Health and Wellness in Healthcare Providers Post-disaster
An Evaluation of a Tiered Approach to Increase Well-Being in Healthcare and Social Service Providers in a Post-Disaster Context
1 other identifier
interventional
1,100
2 countries
2
Brief Summary
The purpose of this evaluation is to understand the impact of mental health and psychosocial support (MHPS) programming that AmeriCares (a non-profit disaster response organization) is currently providing to healthcare and social service providers in Southeast Texas and Puerto Rico. The MHPS services are designed to provide skills to reduce stress, improve coping and reduce symptoms of burnout (compassion fatigue).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Jul 2018
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 1, 2018
CompletedFirst Submitted
Initial submission to the registry
October 16, 2018
CompletedFirst Posted
Study publicly available on registry
October 26, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 30, 2019
CompletedStudy Completion
Last participant's last visit for all outcomes
June 30, 2019
CompletedAugust 26, 2019
August 1, 2019
10 months
October 16, 2018
August 21, 2019
Conditions
Outcome Measures
Primary Outcomes (1)
ProQol--Assessing change over time
The ProQOL 5 is a 30-item scale for measuring professional quality of life among people who work in the helping professions (Stamm, 2010). The tool measures the positive aspect of compassion satisfaction (the pleasure you derive from being able to do your work well), and the negative aspect of compassion fatigue, which is composed of two parts: burnout (exhaustion, frustration and anger) and secondary trauma (work-related secondary exposure to people who have experienced traumatic events).
Baseline, 6 weeks, 12 weeks, 18 weeks
Secondary Outcomes (5)
Social Provisions Scale--Assessing change over time
Baseline, 6 weeks, 12 weeks, 18 weeks
Brief Resilience Scale--Assessing change over time
Baseline, 6 weeks, 12 weeks, 18 weeks
Perceived Stress Scale (PSS) (10)--Assessing change over time
Baseline, 6 weeks, 12 weeks, 18 weeks
Impact of Events Scale-Revised--Assessing change over time
Baseline, 6 weeks, 12 weeks, 18 weeks
Brief Cope--Assessing change over time
Baseline, 6 weeks, 12 weeks, 18 weeks
Study Arms (3)
RCHC
EXPERIMENTALParticipation in the Resilience and Coping of the Healthcare Community Intervention.
RCHC+
EXPERIMENTALParticipation in the Resilience and Coping of the Healthcare Community Intervention, support groups and one on one counseling.
Waitlist Control
OTHERThis group will receive treatment as usual and will be offered services once the study is complete.
Interventions
The RCHC group will receive a three hour psychoeducational intervention on common stress responses among healthcare providers and coping skills. They will also receive a booster session one month later which will reinforce these skills. This intervention group will also receive on-going support groups and one on one counseling as needed.
This group will served as the control group and will receive treatment as usual until the end of the study. At the end of the study they will have the opportunity to take part in the RCHC or RCHC+
Eligibility Criteria
You may qualify if:
- Healthcare workers will be eligible for the study if they are:
- over 18 years of age at the time of admission into the study;
- speak and read English or Spanish;
- have been identified as having experienced Hurricane Harvey or Maria or providing care to people living in areas affected by the storms;
- are employed by a participating Community Health Center or partnering agency;
- participate in AmeriCares MHPS programs.
You may not qualify if:
- do not give consent to participate in the study.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Illinois at Urbana-Champaignlead
- Americarescollaborator
- Louisiana State University Health Sciences Center in New Orleanscollaborator
- Colorado State Universitycollaborator
Study Sites (2)
Americares
Houston, Texas, 77077, United States
Americares Puerto Rico
San Juan, 00901, Puerto Rico
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Tara Powell, PhD
University of Illinois at Chicago
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- FACTORIAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
October 16, 2018
First Posted
October 26, 2018
Study Start
July 1, 2018
Primary Completion
April 30, 2019
Study Completion
June 30, 2019
Last Updated
August 26, 2019
Record last verified: 2019-08