Skip to main content
OpenTrials
Completed

NCT Number: NCT02189031

Sensory Feedback for Touch and Proprioception With Prosthetic Limbs

Upper limb amputation is a devastating injury that leaves many thousands of typically young and active individuals in the US to rely on artificial arms and hands to help restore their lost function. The investigators research is focused on helping these individuals to feel where their prosthetic limbs are moving without having to look at them by developing devices and approaches to provide sensory feedback of limb movement through the nerves that once served the missing limb.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

University of Alberta Glenrose Rehabilitation Hospital, Edmonton, Alberta, Canada

Loading trial locations.

About this study

In the investigators research the investigators seek to understand the organization and (function/operation) of sensory neural systems in order to develop methods for restoring function to injured populations. One of the primary focus areas of the investigators research is working to integrate physiologically relevant sensory feedback with prosthetic limbs. To this end the investigators employ a variety of approaches that interweave disciplines such as electrophysiology, psychophysics, biomedical engineering and cognition. The investigators research team is composed of an interconnected and communicative network of clinicians, engineers, and scientists. This helps us to provide pathways from basic science discoveries that can be used to address clinical needs with transition directly to patient care.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Amputee criteria:

  • Must be over 18 years of age
  • Must be upper extremity amputee who has undergone targeted sensory reinnervation.

Able Bodied participants:

  • Must be over 18 years of age

Treatment and study plan

Tactor array

Device

Bypass Tactor

Device

Primary outcomes

  1. Embodiment of the Prosthetic limb

    Time frame: Ten months

    Visual loading for fine motor tasks,questionnaires, and residual limb temperature will be assessed after 10 months of in home every day use of a custom robust tactor array for sensory feedback.

Secondary outcomes

  1. Investigate the perceptions of limb movement

    Time frame: 6 months

    Test how closely both targeted reinnervation amputees and able bodied study participants are able to interpret limb movement using the kinesthetic perceptual illusion and physiologically relevant kinesthetic feedback.

Sponsors and collaborators

Lead sponsor

Louis Stokes VA Medical Center

Fed

Collaborators

  • Defense Advanced Research Projects Agency
  • HDT Global
  • National Institute of Neurological Disorders and Stroke (NINDS)
  • National Institutes of Health (NIH)
  • Shirley Ryan AbilityLab
  • The Cleveland Clinic
  • University of Alberta

Registry information

Official study title

Sensory Feedback Tactor Systems for Implementation of Physiologically Relevant Cutaneous Touch and Proprioception With Prosthetic Limbs

Important dates

Study start
2013
Primary completion
2023
Study completion
2023
First posted
Jul 14, 2014
Registry last updated
Sep 1, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.