Breast Cancer Clinical Trial
Mobile Behavior Change Program for Weight Loss in Breast Cancer Survivors
Summary
The purpose of this study is to evaluate the preliminary efficacy of a Noom Breast Cancer Weight Loss Program on weight loss outcomes, quality of life, and physical activity. Also, to qualitatively determine acceptability of this novel program among breast cancer survivors with overweight or obesity.
Eligibility Criteria
Inclusion Criteria:
Able to understand and provide informed consent
18 years and older
Overweight or obesity (BMI ≥ 27.5)
Not 6 months postpartum
Not planning to become pregnant in the next 7 months
Have a smartphone that is compatible with Noom's mobile app
Breast cancer survivor with stage I, II, or III
Completed active treatment (e.g, surgery, chemo, radiation, etc.) > 6 months ago
Exclusion Criteria:
Inability or unwillingness of a participant to give written informed consent
Currently pregnant or < 6 months postpartum
Plans to become pregnant within the next 7 months
Stage IV, metastatic cancer or DCIS
Currently taking insulin
Uncontrolled hypertension
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There is 1 Location for this study
New York New York, 10001, United States
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