angstsymptomen anxiety Depression
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) age * 16 years 2) experience mild self-reported symptoms of depression (CES-D between 16 and 28) and/or anxiety (GAD-7 between 5 and 14)
Exclusion criteria
Exclusion criteria: 1) being on a waitlist for, currently receiving, or having received psychotherapy within the past 12 months for any mental health condition 2) having a lifetime bipolar or psychotic disorder (assessed by M.I.N.I.) 3) being at moderate-high suicide risk (M.I.N.I.) 4) self-reported inability to read or write Dutch or English 5) No access to the Internet 6) no informed consent 7) participation in similar studies at time of inclusion
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary ouctome is disorder specific symptom severity at post-intervention. This will be assessed by the QIDS for depression and the HAM-A for anxiety. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary endpoints include: * CMHD onset within 6 and 12 months follow-up (outcome) * CMHD free days (outcome) * Costs (outcome) * Health related quality of life (outcome) * Self-esteem (moderator) * Motivation (mediator) * Program evaluation (mediator) * Wellbeing (outcome) * Alcohol use (outcome) * Socioeconomic/demographic characteristics (moderators) * Risk factors (optional, moderators) * Negative effects of treatment (outcome) * Sleep quality (outcome) * Worry (outcome) * Emotion regulation (outcome) * Incongruence (outcome) * Personality (moderator) * Supporting accountability (mediator) * Resilience (moderator) * Treatment satisfaction (mediator) * Behavioural activation (outcome) | — |
Countries
Netherlands