Methods | Allocation: random, no further details. Blindness: double, no further details. Duration: 8 weeks (last 4 weeks observed). Design: parallel. Location: single centre. |
|
Participants | Diagnosis: (DSM-IV) schizophrenia disorganised (n = 23), paranoid (n = 10), undifferentiated (n = 34). N = 77. Sex: 39 M, 38 F. Age: 28-84 years (mean = 59.9 years). History: duration ill mean = 34.51 years, age at onset: not reported. Setting: inpatient. |
|
Interventions |
|
|
Outcomes | Mental State: PANSS total score, PANSS positive subscore, PANSS negative subscore. Cognitive functioning: digit span distractibility test. |
|
Notes | ||
Risk of bias | ||
Bias | Authors’ judgement | Support for judgement |
Adequate sequence generation? | Unclear risk | Random, no further details. |
Allocation concealment? | Unclear risk | No further details. |
Blinding? subjective outcomes |
Unclear risk | Double, no further details. Whether blinding was successful has not been examined, but the compounds differ quite substantially in side effects. This can be a problem for blinding |
Blinding? objective outcomes |
Low risk | Objective outcomes such as laboratory measures or death are unlikely to have been much affected by problems of blinding |
Incomplete outcome data addressed? All outcomes |
High risk | There was no data on attrition available. |
Free of selective reporting? | High risk | Adverse events were not reported. Numbers on use of antiparkinson medication have not been presented |
Free of other bias? | High risk | There was no wash-out period. The previous antipsychotic treatment was gradually tapered over 4 weeks. Thus, during a period of 4 weeks the participants were on two drugs |