Compassion overload? study tests if kindness training can beat burnout for doctors and nurses
NCT ID NCT07698379
First seen Jul 13, 2026 · Last updated Aug 27, 2026 · Updated 3 times
Summary
This study investigates whether an intensive compassion-based therapy program can reduce burnout and improve well-being in healthcare professionals. Around 180 doctors and nurses with symptoms of burnout, anxiety, depression, or stress will be randomly assigned to either an 8-session compassion therapy group or a relaxation program. Researchers will measure changes in burnout, emotional exhaustion, and personal accomplishment before, right after, and three months after the program.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Attachment-based compassion therapy
- What this could lead to
- If effective, this could offer a practical, short-term program to reduce burnout and improve mental health among healthcare workers.
- What could go wrong
- This is a small, early-stage study with 180 participants, and the results may not apply to all healthcare settings. The intervention is intensive (8 sessions over a weekend) and may not suit 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 180 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Apr 2028
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 75 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: 1. Active healthcare professionals (physicians and nurses) of both sexes. 2. Understanding of spoken and written Spanish. 3. Availability of a computer and internet connection. 4. Written informed consent. Exclusion Criteria: * Previous psychological treatment within the last year, or current psychological treatment. Presence of a severe uncontrolled medical, infectious, or degenerative disease that may interfere with affective symptoms. Presence of a mental disorder related to substance dependence/abuse, or any other disease affecting the central nervous system. Suicide risk, defined as a score of ≥2 on item 9 of the PHQ-9. Scheduled surgical intervention during the course of the study.
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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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Miguel Servet University Hospital
RECRUITINGZaragoza, Spain, 50009, Spain
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