Mindfulness breathing tested for spinal cord injury – but study never started
NCT ID NCT06003712
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study aimed to see if a simple mindfulness breathing exercise could improve health and quality of life in people with spinal cord injury. Participants would have done a 10-15 minute guided breathing session three times a week for a month. However, the trial was withdrawn before any participants were enrolled, so no data was collected.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- mindfulness breathing exercise
- What this could lead to
- If it works, this could point toward a simple, low-cost way to help people with spinal cord injury feel better and improve their quality of life.
- What could go wrong
- This trial was withdrawn before enrolling anyone, so no results are available. The approach is very early and unproven, and any benefits are uncertain.
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
-
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.
- Expected to start
-
Aug 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2026
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 to 70 years
- 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: * Adult males and females aged 18-70 who are living with spinal cord injury * C5 to the T10 levels * Self-reported American Spinal Cord Injury Association (ASIA) Impairment Scale (AIS) A-D * Eligible participants must be able to understand and provide consent, be in good health operationalized as free from acute treatable illness, pressure injury, and cardiovascular disease. Exclusion Criteria: * Participants taking medications that alter chronotropic and pressor responses will be excluded. * Pregnant women will not be eligible to participate
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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.
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