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Clinical Trials/NCT05553210
NCT05553210
Completed
Not Applicable

Effects of Intervention Plan on Outcomes of Stress Recovery Program FOREST+ for Healthcare Workers: A Randomized Controlled Trial

Vilnius University1 site in 1 country91 target enrollmentSeptember 11, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Stress, Psychological
Sponsor
Vilnius University
Enrollment
91
Locations
1
Primary Endpoint
Change on Recovery Experience Questionnaire
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The study aims to assess the efficacy of an internet-based stress recovery intervention for healthcare workers receiving therapist support with or without an intervention plan.

Detailed Description

The intervention will be delivered as an internet-based stress recovery program for healthcare workers, comprising of six modules: introduction, psychological detachment, distancing, mastery, control, and keeping the change alive. These modules have been chosen after considering themes that could be most useful for healthcare workers under high stress. Each module consists of a psychoeducational and an exercise component. An intervention plan will be drawn up with the therapist prior to the start of the program, setting the intensity of engagement and the frequency of reminders. During the program, a therapist provides individual feedback on the completed exercises and can also be available on request. The effect of the intervention will be compared with a control group that will use the program without an intervention plan. The intervention will be delivered in Lithuanian.

Registry
clinicaltrials.gov
Start Date
September 11, 2022
End Date
June 30, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • licensed healthcare professionals currently working under license;
  • at least 18 years old;
  • comprehending Lithuanian language;
  • access to internet.

Exclusion Criteria

  • acute psychiatric crisis;
  • high suicide risk;
  • interpersonal violence.

Outcomes

Primary Outcomes

Change on Recovery Experience Questionnaire

Time Frame: Pre-treatment, post-treatment (after 6 weeks), 6 months follow-up

Changes on stress recovery are measured. Recovery Experiences Questionnaire (Sonnentag \& Fritz, 2007) is a selfreport measure consisting of 16 questions. All items are answered on a 5-point Likert scale ranging from 1 (Totally disagree) to 5 (Totally agree). A higher score indicates more pronounced recovery.

Secondary Outcomes

  • Change on Well-being Index(Pre-treatment, post-treatment (after 6 weeks), 6 months follow-up)
  • Change on Perceived Stress Scale(Pre-treatment, post-treatment (after 6 weeks), 6 months follow-up)
  • Change on Patient Health Questionnaire(Pre-treatment, post-treatment (after 6 weeks), 6 months follow-up)

Study Sites (1)

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