Blended depression treatment is as effective as regular treatment, but teh blended treatment is more cost-effective.
ID
Bron
Aandoening
Depression, major depressive disorder.
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Level of depressive symptoms (PHQ-9)
Achtergrond van het onderzoek
In this study, a randomized controlled trial will be conducted comparing blended Cognitive Behavioural Therapy (bCBT) to treatment as usual (TAU), among patients referred to specialised mental healthcare with a diagnosis of major depressive disorder (MDD) in The Netherlands. The study is part of a large European project (“European Comparative Effectiveness Research on Internet-Based Depression Treatment” (E-COMPARED); www.ecompared.eu), carrying out comparable trials in eight countries.
Doel van het onderzoek
Blended depression treatment is as effective as regular treatment, but teh blended treatment is more cost-effective.
Onderzoeksopzet
Baseline, 3, 6 and 12 months
Onderzoeksproduct en/of interventie
Blended Cognitive Behavioural Therapy (bCBT): combines individual face-to-face CBT with CBT delivered through an Internet-based treatment platform (ICT4Depression). This platform is connected to a mobile phone application which will be used for the monitoring of patients mood state (ecological momentary assessment: EMA) and automated feedback and motivational messages (ecological momentary intervention: EMI). Eighteen alternating face-to-face and online sessions will be delivered over a period of 18-20 weeks.
Treatment as ususal (TAU): the routine care that subjects receive when they are treated for depression in specialised mental healthcare.
Algemeen / deelnemers
Wetenschappers
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
- Being 18 years of age or older.
- Meet DSM-IV diagnostic criteria for MDD as confirmed by the telephone administered MINI International Neuropsychiatric Interview version 5.0 and a score of 5 or higher on the PHQ-9 screening questionnaire.
- Provide signed informed consent.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
- Having current high risk for suicide according to the M.I.N.I. Interview section C.
- Having serious psychiatric co-morbidity as established in the M.I.N.I. interview, i.e. bipolar affective disorder, psychotic illness, substance dependence and obsessive compulsive disorder.
- Currently receiving psychological treatment for depression in primary or specialised mental health care.
- Being unable to comprehend the spoken and written Dutch language.
- Not having access to an internet connection.
- Not willing to carry an Android smartphone during the duration of treatment.
Opzet
Deelname
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Geen registraties gevonden.
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
| Register | ID |
|---|---|
| NTR-new | NL4838 |
| NTR-old | NTR4962 |
| Ander register | Grant agreement nr for Collaborative Project, funded by EU-FP7 : 603098 |