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. |
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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. |
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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. |