ACRinCKD: Automated Clinical Reminders in the Care of Chronic Kidney Disease Patients

Sponsor
University of Pittsburgh (Other)
Overall Status
Completed
CT.gov ID
NCT00688285
Collaborator
(none)
248
1
2
12
20.7

Study Details

Study Description

Brief Summary

To determine whether the use of educational sessions and computerized clinical reminders can improve primary care doctors' delivery of care to CKD patients compared to educational sessions alone. Hypothesis: Clinical reminders will improve the care delivered to CKD patients

Condition or Disease Intervention/Treatment Phase
  • Other: automated clinical alerts
  • Other: provider education
N/A

Detailed Description

Literature supports that most chronic kidney disease (CKD) patients are cared for by primary care physicians (PCP) without the help of a kidney specialist. Many of these patients fail to achieve targeted outcomes and late referral to a nephrologist has been associated with an increased risk of death. Automated computerized clinical reminders have been shown to improve physician compliance with recommended guidelines in other settings.

Aims: To determine if clinical reminders can help PCPs decrease the rate of late referrals, improve urine albumin checks in CKD patients

Design: prospective randomized controlled, single-blinded study with additional historical control

Methods: Two 20-minute teaching sessions aimed at all GIM PCPs in the UPMC clinic followed by randomization of the eligible GIM providers to receive automated clinical reminders (CR) for their CKD stage 3b-5 patients versus routine care.

Outcomes: Using a database search, individuals with an eGFR<45ml/min/1.73m2 (not seen by a nephrologist) will have data collected on: PCP referral to a nephrologist, urinary albumin (or protein) quantification in the past year, PCP recognition of patients with eGFR<45ml/min, ACE/ARB usage.

Study Design

Study Type:
Interventional
Actual Enrollment :
248 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Health Services Research
Official Title:
Automated Clinical Reminders in the Care of Chronic Kidney Disease Patients
Study Start Date :
Dec 1, 2008
Actual Primary Completion Date :
Dec 1, 2009
Actual Study Completion Date :
Dec 1, 2009

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: 1

education and automated clinical alerts

Other: automated clinical alerts
automated clinical alerts in the electronic medical record

Other: provider education
PCP education session on CKD

Active Comparator: 2

education session alone

Other: provider education
PCP education session on CKD

Outcome Measures

Primary Outcome Measures

  1. referral to a nephrologist [12 months]

    Referral to a nephrologist within the 12 months following decision support system activation.

Secondary Outcome Measures

  1. Use of ACE/ARB [12 months]

    Active use of ACE/ARB at the end of the 12 month period following decision support system activation.

  2. Annual ACR or PCR check [12 months]

    ACR or PCR within 12months of the decision support system activation

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • For PCPs: all GIM attending physicians with a weekly continuity clinic.

  • For patients: >= 18 years-old with an eGFR<45ml/min/1.73m2 being seen in the UPMC GIM clinic by a faculty member during the 10-month intervention period

Exclusion Criteria:
  • for PCPs: imminent plans to leave the department

  • patients with a renal transplant, on any form of dialysis, or with a previous nephrology evaluation.

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Pittsburgh Pittsburgh Pennsylvania United States 15261

Sponsors and Collaborators

  • University of Pittsburgh

Investigators

  • Principal Investigator: Khaled Abdel-Kader, MD, University of Pittsburgh
  • Principal Investigator: Mark Unruh, MD, MSc, University of Pittsburgh

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00688285
Other Study ID Numbers:
  • PRO07110299
First Posted:
Jun 2, 2008
Last Update Posted:
Mar 25, 2011
Last Verified:
Mar 1, 2011

Study Results

No Results Posted as of Mar 25, 2011