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. 2017 Sep 12;2017(9):CD006211. doi: 10.1002/14651858.CD006211.pub3
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
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