Feasibility of Implementing the Internet-Delivered Stress Recovery Intervention FOREST for Healthcare Staff in a Real-World Healthcare Setting (FOREST-IN)
調査の概要
詳細な説明
The feasibility of implementing the evidence-based, internet-delivered stress recovery intervention FOREST for healthcare staff in a real-world healthcare setting will be evaluated using a single-arm pre-post study design. The study aims to assess the feasibility of implementing the intervention within a hospital setting and to obtain preliminary estimates of changes in stress recovery and mental health outcomes to inform broader implementation across healthcare settings. Information about the intervention and the study will be disseminated within participating healthcare settings. Interested healthcare staff will complete an online eligibility screening. Individuals who meet the inclusion criteria will be invited to provide informed consent and complete the baseline assessment before being enrolled in and granted access to the FOREST intervention.
The FOREST intervention consists of six sessions (Introduction, Psychological Detachment, Distancing, Mastery, Control, and Keeping the Change Alive) delivered over a four-week period. Each session includes psychoeducational content presented through text and video materials, as well as practical stress recovery exercises. Participants will also have access to support from a trained psychologist on demand throughout the intervention.
Assessments will be conducted at baseline, immediately after the four-week intervention, and at a 12-week follow-up after baseline. The study's primary outcomes will assess implementation at the individual level, guided by Proctor et al.'s Implementation Outcomes Framework to evaluate acceptability and appropriateness, alongside intervention uptake (initiation), and complemented by feasibility and process indicators capturing reach, recruitment, engagement, and retention. Secondary outcomes will provide preliminary estimates of changes in stress recovery and other mental health outcomes.
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：Austeja Dumarkaite, PhD
- 電話番号：+37052686952
- メール：austeja.dumarkaite@fsf.vu.lt
研究連絡先のバックアップ
- 名前：Evaldas Kazlauskas, PhD
- 電話番号：+37052686952
- メール：evaldas.kazlauskas@fsf.vu.lt
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:
- being at least 18 years old
- working in a healthcare setting;
- understanding Lithuanian;
- living in Lithuania;
- having access to an internet-enabled device.
Exclusion Criteria: No additional exclusion criteria will be applied in order to maximize inclusiveness and reflect real-world implementation.
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 |
|---|---|
|
実験的：Intervention group
The intervention group will get a four-week internet-delivered stress recovery intervention FOREST.
|
The internet-delivered stress recovery intervention FOREST consists of six sessions (Introduction, Psychological Detachment, Distancing, Mastery, Control, and Keeping the Change Alive) delivered over a four-week period.
Each session includes psychoeducational content presented through text and video materials, as well as practical stress recovery exercises.
Participants also have access to support from a trained psychologist on demand throughout the intervention.
|
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 |
|---|---|---|
|
Reach
時間枠：Through completion of recruitment, up to 9 months.
|
Measurement: study recruitment records. Reach will be assessed as the proportion of the target healthcare workforce that enrolls in the intervention. It will be calculated as the number of enrolled participants divided by the estimated number of healthcare staff in the target workforce, expressed as a percentage. |
Through completion of recruitment, up to 9 months.
|
|
Recruitment
時間枠：Through completion of recruitment, up to 9 months.
|
Measurement: Study screening, eligibility, and informed consent records. Recruitment will be assessed as the number and proportion of eligible healthcare staff who provide informed consent and enroll in the study. |
Through completion of recruitment, up to 9 months.
|
|
Intervention uptake
時間枠：Through completion of the intervention period, up to 10 months.
|
Measurement: FOREST intervention platform usage records. Intervention uptake will be assessed as the number and proportion of enrolled participants who initiate the intervention by completing the first FOREST session. |
Through completion of the intervention period, up to 10 months.
|
|
Number of intervention sessions completed
時間枠：Through completion of the intervention period, up to 10 months.
|
Number of intervention sessions completed will be assessed using FOREST intervention platform usage records.
