Can biofeedback or movement therapy ease nurse burnout?

NCT ID NCT07827092

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

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Expanded access
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Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

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First seen Sep 18, 2026 ยท Last updated Sep 18, 2026

Summary

Researchers compare two six-week stress-management programs for female hospital nurses and midwives: heart rate variability biofeedback and eurythmy therapy. Participants are assigned at random to one program. Before and after, questionnaires and heart rate measurements track changes in burnout, stress, depression, sleep quality, and quality of life.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
heart rate variability biofeedback and eurythmy therapy
What this could lead to
If one approach works better, hospitals could offer nurses and midwives a practical way to lower burnout and improve sleep. That could help staff stay well in a job with heavy emotional demands.
What could go wrong
The trial is small, with 24 participants, so results may not apply to all nurses or midwives. Both programs take daily practice, and some people may not stick with them long enough to see a benefit.

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.

Participants

24 people

The number who actually took part.

Started

Jan 2012

Finished

Mar 2012

Lead sponsor

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

18 years and older

Sex

Female participants only

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show 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: * Written informed consent; Female; Working as a nurse or midwife Exclusion Criteria: * Cardiac pacemaker; Severe cardiac arrhythmias (assessed based on medical history)

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Conditions

The condition(s) this trial relates to.

Burnout, Psychological insomnia Occupational Stress

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • ARCIM Institute

    Filderstadt, Baden-Wurttemberg, 70794, Germany