N/A N=10 Supportive Care

First Responder Resiliency Program During COVID-19

Resilience · Stress · Sleep

Bottom Line

View on ClinicalTrials.gov: NCT04536376 ↗

Enrolled (actual)

Serious AEs

0.0%

Results posted

May 2024

Primary outcome: Primary: Perceived Stress Scale — -3.2 units on a scale

Study Design & Population

Study type: Interventional
Phase: N/A
Interventions: Resilience Program (Behavioral)
Age: Adult, Older Adult · 18+ yrs
Sex: All
Sponsor: Mayo Clinic
Primary completion: Sep 2021

Outcome Measures

Outcome	Result	p-value
PRIMARY Perceived Stress Scale	-3.2	—

Summary

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

Eligibility Criteria

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

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04536376). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.