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Corrections Work's Adverse Effects and a Total Worker Health Program to Enhance Well-being

Corrections Work's Adverse Effects and a Total Worker Health Program to Enhance Well-being

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05608889
Enrollment
100
Registered
2022-11-08
Start date
2022-11-09
Completion date
2023-12-31
Last updated
2023-02-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Behavior, Mental Health Wellness 1, Occupational Stress, Safety Issues

Keywords

Health Promotion, Mindfulness, Occupational Health, Total Worker Health, Safety

Brief summary

Conduct a quasi-experimental pre-post study of a mindfulness-enhanced, web/app-enabled, scalable Total Worker Health (TWH) program among higher stress Corrections Professionals. The primary outcomes relate to behaviors promoted by the program: being mindful/reduced stress/improved mood; healthier eating; more physical activity; greater restorative sleep; improved work-life balance and greater positive feelings about the organization.

Detailed description

This proposed project will assess an innovative, scalable total worker health and wellness intervention among high stress Corrections Professionals. As stated in the proposal request, organizational and interpersonal factors have been associated with significant stress among Corrections Professionals, but there is limited assessment of effective and feasible interventions to mitigate these stress factors. Our current research has established robust constructs for characteristics of the organization and work environment, noting significant relationships with perceived stress. This critical understanding along with corresponding adverse mental and physical effects informs our proposed intervention to reduce potential stressors, enhance wellbeing, improve work performance, and reduce health care costs. This project will include a prospective interrupted time-series effectiveness trial of a mindfulness-enhanced, website/application-based, scalable Total Worker Health (TWH) program among higher risk corrections personnel working in restrictive housing units. Quantitative outcomes will include process measures; validated self-report indices of primary and secondary outcomes, and proximal potentially mediating factors; anthropometrics; laboratory studies of inflammation, vascular reactivity, and cellular aging; measures of job performance and health care costs. Qualitative measures will provide a deeper understanding of the quantitative findings. At program conclusion, there will be a cost effective easy to use work based health and wellness program tailored to corrections departments ready for dissemination. The robust dissemination plan includes coordinating the website and digital materials with the American Correctional Association marketing and media campaign site along with presentations at national corrections conferences making this freely available to all law enforcement and corrections personnel and agencies.

Interventions

BEHAVIORALTotal Worker Health Mindfulness Enhanced Program

The intervention will be delivered during 12, 45-minute weekly meetings of Correctional Professionals while on shift. Those sessions will be a combination of a video, mindfulness activity, and a group learning activity. It will conclude with members stating personal goals that will be followed up at the next meeting. Sessions will be scripted to make them easy to implement with high fidelity, and include tasks, learning activities, and wrap-up with practice instructions for each week. Coworkers will be responsible for running the sessions, which promotes shared norms and social support.

Sponsors

Kerry Kuehl
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

This study will use a quasi-experimental pre-post design to compare values of outcome measures at the three times points: baseline, immediately post-intervention (3 months after baseline), and follow-up (9 months after baseline). Randomization of the intervention is not feasible at the individual level due to contamination effects within a site and no appropriate control condition. Furthermore, as each of the sites is unique, a randomized cluster design would not be able to account for confounders since there are only three sites, each with institutional differences. An advantage of the pre-post design is that each participant will act as their own control, increasing the power of the study.

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

\- Currently employed as a corrections professional at participating Oregon Department of Corrections facilities (Coffee Creek Correctional Facility and Oregon State Correctional Institution) for at least one month

Exclusion criteria

\- Those who are not employed with participating Oregon Department of Corrections facilities listed above.

