Intervention 1: Resilience and Coping for Healthcare Group Clinical Trial
Official title:
An Evaluation of a Tiered Approach to Increase Well-Being in Healthcare and Social Service Providers in a Post-Disaster Context
NCT number | NCT03722368 |
Other study ID # | 18699 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | July 1, 2018 |
Est. completion date | June 30, 2019 |
Verified date | August 2019 |
Source | University of Illinois at Urbana-Champaign |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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).
Status | Completed |
Enrollment | 1100 |
Est. completion date | June 30, 2019 |
Est. primary completion date | April 30, 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion criteria: Healthcare workers will be eligible for the study if they are: 1. over 18 years of age at the time of admission into the study; 2. speak and read English or Spanish; 3. have been identified as having experienced Hurricane Harvey or Maria or providing care to people living in areas affected by the storms; 4. are employed by a participating Community Health Center or partnering agency; 5. participate in AmeriCares MHPS programs. Exclusion criteria: Healthcare workers will be excluded if they: 1. do not meet the inclusion criteria, or 2. do not give consent to participate in the study. |
Country | Name | City | State |
---|---|---|---|
Puerto Rico | Americares Puerto Rico | San Juan | |
United States | Americares | Houston | Texas |
Lead Sponsor | Collaborator |
---|---|
University of Illinois at Urbana-Champaign | Americares, Colorado State University, Louisiana State University Health Sciences Center in New Orleans |
United States, Puerto Rico,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | 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 | Social Provisions Scale--Assessing change over time | Subscales of the Social Provisions Scale (SPS) (Cutrona & Russel, 1987) (8 items): Reliable Alliance (4), Guidance (4) For the purposes of our study, the instructions leading into the SPS were changed to restrict participants to thinking about co-workers. The measure asks respondents to rate the degree to which their social relationships are currently supplying each of the provisions. Each provision is assessed by four items, two that describe the presence and two that describe the absence of the provision. Respondents indicate on 4-point scales (ranging fromcompletely true to not at all true ) the extent to which each statement describes their current social relationships. For scoring purposes, the negative items are reversed and summed together with the positive items to form a score for each social provision. Reliability for the total support score in a previous study was .92, with reliabilities of the 4-item subscales ranging from .76 to .84 (Cutrona, Russell, & Rose, 1986). | Baseline, 6 weeks, 12 weeks, 18 weeks | |
Secondary | Brief Resilience Scale--Assessing change over time | The brief resilience scale (BRS) was created to assess the ability to bounce back or recover from stress. The BRS has been tested and is reliable as a unitary construct. It is predictably related to personal characteristics, social relations, coping, and health in all samples. It was negatively related to anxiety, depression, negative affect, and physical symptoms when other resilience measures and optimism, social support. | Baseline, 6 weeks, 12 weeks, 18 weeks | |
Secondary | Perceived Stress Scale (PSS) (10)--Assessing change over time | The PSS is a widely used measure of the degree to which situations in one's life are appraised as stressful (Cohen, Kessler, & Underwood Gordon, 1994) . | Baseline, 6 weeks, 12 weeks, 18 weeks | |
Secondary | Impact of Events Scale-Revised--Assessing change over time | Six item screen derived from the PTSD Checklist-Civilian Version to help primary care settings screen for persons with possible PTSD symptoms. The six items evaluate reexperiencing, avoidance, and hyperarousal which are highly correlated with the PCL-C. The full checklist was studied and utilized to screen for PTSD in countries such as China , Armenia, and Nepal. | Baseline, 6 weeks, 12 weeks, 18 weeks | |
Secondary | Brief Cope--Assessing change over time | The Brief COPE measures 14 identified coping responses: Self-distraction, Active coping, Denial, Substance use, use of instrumental support, use of emotional support, behavioral disengagement, venting, positive reframing, acceptance, planning, humor, religion, and Self-blame. It represents a way to rapidly measure coping responses because it is a short 28-item self-report questionnaire with two items for each of the measured coping strategies. | Baseline, 6 weeks, 12 weeks, 18 weeks |