Obesity Prevention After Smoking Cessation in Menopause

Sponsor
National Institute on Aging (NIA) (NIH)
Overall Status
Completed
CT.gov ID
NCT00064961
Collaborator
(none)
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Study Details

Study Description

Brief Summary

This study addresses the high risk of weight gain associated with smoking cessation in women. The obesity prevention pilot study is designed for the primary prevention of weight gain that can lead to overweight in normal-weight women, that can progress to obesity in women who are already overweight, and for the prevention of additional weight gain in obese women with BMI greater than or equal to 30.0. Fat and other macronutrient intake, specifically, sugar, complex carbohydrates, and protein, are analyzed as a target for individually tailored, weight control intervention following smoking cessation in Caucasian and African American women.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Individualized dietary-control and exercise program
  • Behavioral: Weight-management and smoking cessation maintenance
  • Behavioral: Smoking Cessation program
N/A

Detailed Description

Middle-aged women, especially African Americans, who quit smoking are at high risk for weight gain, overweight, and obesity. Postcessation weight gain has been attributed to increased food intake, which in turn, has been ascribed to a selective increase in high-sugar and other high-carbohydrate foods with a high-fat content. This study compares the relative effectiveness, for postmenopausal Caucasian and African American women, of following an empirically validated smoking cessation program with either 1) a group cessation maintenance program with standard exercise advice and food pyramid instructions for healthy eating or 2) an individually tailored, dietary-control, exercise, weight-management and cessation-maintenance program. Effectiveness is assessed by weight change from baseline to postcessation months 6, 12, and 20.

The second aim is to assess overall fat and other specific macronutrient intake (sugar, complex carbohydrates, and protein) and total caloric intake with the use of a novel macronutrient self-selection paradigm in Caucasian and African-American postmenopausal women at baseline prior to smoking cessation, after being abstinent for one week, and again at 6, 12, and 20 months postcessation.

The third aim is to assess whether there is differential responsiveness on the above measures in postmenopausal Caucasian vs. African-American women.

Study Design

Study Type:
Interventional
Intervention Model:
Parallel Assignment
Masking:
Single
Primary Purpose:
Prevention
Study Start Date :
Mar 1, 2000
Actual Primary Completion Date :
Feb 1, 2006
Actual Study Completion Date :
Feb 1, 2006

Outcome Measures

Primary Outcome Measures

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    45 Years to 59 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Female aged 45 - 59 at time of enrollment

    • African-American or Caucasian; able to confirm racial heritage of past two generations in family

    • Postmenopausal

    • Smokers (more than 10 cigarettes per day for 1 year or more)

    • Written physician approval to participate in program and medical clearance that use of over-the-counter nicotine replacement is not contraindicated based on patient's medical status

    Exclusion Criteria

    • Men

    • Age below 45 or above 59

    • Nonsmokers

    • Currently in a standardized weight-reduction program or taking medications for weight loss

    • History or presence of significant psychiatric illness (e.g., eating disorders, psychosis, psychoactive substance abuse, major depression)

    • History of presence of severe physical illness (e.g., renal failure, hepatic failure, cancer, immunological disease)

    • Unable to complete long-term study commitment, including anticipating moving out of study area prior to completion of the study

    • Unable to confirm racial heritage of past two generations in family.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 LSU Pennington Biomedical Research Center Baton Rouge Louisiana United States 70808

    Sponsors and Collaborators

    • National Institute on Aging (NIA)

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT00064961
    Other Study ID Numbers:
    • AG0004
    First Posted:
    Jul 17, 2003
    Last Update Posted:
    Dec 11, 2009
    Last Verified:
    Dec 1, 2009
    Keywords provided by , ,
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Dec 11, 2009