Design outcomes

Primary

MeasureTime frameDescription
Change in Perceived stressChange between timepoints: Before intervention implementation, 3 months after the intervention completion, and 9 months after intervention completionPerceived Stress Scale Short Form (PSS-4)
Change in MoodChange between timepoints: Before intervention implementation, 3 months after the intervention completion, and 9 months after intervention completionThe Positive and Negative Affect Schedule (PANAS); Profile of Mood States Short Form (POMS-SF)
Change in Eating HabitsChange between timepoints: Before intervention implementation, 3 months after the intervention completion, and 9 months after intervention completionRelevant excerpts from the National Cancer Institute's fruit and vegetable all day screener and Diet History Questionnaire (DHQ), percent calories from fat, and health dietary behaviors (Elliot et al., 2007; Kuehl et al., 2014)
Change in Physical ActivityChange between timepoints: Before intervention implementation, 3 months after the intervention completion, and 9 months after intervention completionChange in physical activity will be assessed using this survey question: How many days per week did you exercise or take part in moderate physical activities that increased your breathing a bit for a total of at least 30 minutes during the day (such as brisk walking or bicycling)?. This is measured in days per week (with a scale of 0-7 days). Relevant excerpts from previous research on physical activity behaviors (Elliot et al., 2007).
Change in SleepChange between timepoints: Before intervention implementation, 3 months after the intervention completion, and 9 months after intervention completionChange in sleep will be assessed using this survey question: In the past seven days, I had trouble sleeping measures in a scale of 1-5 (1=very good, 2=good, 3=fair, 4=poor, 5=very poor). Short Form from the National Institutes of Health's Patient-Reported Outcomes Information System's Sleep Disturbance (PROMIS-SD-SF); Pittsburgh Sleep Quality Index (PSQI)
Change in Work-life balanceChange between timepoints: Before intervention implementation, 3 months after the intervention completion, and 9 months after intervention completionChange in work-life balance will be assessed using this survey question: In the past month, how often have you felt that you were able to control the important things in your life? measured in a scale of 1-5 (1=none of the time, 2=a little of the time, 3=some of the time, 4=most of the time, 5=all of the time). Ballin et al., 2021.
Change in Feelings about organizationChange between timepoints: Before intervention implementation, 3 months after the intervention completion, and 9 months after intervention completionChange in feelings about organization will be assessed using this survey question: The Department of Corrections has processes in place that improve my work environment measured with a scale from 1-5 (1=strongly disagree, 2=disagree, 3=neither disagree or agree, 4=agree, 5=strongly agree). Ballin et al., 2021.

Secondary

MeasureTime frameDescription
Change in Tumour Necrosis Factor alphaChange between timepoints: Before intervention implementation, 3 months after the intervention completion, and 9 months after intervention completionChanges in Tumour Necrosis Factor alpha will be measured in pg/mL.
Change in Blood PressureChange between timepoints: Before intervention implementation, 3 months after the intervention completion, and 9 months after intervention completionChanges in blood pressure will be measured in mmHg.
Change in Worker's Compensation ClaimsChange between timepoints: Before intervention implementation, 3 months after the intervention completion, and 9 months after intervention completionChange in Worker's Compensation Claims from Oregon Department of Corrections Human Resources data that report the number of worker's compensation claims there are.
Change in telomere lengthChange between timepoints: Before intervention implementation, 3 months after the intervention completion, and 9 months after intervention completionChanges in telomere length will be measured in kb.
Change in Life SatisfactionChange between timepoints: Before intervention implementation, 3 months after the intervention completion, and 9 months after intervention completionChange in life satisfaction will be assessed with the survey question: Would you say your general health is: with a scale of a)excellent, b)very good, c)good, d)fair, and e)poor.
Change in Body Mass IndexChange between timepoints: Before intervention implementation, 3 months after the intervention completion, and 9 months after intervention completionChange in Body mass index will measured in kg/m2.
Change in Vascular ReactivityChange between timepoints: Before intervention implementation, 3 months after the intervention completion, and 9 months after intervention completionChanges in Vascular reactivity will be measured in adjusted temperature rebound (aTR) between 0-2.
Change in C-reactive ProteinChange between timepoints: Before intervention implementation, 3 months after the intervention completion, and 9 months after intervention completionChanges in C-reactive protein will be measured in mg/L.
Change in Cytokine Interleukin IL-6Change between timepoints: Before intervention implementation, 3 months after the intervention completion, and 9 months after intervention completionChanges in cytokine Interleukin IL-6 will be measured in pg/mL.
Change in Days InjuredChange between timepoints: Before intervention implementation, 3 months after the intervention completion, and 9 months after intervention completionChange in Worker's Compensation Claims from Oregon Department of Corrections Human Resources data that report the number of missed days due to work-related illness or injury

Countries

United States

Contacts

Primary ContactKerry S. Kuehl, MD, Dr.PH
kuehlk@ohsu.edu503-494-5991
Backup ContactCarol Defrancesco, MALS, RDN, LD
defrance@ohsu.edu503-310-5036

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026