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The Professional Peer Resilience Initiative

NCT04396600 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 87

Last updated 2025-04-04

No results posted yet for this study

Summary

The Professional Peer Resilience Initiative (PPRI) study is an observational study aimed at understanding how symptoms of traumatic stress and resilience evolve over time in the University of Minnesota (UMN) healthcare workforce during the coronavirus disease 2019 (COVID-19) pandemic. The study is being conducted concurrently with a UMN peer support program called the MinnRAP program and will remotely administer quality of life and mental health surveys to healthcare workers before they start the MinnRAP program and throughout their participation in the program.

Conditions

  • Stress
  • Stress Disorder
  • Stress, Psychological
  • Trauma, Psychological
  • Anxiety
  • Anxiety State
  • Post Traumatic Stress Disorder
  • Secondary Traumatic Stress
  • Professional Quality of Life
  • Stress Related Disorder
  • Stress Reaction
  • Stress Risk
  • Mental Resilience
  • Emotional Resilience

Interventions

BEHAVIORAL

MinnRAP Peer Support Program

The behavioral intervention consists of 1) pairing healthcare workers into "Battle Buddies" who maintain daily dialogue to detect stress and anxiety and 2) assigning a mental health consultant to each department to facilitate Battle Buddies and provide both small group sessions and individual psychological triage/referrals.

Sponsors & Collaborators

  • University of Minnesota

    lead OTHER

Principal Investigators

  • Cristina S Albott, MD · University of Minnesota

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-06-08
Primary Completion
2024-11-10
Completion
2024-11-10

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04396600 on ClinicalTrials.gov