Breast Cancer Clinical Trial

Behavioral Weight Loss Program for Cancer Survivors in Maryland

Summary

Behavioral Weight Loss for Overweight and Obese Cancer Survivors in Maryland: A Demonstration Project

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Full Description

The objective of the ASPIRE Project is to design, implement, and evaluate a real-world, lifestyle-based, support for overweight or obese cancer survivors in both urban and rural areas of Maryland. The project will provide three options of support to encourage lifestyle change to achieve and maintain a healthy weight for cancer survivors:

Self-Directed Weight Loss: educational materials only;
App-Directed Weight Loss: educational materials, weight loss app with weekly e-mail support; and
Coach-Directed Weight Loss: educational materials, weight loss app, weekly e-mail support and one-to-one weekly telephonic coach support.

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Eligibility Criteria

Inclusion Criteria:

previously diagnosed with a malignant solid tumor,
completed all required surgical, and/or chemotherapy and/or radiation curative intent therapy at least three months prior to enrollment,
anticipated treatment-free life span of 12 months or longer.
chemoprophylaxis with tamoxifen or aromatase inhibitors for breast cancer in women will be permitted
anti- Luteinizing-hormone releasing therapy for prostate cancer in men will be permitted.
BMI ≥ 25 kg/m2 (BMI ≥ 23 kg/m2 for Asians) and weight ≤ 400 lbs.
have an email address for regular personal use

Additional criteria for participants in weight tracking (self-directed or app directed)

willingness to record/transmit quarterly weights for 12 months

Additional criteria for App-Directed Program:

willingness to change diet and increase physical activity and track weight, diet and physical activity
have a smart phone for personal use
sufficient data plan/Internet to support daily use of weight loss app*

Additional Criteria for Coach-Directed Weight Loss Program

willingness to lose weight by changing diet and physical activity habits
willingness to track weight, diet and physical activity
willingness to record/transmit quarterly weights for 12 months
smart phone for personal use
data plan/Internet to support daily use of weight loss app*
willingness to complete coaching calls (12 weekly calls and 3 monthly calls)

sufficient call plan to support coaching calls

a corresponding website could be used, then daily Internet access is required for person use.

Exclusion Criteria:

received any chemotherapy (unless anti-hormonal therapy) and/or radiation three months or less prior to the proposed program date
women who are breastfeeding, pregnant, or planning pregnancy within the next year

Additional exclusion criteria for participants in weight tracking and/or Coach-Directed Program

self-identification of uncontrolled concurrent medical condition likely to limit compliance with the program as determined by investigators.
current involvement in another organized weight loss program
current use of steroids or other medication known to affect body weight
bariatric surgery scheduled within the next 6 months, or
plan to move outside the continental US in the next 12 months

Study is for people with:

Breast Cancer

Estimated Enrollment:

340

Study ID:

NCT04534309

Recruitment Status:

Completed

Sponsor:

Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins

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There is 1 Location for this study

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Johns Hopkins ProHealth
Baltimore Maryland, 21207, United States

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Estimated Enrollment:

340

Study ID:

NCT04534309

Recruitment Status:

Completed

Sponsor:


Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins

How clear is this clinincal trial information?

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