Skip to main content
Clinical Trials/NCT06518616
NCT06518616
Recruiting
Phase 2

Reducing Psychological Distress in Fire Fighters With an Asynchronous App- Based Meditation Intervention

University of Arizona1 site in 1 country192 target enrollmentDecember 3, 2024

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Psychological Distress
Sponsor
University of Arizona
Enrollment
192
Locations
1
Primary Endpoint
anxiety features
Status
Recruiting
Last Updated
5 months ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
December 3, 2024
End Date
February 28, 2027
Last Updated
5 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

anxiety features

Time Frame: before, 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 Outcomes

  • depression features(before, immediately after, 30 days after, and 3 months after the 10-day interventions)

Study Sites (1)

Loading locations...

Similar Trials