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. 2018 Dec 20;2018(12):CD007964. doi: 10.1002/14651858.CD007964.pub2

Pan 2012.

Methods Allocation: randomised
Blinding: not addressed
Location: inpatients, China
Length of follow‐up: 1 year
Participants Diagnosis: schizophrenia with depression (CCMD‐3)
N = 68
Sex: 39 M, 29 F
Age: mean ˜ 31.36 years, SD ˜ 10.78 years
Included: length of illness not reported; total score of HAMD ≥ 17
Excluded: participants with severe physical disorder, epilepsy or depression induced by other reasons; drug abuse, allergic to antipsychotics or suicidal attempts; abnormal laboratory tests; extrapyramidal side effects induced by antipsychotics
Interventions 1. CBT group*: N = 34
Content: not reported
Delivered by: not reported
Frequency: not reported
Treatment duration: 6 weeks
2. Standard care group: N = 34
Content: not reported
Delivered by: not reported
Frequency: not reported
Treatment duration: 6 weeks
All participants received antipsychotics.
Outcomes Global state: relapse
Mental state: general (BPRS scores), negative symptoms (SANS scores), depression (clinically important change (no improvement)**, depression (HAMD scores)
Adverse events: any adverse event
Engagement with services: compliance to medication
Notes *Participants in the CBT group also received the standard care intervention.
**Defined as reduction in HAMD score < 25%
Risk of bias
Bias Authors' judgement Support for judgement
Random sequence generation (selection bias) Unclear risk Quote: "Participants were randomly assigned..." (p.206).
Comments: insufficient information about the sequence generation process to permit judgement of 'Low risk' or 'High risk'
Allocation concealment (selection bias) Unclear risk Comments: The method of concealment was not described.
Blinding of participants and personnel (performance bias) 
 All outcomes High risk Comments: The author did not address this information. However, participants and personnel were not likely to be blinded because participants in the treatment group received CBT, and the control group only received standard care.
Blinding of outcome assessment (detection bias) 
 All outcomes Unclear risk Comments: The method of blindness was not described.
Incomplete outcome data (attrition bias) 
 All outcomes Low risk Comments: no attrition
Selective reporting (reporting bias) Low risk Comments: All measured outcomes were reported.
Other bias Low risk Comments: none obvious