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Talking it out: balint groups may ease nurse burnout

NCT ID NCT07278219

What the study statuses mean

This study's is highlighted.

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 Results may not be published yet.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.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
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.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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

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

30 people

The number who actually took part.

Started

Dec 2024

Finished

Apr 2025

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

Anyone

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: * 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.

Burnout, Psychological

As listed by the trial registrant

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

Contacts and locations

Locations

  • Bilecik Şeyh Edebali University, Faculty of Health Sciences

    Bilecik, Turkey (Türkiye)

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Other studies related to the condition(s) this trial covers.