MedPath

Meditation to Reduce Firefighter Distress

Phase 2
Recruiting
Conditions
Psychological Distress
Interventions
Behavioral: 10-day meditation intervention
Behavioral: 10-day health education intervention
Registration Number
NCT06518616
Lead Sponsor
University of Arizona
Brief Summary

The more than one million firefighters in the United States provide critical emergency medical services in communities they serve and are on the front lines of healthcare delivery, including in the post-pandemic world. As a result of exposure to occupational stressors, a high proportion of firefighters experience considerable stress-related burden including psychological distress (i.e., increased features of anxiety and depression). To address this need, this project will test the efficacy of a 10-day meditation intervention (i.e., 10 individual prerecorded audio units delivered by smartphone app) among career firefighters to decrease psychological distress (i.e., anxiety and depression).

Detailed Description

The goal of this study is to test the efficacy of a 10-day meditation intervention (i.e., 10 individual prerecorded audio units delivered by smartphone app) versus an active attention control (i.e., 10-day health education intervention with 10 individual prerecorded audio units delivered by smartphone app) to reduce psychological distress among N=160 career firefighters (to address possible attrition, N=192 firefighters will be consented and enrolled). The following specific aims will guide the research:

Aim 1. Examine whether firefighters' psychological distress (i.e., features of anxiety \[primary outcome\], depression) is reduced at 10 days, 30 days, and 3 months after the meditation intervention versus an active attention control. Features of anxiety, features of depression will be assessed at baseline (T1), after the 10-day intervention (T2), 30 days later (T3), and 3 months later (T4).

Aim 2: Explore the extent to which reductions in psychological distress from the meditation intervention are mediated by mindfulness and perceived social connection.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
192
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
10-day meditation intervention10-day meditation interventionprerecorded meditation units, 10 units, one per day, delivered by smartphone app
10-day health education intervention10-day health education interventionprerecorded health education units, 10 units, one per day, delivered by smartphone app
Primary Outcome Measures
NameTimeMethod
anxiety featuresbefore, immediately after, 30 days after, and 3 months after the 10-day interventions

PROMIS (Patient Reported Outcomes Measurement Information System) Short Form Emotional Distress - Anxiety - 8a

Secondary Outcome Measures
NameTimeMethod
depression featuresbefore, immediately after, 30 days after, and 3 months after the 10-day interventions

PROMIS Short Form Emotional Distress - Depression - 8a

Trial Locations

Locations (1)

University of Arizona

🇺🇸

Tucson, Arizona, United States

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