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 * About the InBody BWA ON Study
 * About Lymphedema
 * Study Locations
 * FAQs

See if You Pre-Qualify
See if You Pre-Qualify
 * About the InBody BWA ON Study
 * About Lymphedema
 * Study Locations
 * FAQs

Main Menu
See if You Pre-Qualify
See if You Pre-Qualify
 * About the InBody BWA ON Study
 * About Lymphedema
 * Study Locations
 * FAQs

 * About the InBody BWA ON Study
 * About Lymphedema
 * Study Locations
 * FAQs

See if You Pre-Qualify
See if You Pre-Qualify
 * About the InBody BWA ON Study
 * About Lymphedema
 * Study Locations
 * FAQs

Main Menu
See if You Pre-Qualify
See if You Pre-Qualify
 * About the InBody BWA ON Study
 * About Lymphedema
 * Study Locations
 * FAQs


THE INBODY BWA ON LYMPHEDEMA CLINICAL RESEARCH STUDY

Consider Enrolling in a Clinical Trial for breast cancer survivors who are at
risk of developing Lymphedema Today!

Learn about the study
Take the Prescreener


THE INBODY BWA ON LYMPHEDEMA CLINICAL RESEARCH STUDY

Consider Enrolling in a Clinical Trial for breast cancer survivors who are at
risk of developing Lymphedema Today!

Learn about the study
Take the Prescreener


ABOUT THE INBODY BWA ON STUDY

The InBody BWA ON research study is evaluating if the use of a body composition
assessment device, called the InBody BWA ON, is effective in detecting and
monitoring lymphedema in adults, who have had breast cancer-related surgery
within the last 12 months prior to enrollment.

The InBody BWA ON device will be given for at-home use to all adults who
participate, and is used twice daily through the study, in the morning and
evening. Participants will be asked to attend 5 in-clinic visits throughout the
study. The study will last approximately 12 months, including the initial visit
and follow-up visits.

Participants who successfully enroll into the study will be given the InBody BWA
ON device for use in the comfort of their own home for the entirety of the
study. If appropriate, some participants will be allowed to continue using the
at-home device after the study is completed.


STUDY CRITERIA

If you, or someone you know, is interested in enrolling in this study, you or
they may be eligible if you:


ARE AN ADULT AGED 18 OR OLDER


HAVE A MEDICAL DIAGNOSIS OF UNILATERAL (ON ONE SIDE) BREAST CANCER


HAVE HAD BREAST CANCER-RELATED SURGERY WITHIN THE LAST 12 MONTHS PRIOR TO
ENROLLMENT

*Other eligibility criteria apply. Participants receive in-home BWA ON device at
no cost. Compensation for study-related time and travel may be provided.


PARTICIPATION OVERVIEW

This study’s main purpose it to evaluate if the use of a body composition
assessment device, called the InBody BWA ON, is effective in detecting and
monitoring lymphedema in adults who have had breast cancer-related surgery
within the last 12 months prior to enrollment. All participants enrolled in this
study will be supplied the InBody BWA ON device for use in the comfort of their
own home, to be used twice daily (morning and evening) every day through the
study. 

All participants who are eligible and successfully enroll in this study will
participate for up to 12 months. This includes an initial screening visit to
determine if you are eligible for the study.  This visit is when the
participants receive the InBody BWA ON device and are shown how to use it. 
Visit 2 occurs at month 3 and involves follow-up surveillance for standard of
care with the InBody 770 and circumference tape. OT/PT treatment is included if
needed.  The last 3 visits occur at month 6, month 9, and month 12 respectively,
and include standard of care for complete decongestive therapy, with InBody 770
testing and circumference tape measurements.

Am I eligible?


REFER A FRIEND

Do you know someone age 18 or older who has had breast cancer related surgery in
the last 12 months? They may be eligible to participate in this clinical study.
Consider sharing information with them about how they can learn more.

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