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CompletedNCT07502092Updated Jun 16, 2026

Mindfulness in Motion Targeted to Sustaining the Mental and Physical Resilience of First Responders

An interventional study of Mindfulness in Motion for First Responders in Stress, Resilience and Mental Health of First Responders and Work Engagement, sponsored by Ohio State University. Completed at 1 site in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-06-16.

Sponsored by Ohio State University · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Registered 2 years 7 months after the study started (first participant enrolled Aug 2023, registered Mar 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
29
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

High levels of chronic and recurrent workplace stress can profoundly impact the physical, mental, and emotional health of first responders. A multi-modal evidence-based mindfulness intervention was delivered to cohorts of first responders to evaluate effects on perceived stress, resilience, work engagement, and musculoskeletal pain.

Read the detailed description

The occupational stress experienced by first responders can result in decreased quality and safety of patient care, increased risk of first responder injury, and decreased organizational performance. Worksite mindfulness interventions have been shown to support decreases in occupational stress, as well as improved resilience and work engagement for other high stress professions. Mindfulness in Motion (MIM), an evidence-based mindfulness intervention, was adapted to target the specific occupational needs of first responders in a format that could be easily integrated into their workdays. Three cohorts of first responders received eight weekly synchronous mindfulness sessions with full access to the companion smartphone MIM app for six months after the core eight-week sessions were completed. Adaptations to the MIM content and experiential practices were informed by first responder feedback prior to the study. Self-report surveys to assess perceived stress, resilience, work engagement, and musculoskeletal pain were completed by first responder participants before participation in the intervention, at the end of the eight week intervention, and again six months after the intervention was completed.

02

Conditions studied

  • Stress
  • Resilience and Mental Health of First Responders
  • Work Engagement
  • Musculoskeletal Discomfort
  • First Responders

Keywords

  • first responders
  • mindfulness
  • resilience
  • occupational stress
  • mental health
  • physical health
03

In context

Occupational Stress

236 studies on the registry are indexed under Occupational Stress; 64 are open to participants now.

This study's enrollment of 29 is below the median of 89 across 167 interventional studies indexed under Occupational Stress.

Browse Occupational Stress studies →

Lead sponsor

Ohio State University is the lead sponsor of 640 studies on the registry; 144 are open to participants now.

Of its 60 completed or terminated interventional studies of FDA-regulated products, 45 (75%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Actively working as a community First Responder
  • 18 years or older
  • Ability to understand and read English
  • Commitment to participation in the eight weekly virtual sessions, download the MIM smartphone app
  • Adequate Wi-Fi to access the MIM app content

Exclusion criteria

Exclusion Criteria:

  • First responder working in a hospital or healthcare setting
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
29 participants (actual)

Study arms

  • Experimental
    Intervention Group

    First responders participate in an eight-week, synchronous virtual mindfulness intervention, during work hours, with access to companion smartphone app to reinforce virtually presented content and support individual mindfulness practices.

    Behavioral: Mindfulness in Motion for First Responders

Interventions

  • BehavioralMindfulness in Motion for First Responders

    Mindfulness in Motion (MIM) is an eight-week, evidence-based workplace intervention designed to provide participants with practical strategies to reduce stress and burnout, and improve resilience. Offered virtually, MIM was adapted to support first responders relative to their occupational stressors and unique work characteristics. A companion smartphone app supplemented the eight weekly synchronous sessions and offered content informed by first responders and experiential practices that were modeled by first responders.

06

What researchers measure

Primary outcomes

  1. Perceived Stress Scale (PSS-10)

    The Perceived Stress Scale-10 is a self-report measure of perceived stress that measures the degree to which situations in one's life over the past month are appraised as stressful. The 4-point Likert scale responses are 0=Never, 1=Almost Never, 2=Sometimes, 3=Fairly Often, and 4=Very Often. Individual scores are summed and range from 0 to 40 with higher scores indicating higher perceived stress.

