About this trial
The project endeavours to investigate the feasibility and acceptability of a psychoeducational training intervention for professional burnout and related psychological variables among both medical and non-medical workers in Ukraine during wartime. A secondary aim is to assess the outcomes of the intervention at baseline (T0), post-intervention (T1), and follow-up (single-arm feasibility design). The participants receive two days of a psychoeducational training focusing on different facets of burnout prevention.
Eligibility criteria
Qualifiers
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.
Disqualifiers
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.
Trial design
Treatments tested in this trial
- Burnout prevention
Treatment groups
Locations
1Map coordinates are unavailable for these locations. Locations are shown below instead.
Sponsors and collaborators
Charite University, Berlin, Germany
Lead sponsor
Bogomolets National Medical University
Collaborator