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OpenTrials
Completed

NCT Number: NCT00827710

Automated Diabetes Registry Tools to Enhance Patient Self-Management and Provider Performance Feedback

Can we improve diabetes outcomes through 1) report card mailings to patients 2) point of care distribution of report cards to patients and 3) provider performance feedback with patient level data?

Completed

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Denver Health Medical Center

Denver, Colorado, 80204, United States

About this study

Our federally qualified health care center serves over 7000 diabetic patients, many of whom are uninsured (43%) or on medicaid (18%) or medicare (26%). The population is 54% Latino, 25% Caucasian, and 14% African American. We excluded patients older than 75; those without English or Spanish as a first language; and the homeless. The remaining 5457 patients were randomized to this one-year study which ended January 1, 2009. One-half of the enrolled patients received quarterly mailed report cards on their HgA1c, blood pressure, and lipid performance. They were asked to pick from a list of self-management goals and to see their provider if their last visit was more than 2 months prior to the mailing. In a 2x2 design, our eight clinics were randomized to i) on-site printing of patient report cards or no on-site printing and ii) standard provider performance report cards or enhanced provider report cards. The standard provider report cards included data on provider performance on HgA1c, LDL, and blood pressure compared to other providers. The enhanced provider report card also included a list of up to 10 patients not at HgA1c, LDL, or blood pressure goal. The provider report cards were distributed on a quarterly basis, and the point of care patient report cards were distributed at every clinic visit.

We are analyzing the impact of the intervention on the percent of patients at expert recommended goals for glycemic, lipid, and blood pressure control. We are also performing a qualitative analysis to describe provider and patient attitudes toward the interventions.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • icd9 code for diabetes
  • primary care visit in the past 18 months
  • English or Spanish as primary language

Exclusion criteria

  • age more than 75
  • No working address

Treatment and study plan

point of care patient report cards

Behavioral

gives patient feedback on performance on glycemic, lipid, and blood pressure control relative to expert recommended goals

Provider performance report card

Behavioral

Gives provider feedback on performance on their diabetes panel of patients and includes patient level data

Primary outcomes

  1. Percent of patients with HgA1c < 7

    Time frame: january 2009

  2. Percent of patients with LDL < 100 mg/dL

    Time frame: january 2009

  3. Percent of patients with BP < 130/80

    Time frame: january 2009

Secondary outcomes

  1. Percent of patients with A1c checked in last 6 months

    Time frame: january 2009

  2. Percent of patients with LDL checked in past year

    Time frame: january 2009

  3. Percent of patients with BP checked in past year

    Time frame: january 2009

Sponsors and collaborators

Lead sponsor

Denver Health and Hospital Authority

Other

Collaborators

  • Agency for Healthcare Research and Quality (AHRQ)

Registry information

Important dates

Study start
2007
Primary completion
2009
Study completion
2009
First posted
Jan 23, 2009
Registry last updated
May 1, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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