MOtiVating Endometrial Cancer Survivors With Activity Monitors and Tailored Feedback



Status:Recruiting
Conditions:Cervical Cancer, Cancer, Endometrial Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:18 - Any
Updated:2/1/2019
Start Date:September 28, 2018
End Date:August 2020
Contact:Luz Cuaboy, MS
Email:luz_cuaboy@med.unc.edu
Phone:919-966-7051

Use our guide to learn which trials are right for you!

The MOVES Trial: MOtiVating Endometrial Cancer Survivors With Activity Monitors and Tailored Feedback

Overweight and obese endometrial cancer (EC) survivors at the University of North Carolina
(UNC) at Chapel Hill will be approached for tailored feedback fitness intervention. The
investigators plan to enroll 36 women (18 in each arm) to evaluate if receipt of weekly
tailored feedback messages can improve physical activity in EC survivors. It is hypothesized
that women receiving the feedback message intervention will increase step counts from
baseline more than 2,000 steps compared to women in the non-intervention arm.

Objectives:

- To assess if a tailored feedback fitness intervention can increase physical activity in
EC survivors from baseline to 12 weeks post-baseline

- To determine the acceptability of the fitness intervention in EC survivors through a
completion survey.

- To assess if a tailored feedback message fitness intervention can (1) decrease BMI, (2)
reduce waitst to hip (W.H) ratios, (3) improve quality of life (QOL) and (4) improve
serum metabolic markers (insulin, glucose and low density lipoprotein (LDL) in EC
survivors.

Inclusion Criteria:

- Be over the age of 18 years

- Have a confirmed diagnosis of endometrial cancer and have completed therapy (surgery,
chemotherapy or radiation) within the past 6 months

- Have no current evidence of endometrial cancer

- Have a BMI 25 kg/m2 or greater

- Have approval from their treating physician to engage in moderate-intensity physical
activity.

- Have a smart phone with Bluetooth capabilities turned on

- Have access to email

Exclusion Criteria:

- Are currently undergoing treatment for their cancer

- Are unable to read a sample message aloud

- Do not have a computer or smart phone with Bluetooth capabilities

- Are pregnant

- Have a history of angina or palpitations with exertion

- Have a history of uncontrolled pulmonary disease (COPD or asthma)

- Have one or more significant medical conditions that in the physician's judgment
preclude participation in the walking intervention.
We found this trial at
1
site
101 Manning Drive
Chapel Hill, North Carolina 27514
Principal Investigator: Leslie Clark, MD
?
mi
from
Chapel Hill, NC
Click here to add this to my saved trials