Can relaxation techniques beat workplace stress? hospital trial halted early
NCT ID NCT05425511
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This study tested whether sophrology and neurolinguistic programming (NLP) could help hospital workers feel less stressed and improve their well-being. It included 103 staff members who reported high stress levels. The intervention involved breathing exercises, visualization, and relaxation sessions. However, the trial was terminated early, so the full results are not available.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- sophrology and neurolinguistic programming (NLP) sessions
- What this could lead to
- If successful, this could offer a simple, non-drug way to reduce stress and improve well-being for hospital staff.
- What could go wrong
- The trial was terminated early, so results are limited. It was a small, single-site study, and the benefits may not apply to all workers.
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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103 people
The number who actually took part.
- Started
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Mar 2023
- Finished
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Aug 2025
- 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 65 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: * worker (HCW or NHCW) from a hospital, * age between 18-65 years, * with a stress greater than 50 on a visual analogue scale (VAS) of stress, * person able to give an informed consent to participate in research and * affiliated with a Social Security scheme Exclusion Criteria: * Psychiatric, cardiovascular (heart failure, arrhythmia, etc.), hepatic (liver failure, etc.), renal (kidney failure, etc.), or endocrinological diseases (diabetes, etc.) judged by the investigator to be incompatible with the study because they may interfere with the measurements * Non-affiliated to a health insurance * Protected persons (minors, pregnant women, breastfeeding women, guardianship, curatorship, deprived of freedoms, safeguard of justice) * Refusal to participate
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Genom att skicka in godkänner du våra Användarvillkor
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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CHU clermont-ferrand
Clermont-Ferrand, France