Learning How to Recover From Stress - Pilot RCT
Adjustment Disorders
About this trial
This is an interventional prevention trial for Adjustment Disorders focused on measuring Recovery, Stress, Internet-based, Prevention, Intervention, Work
Eligibility Criteria
Inclusion Criteria:
All participants were volunteers. To be eligible for the study, each participant had to fulfill the following criteria:
- at least 18 years old; (ii) fluent in Swedish
- have access to a computer or handheld device with internet access
- currently be employed
- >14 points on the Perceived Stress Scale
- <5 points on the Shirom Melamed Burnout Questionnaire (SMBQ)
- <20 points on the Montgomery Åsberg Depression Rating Scale-Self-Rated (MADRS-S)
- <21 points on the Insomnia Severity Index (ISI)
- <14 points on the Alcohol Use Disorders Identification Test (AUDIT).
Exclusion Criteria:
Participants were excluded from the study if they:
- currently were in treatment for stress or burnout;
- currently were suffering from bipolar disorder, psychosis, post-traumatic stress disorder (PTSD), eating disorders, substance abuse, severe forms of depression, anxiety disorder or personality disorders as assessed in a telephone interview (MINI)
- suicidal ideation based on Item 9 on the MADRS-S.
- If on medication (e.g., antidepressants or sleep medication) this should be held constant medication constant during the study period.
Sites / Locations
- Department of Behavioral Sciences and Learning, Linköping University
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Internet-based recovery training program (n=35)
Wait-list control group (n=34)
The iRTP was based on recovery experiences (psychological detachment, relaxation, mastery, and control), converted into a recovery training intervention inspired by Hahn et al. (2011). The iRTP comprised five modules distributed over five weeks, with modules lasting 60-120 minutes per week.
Wait-list control group received equal and parallell assessment and eligibility procedure as the experimental conditions. Wait-list control group gained access to iCBT/W-iCBT program after the six months follow-up.