The number of FOREST intervention sessions completed by each participant will be recorded.
|
Through completion of the intervention period, up to 10 months.
|
|
Percentage of participants completing all six intervention sessions
時間枠：Through completion of the intervention period, up to 10 months.
|
Percentage of participants completing all six FOREST intervention sessions will be assessed using FOREST intervention platform usage records.
The percentage of participants who complete all six FOREST intervention sessions will be calculated as the number of participants completing all six sessions divided by the total number of participants who initiated the intervention, multiplied by 100.
|
Through completion of the intervention period, up to 10 months.
|
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Retention
時間枠：Through completion of the 12-week follow-up, up to 12 months.
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Measurement: Study assessment completion records. Retention will be assessed as the number and proportion of enrolled participants who complete the post-intervention assessment and the 12-week follow-up assessment. Unit of Measure: Number and percentage of participants completing each assessment time point. |
Through completion of the 12-week follow-up, up to 12 months.
|
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Intervention acceptability
時間枠：Through completion of the post-intervention assessment period, up to 10 months.
|
Measurement: Post-intervention acceptability questions developed by study researchers. Acceptability will be assessed using post-intervention participant questions evaluating satisfaction with the FOREST intervention, perceived usefulness, and likelihood of recommending the intervention to colleagues. Each item will be reported according to its response scale, with descriptive summary statistics presented for participant responses. Higher scores indicate more pronounced acceptability. |
Through completion of the post-intervention assessment period, up to 10 months.
|
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Intervention appropriateness
時間枠：Post-intervention assessment, up to 10 months.
|
Measurement: Post-intervention appropriateness question developed by study researchers. Appropriateness will be assessed using a post-intervention participant question evaluating participants' perceptions of whether the FOREST intervention is relevant and suitable for healthcare staff working in a hospital setting. The item will be reported according to its response scale, with descriptive summary statistics presented for participant responses. A higher score indicates more pronounced appropriateness. |
Post-intervention assessment, up to 10 months.
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Changes in stress recovery
時間枠：Baseline, post-test after four weeks, follow-up after 12 weeks
|
Changes in stress recovery are measured.
The Recovery Experiences Questionnaire (Sonnentag & Fritz, 2007) is a self-report measure consisting of 16 questions.
All items are answered on a 5-point Likert scale ranging from 1 (Totally disagree) to 5 (Totally agree).
A higher score indicates more pronounced stress recovery.
|
Baseline, post-test after four weeks, follow-up after 12 weeks
|
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Changes in perceived stress
時間枠：Baseline, post-test after four weeks, follow-up after 12 weeks
|
Changes in perceived stress are measured.
Perceived Stress Scale (PSS-4, Cohen et al., 1983) is a self-report measure consisting of four questions.
All items are answered on a 5-point Likert scale ranging from 0 (Never) to 4 (Very often).
A higher score indicates more pronounced perceived stress.
|
Baseline, post-test after four weeks, follow-up after 12 weeks
|
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Changes in symptoms of anxiety and depression
時間枠：Baseline, post-test after four weeks, follow-up after 12 weeks
|
Changes in symptoms of anxiety and depression are measured.
The Patient Health Questionnaire-4 (PHQ-4; Kroenke et al., 2009) is a self-report measure consisting of four questions.
All items are answered on a 4-point Likert scale ranging from 0 (Not at all) to 3 (Nearly every day).
A higher score indicates more pronounced symptoms of anxiety and depression.
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Baseline, post-test after four weeks, follow-up after 12 weeks
|
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Changes in mental well-being
時間枠：Baseline, post-test after four weeks, follow-up after 12 weeks
|
Changes in mental well-being are measured.
Well-being Index (WHO-5, Bech, 2004) is a self-report measure consisting of five questions.
All items are answered on a 6-point Likert scale ranging from 0 (At no time) to 5 (All of the time).
A higher score indicates more pronounced mental well-being.
|
Baseline, post-test after four weeks, follow-up after 12 weeks
|
協力者と研究者
スポンサー
捜査官
- 主任研究者：Austeja Dumarkaite, PhD、Vilnius University
研究記録日
主要日程の研究
研究開始 (推定)
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
本研究に関する用語
その他の研究ID番号
- 3.7 E-10000-KT-2858
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