PPRI: The Professional Peer Resilience Initiative

Sponsor
University of Minnesota (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT04396600
Collaborator
(none)
1,200
1
23.5
51

Study Details

Study Description

Brief 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.

Study Design

Study Type:
Observational
Anticipated Enrollment :
1200 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
The Professional Peer Resilience Initiative: Leveraging a Data-Driven Model to Maximize the Resilience of Healthcare Workers During the COVID-19 Pandemic
Actual Study Start Date :
Jun 8, 2020
Anticipated Primary Completion Date :
May 25, 2022
Anticipated Study Completion Date :
May 25, 2022

Arms and Interventions

Arm Intervention/Treatment
Healthcare Workers Already Starting Peer Support Program

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.

Healthcare Workers Starting Peer Support Program Later

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.

Outcome Measures

Primary Outcome Measures

  1. Change in professional quality of life [Before peer support program, through study completion (an average of 7 months)]

    Professional Quality of Life Questionnaire (proQOL): min score of 10; max score of 50; higher scores mean worse outcome

Secondary Outcome Measures

  1. Change in mental health symptoms and resilience markers [Before peer support program, through study completion (an average of 7 months)]

    Stress Risk & Resilience Self-Index: min score 0; max score of 12; higher scores mean worse outcome

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Healthcare workers (HCWs) and mental health consultants (MHCs) in UMN medical school departments
Exclusion Criteria:
  • None

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Minnesota Minneapolis Minnesota United States 55455

Sponsors and Collaborators

  • University of Minnesota

Investigators

  • Principal Investigator: Cristina S Albott, MD, University of Minnesota

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Minnesota
ClinicalTrials.gov Identifier:
NCT04396600
Other Study ID Numbers:
  • PSYCH-2020-28762
First Posted:
May 20, 2020
Last Update Posted:
Sep 8, 2021
Last Verified:
Sep 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University of Minnesota
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 8, 2021