Breast Cancer Clinical Trial

Addressing Modifiable Breast Cancer Risk Factors With Project CONECT

Summary

The objective of this protocol is to adapt and pilot test an existing lifestyle modification intervention for weight loss for women with overweight or obesity who have had a recent false positive mammography screen. The purpose of this pilot trial is to establish feasibility of Connect Online to Engage Change Tool (CONECT) to promote weight loss through increased physical activity and diet change.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Female
40-65 years of age,
Received a negative mammography screening result in the previous four weeks
Moderately sedentary lifestyle (less than 120 minutes/week moderate intensity activity),
Answer "no" to all questions on the Physical Activity Readiness Questionnaire (PAR-Q).
BMI 25-40 kg/m2
Has access to a computer or mobile device with wireless internet
Able to speak and read English (language requirements are necessary because we cannot accommodate additional languages in prototype development phase.)

Exclusion Criteria:

Previous history or current diagnosis of breast cancer
Pregnancy or lactation
Involvement in a weight loss program
Major co-morbidities (e.g.,diabetes, hypertension, etc.)
History of disordered eating
Currently taking medication that may impact weight (e.g., synthroid, metformin)

Study is for people with:

Breast Cancer

Estimated Enrollment:

14

Study ID:

NCT02871388

Recruitment Status:

Completed

Sponsor:

Virginia Commonwealth University

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There is 1 Location for this study

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Virginia Commonwealth University/Massey Cancer Center
Richmond Virginia, 23298, United States

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Estimated Enrollment:

14

Study ID:

NCT02871388

Recruitment Status:

Completed

Sponsor:


Virginia Commonwealth University

How clear is this clinincal trial information?

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