Can a smartphone app tame chronic pain after spinal injury?
NCT ID NCT06891989
First seen Aug 20, 2026 · Last updated Aug 21, 2026 · Updated 1 time
Summary
This study tests whether a 6-week mindfulness meditation app can reduce pain intensity and improve mood in people with spinal cord injury who have chronic pain. Participants are randomly assigned to either use the mindfulness app or a health education app. The goal is to see if the mindfulness approach helps with pain, depression, and anxiety.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Mindfulness Coach app-based mindfulness meditation
- What this could lead to
- If effective, this app-based mindfulness program could offer a low-cost, accessible way to help people with spinal cord injury manage chronic pain and improve emotional well-being.
- What could go wrong
- The trial is still in progress, and results may not show a clear benefit. Also, the intervention requires daily internet access and may not work for everyone.
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 282 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Oct 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2029
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: * Traumatic SCI of at least 6 months duration * Chronic pain \[defined as pain lasting at least 3 months with a pain intensity rating of 4 or higher on a 10-point visual analog scale\] * Understand spoken and written English sufficiently to provide informed consent, participate in the intervention and complete study surveys Exclusion Criteria: * Lack of daily internet access * Inability to demonstrate comprehension of informed consent by correctly answering 4 out of 5 questions about the study * Significant visual/hearing impairment that does not allow use of the MM app's audiovisual presentations * Use of any meditation more than once a week in the last 3 months * Inability to provide or obtain an email address for registration to the AC intervention and/or communication with study staff * Inability to provide a phone number for communication with study staff
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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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Mayo Clinic
Jacksonville, Florida, 32224, United States
More trials for these conditions
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