Health Protection & Promotion for Oregon Correctional Officers (DOC HEALTH)
調査の概要
詳細な説明
Investigators will enroll up to 100 Correctional Officers from four Oregon Department of Corrections facilities for a randomized controlled 1-year assessment of the intervention. Participants will be evaluated at baseline, 6, and 12 months.
Primary study aims are; 1) Implement a randomized controlled efficacy trial of the Team-centered health promotion intervention, and assess its behavioral and occupational outcomes among COs, 2) Perform a cost analysis to determine the potential economic impact of this CO worksite health promotion program on illness/injury rates and disability claims, and 3) Determine relationships among specific intervention components with changes to behavior and occupational outcomes and assess by mediation analysis.
The intervention involves a scripted peer-taught interactive curriculum, which is delivered as twelve, 30 minute weekly sessions incorporated into a team's usual work time activities. The curriculum is designed to build understanding, healthy decision making skills and engender the social support of teammates; its content and scope reflects the core lifestyles activities used with fire fighters and law enforcement, along with adaptations for the needs of Correctional Officers in domains of the team-building, family support and psychological health.
Participant assessments include established survey instruments, physiological measures and selected laboratory parameters of outcomes and potential mediating variables at the individual, interpersonal and organizational levels. Intervention delivery and fidelity will be assessed. Multilevel and latent growth modeling and mediation analyses will be used to assess outcomes and the relationships among variables. At proposal completion there will be an evidenced-based, exportable occupational safety and health program for COs. Its critical components will be defined, and its benefits clearly determined.
研究の種類
入学 (実際)
段階
- 適用できない
連絡先と場所
研究場所
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Oregon
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Portland、Oregon、アメリカ、97239
- Oregon Health and Science University
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参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
Inclusion Criteria:
- security employee of a participating facility in the Oregon Department of Corrections
Exclusion Criteria:
- none
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：ランダム化
- 介入モデル：並列代入
- 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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介入なし：テストのみ
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実験的：検査と介入
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Intervention involves a scripted peer-taught interactive curriculum, which is delivered as twelve, 30 minute weekly sessions incorporated into a team's usual work time or overtime activities.
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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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Change from baseline in BMI at 6 and 12 months
時間枠：Baseline, 6 months, 12 months
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calculation of direct measurement of height and weight
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Baseline, 6 months, 12 months
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Change from baseline in Fruit and Vegetable Intake at 6 and 12 months
時間枠：Baseline, 6 months, 12 months
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questionnaire, NCI fruit/vegetables (Thompson et al., 2002)
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Baseline, 6 months, 12 months
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Change from baseline in Physical Activity at 6 and 12 months
時間枠：Baseline, 6 months, 12 months
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questionnaire; Elliot et al., 2007
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Baseline, 6 months, 12 months
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Change from baseline in Stress at 6 and 12 months
時間枠：Baseline, 6 months, 12 months
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questionnaire; Netemeyer RG et al, 1996; Cohen et al., 1983; Stanton et al, 2001
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Baseline, 6 months, 12 months
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Change from baseline in Sleep at 6 and 12 months
時間枠：Baseline, 6 months, 12 months
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questionnaire; Sorenson et al., 2011; Buysee et al., 1989; Buxton et al.; Rajaratnam et al., 2011
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Baseline, 6 months, 12 months
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Change from baseline in Alcohol Use at 6 and 12 months
時間枠：Baseline, 6 months, 12 months
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questionnaire
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Baseline, 6 months, 12 months
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Change from baseline in Tobacco Use at 6 and 12 months
時間枠：Baseline, 6 months, 12 months
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questionnaire; study specific development
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Baseline, 6 months, 12 months
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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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Change from baseline in Blood Pressure at 6 and 12 months
時間枠：Baseline, 6 months, 12 months
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direct measurement
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Baseline, 6 months, 12 months
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Change from baseline in Percent Body Fat at 6 and 12 months
時間枠：Baseline, 6 months, 12 months
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direct measurement via Bioelectric Impedance Analysis scale
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Baseline, 6 months, 12 months
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Change from baseline in Lipids and Lipoproteins at 6 and 12 months
時間枠：Baseline, 6 months, 12 months
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direct measurement via Cholestech LDX analyzer
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Baseline, 6 months, 12 months
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Change from baseline in Glucose at 6 and 12 months
時間枠：Baseline, 6 months, 12 months
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direct measurement via Cholestech LDX analyzer
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Baseline, 6 months, 12 months
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Cost-Effective Analysis
時間枠：12 months
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analysis of departmental aggregate data of injury rates and workers compensation claims
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12 months
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協力者と研究者
協力者
捜査官
- 主任研究者：Kerry S Kuehl, MD, DrPH、Oregon Health and Science University
研究記録日
主要日程の研究
研究開始
一次修了 (実際)
研究の完了 (実際)
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 (見積もり)
学習記録の更新
投稿された最後の更新 (見積もり)
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。