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Completed

NCT Number: NCT03784846

Mindfulness-Based Resilience Training for Aggression, Health, and Stress Among Law Enforcement Officers

Law enforcement officers (LEOs) are exposed to significant stressors, elevating their risk for aggression and excessive use of force, as well as mental health consequences, including post-traumatic stress disorder, burnout, alcohol misuse, depression, and suicide. The proposed study will identify, optimize and refine best clinical and research practices across two sites to ensure success in a future multisite efficacy trial assessing preventative effects of Mindfulness-Based Resilience Training on physiological, behavioral, and psychological outcomes.

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Key information

Age range

21 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of New Mexico, Albuquerque, New Mexico, United States

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About this study

Law enforcement officers (LEOs) are exposed to significant stressors, elevating their risk for aggression and excessive use of force. Such dysfunctional stress reactivity can lead to devastating consequences for their community, including unjustified shootings, severe beatings, and fatal chokings. It can also lead to serious consequences for the LEOs, including elevated incidence of post-traumatic stress disorder, burnout, alcohol misuse, depression, and suicide. A recent meta-analysis of LEO stress reduction programs found little evidence to demonstrate that such approaches are effective, highlighting the urgent need for preventive interventions targeting the stress inherent to policing. Mindfulness training is a promising approach with high-stress populations that has been shown effective in reducing stress and increasing resilience. In a recent pilot feasibility study (R21AT008854), the study team established initial feasibility, acceptability, and adherence to procedures in a single-site RCT assessing Mindfulness-Based Resilience Training (MBRT), a preventive intervention designed to improve LEO mental health and resilience, and reduce aggression and excessive use of force. The R21 data suggest physiological mechanisms and potential clinical benefit in a sample of LEOs. Relative to waitlist control, MBRT participants showed improvements in stress reactivity, aggression, burnout, occupational stress, sleep disturbance, and psychological flexibility. Implemented at two sites, the proposed study is designed to establish optimal protocols and procedures for a future full-scale, multi-site trial assessing effects of MBRT versus an attention control (Stress Management Education) and a no-intervention control, on physiological, behavioral, and psychological outcomes. To prepare for this future clinical trial, this study will: a) enhance efficiency of recruitment, engagement and retention; b) optimize lab, assessment, and data management procedures; c) optimize intervention training and ensure fidelity to intervention protocols; and d) assess participant experience and optimize outcome measures across sites. The long-term objective of this line of research is to develop an intervention that will reduce violence and increase resilience among LEOs, as well as yield significant benefits for communities and residents they serve.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • be 21-65 years old (age limitations for both police departments),
  • demonstrate English fluency,
  • be a sworn, full-time, active status law enforcement officer,
  • agree to random assignment to condition, and
  • be willing to complete assessments at multiple time points and attend intervention groups

Exclusion criteria

  • previous participation in MBSR, MBRT or a similar mindfulness course,
  • score in the severe range on brief screening measures of depression, suicidal ideation, alcohol use, or PTSD, or
  • unable or unwilling to give written informed consent.

Treatment and study plan

Mindfulness-Based Resilience Training

Behavioral

MBRT is an 8-week program combining training in standardized mindfulness practices targeting factors that facilitate resilience, CBT, and psychoeducation. It contains experiential and didactic exercises including body scan, sitting and walking meditation, mindful movement and discussions.

Stress Management Education

Behavioral

SME was designed as an active control condition for other Mindfulness-Based Intervention trials. SME uses a group-based didactic approach with modules on physiological and dietary effects of stress, time management, sleep physiology and insomnia, nutrition, exercise, stress hardiness, and factors mitigating impacts of stress.

Primary outcomes

  1. Change in Aggression

    Time frame: baseline, post-intervention (week 8), 3-month followup, 6-month followup

    Buss-Perry Aggression Questionnaire-Short Form. Scores range from 1-5, with higher scores indicating greater aggression.

Secondary outcomes

  1. Change in C-reactive Protein

    Time frame: baseline, post-intervention (8 weeks), 3 month followup

    Blood spot analysis of high-sensitivity C-reactive protein.

  2. Change in Interleukin-6

    Time frame: baseline, post-intervention (8 weeks), 3 month followup

    Blood spot analysis of interleukin-6.

  3. Change in Interleukin-10

    Time frame: baseline, post-intervention (8 weeks), 3 month followup

    Blood spot analysis of interleukin-10.

  4. Change in Tumor Necrosis Factor-alpha

    Time frame: baseline, post-intervention (8 weeks), 3 month followup

    Blood spot analysis of tumor necrosis factor-alpha.

  5. Change in Psychological Resilience

    Time frame: baseline, post-intervention (8 weeks), 3 month followup, 6 month followup

    Brief Resilience Scale. Scores range from 1-5, with higher scores indicating greater resilience.

