Electric suit aims to silence phantom pain
NCT ID NCT07759219
First seen Aug 12, 2026 · Last updated Aug 13, 2026 · Updated 1 time
Summary
This trial tests whether a wearable suit delivering gentle electrical stimulation can reduce pain and improve daily function in adults with lower-limb amputation who have pain in multiple body areas. Participants will receive 10 treatment sessions over 2-3 weeks, comparing a 'strong but comfortable' stimulation level to a barely noticeable one. The study measures changes in pain intensity, pain interference, and overall improvement to see if this approach is a viable pain management option.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Transcutaneous electrical nerve stimulation (TENS) delivered via a wearable suit at two different intensities
- What this could lead to
- If it works, this wearable suit could offer a drug-free way to manage chronic pain and improve mobility for people with limb loss.
- What could go wrong
- This is a small early-stage trial, and results may not apply to everyone. The effect may be modest, and not all participants may find the stimulation comfortable.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 40 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Aug 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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: * English-speaking and reading to enable informed consent and participation * Report of pain in 2/more body regions for at least 3 months duration per site • Report of at least moderate intensity pain over the past 7 days Exclusion Criteria: * An amputation of the contralateral lower-limb \> toe-level * Do not currently use a prosthesis to ambulate * Diagnosed cognitive impairment (e.g., dementia, traumatic brain injury) * Severe vision (e.g., blind) or hearing loss (e.g., deaf) * Are currently pregnant * Active cancer/malignancy * Open wound in any area that is covered by the suit * An acute infection or injury (e.g., fracture) * Deep vein thrombosis * Bowel and/or bladder incontinence
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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International Institute of Orthotics and Prosthetics
Tampa, Florida, 33634, United States