Status:
COMPLETED
Lifestyle Intervention for High Risk Cancer Survivors
Lead Sponsor:
M.D. Anderson Cancer Center
Collaborating Sponsors:
National Cancer Institute (NCI)
Conditions:
Breast Cancer
Eligibility:
FEMALE
18-80 years
Phase:
NA
Brief Summary
The goal of this behavioral research study is to find out more about the health behaviors of cancer survivors. Researchers want to understand the cultural, social, and environmental factors related to...
Detailed Description
If you agree to take part in this study, you will have a baseline study visit. This visit will include a physical exam, including measurements of your height and weight. Your hips, wrist, mid-arm, and...
Eligibility Criteria
Inclusion
- 18-80 years old at diagnosis
- diagnosed with operable invasive cancer
- have access to high speed internet
- Phase 2 only: be currently sedentary (i.e., engage in \< or = 60 minutes of purposeful moderate-intensity PA/week)
- Phase 2 only: be overweight or obese (i.e., have a body mass index (BMI) \> or = 25 kg/m\^2)
- speak English
Exclusion
- watch less than 3 hours of television per day
- be currently enrolled in another intervention study or recently completed a study promoting healthy lifestyle behaviors (diet and/or exercise)
- participants answering 'Yes' to one or more of the questions on the physical activity readiness questionnaire (PAR-Q) will need to obtain approval from a physician before they can participate in the intervention.
Key Trial Info
Start Date :
May 1 2012
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 1 2015
Estimated Enrollment :
1150 Patients enrolled
Trial Details
Trial ID
NCT01508273
Start Date
May 1 2012
End Date
December 1 2015
Last Update
December 2 2016
Active Locations (3)
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1
The University of North Texas Health Science Center
Fort Worth, Texas, United States, 76107
2
Memorial Herman Health Care System
Houston, Texas, United States, 77030
3
University of Texas MD Anderson Cancer Center
Houston, Texas, United States, 77030