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. Author manuscript; available in PMC: 2014 Jul 22.
Published in final edited form as: Cochrane Database Syst Rev. 2011 Jun 15;(6):CD006374. doi: 10.1002/14651858.CD006374.pub2
Methods Allocation: random, no further details.
Blinding: single.
Duration: until discharge or 6-12 months.
Post-discharge follow up to 5 years.
Participants Diagnosis: schizophrenia (clinical consensus); selected ‘middle third of prognostic spectrum’ (selection criteria unspecified).
N=228.
Age: range 16-45 years.
Sex: male and female.
History: first admission, ‘middle prognostic range’, not remitted with average 14 day observation period.
Excluded: people who were assessed as unlikely to be discharged within 2 years, and those whose illness went into remission during 14 day average assessment period
Interventions 1. Individual psychotherapy. N=46.
2. Ataraxic drugs (trifluoperazine). N=48.
3. Individual psychotherapy and ataraxic drugs. N=44.
4. ECT. N=47.
5. Milieu therapy and ataraxic drugs. N=43.
Outcomes Leaving the study early
Menninger Health-Sickness Rating Scale (HSRS).
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 further details.
Blinding (performance bias and detection bias)
All outcomes
High risk Open study.
Incomplete outcome data (attrition bias)
All outcomes
Unclear risk Study attrition not reported. Successive follow-up studies have diminishing sample size
Selective reporting (reporting bias) Unclear risk No details.
Other bias High risk Criteria used to select the “middle third of prognostic spectrum” not specified