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Completed

NCT Number: NCT00023543

Reduction of Triglycerides in Women on Hormone Replacement Therapy

The purpose of this study is to test the effect of lifestyle intervention on subclinical cardiovascular disease measures in women taking hormone replacement therapy (HRT).

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Key information

Age range

52 year–60 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 2

Primary location

University of Pittsburgh

Pittsburgh, Pennsylvania, 15261, United States

About this study

BACKGROUND:

Cardiovascular disease is a common cause of morbidity and mortality in older women. Better methods of prevention via health promotion are needed. Estrogen HRT may beneficially affect women's cardiovascular health, based on evidence from observational studies, but recent trial evidence suggests HRT may actually lead to increased risk of cardiovascular disease in new users. Understanding this untoward effect of HRT and how to prevent it is a significant aim.

DESIGN NARRATIVE:

This randomized trial of 500 women on HRT for at least two years, aged 52-60 years, and three or more years postmenopausal will test whether reduction in waist circumference, triglycerides, dense low density lipoprotein cholesterol (LDLc), number of LDL particles, C-reactive protein, and plasminogen activator inhibitor-I (PAI-I) by aggressive diet and exercise, versus a health education control, and will decrease progression or result in regression of measures of subclinical vascular disease. The intervention is designed to reduce total fat intake to 17 percent of calories, 1300 kilo calories, and increase moderate activity to 150-240 minutes per week to obtain a 10 percent reduction in weight. The primary endpoint will be a 20 percent or at least a 20 mg decrease in triglyceride levels, a 5 cm decrease in waist circumference, and a 10 percent decrease in LDLc. This will result in changes in subclinical measurements, including carotid ultrasound, electron beam computer tomography of the coronary artery and aorta, pulse wave velocity, endothelial function, and tonometry of the radial artery. Nuclear magnetic resonance spectroscopy of lipoproteins, inflammatory markers, and estrogen metabolites will also be evaluated.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • On HRT for at least two years
  • Women 52 to 60 years of age
  • Three or more years postmenopausal
  • Waist circumference greater than 80 cm
  • LDLc between 100 and 160 mg/dl
  • Body mass index 25-39.9 kg/m2
  • Blood Pressure less than 160/95 mm Hg
  • Beck Depression Inventory Score less than 20

Exclusion criteria

  • Current use of cholesterol-lowering medication
  • Diagnosis of diabetes
  • On diabetes medication

Treatment and study plan

diet, fat-restricted

Behavioral

Reduction in total, saturated, trans fat, cholesterol, calories. Increase in fiber. Promotion of nutrient-dense, high-volume, low calorie foods.

Exercise

Behavioral

Rigorous, stepped care approach to reach 150 min/week of physical activity.

Primary outcomes

  1. Measures of subclinical disease

    Time frame: 5 years

  2. Change in coronary calcium (EBCT)

    Time frame: 5 years

  3. Change in carotid intima media wall thickness

    Time frame: 5 years

  4. Change in vascular stiffness (PWV)

    Time frame: 5 years

Secondary outcomes

  1. Change in waist circumference and weight

    Time frame: 5 years

  2. Change in LDL particles, triglycerides and small, medium and large LDL particles

    Time frame: 5 years

  3. Change in HDL particles

    Time frame: 5 years

  4. Change in insulin and glucose

    Time frame: 5 years

  5. Change in systolic blood pressure, diastolic blood pressure

    Time frame: 5 years

Sponsors and collaborators

Lead sponsor

University of Pittsburgh

Other

Collaborators

  • National Heart, Lung, and Blood Institute (NHLBI)

Registry information

Official study title

Reduction of Triglycerides in Women on HRT

Important dates

Study start
2001
Primary completion
2010
Study completion
2010
First posted
Sep 7, 2001
Registry last updated
Jun 19, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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