Breast Cancer Clinical Trial

BCRL Prevention Pilot

Summary

The purpose of this study is to establish feasiblity of recruiting obese breast cancer survivors at the end of treatment, getting those survivors to lose weight and attend follow-up visits for 6 months.

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Full Description

Breast cancer related lymphedema occurs in 20-30% of survivors. Weight loss could prevent onset. We seek to do a pilot study to establish feasibility of 1) recruiting survivors at risk for lymphedema to do a weight loss intervention, 2) achieving 10-15% weight loss over 26 weeks in this population, and 3) attendance at follow-up visits 6 months.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Women
Breast Cancer Survivors who had 5 or more lymph nodes removed and radiation to lymph nodes as part of treatment.
Completed all treatments - no metastatic cancers
Overweight or obese (BMI greater than or equal to 25 kg/m2)
Medically and logistically able to participate in a weight loss and exercise program over 6 months.
Diagnosed with breast cancer within the past 2 years.

Exclusion Criteria:

More than 2 years since breast cancer diagnosis
Medical status that would preclude safety of participation in a weight loss and exercise program
Metastatic cancer
Already enrolled in a weight loss program

Study is for people with:

Breast Cancer

Estimated Enrollment:

20

Study ID:

NCT01166672

Recruitment Status:

Completed

Sponsor:

Abramson Cancer Center of the University of Pennsylvania

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There is 1 Location for this study

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Abramson Cancer Center of the University of Pennsylvania
Philadelphia Pennsylvania, 19104, United States

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Estimated Enrollment:

20

Study ID:

NCT01166672

Recruitment Status:

Completed

Sponsor:


Abramson Cancer Center of the University of Pennsylvania

How clear is this clinincal trial information?

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