DOC HEALTH: Health Protection & Promotion for Oregon Correctional Officers

Sponsor
Oregon Health and Science University (Other)
Overall Status
Completed
CT.gov ID
NCT02098603
Collaborator
National Institute for Occupational Safety and Health (NIOSH/CDC) (U.S. Fed), Oregon Healthy Workforce Center (Other)
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Study Details

Study Description

Brief Summary

More than 530,000 individuals work as US Correctional Officers (COs) responsible for overseeing the approximately 1.6 million offenders who are incarcerated at any given time in the United States. Prison work is regarded as one of the most difficult occupations with CO's having one of the highest nonfatal injury rates of all U.S. occupations. The few studies done on CO's show high levels of stress, cardiovascular disease, high job burnout, increased sick leave rates and absenteeism, and decreased quality of life leading to premature illness/injury and high employer healthcare costs. Many of these conditions could be prevented by specific training activities and healthier lifestyles. The investigators wish to test a worksite-based, health promotion curriculum in COs with the overall hypothesis that the program will improve health and decrease injuries. The program proposed would be the first occupational intervention to improve the safety, and emotional and physical health of those who are charged with the complex task of prison work protecting the investigators communities. If successful, this proposal would result in an exportable, practical occupational safety and health program applicable for use by local, state, and federal correctional facilities.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Testing & Intervention
N/A

Detailed Description

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.

Study Design

Study Type:
Interventional
Actual Enrollment :
86 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Health Protection & Promotion for Oregon Correctional Officers
Study Start Date :
Jan 1, 2013
Actual Primary Completion Date :
Aug 1, 2014
Actual Study Completion Date :
Sep 1, 2014

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Testing Only

Experimental: Testing & Intervention

Behavioral: Testing & Intervention
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.

Outcome Measures

Primary Outcome Measures

  1. Change from baseline in BMI at 6 and 12 months [Baseline, 6 months, 12 months]

    calculation of direct measurement of height and weight

  2. Change from baseline in Fruit and Vegetable Intake at 6 and 12 months [Baseline, 6 months, 12 months]

    questionnaire, NCI fruit/vegetables (Thompson et al., 2002)

  3. Change from baseline in Physical Activity at 6 and 12 months [Baseline, 6 months, 12 months]

    questionnaire; Elliot et al., 2007

  4. Change from baseline in Stress at 6 and 12 months [Baseline, 6 months, 12 months]

    questionnaire; Netemeyer RG et al, 1996; Cohen et al., 1983; Stanton et al, 2001

  5. Change from baseline in Sleep at 6 and 12 months [Baseline, 6 months, 12 months]

    questionnaire; Sorenson et al., 2011; Buysee et al., 1989; Buxton et al.; Rajaratnam et al., 2011

  6. Change from baseline in Alcohol Use at 6 and 12 months [Baseline, 6 months, 12 months]

    questionnaire

  7. Change from baseline in Tobacco Use at 6 and 12 months [Baseline, 6 months, 12 months]

    questionnaire; study specific development

Secondary Outcome Measures

  1. Change from baseline in Blood Pressure at 6 and 12 months [Baseline, 6 months, 12 months]

    direct measurement

  2. Change from baseline in Percent Body Fat at 6 and 12 months [Baseline, 6 months, 12 months]

    direct measurement via Bioelectric Impedance Analysis scale

  3. Change from baseline in Lipids and Lipoproteins at 6 and 12 months [Baseline, 6 months, 12 months]

    direct measurement via Cholestech LDX analyzer

  4. Change from baseline in Glucose at 6 and 12 months [Baseline, 6 months, 12 months]

    direct measurement via Cholestech LDX analyzer

  5. Cost-Effective Analysis [12 months]

    analysis of departmental aggregate data of injury rates and workers compensation claims

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 70 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • security employee of a participating facility in the Oregon Department of Corrections
Exclusion Criteria:
  • none

Contacts and Locations

Locations

Site City State Country Postal Code
1 Oregon Health and Science University Portland Oregon United States 97239

Sponsors and Collaborators

  • Oregon Health and Science University
  • National Institute for Occupational Safety and Health (NIOSH/CDC)
  • Oregon Healthy Workforce Center

Investigators

  • Principal Investigator: Kerry S Kuehl, MD, DrPH, Oregon Health and Science University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Kerry Kuehl, Professor of Medicine, Oregon Health and Science University
ClinicalTrials.gov Identifier:
NCT02098603
Other Study ID Numbers:
  • e7925
  • U19OH010154
First Posted:
Mar 28, 2014
Last Update Posted:
Oct 30, 2015
Last Verified:
Oct 1, 2015
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 30, 2015