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Improving Diabetes Quality of Care:Effectiveness of Physician Profiling and Care Coordination by a Diabetes Resource Nurse

This study has been completed.

Sponsors and Collaborators: Baylor Research Institute
American Diabetes Association
Information provided by: Baylor Research Institute
ClinicalTrials.gov Identifier: NCT00258674
  Purpose

The purpose of this study is to test the effectiveness of physician profiling and care coordination by a diabetes resource nurse in improving the quality of diabetes care.


Condition Intervention Phase
Diabetes Mellitus
Behavioral: Care coordination by a diabetes resource nurse
Behavioral: Physician profiling
Phase III

MedlinePlus related topics:   Diabetes   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study
Official Title:   A Randomized Trial of Strategies to Improve Diabetes Care: Effectiveness and Costs of Physician Profiling and Care Coordination by a Diabetes Resource Nurse

Further study details as provided by Baylor Research Institute:

Primary Outcome Measures:
  • Pre-post intervention change in HbA1c level

Secondary Outcome Measures:
  • Pre-post intervention change in other patient outcomes; Performance of diabetes related processes of care

Study Start Date:   January 2000
Estimated Study Completion Date:   June 2002

Detailed Description:

HealthTexas Provider Network primary care practices with at least 10 Medicare diabetes patients over the age of 65 were randomized to one of 3 intervention arms: physician feedback of process measures using Medicare claims data (“Claims”); feedback of Medicare claims data plus clinical measures from medical record abstraction (“Claims+MR”); or both types of feedback plus a practice-based DRN (“DRN”). For the 12 months prior to the intervention and 12 months post-intervention, performance data on diabetes related processes of care (annual HbA1c testing, annual LDL cholesterol screening, annual hypertension screening, annual eye, foot, and renal assessment) and patient outcomes (HbA1c level, LDL cholesterol level, blood pressure) were collected from medical record abstraction and Medicare claims data. Pre-post change scores will be compared between intervention arms to examine effectiveness of physician profiling and care coordination by a diabetes resource nurse.

  Eligibility
Ages Eligible for Study:   65 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Criteria

Inclusion Criteria:

  • age ≥ 65 years on January 1, 2000
  • diagnosis of diabetes mellitus
  • diabetes related visit to HTPN physician within the past year
  • Resident of Texas
  • Medicare insurance coverage

Exclusion Criteria:

  • Patient chart not available for abstraction
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00258674

Locations
United States, Texas
Baylor Health Care System Institute for Health Care Research and Improvement    
      Dallas, Texas, United States

Sponsors and Collaborators
Baylor Research Institute
American Diabetes Association

Investigators
Principal Investigator:     David J Ballard, MD, MSPH, PhD, FACP     Baylor Health Care System Institute for Health Care Research and Improvement    
  More Information


Publications of Results:

Study ID Numbers:   Baylor IRB #000-113
First Received:   November 23, 2005
Last Updated:   October 4, 2006
ClinicalTrials.gov Identifier:   NCT00258674
Health Authority:   United States: Institutional Review Board

Keywords provided by Baylor Research Institute:
Diabetes  
Care coordination  
Case management  
Physician profiling  

Study placed in the following topic categories:
Metabolic Diseases
Diabetes Mellitus
Endocrine System Diseases
Endocrinopathy
Metabolic disorder
Glucose Metabolism Disorders

ClinicalTrials.gov processed this record on October 06, 2008




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