Effect of a Low-Calorie Diet and/or Exercise Program on Risk Factors for Developing Breast Cancer in Overweight or Obese Postmenopausal Women
Breast Cancer, Obesity, Weight Changes
About this trial
This is an interventional prevention trial for Breast Cancer focused on measuring breast cancer, obesity, weight changes
Eligibility Criteria
DISEASE CHARACTERISTICS:
At increased risk for developing breast cancer due to any of the following lifestyle risk factors:
- Lack of physical activity
- Excess weight
- Obesity
- Weight gain over lifetime
- Body mass index > 25.0
- Physically able to undertake a moderate exercise or calorie reduction program
- No history of invasive or in situ breast cancer
PATIENT CHARACTERISTICS:
- Postmenopausal, defined by the absence of periods for the past 12 months
- Able to attend study clinic visits and classes, and undergo study measurements
- Able to fill out questionnaires and logs in English
- No moderate to high alcohol intake (more than 2 drinks per day)
- No concurrent smoking
- No invasive cancer within the past 10 years except simple basal cell or squamous cell carcinoma
No diabetes mellitus
- Fasting blood sugar < 126 mg/dL (on 2 occasions)
- Hematocrit 32-48%
- WBC 3,000-15,000/mm³
- Potassium 3.5-5.0 mEq/L
- Creatinine ≤ 2.0 mg/dL
- No abnormalities on screening physical that contraindicate study participation
No contraindications for treadmill testing or entry into a training program, including any of the following:
- Myocardial infarction within the past 6 months
- Pulmonary edema
- Myocarditis
- Pericarditis
- Unstable angina
- Pulmonary embolism or deep vein thrombosis
- Uncontrolled hypertension (i.e., blood pressure > 200/100 mm Hg)
- Orthostatic hypotension
- Moderate-to-severe aortic stenosis
- Uncontrolled arrhythmia
- Uncontrolled congestive heart failure
- Third-degree heart block
- Left bundle branch block
- Thrombophlebitis
- ST depression > 3 mm at rest
- History of cardiac arrest or stroke
Normal exercise treadmill testing (ETT)
- Negative thallium or echo ETT required for patients with abnormal ETT (defined as ≥ 1.5 mm ST depression in > 1 lead within 1-minute recovery OR ≥ 1.1 mm ST depression in > 1 lead after 1-minute recovery OR reading of positive test by study doctor)
- No drug abuse
- No significant mental illness
PRIOR CONCURRENT THERAPY:
- More than 6 months since prior and no concurrent menopausal hormone replacement therapy of any type, including vaginal route
- No concurrent participation in any other organized weight loss or exercise program
- No concurrent appetite suppressant medication
- No concurrent medications (e.g., weight-loss medications) likely to interfere with adherence to interventions or study outcomes
Sites / Locations
- Fred Hutchinson Cancer Research Center
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
No Intervention
Other
Other
Other
Control
Caloric Restriction
Exercise Intervention
Caloric Restriction AND Exercise Intervention
Nutritionist-delivered weight loss intervention though diet modification with an aim of 10% weightloss over a year long intervention based on the DPP and LookAHEAD interventions. Participants meet with a nutritionist individually and in small groups. Participants receive general information about diet and behavior strategies such as self-monitoring, goal-setting, stimulus-control, problem-solving, and relapse-prevention training. Participants learn to set a calorie goal and a fat gram goal and how to achieve the goal calorie reduction. Meetings are held weekly during the first 6 months of the diet program but taper off over the course of the study.
Participants exercise 3 days per week under the supervision of a physiologist and 2 days per week independently at home, for a total of 5 exercise sessions (at least 45 minutes of moderate-intensity exercise per session) weekly over 12 months
Combined caloric restriction & exercise intervention