BridgeMD
New treatment option for Burnout Risk
Official title Burnout Intervention During War for Hospital Staff in Ukraine
ClinicalTrials.gov ID: NCT07620756
What this study is testing
- What it's testing
- 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).
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 99. Healthy volunteers may be eligible.
You may be able to join if
- 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).
You likely can't join if
- 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...
- 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...
- Refusal to participate or withdrawal of informed consent at any stage of the study.
See the full eligibility 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).
- 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...
- 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.
The study team makes the final eligibility decision.
Where it's taking place
- Kyiv, Kyiv Oblast, Ukraine
Compensation & support
A stipend or compensation may be offered.
Compensation mentioned.
ClinicalTrials.gov doesn't provide a reliable structured field for payment or travel support - confirm details with the study team.
Questions & answers
Do participants get paid in this trial?
This study's listing includes signals that participants may be compensated or receive a stipend. Amounts vary and are set by the study team - confirm the details with them.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years to 99 years. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Kyiv, Kyiv Oblast, Ukraine. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.