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Improving Medication Adherence in Co morbid Conditions

This study is currently recruiting patients.

Sponsored by: National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Information provided by: National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Purpose

This study is designed to study how adults with Type 2 Diabetes and either high blood pressure and/or high blood cholesterol manage their treatment regimen. It is also called the Diabetes Management Study. Individuals need to be 40 years of age or older and on oral medication (pills) management for two of the three conditions of interest. They may also be on other treatment such as insulin, diet and/or exercise programs. Individuals will be followed for approximately 12 months. About 1/4 of the persons in the study will receive a telephone counseling program with a nurse focused upon their management of their treatment program.

Condition Treatment or Intervention
Diabetes Mellitus, Type 2
Hypertension
Hyperlipidemia
 Behavior: telephone counseling

MedlinePlus related topics:  Diabetes;   High Blood Pressure;   Metabolic Disorders

Study Type: Interventional
Study Design: Educational/Counseling/Training, Randomized, Open Label, Active Control, Single Group Assignment, Efficacy Study

Eligibility

Ages Eligible for Study:  40 Years and above,  Genders Eligible for Study:  Both

Criteria


Location and Contact Information

Lisa Tamres, MS      1-866-247-2611    dms@pitt.edu
Maura McCall, BS, RN      1-866-247-2611    dms@pitt.edu

Pennsylvania
      University of Pittsburgh School of Nursing, Pittsburgh,  Pennsylvania,  15261,  United States; Recruiting
Jacqueline M Dunbar-Jacob, PhD, RN  866-247-2611    dms@pitt.edu 
Lisa Tamres, MS  1-866-247-2611    dms@pitt.edu 
Jacqueline M Dunbar-Jacob, PhD, RN,  Principal Investigator

More Information

Study ID Numbers:  59048DK
Record last reviewed:  May 2004
Record first received:  November 12, 2003
ClinicalTrials.gov Identifier:  NCT00072891
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2004-10-27
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