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. 2011 Jun 15;2011(6):CD006374. doi: 10.1002/14651858.CD006374.pub2

Simon 1965.

Methods Allocation: random.
 Blinding: unclear.
 Duration: 30 days.
 Setting: hospital.
Participants Diagnosis: DSM‐I schizophrenia (no further details), no prior treatment for schizophrenia, an average of 32.7 days treatment prior to evaluation for this study.
 N=80.          
 Age: average ˜ 31 years.
 Sex: all male.
Interventions 1. Chlorpromazine: dose minimum 200 mg/day, maximum 1200 mg/day, average 400mg/day.  n=20.
2. Hospital routine care (occupational and manual arts therapy, special services activities). N=20
3. Reserpine: dose minimum 2 mg/day, maximum 16 mg/da, average 6 mg/day. N=20.
4. Clinical judgement. N=20.
Outcomes Leaving the study early.
 Not improved (Psychiatric improvement rating scale).
Unable to use.
 Behaviour rating scale ‐ no usable data.
 Minnesota Multiphasic Personality Iinventory (MMPI) ‐ no usable data.
Notes  
Risk of bias
Bias Authors' judgement Support for judgement
Random sequence generation (selection bias) Low risk Randomised ‐ no further details.
Allocation concealment (selection bias) Unclear risk No details.
Blinding (performance bias and detection bias) 
 All outcomes Unclear risk No details.
Incomplete outcome data (attrition bias) 
 All outcomes Unclear risk No details.
Selective reporting (reporting bias) Unclear risk No details.
Other bias Unclear risk No details.