Methods | Year: 1990 Location: Providence, Rhode Island, USA (Teaching Hospital) Team/ward?: ward Timing: direct Trial method: randomised trial | |
Participants | Number (total): 436 Mean age: 83 years Male:female proportion: 28% male Inclusion criteria: > 75 years of age; physician given consent; did not require CCU or ICU Exclusion criteria: none given | |
Interventions |
Team members: specialist nurses, ward nurses, senior geriatrician,
pharmacist, physiotherapist, dietician, social worker Team organisation: at least weekly multi‐disciplinary
meetings, goal setting, standardised assessment tools Control: usual hospital care |
|
Outcomes | Death Cognition Dependence Mood Costs Institutionalisation Trial conclusions: no significant differences between groups observed |
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Notes | ||
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Insufficient information on the sequence generation process |
Allocation concealment (selection bias) | Unclear risk | Method of allocation concealment not described |
Blinding of participants and personnel (performance bias) | High risk | Blinding of participants and personnel not possible |
Blinding of outcome assessment (detection bias) for objective outcome measures | Low risk | Objective outcome measures (e.g. living at home) unlikely to be influenced by lack of blinding |
Blinding of outcome assessment (detection bias) for subjective outcome measures | Unclear risk | Few details of outcome assessors given |
Incomplete outcome data (attrition bias) All outcomes | Low risk | Attrition rates after entry clearly described and balanced and apparently negligible |
Selective reporting (reporting bias) | Unclear risk | No a priori documentation found to judge this item |
Other bias | Low risk | Little evidence of contamination of control group |