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Clinical Trials/NCT02274298
NCT02274298UnknownNot Applicable

Improving Care for Patients With Chronic Kidney Disease Using Electronic Medical Record Interventions: A Pragmatic Cluster Randomized Trial

Sunnybrook Health Sciences Centre0 sites221 target enrollmentStarted: October 1, 2014Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Enrollment
221
Primary Endpoint
Proportion of patients age 50-80 with Stage 3+ CKD and a statin prescription

Study Overview

Brief Summary

This pragmatic cluster randomized controlled trial will test the impact of feedback and a toolkit aimed at improving the management of chronic kidney disease (CKD) in the primary care setting. This trial will use family physicians in Ontario participating in the Electronic.

Detailed Description

This trial will use family physicians in Ontario participating in the Electronic Medical Record Administrative data Linked Database (EMRALD) and receiving the System for Audit and Feedback to Improve caRE (SAFIRE) along with other decision support tools. Performance on CKD quality indicators for family physicians receiving the CKD feedback and tools will be compared to physicians not receiving the CKD feedback or tools.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Family physicians participating in EMRALD, on the EMR for >=2 years, roster size >=100 patients
  • •Patient criteria, rostered and actively seeing an EMRALD physician, on the EMR for .=1 year

Exclusion Criteria

  • •Updated data available at the time of study commencement

Arms & Interventions

CKD feedback and tools

Active Comparator

Physicians in these clinics/clusters will receive feedback on their performance for screening and managing CKD quality indicators as well as EMR tools to aid in their performance

Intervention: CKD feedback and tools (Behavioral)

No Intervention

No Intervention

Physicians in these clinics/clusters will not receive CKD feedback or tools

Outcomes

Primary Outcomes

Proportion of patients age 50-80 with Stage 3+ CKD and a statin prescription

Time Frame: 24 months

Comparison of proportion of patients age 50-80 years with Stage 3+ CKD (no dialysis or renal transplant) and receiving a statin prescription at baseline and at the end of the trial

Secondary Outcomes

  • Proportion of patients with an initial eGFR <60 and a f/u eGFR or an ACR(24 months)
  • Proportion of patients meeting eGFR criteria for CKD and documentation of CKD in the cumulative patient profile (CPP)(24 months)
  • Proportion of patients age less than 80 years and an eGFR<30 being seen by or with a referral to a Nephrologist(24 months)
  • Proportion of patients at high risk screened for CKD with an eGFR and/or ACR(24 months)
  • Proportion of patients with diabetes and albuminuria and on an ACE or ARB(24 months)
  • Proportion of patients with an ACR in the past 18 months and meeting bp targets(24 months)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Dr. Karen Tu

Senior Scientist

Sunnybrook Health Sciences Centre

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