination with a myoelectric prosthesis in conveying information on grasp strength to the user, as well as the user's preference regarding the feature.

Conditions

  • Amputation, Traumatic
  • Limb Defect

Interventions

DEVICE

SoftHand Pro with CUFF force feedback device

Participants will complete various movement and activity of daily living (ADL) assessments to test the effectiveness of the CUFF device in combination with the Soft Hand Pro (SHP) in conveying haptic force feedback to patients with transradial limb loss, and to assess the extent to which the grip force feedback improves the embodiment of the prosthetic device.

Sponsors & Collaborators

  • Arizona State University

    collaborator OTHER

  • University of Pisa

    collaborator OTHER

  • Kristin Zhao, PhD

    lead OTHER

Principal Investigators

  • Kristin D. Zhao, Ph.D. · Mayo Clinic

  • Karen L. Andrews, M.D. · Mayo Clinic

Study Design

Allocation
NON_RANDOMIZED
Purpose
DEVICE_FEASIBILITY
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-10-17
Primary Completion
2019-06-14
Completion
2019-06-14
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 NCT03412656 on ClinicalTrials.gov