ICare Prevent is more effective than care as usual in preventing episodes of depression and/or anxiety.
ID
Bron
Verkorte titel
Aandoening
Depression, Anxiety, Prevention
Depressie, Angst, Preventie
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Disorder specific symptom severity at post-intervention (Quick Inventory for Depression Scale + Hamilton Anxiety Rating Scale)
Achtergrond van het onderzoek
A three-arm randomized controlled trial is conducted comparing the (cost-)effectiveness of a) a guided version of ICare Prevent, b) an unguided version of ICare Prevent, to c) care as usual for the prevention of depression and anxiety. A specific focus is put on student populations. 252 participants will be randomized into either of the three groups, resulting in 84 participants per condition. This study is part of a large European project (ICare); www.icare-online.eu/nl).
Doel van het onderzoek
ICare Prevent is more effective than care as usual in preventing episodes of depression and/or anxiety.
Onderzoeksopzet
T0 - screening
T1 - baseline
T2 - mid-intervention
T3 - post-intervention
T4 - 6 months follow-up
T5 - 12 months follow-up
Onderzoeksproduct en/of interventie
Acces to ICare Prevent, a transdiagnostic Internet-based intervention. The intervention is based on CBT principles. One arm of the RCT is self-guided, the other arm receives feedback on exercises by a trained eCoach. All three groups in the RCT have access to usual care.
Publiek
Felix Bolinski
Van der Boechorstraat 1
Amsterdam 1081 BT
The Netherlands
+31 (0)20 59 85204
f.bolinski@vu.nl
Wetenschappelijk
Felix Bolinski
Van der Boechorstraat 1
Amsterdam 1081 BT
The Netherlands
+31 (0)20 59 85204
f.bolinski@vu.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
Age > 16;
subclinical symptoms of depression (Center for Epidemiologic Studies Depression Scale ≥ 16) and/or anxiety (7-item Generalized Anxiety Disorder scale ≥ 5);
not meeting criteria for a full syndrome presentation of any common mental health disorder within the past six months, in the absence of cardinal symptoms during the past three weeks (assessed by the MINI International Neuropsychiatric Interview)
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
being on a waitlist for, currently receiving or having received psychotherapy within the past 12 months for any mental condition;
having a lifetime bipolar or psychiatric disorder (assessed by the MINI International Neuropsychiatric Interview);
being at moderate to severe risk for suicide (assessed by the MINI International Neuropsychiatric Interview);
self-reported inability to read or write Dutch;
no access to a computer or the Internet;
participation in similar studies at time of inclusion
Opzet
Deelname
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In overige registers
| Register | ID |
|---|---|
| NTR-new | NL6378 |
| NTR-old | NTR6562 |
| CCMO | NL60705.029.17 |
| OMON | NL-OMON47514 |