  6. Change in Alcohol Use

    Time frame: baseline, post-intervention (8 weeks), 3 month followup, 6 month followup

    Patient Reported Outcome Measurement System (PROMIS) Alcohol Use. Scores range from 39-77, with higher scores indicating greater alcohol use.

  7. Change in Alcohol Use Negative Consequences

    Time frame: baseline, post-intervention (8 weeks), 3 month followup, 6 month followup

    Patient Reported Outcome Measurement System (PROMIS) Alcohol Use Negative Consequences.Scores range from 39-77, with higher scores indicating greater alcohol use negative consequences.

  8. Change in Depression

    Time frame: baseline, post-intervention (8 weeks), 3 month followup, 6 month followup

    Patient Reported Outcome Measurement System (PROMIS) Depression. Scores range from 38-80, with higher scores indicating more depression.

  9. Change in Suicidal Thinking

    Time frame: baseline, post-intervention (8 weeks), 3 month followup, 6 month followup

    Concise Heath Risk Tracking Scale-Self-Report. Scores range from 7-35, with higher scores indicating greater suicidal ideation.

  10. Change in Trauma Symptoms

    Time frame: baseline, post-intervention (8 weeks), 3 month followup, 6 month followup

    PTSD Checklist for DSM-5. Scores ranges from 0-80, with higher scores indicating greater PTSD symptoms.

  11. Change in Burnout

    Time frame: baseline, post-intervention (8 weeks), 3 month followup, 6 month followup

    Oldenburg Burnout Inventory. Scores range from 1-4, with higher scores indicating greater burnout.

  12. Change in Sustained Attention

    Time frame: baseline, post-intervention (8 weeks), 3 month followup, 6 month followup

    Sustained Attention to Response Task. A computer-based go/no-go task that requires participants to withhold behavioral response to a single, infrequent target presented amongst a background of frequent non-targets. Increased errors indicates less sustained attention.

  13. Change in Perceived Stress

    Time frame: baseline, post-intervention (8 weeks), 3 month followup, 6 month followup

    Perceived Stress Scale-10. Scores range from 0-40, with higher scores indicating greater perceived stress.

  14. Change in Sleep Disturbance

    Time frame: baseline, post-intervention (8 weeks), 3 month followup, 6 month followup

    Patient Reported Outcome Measurement System (PROMIS) Sleep Disturbance. Scores range from 32-76, with higher scores indicating greater sleep disturbance.

  15. Change in Self-Compassion

    Time frame: baseline, post-intervention (8 weeks), 3 month followup, 6 month followup

    Self-Compassion Scale-Short Form. Scores range from 1-5, with higher scores indicating greater self-compassion.

  16. Change in Mindfulness

    Time frame: baseline, post-intervention (8 weeks), 3 month followup, 6 month followup

    Five Facet Mindfulness Questionnaire-Short Form. Scores range from 1-5, with higher scores indicating greater mindfulness.

  17. Change in Interoceptive Awareness

    Time frame: baseline, post-intervention (8 weeks), 3 month followup, 6 month followup

    Multidimensional Assessment of Interoceptive Awareness-II. Scores range from 1-6, with higher scores indicating greater interoceptive awareness.

  18. Treatment Acceptability

    Time frame: post-intervention (8 weeks)

    Postcourse satisfaction survey. Scores range from 4-16, with higher scores indicating greater treatment acceptability. Measure only administered to Mindfulness-Based Resilience Training and Stress Management Education arms.

  19. Treatment Compliance

    Time frame: post-intervention (8 weeks)

    Objective assessment of duration of homework practice. Measure only administered to Mindfulness-Based Resilience Training and Stress Management Education arms.

  20. Treatment Expectancy and Credibility

    Time frame: baseline

    Expectancy/Credibility Questionnaire. Scale for measuring treatment expectancy and rationale credibility for use in clinical outcome studies. Scores range from 7-21, with higher scores indicating greater expectancy and credibility.

  21. Global Impression of Change

    Time frame: post-intervention (8 weeks)

    Clinical Global Impressions Scale. Measure of perceived change in functioning as a result of the intervention. Scores range from 3-21, with higher scores indicating a greater impression of change. Measure only administered to Mindfulness-Based Resilience Training and Stress Management Education arms.

Sponsors and collaborators

Lead sponsor

Pacific University

Other

Collaborators

  • National Center for Complementary and Integrative Health (NCCIH)
  • National Institutes of Health (NIH)

Registry information

Important dates

Study start
2019
Primary completion
2022
Study completion
2022
First posted
Dec 24, 2018
Registry last updated
Jul 3, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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