Feasibility and Impact of "ABCs of Diabetes" Self-Management Education Program at an Urban Public Library

NCT00822471 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 360

Last updated 2020-08-25

No results posted yet for this study

Summary

A concise diabetes self-management education (DSME) program on the "ABCs of Diabetes" will be placed in an urban public library to assess the feasibility of using this community setting for the delivery of health care education in an urban African American population. Impact on knowledge of, prescriptions for, and control of blood sugar (A1C), blood pressure (BP) and LDL cholesterol (LDL-C)before and after participation in the program will be assessed. We will also examine the frequency of emergency department (ED) visits and hospitalizations for uncontrolled diabetes at 6 months post-DSME intervention.

Conditions

Interventions

BEHAVIORAL

Diabetes Self-Management Education

DSME intervention consisting of two interactive 2-1/2 hour classes taught by a diabetes educator focusing on the "ABCs of diabetes" and training in how to talk to your doctor.

Sponsors & Collaborators

  • Medstar Diabetes Institute;

    collaborator UNKNOWN
  • American Diabetes Association

    collaborator OTHER
  • Bayer

    collaborator INDUSTRY
  • CareFirst BlueCross Blue Shield;

    collaborator UNKNOWN
  • District of Columbia, Department of Health Block Grants Program;

    collaborator UNKNOWN
  • Charles and Mary Latham Trust Fund;

    collaborator UNKNOWN
  • Eli Lilly and Company

    collaborator INDUSTRY
  • Hewlett-Packard

    collaborator INDUSTRY
  • Meltzer Entities;

    collaborator UNKNOWN
  • NBC Washington

    collaborator OTHER
  • Novo Nordisk A/S

    collaborator INDUSTRY
  • Aventis Pharmaceuticals

    collaborator INDUSTRY
  • Takeda Pharmaceuticals North America, Inc.

    collaborator INDUSTRY
  • Pfizer

    collaborator INDUSTRY
  • Medstar Health Research Institute

    lead OTHER

Principal Investigators

  • Michelle F. Magee, MD, LRCPSI · Medstar Health Research Institute

Study Design

Allocation
NON_RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2003-01-31
Primary Completion
2005-01-31
Completion
2005-07-31

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00822471 on ClinicalTrials.gov