Burnout Intervention During War for Hospital Staff in Ukraine
Professional Burnout Among Socially Significant Services in Ukraine in Wartime and Its Dynamics Within the Framework of Training Intervention for Burnout Prevention
調査の概要
詳細な説明
The investigators will identify eligible participants. An eligibility screening conducted in person or by telephone to ensure the inclusion criteria and to introduce the study is held by the study assistant. All participants must sign an informed consent after written and verbal study clarification. Participants will carry out self-reported measurements at baseline (T0), after the intervention phase of 2-5 days (T1; depending on the date of the second workshop day) and two weeks after finishing the intervention (T2). The group of participants participates in two workshop sessions lasting 2.5-3 hours each and occuring on separate days.
The training is practical in nature and aims to build and/or increase motivation to implement effective strategies for preventing burnout syndrome. Participants learn about scientifically proven methods of supporting mental health and receive tools for applying them in their professional and everyday lives.
The training program covers, in particular, the following areas: managing working time and workload; effective professional communication; developing stress-resistant thinking patterns; forming healthy lifestyle habits; methods of relaxation and overcoming stressful situations. .
The data management plan includes standard procedures for data-handling such as using anonymized identification codes for patient data. The data is being saved in an online database, only allowing researchers involved in the study to access the data.
研究の種類
入学 (推定)
段階
- 適用できない
連絡先と場所
研究連絡先
- 名前：Solveig Kemna, Dr. med.
- 電話番号：+49 30 450 517 542
- メール：solveig.kemna@charite.de
研究場所
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Kyiv Oblast
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Kyiv、Kyiv Oblast、ウクライナ、01601
- 募集
- National Medical University Bogomolets, Kyiv, Kyiv
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コンタクト：
- Lesia Sak
- 電話番号：(044) 234-92-76
- メール：lesia.sak@gmail.com
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参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
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.
研究計画
研究はどのように設計されていますか？
デザインの詳細
- 主な目的：防止
- 割り当て：なし
- 介入モデル：単一グループの割り当て
- マスキング：なし（オープンラベル）
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
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実験的：Burnout prevention intervention
The training is practical in nature and aims to build and/or increase motivation to implement effective strategies for preventing burnout syndrome. Participants learn about scientifically proven methods of supporting mental health and receive tools for applying them in their professional and everyday lives. The training program covers, in particular, the following areas: managing working time and workload; effective professional communication; developing stress-resistant thinking patterns; forming healthy lifestyle habits; methods of relaxation and overcoming stressful situations. |
The training is practical in nature and aims to build and/or increase motivation to implement effective strategies for preventing burnout syndrome. Participants learn about scientifically proven methods of supporting mental health and receive tools for applying them in their professional and everyday lives. The training program covers, in particular, the following areas: managing working time and workload; effective professional communication; developing stress-resistant thinking patterns; forming healthy lifestyle habits; methods of relaxation and overcoming stressful situations. |
この研究は何を測定していますか？
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Acceptability of the intervention
時間枠：Post-Intervention (after completion of 2 workshop sessions; 2-5 weeks from baseline)
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Feasibility will be indexed by participants attendance of the workshop sessions (>25% of sessions).
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Post-Intervention (after completion of 2 workshop sessions; 2-5 weeks from baseline)
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Feasibility of intervention
時間枠：Post-intervention (after completion of 2 workshop sessions; 2-5 days from baseline)
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Feasibility will be indexed by drop-out rate (<50% of participants); dropout is defined as having attended none of the sessions
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Post-intervention (after completion of 2 workshop sessions; 2-5 days from baseline)
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Acceptability of the intervention
時間枠：Post-intervention (after completion of 2 workshop sessions; 2-5 days from baseline)
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Acceptability will be indexed by the retention rate (having filled out the post-intervention questionnaire) of participants to the study (>30% of questionnaires).
