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Table 2 Baseline and outcome measures

From: Precision computerised cognitive behavioural therapy (cCBT) for adolescents with depression: a pilot and feasibility randomised controlled trial protocol for SPARX-UK

Months post-randomisation

0

0

1

2

Time point

Telephone/videoconference screening

Baseline

Mid-intervention (4 weeks)

Primary end point (8–10 weeks)

Consent

 

R (P+A)

  

Randomisation

 

R

  

PHQ-A

 

R (A/P)

A/P

R (A/P)

CAIDS-Q

 

R (A/P)

  

RCADS

 

R (A/P)

 

R (A/P)

Screening for eligibility

R (P)

R

  

SDQ & DAWBA (conducted post telephone/videoconference screen & prior to baseline)

P

   

CGI-S/I

 

R (A/P)

 

R (A/P)

EQ-5D-Y

 

R (A)

 

R (A)

EQ-5D-Y (proxy version)

 

R (P)

 

R (P)

Demographics

 

R (A/P)

  

Concomitant interventions

 

R (A/P)*

 

R (A/P)

Adverse events

 

R (A/P)

A/P

R (A/P)

Interview (process evaluation)

   

R

  1. P parent: A adolescent: R researcher: PHQ-A Patient Health Questionnaire modified for adolescents: CAIDS-Q Child and Adolescent Intellectual Disability Screening Questionnaire: RCADS Revised Child Anxiety and Depression Scale: SDQ Strengths and Difficulties Questionnaire: DAWBA Development and Wellbeing Assessment: CGI-S/I Clinical Global Impressions Severity/Improvement.*Taken as part of demographic questionnaire at baseline