Lok 2020.
Study characteristics | ||
Methods | RCT | |
Participants | N = 60 (30F/30M) Typical Alzheimer's disease in accordance with International Working Group‐2 diagnostic criteria All receiving AChEI medication Mean MMSE 16.9 (SD 4.3) Age ‐ no information provided Community residents |
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Interventions | CST groups based on Roy's adaptation model (RAM) (N = 30) Treatment‐as‐usual controls (N = 30) |
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Outcomes | Cognition: Standardised MMSE Quality of Life: QoL‐AD Coping and Adaptation Processing Scale (CAPS) |
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Notes | 45 minutes, twice a week for 7 weeks | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Electronic randomisation programme used |
Allocation concealment (selection bias) | Unclear risk | No information about allocation concealment and independence of randomisation |
Blinding of outcome assessment (detection bias) All outcomes | High risk | "Pre‐test and post‐test data were collected and RAM‐based CST was applied by the same person". |
Incomplete outcome data (attrition bias) All outcomes | Low risk | Attrition reported as zero and no cases were excluded from analysis |
Selective reporting (reporting bias) | Low risk | All outcome measures mentioned in methods were reported. |
Other bias ‐ training and supervision | Unclear risk | Intervention delivered by first author of the paper but little information about receiving training in CST |
Other bias ‐ treatment manual | Low risk | Based on the manualised CST programme (Spector 2006) |