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Improving Care for Patients With Chronic Kidney Disease Using EMRALD

S

Sunnybrook Health Sciences Centre

Status

Unknown

Conditions

Chronic Kidney Disease

Treatments

Behavioral: CKD feedback and tools

Study type

Interventional

Funder types

Other

Identifiers

NCT02274298
074-2013-2

Details and patient eligibility

About

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.

Full 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.

Enrollment

221 patients

Sex

All

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

221 participants in 2 patient groups

CKD feedback and tools
Active Comparator group
Description:
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
Treatment:
Behavioral: CKD feedback and tools
No Intervention
No Intervention group
Description:
Physicians in these clinics/clusters will not receive CKD feedback or tools

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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