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Clinical Trials/NCT04817995
NCT04817995CompletedNot Applicable

Stress Recovery Program FOREST for Healthcare Staff: A Randomized Controlled Trial

Vilnius University1 site in 1 country208 target enrollmentStarted: April 22, 2021Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
208
Locations
1
Primary Endpoint
Change on Recovery Experience Questionnaire

Study Overview

Brief Summary

The aim of the study is to assess the efficacy of an internet-based stress recovery intervention among healthcare staff during COVID-19 pandemic.

Detailed Description

Intervention is going to take the form of an internet-based stress recovery intervention consisting of six modules. The themes include introduction, psychological detachment, distancing, mastery, control, and keeping the change alive. These themes were chosen after considering topics that might be the most useful for healthcare staff experiencing high levels of stress. Each module consists of psychoeducation and exercise parts. Psychologist provide individual feedback on completed exercises as well as can be reached on demand.

The effect of the intervention will be compared against a waiting list control group. Intervention is in Lithuanian.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •at least 18 years old;
  • •comprehending Lithuanian language;
  • •access to internet;
  • •high levels of stress.

Exclusion Criteria

  • •acute psychiatric crisis;
  • •high suicide risk;
  • •interpersonal violence;
  • •alcohol / drug addiction.

Arms & Interventions

Intervention group

Experimental

The intervention group will get a 6-week internet-based stress recovery intervention.

Intervention: FOREST (Behavioral)

Control group

No Intervention

The waiting list will get no intervention while the intervention group is getting the intervention. The waiting list has the possibility to get an intervention after the intervention group finishes it.

Outcomes

Primary Outcomes

Change on Recovery Experience Questionnaire

Time Frame: Pre-treatment, after 6 weeks, 3 months post-treatment

Changes on stress recovery are measured. Recovery Experiences Questionnaire (Sonnentag \& Fritz, 2007) is a self-report measure and consists of 16 questions. All items are answered on a 5-point Likert scale that ranges from 1 (Totally disagree) to 5 (Totally agree). Higher score indicates more pronounced recovery.

Secondary Outcomes

  • Change on Perceived Stress Scale(Pre-treatment, after 6 weeks, 3 months post-treatment)
  • Change on Well-being Index(Pre-treatment, after 6 weeks, 3 months post-treatment)
  • Change on Patient Health Questionnaire(Pre-treatment, after 6 weeks, 3 months post-treatment)
  • Change on International Trauma Questionnaire(Pre-treatment, after 6 weeks, 3 months post-treatment)
  • Change on Moral Injury Outcome Scale(Pre-treatment, after 6 weeks, 3 months post-treatment)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Evaldas Kazlauskas

Professor

Vilnius University

Study Sites (1)

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