NCT04396600

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
87

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jun 2020

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

April 23, 2020

Completed
27 days until next milestone

First Posted

Study publicly available on registry

May 20, 2020

Completed
19 days until next milestone

Study Start

First participant enrolled

June 8, 2020

Completed
4.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 10, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 10, 2024

Completed
Last Updated

April 4, 2025

Status Verified

April 1, 2025

Enrollment Period

4.4 years

First QC Date

April 23, 2020

Last Update Submit

April 2, 2025

Conditions

Keywords

ResilienceCOVID-19Coronavirus Disease 2019CoronavirusHealthcare WorkersFrontlineTraumatic Stress

Outcome Measures

Primary Outcomes (1)

  • Change in professional quality of life

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

    Before peer support program, through study completion (an average of 7 months)

Secondary Outcomes (1)

  • Change in mental health symptoms and resilience markers

    Before peer support program, through study completion (an average of 7 months)

Study Arms (2)

Healthcare Workers Already Starting Peer Support Program

Behavioral: MinnRAP Peer Support Program

Healthcare Workers Starting Peer Support Program Later

Behavioral: MinnRAP Peer Support Program

Interventions

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 Already Starting Peer Support ProgramHealthcare Workers Starting Peer Support Program Later

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

The study population consists of healthcare workers and mental health consultants in the University of Minnesota healthcare workforce.

You may qualify if:

  • Healthcare workers (HCWs) and mental health consultants (MHCs) in UMN medical school departments

You may not qualify if:

  • None

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Minnesota

Minneapolis, Minnesota, 55455, United States

Location

MeSH Terms

Conditions

Stress Disorders, TraumaticStress, PsychologicalPsychological TraumaAnxiety DisordersStress Disorders, Post-TraumaticCompassion FatigueFractures, StressCOVID-19Coronavirus Infections

Condition Hierarchy (Ancestors)

Trauma and Stressor Related DisordersMental DisordersBehavioral SymptomsBehaviorMental FatigueFatigueSigns and SymptomsPathological Conditions, Signs and SymptomsOccupational StressFractures, BoneWounds and InjuriesPneumonia, ViralPneumoniaRespiratory Tract InfectionsInfectionsVirus DiseasesCoronaviridae InfectionsNidovirales InfectionsRNA Virus InfectionsLung DiseasesRespiratory Tract Diseases

Study Officials

  • Cristina S Albott, MD

    University of Minnesota

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

April 23, 2020

First Posted

May 20, 2020

Study Start

June 8, 2020

Primary Completion

November 10, 2024

Study Completion

November 10, 2024

Last Updated

April 4, 2025

Record last verified: 2025-04

Locations