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Improving Care for Patients With Chronic Kidney Disease Using EMRALD

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

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02274298
Enrollment
221
Registered
2014-10-24
Start date
2014-10-31
Completion date
2017-04-30
Last updated
2016-10-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Kidney Disease

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.

Interventions

BEHAVIORALCKD feedback and tools

people in the intervention arm will receive feedback on ckd quality indicators and tools to help in the detection and management of ckd

Sponsors

Ontario Renal Network
CollaboratorUNKNOWN
Sunnybrook Health Sciences Centre
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
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

Design outcomes

Primary

MeasureTime frameDescription
Proportion of patients age 50-80 with Stage 3+ CKD and a statin prescription24 monthsComparison 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

MeasureTime frameDescription
Proportion of patients with an initial eGFR <60 and a f/u eGFR or an ACR24 monthscompare baseline rates to end of intervention rates
Proportion of patients with diabetes and albuminuria and on an ACE or ARB24 monthscompare baseline rates to end of intervention rates
Proportion of patients at high risk screened for CKD with an eGFR and/or ACR24 monthscompare baseline rates to end of intervention rates
Proportion of patients with an ACR in the past 18 months and meeting bp targets24 monthscompare baseline rates to end of intervention rates
Proportion of patients age less than 80 years and an eGFR<30 being seen by or with a referral to a Nephrologist24 monthscompare baseline rates to end of intervention rates
Proportion of patients meeting eGFR criteria for CKD and documentation of CKD in the cumulative patient profile (CPP)24 monthscompare baseline rates to end of intervention rates

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 27, 2026