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. 2012 Oct 17;2012(10):CD006525. doi: 10.1002/14651858.CD006525.pub2

Clarke 2005.

Methods Study design: Randomised controlled trial
Participants Setting: Primary care
Diagnosis: At least one recent dispense of an SSRI antidepressant medication prescribed by a paediatric PCP. Current, research‐ascertained DSM episode of major depression
Inclusion criteria:  Adolescents 12 to 18 years old
Exclusion criteria:  Chart indication of schizophrenia or significant developmental/intellectual disability.  Extreme suicidal risk that resulted in hospitalisation
Age: Mean 15.3 years
Gender: 78% female
Ethnicity: 14% ethnic minority
Country: United States
Sample size (randomised): Total participants 152, intervention 77, control 75
Interventions Treatment: Brief CBT plus treatment as usual SSRIs
Contains the four elements of collaborative care:
1) a multi‐professional approach to patient care: Paediatric primary care provider (PCP), psychologist/CBT (CM), psychologist (MH specialist)
2) a structured management plan: All patients were being treated with an SSRI at enrolment. In addition those in the treatment group received brief CBT based on adult and adolescent depression programmes. Acute phase: After initial decision making session (session 1), CBT began with a choice of either four sessions of cognitive restructuring or four sessions of behavioural activation. A workbook was provided. After completion of the first module (sessions 2–5) progress was evaluated and if appropriate the second module commenced (if recovered the youth entered maintenance phase). The second module (sessions 6–9) consisted of the skills training approach not delivered in the first module. The acute phase also aimed to maximise SSRI medication adherence by reviewing compliance, reported benefits/side effects, and risk of discontinuation. Limited psychoeducation about the benefits of SSRI medication and the importance of adherence was provided
Maintenance phase: CM made brief telephone calls after completing acute sessions
3) scheduled patient follow‐ups: Acute phase: 6‐9 sessions of CBT delivered by CM; maintenance phase: CMs made brief telephone calls to patients 1, 2, 3, 5, 7, and 9 months after completing acute sessions. Also option to request as many as six additional, in‐person sessions during the year long continuation phase
4) enhanced inter‐professional communication: On‐going communication with PCP was part of protocol. CMs received weekly supervision from study psychologists
Control: Treatment as usual enhanced as all patients were being treated with an SSRI at enrolment
Outcomes Depression (CES‐D): 6, 12, 26, 52 weeks
Medication use: 12 weeks
Quality of Life (mental and physical health): 6, 12, 26, 52 weeks
Satisfaction: 6, 12, 26, 52 weeks
Notes CM: case manager; CBT: cognitive behaviour therapy; CES‐D: Centre for Epidemiological Studies Depression; DSM: Diagnostic and Statistical Manual; MH: mental health; PCP: primary care provider; SSRI: selective serotonin reuptake inhibitor
Risk of bias
Bias Authors' judgement Support for judgement
Random sequence generation (selection bias) Unclear risk Block randomisation. Insufficient information available to assess
Allocation concealment (selection bias) Unclear risk Insufficient information available to assess
Incomplete outcome data (attrition bias) 
 All outcomes Unclear risk Short‐term loss to follow‐up based on primary depression outcome (CES‐D) was: overall 25/152(16%), 12/77(16%) intervention and 13/75(17%) control. Reasons for loss to follow‐up not provided. Used intention‐to‐treat analysis.
Selective reporting (reporting bias) Unclear risk Insufficient information available to assess
Other bias Unclear risk Insufficient information available to assess
Implementation Integrity Low risk Attempts were made to assess implementation integrity (e.g. direct observation or rating of tapes)
Blinding of participants and personnel (performance bias) 
 All outcomes High risk Participants and personnel could not be blinded, outcome likely to be influenced by lack of blinding
Blinding of outcome assessment (detection bias) 
 All outcomes Low risk Assessor was not aware of treatment allocation