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. 2011 Sep 7;2011(9):CD008012. doi: 10.1002/14651858.CD008012.pub3

Fang 2003.

Methods RCT design: Parallel‐group trial
Total N randomised: 57
Length of follow‐up: 8 weeks
Analysis: unclear
Participants Location: China
Number of study centres: Patients selected from 2 hospitals
CAD diagnosis: Myocardial infarction (MI) confirmed by an electronic radiograph
Depression diagnosis: Sung's self‐rating depressive scale (SDS) score > 43
Other entry criteria: Sung's self‐rating anxiety scale (SAS) score > 38
Exclusion criteria: unclear
Treatment N: 27 (sex and age distribution unclear)
Control N: 30 (sex and age distribution unclear)
Comparability of the groups: unclear
Interventions Treatment: Health education and psychological intervention in addition to standard medication. Health education included basic myocardial infarction knowledge and related subjects such as healthy diet, exercise, cholesterol control. Psychological intervention comprised support (5 times a week, 30 ‐ 40 minutes per meeting), various psychological treatments tailored according to the patients needs (twice a week for 30 ‐ 40 minutes), and mind and body relaxation time using breathing exercises, and various relaxation techniques (twice daily, 15 ‐ 20 minutes)
Control: Usual care
Duration of treatment: 8 weeks
Outcomes Review outcomes: Sung's self‐rating depressive scale (SDS) score
Other outcomes: Sung's self‐rating anxiety scale (SAS) score, New York Heart Association (NYHA) functional class, Left Ventricular Ejection Fraction (LVEF)
Funding unclear
Notes  
Risk of bias
Bias Authors' judgement Support for judgement
Random sequence generation (selection bias) Unclear risk not applicable
Allocation concealment (selection bias) Unclear risk not applicable
Blinding (performance bias and detection bias) 
 All outcomes Unclear risk not applicable
Incomplete outcome data (attrition bias) 
 All outcomes Unclear risk not applicable
Selective reporting (reporting bias) Unclear risk not applicable
Other bias Unclear risk not applicable