The BWEL Breast Cancer Weight Loss Study. Randomized Phase III Trial Evaluating the Role of Weight Loss in Adjuvant Treatment of Overweight and Obese Women with Early Breast Cancer (ALLIANCE A011401)

  • STATUS
    Recruiting
Updated on 24 November 2020
cancer
breast cancer
overweight or obesity
weight loss diet

Summary

The BWEL Breast Cancer Weight Loss Study. Randomized Phase III Trial Evaluating the Role of Weight Loss in Adjuvant Treatment of Overweight and Obese Women with Early Breast Cancer (ALLIANCE A011401)

Description

The BWEL Breast Cancer Weight Loss Study will look at whether losing weight, by eating less and exercising more, changes the risk of cancer recurrence in women who have been diagnosed with early breast cancer. The study will enroll more than 3,000 patients with breast cancer in the United States and Canada.

Participants will receive regular mailings on breast cancer topics and general health as well as invitations to attend online seminars that focus on breast cancer.

Participants will complete health questionnaires and take height and weight measurements and a fasting blood draw at different points throughout the study.

Details
Clinical Study IdentifierTX149689
Last Modified on24 November 2020

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Eligibility

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Inclusion Criteria

Are you female?
Do you have any of these conditions: Breast Cancer or Weight Loss?
You have been diagnosed with stage II-III breast cancer within the last 12 months
You have completed surgery and chemotherapy (if applicable)
You are interested in taking part in a weight loss program
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How to participate?

Step 1 Connect with a site
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

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Step 2 Get screened

Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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Step 3 Enroll in the clinical study

If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Step 4 Get your study results

Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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