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ID
Source
Brief title
Health condition
Mild to moderate symptoms of depression and/ or anxiety
Sponsors and support
Protestants Fonds voor de Geestelijke Volksgezondheid
Intervention
Outcome measures
Primary outcome
Primary outcomes are the Patient Health Questionnaire (PHQ-9) for depression, the Generalised Anxiety Disorder - 7 items scale (GAD-7) for anxiety and the Mini - International Neuropsychiatric Interview (MINI)
Secondary outcome
Secondary outcomes are the EuroQol - 5 Dimensions (EQ-5D) for the quality of life and the Client satisfaction with treatment - 8 items questionnaire (CSQ-8). In addition, university dropout and educational achievement will be assessed.
Background summary
The aim of the present study is to conduct a randomised controlled trial (RCT) to assess the effectiveness of a guided web-based transdiagnostic intervention in treating college student depression and anxiety.The intervention will be compared to care as usual. Approximately 100 participants from a Dutch university or college will be randomised into the two trial arms.
Study objective
The web-based transdiagnostic interventions will be more effective compared to usual care in reducing symptoms of depression and anxiety in college students.
Study design
T0 - screening
T1 - baseline
T2 - post-treatment
T3 - 6 months follow up
T4 - 12 months follow up
Intervention
The intervention will be a guided web-based transdiagnostic intervention targeted at symptoms of depression and/ or anxiety. The intervention consists of 7 online sessions with duration ranging from 4 to 7 weeks depending on individual progress. A booster session will be administered after the completion of the 7th online session.
van der Boechorststraat 1
Amsterdam 1081 BT
The Netherlands
+31 20 59 87282
e.karyotaki@vu.nl
van der Boechorststraat 1
Amsterdam 1081 BT
The Netherlands
+31 20 59 87282
e.karyotaki@vu.nl
Inclusion criteria
In order to be eligible to participate in this RCT, a subject must meet all of the following criteria:
(a) Participation who have given their consent to be contacted after completing an online survey assessing their mental health.
(b) Being 18 years of age or older
(c) Being enrolled as a student at a Dutch university or college
(d) Speak Dutch or English fluently
(e) Students who experience mild to moderate depression (as defining by scoring above the cut-off score of 4 on the Patient health questionnaire [PhQ-9]) and/ or anxiety symptoms (as defining by scoring above the cut-off score of 4 on the Generalised Anxiety Disorder scale – 7 items [GAD – 7])
(f) Provide informed consent before participation
Exclusion criteria
A potential subject who meets any of the following criteria will be excluded from participation in this RCT:
(a) Co-morbid bipolar disorder according to the MINI International Neuropsychiatric Interview (MINI).
(b) Students with severe depression (as defined by scoring above the cut-off score of 14 on the PhQ-9) and/ or anxiety symptoms (as defined by scoring above the cut-off score of 14 on the GAD-7 scale).
(c) Currently receiving/ have received psychological treatment for depression and/or anxiety in the past 12 months
(d) Having slow or no Internet connection (e.g. no broadband Internet or something comparable)
Design
Recruitment
Followed up by the following (possibly more current) registration
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
NTR-new | NL6613 |
NTR-old | NTR6797 |
CCMO | NL60156.029.16 |
OMON | NL-OMON47291 |