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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT04396600
Other study ID # PSYCH-2020-28762
Secondary ID
Status Enrolling by invitation
Phase
First received
Last updated
Start date June 8, 2020
Est. completion date December 1, 2024

Study information

Verified date September 2023
Source University of Minnesota
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 1200
Est. completion date December 1, 2024
Est. primary completion date December 1, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Healthcare workers (HCWs) and mental health consultants (MHCs) in UMN medical school departments Exclusion Criteria: - None

Study Design


Intervention

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.

Locations

Country Name City State
United States University of Minnesota Minneapolis Minnesota

Sponsors (1)

Lead Sponsor Collaborator
University of Minnesota

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary 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 Change in mental health symptoms and resilience markers Stress Risk & Resilience Self-Index: min score 0; max score of 12; higher scores mean worse outcome Before peer support program, through study completion (an average of 7 months)
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