Expired Study
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Chicago, Illinois 60611


Purpose:

RATIONALE: Lifestyle factors, such as physical activity, diet, and obesity, and hormone function may affect breast density. Screening tests, such as mammography, may help doctors find tumor cells early and plan better treatment for breast cancer. PURPOSE: This clinical trial is studying the effect of lifestyle factors and hormone function on breast density in healthy Hispanic women who are undergoing mammography for breast cancer screening.


Study summary:

OBJECTIVES: - Correlate physical activity, diet, and obesity, as measured by body mass index and waist circumference, with percent breast density and the absolute estimate of total dense breast area in healthy Hispanic women undergoing screening mammography. - Correlate fasting serum insulin growth factor (IGF)-1 and the molar ratio of IGF-1 to IGF binding protein-3 with breast density in participants undergoing screening mammography. - Correlate insulin concentration and insulin resistance with breast density in participants undergoing screening mammography. OUTLINE: This is a multicenter study. Participants undergo blood collection and physical examination. Participants also complete breast cancer risk factor, food frequency, and physical activity questionnaires and receive breast health and physical activity education. Participants then undergo a digital screening mammogram. Participants are notified of mammogram results. PROJECTED ACCRUAL: A total of 114 participants will be accrued for this study.


Criteria:

DISEASE CHARACTERISTICS: - Healthy Hispanic women - Registered patient at the Erie Family Health Centers' West Town or Humboldt Park clinics - No screening mammography within the past 12 months - No abnormality on clinical breast exam - No history of breast cancer - Hormone receptor status: - Not specified PATIENT CHARACTERISTICS: Age - 40 and over Sex - Female Menopausal status - Not specified Performance status - Not specified Life expectancy - Not specified Hematopoietic - Not specified Hepatic - Not specified Renal - Not specified Other - Not pregnant PRIOR CONCURRENT THERAPY: Biologic therapy - Not specified Chemotherapy - Not specified Endocrine therapy - Not specified Radiotherapy - Not specified Surgery - Not specified


NCT ID:

NCT00131950


Primary Contact:

Principal Investigator
Susan M. Gapstur
Robert H. Lurie Cancer Center


Backup Contact:

N/A


Location Contact:

Chicago, Illinois 60611
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: December 10, 2017

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