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Post-intervention (after completion of 2 workshop sessions; 2-5 days from baseline)
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Acceptability of the intervention
時間枠：Post-intervention (after completion of 2 workshop sessions; 2-5 days from baseline)
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Acceptability will be assessed by using the Client Satisfaction Questionnaire (Attkisson & Zwick, 1982)
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Post-intervention (after completion of 2 workshop sessions; 2-5 days from baseline)
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Stress, anxiety and depression
時間枠：At baseline, post-intervention (after completion of 2 workshop sessions; 2-5 from baseline), and follow-up (2 weeks after last workshop session)
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The Depression Anxiety Stress Scale (Nilges & Essau, 2015) will be used to analyse symptoms of stress, anxiety and depression.
The main score ranges from 0 to 63, with higher scores indicating higher levels of depressive and anxiety symptoms.
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At baseline, post-intervention (after completion of 2 workshop sessions; 2-5 from baseline), and follow-up (2 weeks after last workshop session)
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Resilience
時間枠：At baseline, post-intervention (after completion of 2 workshop sessions; 2-5 from baseline), and follow-up (2 weeks after last workshop session)
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The Brief Resilience Scale (Smith 2009) will be used to assess the ability to bounce back or recover from stress.
The scale consists of six items rated on a 5-point Likert scale.
For interpretation, a mean score is calculated ranging from 1 to 5, with higher scores indicating greater resilience.
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At baseline, post-intervention (after completion of 2 workshop sessions; 2-5 from baseline), and follow-up (2 weeks after last workshop session)
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Traumatic stress
時間枠：At baseline, post-intervention (after completion of 2 workshop sessions; 2-5 days from baseline), and follow-up (2 weeks after last workshop session)
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The International Trauma Questionnaire (Cloitre 2018) will be used to assess traumatic stress.
Scores range from 0 to 25, with higher scores indicating greater somatic symptom burden
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At baseline, post-intervention (after completion of 2 workshop sessions; 2-5 days from baseline), and follow-up (2 weeks after last workshop session)
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Burnout - Exhaustion
時間枠：At baseline, post-intervention (after completion of 2 workshop sessions; 2-5 days from baseline), and follow-up (2 weeks after last workshop session)
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The Masslach Burnout Inventory (Masslach et al., 1997) will be used to assess burnout, with the domain of emotional exhaustion ranging from 0-54.
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At baseline, post-intervention (after completion of 2 workshop sessions; 2-5 days from baseline), and follow-up (2 weeks after last workshop session)
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Burnout - Depersonalization
時間枠：At baseline, post-intervention (after completion of 2 workshop sessions; 2-5 days from baseline), and follow-up (2 weeks after last workshop session)
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The Masslach Burnout Inventory (Masslach et al., 1997) will be used to assess burnout, with the domain of depersonalization ranging from 0-30.
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At baseline, post-intervention (after completion of 2 workshop sessions; 2-5 days from baseline), and follow-up (2 weeks after last workshop session)
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Burnout - Personal Accomplishment
時間枠：At baseline, post-intervention (after completion of 2 workshop sessions; 2-5 days from baseline), and follow-up (2 weeks after last workshop session)
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The Masslach Burnout Inventory (Masslach et al., 1997) will be used to assess burnout, with the domain of Personal Accomplishment ranging from 0-48.
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At baseline, post-intervention (after completion of 2 workshop sessions; 2-5 days from baseline), and follow-up (2 weeks after last workshop session)
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Burnout (custom measure)
時間枠：At baseline, post-intervention (after completion of 2 workshop sessions; 2-5 from baseline), and follow-up (2 weeks after last workshop session)
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The questionnaire consists of a dichotomous (yes/no) with variable scoring (ranging from 0 to 5) depending on the content of each item. Total score: the overall level of emotional burnout is calculated as the sum of scores across 50 items, with a total score range from 0 to 75. |
At baseline, post-intervention (after completion of 2 workshop sessions; 2-5 from baseline), and follow-up (2 weeks after last workshop session)
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協力者と研究者
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。
燃え尽き症候群のリスクの臨床試験
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Institute of Hematology & Blood Diseases Hospital...Hebei Taihe Chunyu Biotechnology Co., Ltd募集形質細胞白血病 | Ultra High Risk MM（UHR-MM）、18〜70歳、ASCTに適しています。次のUHR-MM定義のいずれかを満たします | 細胞遺伝学の超高リスク | 一次難治 | 早期進行 | 非麻痺性髄外浸潤 | R2-ISS-IV /MPSS-IV中国
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