A device that lets amputees feel their prosthetic limb move
NCT ID NCT02189031
First seen Sep 01, 2026 · Last updated Sep 02, 2026 · Updated 1 time
Summary
This trial tests a wearable tactor array that delivers sensory feedback to the nerves of a missing limb, aiming to help upper limb amputees feel where their prosthetic is moving without looking. Participants include amputees who have undergone targeted sensory reinnervation and able-bodied volunteers. Researchers will assess how well the device supports a sense of limb ownership and movement interpretation after daily home use.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- A wearable tactor array device that provides sensory feedback through the nerves of the missing limb
- What this could lead to
- If it works, this could help people with upper limb amputations feel where their prosthetic limb is moving without looking at it, improving control and making the limb feel more like their own.
- What could go wrong
- This is a small, early-stage trial with only 21 participants. The device may not provide clear or reliable sensations for everyone, and results may not apply to all amputees.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
-
21 people
The number who actually took part.
- Start date
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Feb 2013
- Finished
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Nov 2023
- Lead sponsor
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A government agency
The lead sponsor is a US federal agency other than the NIH.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Amputees who have undergone targeted sensory reinnervation
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Cleveland Clinic Lerner Research Institute
Cleveland, Ohio, 44195, United States
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Louis Stokes VA Medical Center
Cleveland, Ohio, 44106, United States
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Rehabilitation Institute of Chicago
Chicago, Ill, 60611, United States
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University of Alberta Glenrose Rehabilitation Hospital
Edmonton, Alberta, T5B0B7, Canada
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