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Protecting the mental and physical well-being of frontline health care workers during COVID-19: Study protocol of a cluster randomized controlled trial.
Dong, Lu; Meredith, Lisa S; Farmer, Carrie M; Ahluwalia, Sangeeta C; Chen, Peggy G; Bouskill, Kathryn; Han, Bing; Qureshi, Nabeel; Dalton, Sarah; Watson, Patricia; Schnurr, Paula P; Davis, Katherine; Tobin, Jonathan N; Cassells, Andrea; Gidengil, Courtney A.
  • Dong L; RAND Corporation, Santa Monica, CA, USA. Electronic address: ldong@rand.org.
  • Meredith LS; RAND Corporation, Santa Monica, CA, USA.
  • Farmer CM; RAND Corporation, Pittsburgh, PA, USA.
  • Ahluwalia SC; RAND Corporation, Santa Monica, CA, USA; UCLA Fielding School of Public Health, Los Angeles, CA, USA.
  • Chen PG; RAND Corporation, Santa Monica, CA, USA.
  • Bouskill K; RAND Corporation, Santa Monica, CA, USA.
  • Han B; Department of Research and Evaluation, Kaiser Permanente Southern California, Pasadena, CA, USA.
  • Qureshi N; RAND Corporation, Santa Monica, CA, USA.
  • Dalton S; RAND Corporation, Santa Monica, CA, USA.
  • Watson P; National Center for PTSD, VT, USA.
  • Schnurr PP; National Center for PTSD, VT, USA; Geisel School of Medicine at Dartmouth, NH, USA.
  • Davis K; Vizient, Inc. TX, USA.
  • Tobin JN; Clinical Directors Network (CDN), NY, USA; The Rockefeller University Center for Clinical and Translational Science, NY, USA.
  • Cassells A; Clinical Directors Network (CDN), NY, USA.
  • Gidengil CA; RAND Corporation, Boston, MA, USA.
Contemp Clin Trials ; 117: 106768, 2022 06.
Article in English | MEDLINE | ID: covidwho-1800167
ABSTRACT

INTRODUCTION:

The COVID-19 pandemic has placed health care workers at unprecedented risk of stress, burnout, and moral injury. This paper describes the design of an ongoing cluster randomized controlled trial to compare the effectiveness of Stress First Aid (SFA) to Usual Care (UC) in protecting the well-being of frontline health care workers.

METHODS:

We plan to recruit a diverse set of hospitals and health centers (eight matched pairs of hospitals and six pairs of centers), with a goal of approximately 50 HCW per health center and 170 per hospital. Participating sites in each pair are randomly assigned to SFA or UC (i.e., whatever psychosocial support is currently being received by HCW). Each site identified a leader to provide organizational support of the study; SFA sites also identified at least one champion to be trained in the intervention. Using a "train the trainer" model, champions in turn trained their peers in selected HCW teams or units to implement SFA over an eight-week period. We surveyed HCW before and after the implementation period. The primary outcomes are posttraumatic stress disorder and general psychological distress; secondary outcomes include depression and anxiety symptoms, sleep problems, social functioning problems, burnout, moral distress, and resilience. In addition, through in-depth qualitative interviews with leaders, champions, and HCW, we assessed the implementation of SFA, including acceptability, feasibility, and uptake.

DISCUSSION:

Results from this study will provide initial evidence for the application of SFA to support HCW well-being during a pandemic. TRIAL REGISTRATION (Clinicaltrials.govNCT04723576).
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Psychological Distress / COVID-19 Type of study: Experimental Studies / Observational study / Prognostic study / Qualitative research / Randomized controlled trials Limits: Humans Language: English Journal: Contemp Clin Trials Journal subject: Medicine / Therapeutics Year: 2022 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Psychological Distress / COVID-19 Type of study: Experimental Studies / Observational study / Prognostic study / Qualitative research / Randomized controlled trials Limits: Humans Language: English Journal: Contemp Clin Trials Journal subject: Medicine / Therapeutics Year: 2022 Document Type: Article