Ancient Mind-Body practice put to the test for spinal cord injury pain
NCT ID NCT06140355
First seen Aug 19, 2026 · Last updated Aug 20, 2026 · Updated 1 time
Summary
This study tests whether a 12-week remote Qigong program is feasible and acceptable for adults with spinal cord injury who have chronic neuropathic pain. Participants will be randomly assigned to either practice Qigong via video or complete a short daily pain survey. The goal is to see if this approach can be used in a larger future trial to potentially offer a non-drug way to manage pain.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Qigong, a mind-body practice involving gentle movement and breathing, delivered remotely via video
- What this could lead to
- If this trial shows that Qigong is feasible and acceptable, it could pave the way for a larger study and eventually a non-drug option to help manage chronic pain after spinal cord injury.
- What could go wrong
- This is a small feasibility study, not a proof of effectiveness. It may not show clear pain relief, and results may not apply to all people with spinal cord injury. Remote practice requires internet access and motivation.
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.
- Started
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Aug 2024
- Expected to finish
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Jan 2027
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: * 18+ years old * medically stable * with neuropathic pain 4 or above on the numeric pain rating scale + screened with painDETECT * willing to participate in a remote Qigong intervention (from any location with internet connection) * fluent in English or Spanish * access to the internet and a computer/iPad or smartphone Exclusion Criteria: * uncontrolled seizure disorder * cognitive impairment and/or communicative disability (e.g., due to brain injury) preventing them from following directions or from learning * ventilator dependency * major medical complications * pressure ulcers hindering prolonged sitting or lying down * (planning to become) pregnant or planning a major surgery during the study (given study duration, regular Qigong practice, and frequent check-ins) * regular Tai Chi or Qigong practice in the past 6 months (3x/week or more) * currently engaged in other rehabilitation programs that would influence outcomes
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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
3 sites. 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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University of Miami
NOT_YET_RECRUITINGMiami, Florida, 33124, United States
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University of Minnesota
RECRUITINGMinneapolis, Minnesota, 55414, United States
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University of Texas - Rio Grande Valley
NOT_YET_RECRUITINGHarlingen, Texas, 78539, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Early detrusor chemodenervation to preserve bladder compliance and longevity after spinal cord injury
- Prevention of thromboembolism using apixaban vs enoxaparin following spinal cord injury
- Can a brain implant let paralyzed people control computers with their minds?
- Can ultrasound dye reveal spinal cord damage Mid-Surgery?
- Can a mindfulness app ease the stress of hospitalization?