3.8 Article

A first remotely-delivered guided brief intervention to reduce intrusive memories of psychological trauma for healthcare staff working during the ongoing COVID-19 pandemic: Study protocol for a randomised controlled trial

Journal

Publisher

ELSEVIER INC
DOI: 10.1016/j.conctc.2022.100884

Keywords

COVID-19; Digital intervention; Healthcare staff; Intrusive memories; Psychological trauma; Randomised controlled trial

Funding

  1. Swedish Research Council [2017-00957, 2020-00873]
  2. Oak Foundation [OCAY-18-442]
  3. AFA Insurance [200342, 200311]
  4. Lupina Foundation
  5. Swiss National Science Foundation [P2BEP1_184378]
  6. Swedish Collegium for Advanced Study
  7. Karolinska Institutet
  8. Karolinska University Hospital
  9. FO Akut, Karolinska University Hospital
  10. Swedish Research Council [2020-00873] Funding Source: Swedish Research Council
  11. Swiss National Science Foundation (SNF) [P2BEP1_184378] Funding Source: Swiss National Science Foundation (SNF)

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Addressing the mental health needs of healthcare staff exposed to traumatic events at work during the COVID-19 pandemic is a global priority. This study aims to evaluate a digitalized form of a brief cognitive task intervention delivered remotely to reduce intrusive memories among healthcare staff. The findings will inform further development and dissemination of the intervention.
Addressing the mental health needs of healthcare staff exposed to psychologically traumatic events at work during the COVID-19 pandemic is a pressing global priority. We need to swiftly develop interventions to target the psychological consequences (e.g., persistent intrusive memories of trauma). Interventions for healthcare staff must be brief, flexible, fitted around the reality and demands of working life under the pandemic, and repeatable during ongoing/further trauma exposure. Intervention delivery during the pandemic should be remote to mitigate risk of infection; e.g., here using a blend of digitalized self-administered materials (e.g., video instructions) and guided (remote) support from a researcher. This parallel groups, two-arm, randomised controlled trial (RCT) with healthcare staff working during the COVID-19 pandemic is the first evaluation of whether a digitalized form of a brief cognitive task intervention, which is remotely-delivered (guided), reduces intrusive memories. Healthcare staff who experience intrusive memories of work-related traumatic event(s) during the COVID-19 pandemic (>= 2 in the week before inclusion) will be randomly allocated (1:1) to receive either the cognitive task intervention or an active (attention placebo) control, and followed up at 1-week, 1-month, 3-months, and 6-months post-intervention. The primary outcome will be the number of intrusive memories reported during Week 5; secondary and other outcomes include the number of intrusive memories reported during Week 1, and other intrusive symptoms. Findings will inform further development and dissemination of a brief cognitive task intervention to target intrusive memories.

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