    Time frame: Baseline, immediately after the 8 week intervention, and 6 months after the completion of the 8-week intervention

  2. Connor-Davidson Resilience Scale-10 (CD-RISC-10)

    The Connor Davidson-Resilience Scale-10 is a 10-item self-report assessment of a person's ability to bounce back after adversity. A 5-point Likert scale for each statement ranges from 0=Not true at all to 4=True nearly all of the time. A respondents's total sum score can range from 0-40 with higher scores indicating higher resilience.

    Time frame: Baseline, immediately after the 8 week intervention, and 6 months after the completion of the 8-week intervention

  3. Utrecht Work Engagement Scale-0 (UWES-9)

    A 9-item assessment of attitudes towards one's job. The Utrecht Work Engagement Scale-9 measures three dimensions: dedication, vigor, and absorption. All items are rated on a 7-point Likert scale ranging from 0=Never, 1=Almost Never, 2=Rarely, 3=Sometimes, 4=Often, 5=Very Often, and 6=Always. Each sub scale time is summed and ranges from 0-18. Higher scores for each sub scale indicate higher dedication, vigor, and absorption with work.

    Time frame: Baseline, immediately after the 8 week intervention, and 6 months after the completion of the 8-week intervention

Secondary outcomes

  1. Modified Nordic Musculoskeletal Questionnaire (mNMQ)

    The Modified Nordic Musculoskeletal Questionnaire is a standardized 14-item tool assessing musculoskeletal symptoms, over the past 12 months and past 7 days, across multiple body regions. Q. 1 asks about musculoskeletal pain in 9 anatomical areas include the neck, shoulders, upper back, elbows, lower back, wrists/hands, hips/thighs, knees, and ankles/feet--yes/no are responses. Q. 2 asks frequency of musculoskeletal issues in the 9 anatomical areas over the past 30 days with Q. 3 asking about length of time related to the musculoskeletal pain and Q. 4 about intensity of the pain that was indicated. With yes/no responses, Q. 5 \& 6 asks if pain has interfered with usual activities; question 7 asks if a healthcare provider was seen. Q. 9, 10, 11 asks if work activities have been disrupted and if a formal diagnosis was determined. Q. 12, 13, and 14 asks about related symptoms. The tool uses a structured, forced-choice format supported by a body map. There is no minimum or maximum score.

    Time frame: Baseline, immediately after the 8 week intervention, and 6 months after the completion of the 8-week intervention

  2. Mindfulness in Motion smartphone app usage

    App usage data in time per participant

    Time frame: Immediately after completion of the 8-week intervention

  3. Mindfulness in Motion videos watched

    Frequency of videos watched by the overall participant sample on the smartphone app

    Time frame: immediately after completion of the 8-week intervention

07

Study locations

1 site
  • The Ohio State University
    Columbus, Ohio 43210, United States
08

References and documents

Study documents

  • Protocol and statistical analysis plan · Sep 8, 2022
  • Informed consent form · Sep 8, 2022

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: Yes — The de-identified data and analysis code will be submitted to the Dryad repository. Human subjects demographics will be limited to three de-identified descriptors. MIM app usage will be submitted as de-identified usage frequencies. Paired t-test and ANOVA analysis for perceived stress, resilience, and work engagement will be submitted as de-identified, cohort data-comparison on means. nNMQ data will be submitted as frequency and comparison of means.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 16, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07502092
Lead sponsor
Ohio State University
Responsible party
Maryanna Klatt (Director of Integrative Health; Professor, Family Medicine, Ohio State University) — Principal investigator
First posted
Mar 30, 2026
Start date
Aug 1, 2023
Primary completion
Jun 30, 2024
Completion
Dec 1, 2025
Last update
Jun 16, 2026

Study contacts

Maryanna Klatt, PhD
principal investigator · Ohio State University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jun 2026. You cannot join it, but the record below documents what was studied.

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