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Can a Two-Day training shield ukrainian workers from burnout?

NCT ID NCT07620756

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 tests whether a two-day psychoeducational training can help prevent burnout among medical and non-medical workers in Ukraine during wartime. Eighty participants will receive the training and be assessed before, after, and at follow-up. The main goal is to see if the program is feasible and acceptable, not yet to prove it works.

What this could mean

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

Active substance
psychoeducational training program for burnout prevention
What this could lead to
If it works, this could provide a practical, low-cost way to reduce burnout among essential workers in high-stress environments like wartime.
What could go wrong
This is a small, early feasibility study with only 80 participants and no control group. Results may not apply broadly, and the training may not reduce burnout significantly.

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

About 80 people

The number the study aims to enrol. It can still change while the study runs.

Started

Mar 2026

Expected to finish

Nov 2026

An estimate. End dates often move.

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 to 99 years

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: * Respondents must be 18 years of age or older. * Sufficient command of the Ukrainian language to understand the materials and complete the questionnaires. * Voluntary informed consent to participate in the study and data processing. * Permanent residence in Ukraine at the time of participation in the study. * Belonging to the working civilian population (medical or non-medical workers). * Technical ability to participate online (access to the internet and an electronic device for completing questionnaires and participating in training). * Skills/ability to attend online sessions and use smartphone chat for communication. * Willingness to complete questionnaires at specified time points (T0, T1, T2). Exclusion Criteria: * Inability to provide informed consent or limited legal capacity. * Presence at the time of inclusion of a condition that significantly complicates participation in the study or adherence to the protocol (acute psychotic episodes, manic states, severe cognitive impairment, decompensated somatic diseases, active dependence on psychoactive substances), Severe mental state or pronounced mental distress requiring urgent specialized care. * Current intensive psychotherapeutic or psychiatric treatment that may significantly affect the assessed indicators. * Lack of technical ability to participate in online training or complete questionnaires at specified times. * Inability to use a smartphone or significant visual, hearing, or speech impairments that prevent interaction with the application and completion of questionnaires. * Refusal to participate or withdrawal of informed consent at any stage of the study.

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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.

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. 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

  • National Medical University Bogomolets, Kyiv, Kyiv

    RECRUITING

    Kyiv, Kyiv Oblast, 01601, Ukraine