Improving Medication Adherence in Comorbid Conditions

NCT ID: NCT00072891

Last Updated: 2010-02-15

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

400 participants

Study Classification

INTERVENTIONAL

Study Completion Date

2005-12-31

Brief Summary

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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.

Detailed Description

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Conditions

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Diabetes Mellitus, Type 2 Hypertension Hyperlipidemia

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SINGLE_GROUP

Blinding Strategy

NONE

Interventions

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telephone counseling

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Type 2 diabetes mellitus, hypertension and/or hyperlipidemia,
* On oral medication for two of the above conditions,
* Manage own medications,
* Must have access to a telephone,
* Not participating in other adherence education or counseling trials
Minimum Eligible Age

40 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

NIH

Sponsor Role lead

Locations

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University of Pittsburgh School of Nursing

Pittsburgh, Pennsylvania, United States

Site Status

Countries

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United States

Other Identifiers

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59048DK (completed)

Identifier Type: -

Identifier Source: org_study_id

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