Clinical trial Recruiting at 1 site Interventional Ages 18 to 89

Home-based rehabilitation for phantom limb pain in veterans with amputations

Official title: Home-based Rehabilitation Intervention for Phantom Limb Pain in Veterans With Lower Limb Amputations

Run by VA Office of Research and Development · NCT06106984 · Data updated 2026-11-12

This study is testing a mobile app that helps veterans with amputations manage their phantom limb pain through home-based exercises and techniques.

Quick facts

Study typeInterventional
Ages18 Years to 89 Years
SexAll
Enrollment36 (estimated)
SponsorVA Office of Research and Development
Federal
Locations1 site (Minneapolis, Minnesota)
StatusRecruiting
StartedApril 1, 2024
Main results expectedNovember 30, 2028
Study endsMarch 31, 2029
Registry record updatedOctober 2, 2026
Trial IDNCT06106984 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are military veterans who are at least 18 years old, have undergone a unilateral below-knee amputation over a year ago, and experience moderate to severe phantom limb pain.

Probably not a fit

Patients with unstable medical conditions, severe mental illness, or other neuropathic pain conditions may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This project aims to address phantom limb pain (PLP) experienced by veterans with lower limb amputations through a home-based intervention using a mobile app for graded motor imagery (GMI). The study will refine the app and pilot test its feasibility and acceptability among veterans suffering from moderate to severe PLP. Participants will engage in a series of sessions using the app, which incorporates techniques like limb laterality training, motor imagery, and mirror therapy. The goal is to develop effective non-drug treatment options for PLP that can enhance the quality of life for veterans.

Why it matters

Potential benefit: If successful, this intervention could significantly reduce phantom limb pain and improve daily functioning for veterans with amputations.

How similar studies have gone: While there are limited studies specifically on graded motor imagery for phantom limb pain, similar non-drug interventions have shown promise in managing chronic pain conditions.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Must be a military Veteran
* \>1 year since unilateral below knee amputation
* Moderate or severe (NRS score 4 on a 0-10 scale) PLP
* Stable medications over the past 2 weeks
* Willing and able to give informed consent
* Able to participate in the telehealth study activities with a personal device

Exclusion Criteria:

* Unstable medical conditions (e.g., uncontrolled diabetes, heart failure exacerbation)
* Unstable mental illness or substance use disorder (e.g., active suicidality or psychosis)
* Unable to give informed consent due to a cognitive impairment
* Fibromyalgia or complex regional pain syndrome-like symptoms

Where it's running

  • Minneapolis VA Health Care System, Minneapolis, MN
    Minneapolis, Minnesota, United States
    Recruiting

Study contacts

  • Principal investigator: Tonya L Rich, PhD MA BS — Minneapolis VA Health Care System, Minneapolis, MN
  • Study coordinator: Tonya L Rich, PhD MA BS
  • Email: Tonya.Rich@va.gov
  • Phone: (612) 467-5463

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.