Can a 13-minute daily chat with a colleague reduce burnout? new study aims to find out.
NCT ID NCT07637422
First seen Jun 27, 2026 · Last updated Sep 16, 2026 · Updated 2 times
Summary
This study tests an 8-week online program where healthcare professionals pair up daily for a 13-minute empathy and compassion exercise. The goal is to see if it improves mental health, resilience, and social skills. 666 healthcare workers in Germany and Austria will participate. The training is done via an app and focuses on listening and sharing emotions.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Empathy- and compassion-based socio-emotional mental training (EmCo)
- What this could lead to
- If it works, this could offer a practical, low-cost way to reduce burnout and loneliness among healthcare workers.
- What could go wrong
- This is a non-randomized waitlist-controlled trial, so results may be less reliable. The training is app-based and relies on daily partner practice, which 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 666 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Sep 2026
- Expected to finish
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Apr 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 to 68 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: 1. Between 18- and 65-years old. 2. Currently practicing a healthcare profession in Germany or Austria 2a. Belongs to one of the eligible state-regulated professions with legally defined independent responsibility for patient care, including diagnosis, treatment, psychotherapy, maternity care, or the overall nursing process (e.g., physician, psychotherapist, midwife, or registered nurse). 2b. Regular direct contact with patients or clients as part of the professional role (3) Proficient in German. (4) Informed consent. (5) No diagnosis of a psychiatric disorder within the past two years. (6) Stable internet access and necessary technical equipment (mobile phone with internet access). (7) No regular contemplative practice (≤ 50 hours total within the past six months); healthy population, non-clinical population. Exclusion Criteria: (8) Insufficient German proficiency. (9) Lack of stable internet access or required devices (mobile phone with internet access). (10) No informed consent. (11) Not currently practicing the profession, or working only in administrative, research, or teaching roles without patient contact. 11a. Professions are excluded if their primary role is supportive, assistive, emergency transport, preventive, counseling-focused, or based on prescribed adjunct therapies rather than independent responsibility for patient care, along with non-human-related professions. This includes, for example, nursing assistants, health psychologists, physiotherapists, occupational therapists, speech therapists, dietitians, massage therapists, paramedics (Sanitäter), and other comparable support or adjunct roles. 11b. No regular direct patient or client contact (12) Regular contemplative practice (\> 50 hours in the past six months (e.g., dyad, mindfulness, compassion-based practices). (13) Current psychiatric diagnosis or therapy, or reaching screening cutoffs on: * Patient Health Questionnaire-9 (PHQ-9 ; Martin et al., 2006 ; Löwe et al., 2004 ; Cutoff ≥ 15 ; or endorsing suicidality on the item 9), * Generalized Anxiety Disorder-7 (GAD-7; Löwe et al., 2007; Spitzer et al., 2006; Cutoff ≥ 15) * Toronto Alexithymia Scale-20 (TAS-20; Bagby et al., 1994; Ritz \& Kannapin, 2000; Cutoff ≥ 61) * Standardized Assessment of Personality - Abbreviated Scale (SAPAS; Moran et al., 2003; Söchtig et al., 2012, Cutoff ≥ 4).
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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
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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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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Social Neuroscience Lab manages the Edu:Social study-based application (app)
Berlin, State of Berlin, 10557, Germany
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Other studies related to the condition(s) this trial covers.
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