Talking it out: balint groups may ease nurse burnout
NCT ID NCT07278219
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether a Balint-based group intervention could reduce burnout and improve communication skills in nurses. Thirty nurses were randomly assigned to either six weekly online Balint sessions or their usual routine. Burnout and communication skills were measured before, right after, and at one and three months after the sessions.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Balint-based group intervention (behavioral)
- What this could lead to
- If it works, this could offer a simple, low-cost way to reduce burnout and improve communication among nurses.
- What could go wrong
- This is a very small study (30 nurses) with no blinding, so results may not apply widely. The intervention is short (6 sessions) and effects may not last.
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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30 people
The number who actually took part.
- Started
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Dec 2024
- Finished
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Apr 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 years and older
- 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: * having worked as a nurse in the same clinical setting for at least one year * providing informed consent to participate Exclusion Criteria: * presence of a communication impairment that could hinder participation (e.g., hearing or speech disorder) Discontinuation Criteria: * Voluntary withdrawal from the study * Failure to attend at least two sessions * Incomplete or missing data on the study instruments
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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.
Contacts and locations
Locations
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Bilecik Şeyh Edebali University, Faculty of Health Sciences
Bilecik, Turkey (Türkiye)
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