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Women's Health Trial: Feasibility Study in Minority Populations

This study has been completed.

Sponsors and Collaborators: National Heart, Lung, and Blood Institute (NHLBI)
National Cancer Institute (NCI)
Information provided by: National Heart, Lung, and Blood Institute (NHLBI)
ClinicalTrials.gov Identifier: NCT00000481
  Purpose

To evaluate the feasibility of recruiting women of different socioeconomic status and minority groups and to determine whether these women could achieve and maintain a modified fat-eating pattern. The full-scale trial sought to determine whether a low-fat diet could decrease the incidence of cancer and coronary heart disease in postmenopausal women. The National Heart, Lung, and Blood Institute contributed funds over a three-year period to measure lipids, lipoproteins, and other cardiovascular disease risk factors.


Condition Intervention Phase
Cardiovascular Diseases
Coronary Disease
Heart Diseases
Myocardial Ischemia
Postmenopause
Behavioral: diet, fat-restricted
Phase III

MedlinePlus related topics:   Heart Disease in Women    Heart Diseases    Women's Health   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Prevention, Randomized

Further study details as provided by National Heart, Lung, and Blood Institute (NHLBI):

Study Start Date:   September 1991
Estimated Study Completion Date:   January 1996

Detailed Description:

BACKGROUND:

The Request for Proposal for the Women's Health Trial: Feasibility Study in Minority Populations was developed and released by the National Cancer Institute with assistance from the National Heart, Lung, and Blood Institute.

DESIGN NARRATIVE:

Randomized. Recruitment began in August 1992 and ended in February 1994. Forty percent of the subjects were randomized to a control group and 60 percent to the dietary intervention group. Dietary counseling aimed to reduce total fat to 20 percent of calories, reduce saturated fat and dietary cholesterol intakes, and to increase the intake of fruits, vegetables, and grain products. Recruitment and randomization were conducted over an 18-month period at three clinical centers. Other objectives of the trial included: development and evaluation of strategies for recruiting and retaining women of different racial and SES groups into a dietary intervention study; identification of factors affecting compliance; assessment of the effects of a modified fat eating pattern on cardiovascular disease risk factors, including fasting blood lipids and lipoproteins, glucose and insulin, body weight and blood pressure; identification and assessment of potential biochemical and/or biological markers for dietary adherence.

Close-out visits began in May 1994 and ended in September 1994. These visits included six, twelve, and eighteen-month follow-up. NCI extended the coordinating center contract through January 1996 to support data analysis and publication of research results.

  Eligibility
Ages Eligible for Study:   50 Years to 69 Years
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   No

Criteria

Postmenopausal women, aged 50 to 69 years, who consumed 38 percent or more of total calories as fat at baseline.

  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00000481

Sponsors and Collaborators

Investigators
Investigator:     Valerie George     University of Miami    
Investigator:     W. Hall     Emory University    
Investigator:     Albert Oberman     University of Alabama at Birmingham    
  More Information


Publications:

Study ID Numbers:   71
First Received:   October 27, 1999
Last Updated:   June 23, 2005
ClinicalTrials.gov Identifier:   NCT00000481
Health Authority:   United States: Federal Government

Study placed in the following topic categories:
Coronary Disease
Heart Diseases
Myocardial Ischemia
Vascular Diseases
Ischemia

Additional relevant MeSH terms:
Pathologic Processes
Cardiovascular Diseases

ClinicalTrials.gov processed this record on October 29, 2008




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