Impact of an Automated Telephone Intervention on Glycosylated Hemoglobin (HbA1c) in Type 2 Diabetes

NCT ID: NCT00700908

Last Updated: 2013-02-22

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

120 participants

Study Classification

INTERVENTIONAL

Study Start Date

2007-06-30

Study Completion Date

2008-06-30

Brief Summary

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Aim 1. Determine the impact of a daily, automated telephone intervention on HbA1c levels compared to standard care in older patients with type 2 diabetes.

Aim 2. Determine the impact of the automated telephone intervention compared to standard care on adherence to prescribed SMBG frequency in older patients with type 2 diabetes.

Aim 3. Determine the impact of the automated telephone intervention compared to standard care on self-reported diabetic control problems in older patients with type 2 diabetes.

Aim 4. Determine the impact of the automated telephone intervention compared to standard care on self-reported attitudes and health beliefs concerning diabetes in older patients with type 2 diabetes

Detailed Description

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Conditions

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Type 2 Diabetes

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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1

Automated telephone intervention

Group Type EXPERIMENTAL

automated telephone intervention vs. usual care

Intervention Type BEHAVIORAL

2

Usual care

Group Type ACTIVE_COMPARATOR

automated telephone intervention vs. usual care

Intervention Type BEHAVIORAL

Interventions

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automated telephone intervention vs. usual care

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Age greater or equal to 55
* Type 2 diabetes
* English speaking
* Ability to use glucose meter

Exclusion Criteria

* Unable to give informed consent
* Unwilling to allow SMBG levels to be shard with primary care physician
Minimum Eligible Age

55 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Novo Nordisk A/S

INDUSTRY

Sponsor Role collaborator

University of Minnesota

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Judith Graziano, PhD, RN

Role: PRINCIPAL_INVESTIGATOR

University of Minnesota

Locations

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Primary Care Center University of Minnesota

Minneapolis, Minnesota, United States

Site Status

Countries

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United States

Other Identifiers

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0701M99406

Identifier Type: -

Identifier Source: org_study_id

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