A relapse prevention programme for patients with (partially) remitted anxiety and depression: the GET READY study
Completed
- Conditions
- Anxiety Disorder, Depression, Major Depressive Disorder, Angststoornis, Depressieve stoornis
- Registration Number
- NL-OMON28629
- Lead Sponsor
- Hogeschool Inholland, GGZ inGeest, VU Medical Center, VU University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 126
Inclusion Criteria
Inclusion criteria are: patients have completed their treatment for anxiety and/or depression within the last two years, have a score on the Global Assessment of Functioning scale (GAF) of 50 or higher, are at least 18 years old, and have sufficient command of the Dutch language.
Exclusion Criteria
Patients are excluded if they participate in another structured psychological intervention, when they do not have access to the internet, or when the severity of a comorbid psychiatric disorder requires specialised treatment.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary outcome will be change in anxiety and depression scores, measured with the BAI, IDS-SR, ASI and weekly diary scores.
- Secondary Outcome Measures
Name Time Method Secondary outcomes will be: use of the relapse prevention programme (log data), self-management strategies (Self-management in depression and anxiety questionnaire), functioning (WHODAS 2.0), healthcare use (TiC-P) and satisfaction with the programme (Satisfaction with treatment measure).