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. 2018 Apr 15;16:52–64. doi: 10.1016/j.invent.2018.04.002

Table 3.

Overview study self-report assessments.

Construct Questionnaire T0 T1 T2 T3 T4 T5
Demographics Socio-demographic data (SozDemo)
Psychopathology
Mental health
Mental health (PG)
Psychopathology
Depression
Center for Epidemiological Studies Depression Scale - Short Version (CES-D)
Psychopathology
Anxiety
General Anxiety Disorder Measurement (GAD-7)
Psychopathology
Depression
Patient Health Questionnaire (PHQ-9)
Psychopathology
Alcohol abuse
The Alcohol Use Disorders Identification Test (AUDIT-C)
Quality of life
Wellbeing
WHO-Five Wellbeing Index (WHO-5)
Quality of life EuroQol (EQ-5D)
Quality of life Assessment Quality of Life (AQoL-8D)
Quality of life
Health economic evaluation
Client Service Receipt Inventory (CSRI)
Training
Expectancy
Credibility/Expectancy Questionnaire (CEQ)
Training
Negative treatment effects
Inventory to assess negative effects of psychotherapy (INEP)
Training
Program evaluation
(Based on) Client Satisfaction Questionnaire (CSQ-8)
Training
Attitudes toward help
Attitudes Toward Seeking Professional Help (ATSPPHS)
Training
Supportive accountability
Supporting Accountability (SA)
Training
Treatment Satisfaction
(adaption of) Working Alliance Inventory SR (WAI-SR)
Risk factors
Risk factors questionnaire
Risk Factor Questionnaire (developed by ICare Prevent team) (RF)
Risk factor
Worry
Penn State Worry Questionnaire – Ultra Brief (PSWQ-3)
Risk factor
Sleep
Pittsburgh Sleep Quality Index (PSQI)
Risk factor
Self-esteem
Rosenberg Self Esteem Scale (RSES)
Risk factor
Resilience
Connor-Davidson Resilience Scale (CD-RISC)
Other
Emotion regulation
Subscales of emotion regulation scale questionnaire (SEK-15)
Other
Incongruence
Incongruence questionnaire (short version) (INK-K)
Other
Personality
Big Five Inventory (BFI-10)
Other
Self-regulation
Self-Regulation Scale (SSRQ)
Other
Behavioral activation
The Behavioral Activation for Depression Scale (BADS-FS-9)
Other Drop-Out Reasons (developed by ICare Prevent team) (DG)
Other Other help (developed by ICare Prevent team) (INH)

T0 = screening, T1 = baseline, T2 = 5 weeks after randomization, T3 = post-intervention, 8 weeks after randomization, T4 = 6-month follow-up, T5 = 12-month follow-up.

Trial site Netherlands will assess the CES-D only at screening and will not assess ATSPPHS, SSRQ and SEK, participation will be optional in the risk factor questionnaire.