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First Responder Resiliency Program During COVID-19

Not Applicable
Completed
Conditions
Stress
Resilience
Sleep
Interventions
Behavioral: Resilience Program
Registration Number
NCT04536376
Lead Sponsor
Mayo Clinic
Brief Summary

Evaluating a wellness program developed to provide effective sustainable solutions for medical professionals providing care to COVID-19 pandemic patients.

Detailed Description

Providing mindfulness training at specific time points during study participation with an emphasis on integrating physical and mental health management. The phase-based program delivers individualized, data-driven and quantifiable solutions that directly address pain points impacting healthcare professionals and organizations.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
10
Inclusion Criteria
  1. 18 years of age or older at the time of consent
  2. Frontline healthcare professional
  3. Have access to an Apple or Android device
  4. Not pregnant by subject self-report at time of consent
  5. Have the ability to provide informed consent
  6. Have no contraindicating comorbid health condition as determined by the clinical investigators
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Exclusion Criteria
  1. Currently (within the past 3 weeks) been practicing mindfulness training on a weekly/regular basis
  2. Currently (within the past 3 weeks) been undergoing an additional program (e.g. CAM) to improve quality of life or sleep
  3. Currently (within 3 weeks) been enrolled in another clinical or research program (e.g. CAM) which intervenes on the patients' QOL, stress or sleep
  4. An unstable medical or mental health condition as determined by the physician investigator
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Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Resilience ProgramResilience Programa 4 week program focused on improving resilience
Primary Outcome Measures
NameTimeMethod
Perceived Stress Scale4 weeks

Perceived Stress Scale (PSS) is a 10-item Likert scale scoring system that measures global life stress by assessing the degree to which experiences are appraised as uncontrollable or unpredictable. Scores can range from 0 to 40, with higher scores indicating greater perceived stress. The outcome was analyzed as change from baseline

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Mayo Clinic

🇺🇸

Rochester, Minnesota, United States

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