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Mindfulness-Based Resilience Training for Aggression

N/A
Waitlist Available
Research Sponsored by Pacific University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
be 21-65 years old (age limitations for both police departments)
demonstrate English fluency
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, post-intervention (week 8), 3-month followup, 6-month followup
Awards & highlights

Study Summary

This trialaims to help LEOs better cope with stress through mindfulness training to reduce aggression, mental health issues, and alcohol misuse.

Eligible Conditions
  • Aggression
  • Stress

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, post-intervention (week 8), 3-month followup, 6-month followup
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline, post-intervention (week 8), 3-month followup, 6-month followup for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Change in Aggression
Secondary outcome measures
Change in Alcohol Use
Change in Alcohol Use Negative Consequences
Change in Burnout
+18 more

Trial Design

3Treatment groups
Experimental Treatment
Active Control
Group I: Mindfulness-Based Resilience TrainingExperimental Treatment1 Intervention
MBRT is an 8-week program combining training in standardized mindfulness practices targeting factors that facilitate resilience, cognitive behavioral therapy (CBT), and psychoeducation. It contains experiential and didactic exercises including body scan, sitting and walking meditation, mindful movement and discussions.
Group II: Stress Management EducationActive Control1 Intervention
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.
Group III: No Intervention ControlActive Control1 Intervention
No contact control condition (other than baseline, post, and follow-up assessments)
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Mindfulness-Based Resilience Training
2019
N/A
~140

Find a Location

Who is running the clinical trial?

Pacific UniversityLead Sponsor
12 Previous Clinical Trials
644 Total Patients Enrolled
1 Trials studying Aggression
40 Patients Enrolled for Aggression
National Institutes of Health (NIH)NIH
2,679 Previous Clinical Trials
6,910,573 Total Patients Enrolled
1 Trials studying Aggression
40 Patients Enrolled for Aggression
National Center for Complementary and Integrative Health (NCCIH)NIH
827 Previous Clinical Trials
668,635 Total Patients Enrolled
2 Trials studying Aggression
80 Patients Enrolled for Aggression

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Are there any positions available for individuals interested in this trial?

"Based on the details available at clinicaltrials.gov, this trial is no longer accepting patients as it was last updated in November 16th 2022. Nevertheless, there are still 171 other active trials which can be found right now."

Answered by AI

What qualifications are necessary to partake in this clinical investigation?

"The study is currently enrolling 109 participants who are aged between 21 and 65, displaying symptoms of aggression."

Answered by AI

Is this research endeavor open to seniors above the age of 65?

"This medical trial is open to adults aged 21 - 65 and there are 37 separate studies for minors under 18, and 124 programs available for seniors above the age of 65."

Answered by AI

What are the desired outcomes of this research initiative?

"This medical trial will observe patients over 12 months with the primary aim of assessing changes in aggression. Secondary objectives are to analyse alterations in interoceptive awareness (scores ranging from 0-185, higher scores indicating greater understanding), acceptance levels of self-report questionnaires (0-12, high scores suggesting increased acceptability) and proinflammatory cytokine levels as measured by tumor necrosis factor alpha."

Answered by AI
~20 spots leftby Mar 2025