Breathe away trauma: simple breathing drill may stop PTSD
NCT ID NCT04701723
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This pilot study tests whether a breathing technique called cardiac coherence can prevent chronic PTSD in people who recently experienced a traumatic event. 44 participants with acute stress disorder will practice the breathing exercises for 3 months. The goal is to see if this simple, drug-free method can stop PTSD from developing.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- cardiac coherence breathing training
- What this could lead to
- If it works, this could offer a simple, drug-free way to prevent chronic PTSD after trauma.
- What could go wrong
- This is a very small pilot study (44 people) with no control group, so results may not be conclusive. The intervention is also early-stage 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 44 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2021
- Expected to finish
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May 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: * patients seen at medico-psychological emergency cell * patients with an acute stress disorder, diagnosed by DSM-5 * patients who have experienced a potentially traumatic event for the last 3-15 days (vctim or witness) * patients able to read and write in French language * person affiliated or beneficiary of a social security scheme. * person who agrees to participate in the study Exclusion Criteria: * patients with respiratory pathology not allowing cardiac coherence training * patients currently practicing a regular respiratory control technique or within the last 6 months * patients taking beta-blocker, betamimetic, anti-arrhythmic, opioid, antidepressant * patients with a pacemaker or suffering from severe cardiac illness * patients with non-stabilized psychiatric disorder at inclusion * patient taking benzodiazepine unable to wean off in the week following the inclusion * patients with addiction * patients with a cognitive deficit * patients under guardianship or curatorship, under judicial supervision
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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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Etablissement Public de Santé Mentale de La Réunion
RECRUITINGSaint-Paul, 97460, Reunion
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