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Clinical Trials/NCT04536376
NCT04536376CompletedNot Applicable

First Responder Resiliency Program for Health Care Professionals During a Pandemic

Mayo Clinic1 site in 1 country10 target enrollmentStarted: January 15, 2021Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
10
Locations
1
Primary Endpoint
Perceived Stress Scale

Study Overview

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.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Supportive Care
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •18 years of age or older at the time of consent
  • •Frontline healthcare professional
  • •Have access to an Apple or Android device
  • •Not pregnant by subject self-report at time of consent
  • •Have the ability to provide informed consent
  • •Have no contraindicating comorbid health condition as determined by the clinical investigators

Exclusion Criteria

  • •Currently (within the past 3 weeks) been practicing mindfulness training on a weekly/regular basis
  • •Currently (within the past 3 weeks) been undergoing an additional program (e.g. CAM) to improve quality of life or sleep
  • •Currently (within 3 weeks) been enrolled in another clinical or research program (e.g. CAM) which intervenes on the patients' QOL, stress or sleep
  • •An unstable medical or mental health condition as determined by the physician investigator

Arms & Interventions

Resilience Program

Experimental

a 4 week program focused on improving resilience

Intervention: Resilience Program (Behavioral)

Outcomes

Primary Outcomes

Perceived Stress Scale

Time Frame: 4 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 Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Ivana T Croghan, PhD

Professor of Medicine, College of Medicine

Mayo Clinic

Study Sites (1)

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