Mobile Behavior Change Program for Weight Loss in Breast Cancer Survivors

Completed · Not applicable

Conditions studied: Weight Loss, Behavior, Health

In brief

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.

Key facts

Study ID

NCT04753268

Run by

Noom Inc.

People needed

30

Starts

2021-03-24

Expected to finish

2021-10-01

Last updated by the study team

2022-10-06

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• 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

You may not qualify if…

• 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

Where it is running

• Noom, Inc — New York, New York, United States

Full record on ClinicalTrials.gov

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