Women's Health Trial: Feasibility Study in Minority Populations

Sponsor
National Cancer Institute (NCI) (NIH)
Overall Status
Completed
CT.gov ID
NCT00000481
Collaborator
National Heart, Lung, and Blood Institute (NHLBI) (NIH)
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Study Details

Study Description

Brief Summary

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 or Disease Intervention/Treatment Phase
  • Behavioral: diet, fat-restricted
Phase 3

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.

Study Design

Study Type:
Interventional
Allocation:
Randomized
Primary Purpose:
Prevention
Study Start Date :
Sep 1, 1991
Study Completion Date :
Jan 1, 1996

Outcome Measures

Primary Outcome Measures

    Eligibility Criteria

    Criteria

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

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

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

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

    Investigators

    • : Valerie George, University of Miami
    • : W. Hall, Emory University
    • : Albert Oberman, University of Alabama at Birmingham

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    National Cancer Institute (NCI)
    ClinicalTrials.gov Identifier:
    NCT00000481
    Other Study ID Numbers:
    • 71
    • N01CN025427-010
    First Posted:
    Oct 28, 1999
    Last Update Posted:
    Feb 14, 2017
    Last Verified:
    Feb 1, 2017

    Study Results

    No Results Posted as of Feb 14, 2017