No registrations found.
ID
Source
Brief title
Health condition
Anxiety Disorder, Depression, Major Depressive Disorder, Angststoornis, Depressieve stoornis
Sponsors and support
Intervention
Outcome measures
Primary outcome
Primary outcome will be change in anxiety and depression scores, measured with the BAI, IDS-SR, ASI and weekly diary scores.
Secondary outcome
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).
Background summary
In this study, a relapse prevention program for patients (partially) in remission from anxiety and depression will be developed, implemented and evaluated. Patients will receive access to an online programme and have contact with a mental health professional every three months. Both quantitative and qualitative data will be collected to measure 1) the extent to which patients make use of the relapse prevention programme; 2) the factors that influence the use of the programme; 3) the association between usage intensity and course of symptoms; 4) barriers and facilitators in implementation of the programme; and 5) how patients evaluate the programme.
Study objective
The aim of this study is to implement and evaluate a guided self-help online relapse prevention programme for patients who are completely or partially in remission from anxiety and/or depressive disorders, and who previously received treatment in mental healthcare services.
Study design
Quantitative data: baseline, 3, 6 and 9 months
Qualititative data: after dropout or completion of the programme
Intervention
Patients receive access to an E-health platform, combined with regular contact with a mental health professional in general practices. The online programme consists of three basic components and 12 optional modules. The three basic components are: ‘Relapse psychoeducation’, ‘Relapse prevention plan’, and ‘Mood & anxiety diary’. The optional modules are for example 'exposure', 'relaxation', 'behavioral activation' and 'sleep. About once every three months patients have face-to-face contact with their mental health professional to discuss the use of the programme and check whether additional support is needed.
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.
Design
Recruitment
IPD sharing statement
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
| Register | ID |
|---|---|
| NTR-new | NL7366 |
| NTR-old | NTR7574 |
| Other | RAAK publiek Regieorgaan SIA : 2015-02-36P |