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OpenTrials
Completed

NCT Number: NCT04536376

First Responder Resiliency Program During COVID-19

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

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Key information

Conditions

Resilience Sleep Stress

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Mayo Clinic

Rochester, Minnesota, 55905, United States

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Resilience Program

Behavioral

Subjects receive program devices, and will be asked to wear during rest and sleep on a nightly basis along with active use during daytime. Notifications are sent daily, individualized approach developed and sent to participants to participate on.

Primary outcomes

  1. 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

Sponsors and collaborators

Lead sponsor

Mayo Clinic

Other

Collaborators

  • PNMedical

Registry information

Official study title

First Responder Resiliency Program for Health Care Professionals During a Pandemic

Important dates

Study start
2021
Primary completion
2021
Study completion
2022
First posted
Sep 2, 2020
Registry last updated
May 13, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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