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Clinical Trials/NCT05379296
NCT05379296
Withdrawn
Not Applicable

Healthy Hearts: Leveraging the Diabetes Prevention Program to Decrease Health Disparities in Women of Reproductive Age

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Prediabetic State
Sponsor
The University of Texas Medical Branch, Galveston
Primary Endpoint
Change from Baseline Triglycerides at 12 months
Status
Withdrawn
Last Updated
3 years ago

Overview

Brief Summary

Nearly half of women have obesity and/or hypertension (HTN). Specific to women, pregnancy creates a vulnerable window for excess gestational weight gain (GWG), exacerbating intergenerational risks for obesity, HTN, type 2 diabetes (T2D), and cardiovascular disease (CVD) across the lifespan. Healthy lifestyles are the first-line recommendations for prevention and treatment of overweight/obesity, HTN, T2D, and CVD. The Diabetes Prevention Program (DPP) is a well-established, Centers for Disease Control and Prevention (CDC)-led public health program focusing on healthy lifestyle changes and is effective at reducing 5-7% of body weight, lowering risks for T2D. Interestingly, research investigating the DPP as a lifestyle intervention for other chronic conditions (i.e., overweight/obesity and HTN) is lacking, demonstrating a missed opportunity. The aim of this study is to determine the initial effects of the first 6-months and after receiving the full 12-months of the virtual DPP compared to the DPP expanded with a CDC-approved HTN prevention component (DPP+) on physical activity, diet, weight, and CVD risk factors in 30 prediabetic women (18-45 years old) with a history of excess GWG, overweight/obesity, and HTN. Participants will be recruited through University of Texas Medical Branch (UTMB) community-based clinics using Epic. The Participants will be randomized into 2 groups (DPP and DPP+) and guided through the 12-month virtual DPP or DPP+ program using UTMB DPP personnel.

Registry
clinicaltrials.gov
Start Date
January 1, 2022
End Date
January 20, 2023
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Eligibility Criteria

Inclusion Criteria

  • Women with prediabetes and eligible for the DPP, overweight/obesity, HTN (diagnosed or 3 successive high blood pressure readings), and history of excess gestational weight gain during most recent pregnancy

Exclusion Criteria

  • Pregnant and lactating women, participants planning to move out of Galveston County within the next year

Outcomes

Primary Outcomes

Change from Baseline Triglycerides at 12 months

Time Frame: Baseline, 12-months

Change from Baseline Low-density lipoproteins at 12 months

Time Frame: Baseline, 12-months

Change from Baseline Systolic Blood Pressure at 6 months

Time Frame: Baseline, 6-months

Change from Baseline High-density lipoproteins at 6 months

Time Frame: Baseline, 6-months

Change from Baseline Low-density lipoproteins at 6 months

Time Frame: Baseline, 6-months

Change from Baseline Diastolic Blood Pressure at 6 months

Time Frame: Baseline, 6-months

Change from Baseline Diastolic Blood Pressure at 12 months

Time Frame: Baseline, 12-months

Change from Baseline Systolic Blood Pressure at 12 months

Time Frame: Baseline, 12-months

Change from Baseline Total cholesterol at 6 months

Time Frame: Baseline, 6-months

Change from Baseline High-density lipoproteins at 12 months

Time Frame: Baseline, 12-months

Change from Baseline Fasting blood glucose at 6 months

Time Frame: Baseline, 6-months

Change from Baseline Triglycerides at 6 months

Time Frame: Baseline, 6-months

Change from Baseline Total cholesterol at 12 months

Time Frame: Baseline, 12-months

Change from Baseline Hemoglobin a1c at 6 months

Time Frame: Baseline, 6-months

Change from Baseline Weight at 12 months

Time Frame: Baseline, 12-months

Change from Baseline Fasting blood glucose at 12 months

Time Frame: Baseline, 12-months

Change from Baseline Hemoglobin a1c at 12 months

Time Frame: Baseline, 12-months

Change from Baseline Weight at 6 months

Time Frame: Baseline, 6-months

Change from Baseline Body mass index at 12 months

Time Frame: Baseline, 12-months

Change from Baseline Body mass index at 6 months

Time Frame: Baseline, 6-months

Change from Baseline Serum insulin at 6 months

Time Frame: Baseline, 6-months

Change from Baseline Serum insulin at 12 months

Time Frame: Baseline, 12-months

Secondary Outcomes

  • Change from Baseline Total portions of Combined Weekly Fruit and Vegetable Consumption at 12 months(Baseline, 12-months)
  • Change from Baseline Total portions of Fried Food Consumption at 6 months(Baseline, 6-months)
  • Change from Baseline Subjective Weekly Physical activity at 6 months(Baseline, 6-months)
  • Change from Baseline Total portions of Combined Weekly Fruit and Vegetable Consumption at 6 months(Baseline, 6-months)
  • Change from Baseline Objective Total Weekly Physical activity minutes at 6 months(Baseline, 6-months)
  • Change from Baseline Visceral adiposity tissue at 6 months(Baseline, 6-months)
  • Change from Baseline C-reactive protein at 12 months(Baseline, 12-months)
  • Change from Baseline Total portions of Fried Food Consumption at 12 months(Baseline, 12-months)
  • Change from Baseline Subjective Weekly Physical activity at 12 months(Baseline, 12-months)
  • Change from Baseline Objective Total Weekly Physical activity minutes at 12 months(Baseline, 12-months)
  • Change from Baseline C-reactive protein at 6 months(Baseline, 6-months)
  • Change from Baseline Visceral adiposity tissue at 12 months(Baseline, 12-months)

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