Mind over phantom pain: brain training offers Drug-Free hope for amputees
NCT ID NCT05880251
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a non-drug approach to help people with phantom limb pain—pain felt in a missing limb. Twenty adults with arm or leg amputations learned to change their brain responses using real-time feedback. The goal was to retrain the brain to reduce pain and improve quality of life.
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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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20 people
The number who actually took part.
- Started
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Jul 2023
- Finished
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Aug 2025
- 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.
- 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * An upper (or lower limb) amputation more than 6 months ago, that has produced a moderate to severe hand/arm (or foot/leg) phantom limb pain, * Male or female age 18 years or older, * Medical clearance to participate, * Reasonable expectation that ongoing medications, if any, will be maintained without change for at least 4 months from the start of the study, * Able to provide informed consent and to understand the study instructions, * Able to participate in the specific study procedures. Exclusion Criteria: * Presence of other medically unstable and/or infectious condition (e.g., uncontrolled diabetes with recent weight loss, diabetic coma, frequent insulin reactions), * A cardiac condition (e.g., history of myocardial infarction or congestive heart failure), * Cognitive and/or attention difficulties affecting participant's ability to follow study directions, * Known skin disorders or damaged skin at the anticipated at the scalp for EEG recording (e.g., unhealed wounds, broken skin). * Metal implants above the chest
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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.
Contacts and locations
Locations
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Albany VA Medical Center Samuel S. Stratton, Albany, NY
Albany, New York, 12208-3410, United States
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Other studies related to the condition(s) this trial covers.
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