The DINE Study-Diet Intervention to Negate Diabetes Study (Improving Weight Loss Outcomes for African Americans)

NCT ID: NCT00599040

Last Updated: 2013-03-18

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

PHASE4

Total Enrollment

113 participants

Study Classification

INTERVENTIONAL

Study Start Date

2005-09-30

Study Completion Date

2010-12-31

Brief Summary

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The purpose of this study is to determine if what you eat affets your insulin sensitivity when you lose a small amount of weight

Detailed Description

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Conditions

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Diabetes Hypertension Insulin Resistance

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

FACTORIAL

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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Weight loss

Weight loss diet focused on the DASH diet

Group Type ACTIVE_COMPARATOR

The DASH diet with weight loss

Intervention Type BEHAVIORAL

A reduced calorie diet is provided to participants based on the DASH diet.

DASH diet

The DASH diet without weight loss

Group Type ACTIVE_COMPARATOR

The DASH diet without weight loss

Intervention Type BEHAVIORAL

participants are given a weight maintainenance diet based on the DASH diet

Diary

Dairy Intervention

Group Type ACTIVE_COMPARATOR

Dairy diet

Intervention Type BEHAVIORAL

participants are given a high dairy, reduced calorie diet

Interventions

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The DASH diet with weight loss

A reduced calorie diet is provided to participants based on the DASH diet.

Intervention Type BEHAVIORAL

The DASH diet without weight loss

participants are given a weight maintainenance diet based on the DASH diet

Intervention Type BEHAVIORAL

Dairy diet

participants are given a high dairy, reduced calorie diet

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* African American adults (age ≥ 19)
* Obese (BMI \> or equal to 30 kg/m2)
* Otherwise generally healthy

Exclusion Criteria

* Diagnoses of diabetes
* Malignancy or other states where weight loss is contraindicated (pregnancy
* Individuals with high blood pressure on medications.
Minimum Eligible Age

19 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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National Institutes of Health (NIH)

NIH

Sponsor Role collaborator

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

NIH

Sponsor Role collaborator

University of Alabama at Birmingham

OTHER

Sponsor Role lead

Responsible Party

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Jamy Ard, MD

Associate Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Jamy D Ard, MD

Role: PRINCIPAL_INVESTIGATOR

University of Alabama at Birmingham

Locations

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University of Alabama at Birmingham Nutrition Sciences Department

Birmingham, Alabama, United States

Site Status

Countries

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United States

Other Identifiers

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1K23DK068223-01

Identifier Type: NIH

Identifier Source: secondary_id

View Link

F040719005

Identifier Type: -

Identifier Source: org_study_id

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