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. 2018 Sep 4;2018(9):CD013102. doi: 10.1002/14651858.CD013102

Clifford 2005.

Methods Randomised trial
Participants Patients: 180 (intervention 92; control 88)
 Professional (delivering intervention): unclear
 Practices: 1
University‐affiliated internal medicine clinic
Australia
 Year of study: February 2001 to November 2002
Interventions Pharmacist assessed patients' drug regimen and clinical parameters, developed therapeutic plan, provided patient education about diet, exercise, compliance and home‐glucose monitoring, and forwarded patient information (medication lists, laboratory results, goals) to primary care pharmacists, vs usual care.
 Length of intervention: 5 to 30 minutes (average 15 minutes)
 Number of interventions: 8 in 12 months (face‐to‐face meetings at baseline, 6, and 12 months; 6‐weekly intervals by phone)
Outcomes HbA1c
Fasting plasma glucose, blood pressure, serum lipids, urinary albumin‐to‐creatinine ratio
Notes Funding source: The Raine Foundation, University of Western Australia, funded the FDS. R.M.C. was the recipient of a National Health and Medical Research Council of Australia PhD scholarship.
Conflict of interest: Not stated
Risk of bias
Bias Authors' judgement Support for judgement
Random sequence generation (selection bias) Unclear risk A subset of patients was randomised to the intervention or usual care by consecutive allocation
Allocation concealment (selection bias) High risk Quote: "randomised...by consecutive allocation"
Blinding of participants and personnel (performance bias) 
 All Outcomes/Outcome 1 Low risk Personnel were not blinded but all differences in behaviour between control and intervention arm appear to be legitimate parts of the intervention.
Blinding of outcome assessment (detection bias) 
 All Outcomes/Outcome 1 Low risk Assessors unblinded, but the main outcome does not allow for significant detection bias. HbA1c is an objective measure.
Incomplete outcome data (attrition bias) 
 All outcomes Low risk Between group attrition < 10%. Overall competion rate >90%
Selective reporting (reporting bias) Low risk Main outcomes reported
Other bias Low risk None