An Exercise RCT Targeting African-American Women With Metabolic Syndrome and High Risk for Breast Cancer
Metabolic Syndrome, Obesity
About this trial
This is an interventional prevention trial for Metabolic Syndrome focused on measuring Breast Cancer, Obesity, African American female, exergaming
Eligibility Criteria
Inclusion Criteria:
- Eligible participants should be female, African-American postmenopausal women between the ages of 45 and 65 with waist circumference greater than 35 inches (88 cm), 5-year invasive breast cancer risk is greater than 1.40% using the CARE model, and have at least one of the following:
- elevated fasting glucose is greater than or equal to 100 mg/dL
- elevated blood pressure is greater than or equal to 130/85 mm/Hg. In addition, they should also have a cell phone with texting capabilities, read and speak English, reside in close proximity to, or can access the Navy Yard stop on the green line, can provide meaningful consent, and medical clearance from a physician or nurse practitioner.
Exclusion Criteria:
- -physical limitations that prevent participant from exercising
- premenopausal
- pregnant or planning to become pregnant within the next year
- history of cancer (except for non-melanoma skin cancer)
- have diabetes
- use anti-diabetic medication (including insulin)
- are currently enrolled in a physical activity and/or dietary clinical trial
- are on a weight loss program
- cannot commit to the intervention schedule
Sites / Locations
- Georgetown Lombardi Office of Minority Health community site
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
No Intervention
Experimental
Facility-Based Exercise Intervention
Control
Home-Based Exercise Intervention
Supervised Facility-Based Exercise Intervention Arm The participants randomized to the exercise group will be required to meet and maintain a goal of 150 min/wk of moderate intensity exercise for 6 months. This intervention will use heart rate and rating of perceived exertion (RPE) to define moderate intensity. Participants will exercise for the prescribed duration at a heart rate in the range of 45-65% of their maximal oxygen consumption (VO2 max), as determined during baseline testing, and with an RPE in the range of 11-14 on the 20-point scale. The exercise will primarily utilize treadmills and exercise bikes.
After baseline testing, the control group will be asked to maintain their current daily activities and exercise habits for the duration of the study (6 months). The control group will have measurements at the same time periods as the participants in the intervention arm through the completion of the study. Participants will be seen for follow-up at 3 and 6 months (study completion). The participants in the control group will receive the same incentives as those in the intervention arms (gift cards). Since the women in the control group are obese, with components of metabolic syndrome, and at relatively high risk for breast cancer, we are providing healthy lifestyle information to the group, via text messages.
Home-Based Exercise Intervention Group The participants randomized to this intervention arm will be required to meet and maintain a goal of 150 min/wk of moderate intensity exercise for 6 months, the same as the supervised intervention group. Their exercise goal will be to achieve a total of 10,000 steps per day, as measured by pedometers. Participants will be required to have a cell phone with text messaging capabilities.