Breast Cancer Clinical Trial

Promoting a Healthier Lifestyle Among Breast Cancer Survivors

Summary

The purpose of this study is to find out if a counseling program the investigators have developed can help breast cancer survivors adopt a healthier lifestyle.

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Full Description

Participants will be randomly assigned to one of two groups. One group of breast cancer survivors will receive general information on how to adopt healthy lifestyle behaviors. The other group of breast cancer survivors will receive counseling on how to increase their level of physical activity.

Participants will have three consultations with a health counselor. The first two consultations will take place in-person and the third consultation will take place via telephone. Participants will also be asked to complete questionnaires assessing their physical and mental well-being, their dietary habits, and their physical activity habits at four time-points: in-person during their first study visit, via mail or through an online survey 6 weeks later, in-person 12 weeks later, and via mail or through an online survey 24 weeks later. Additionally, during their first study visit and 12 weeks later, their level of aerobic fitness will be tested by having participants walk a long hallway for six minutes.

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Eligibility Criteria

Inclusion Criteria:

≥ 18 years of age;
be capable of speaking and reading English;
be diagnosed with stage 0-II breast cancer;
be currently disease free;
have been treated surgically for breast cancer;
have completed chemotherapy and/or radiotherapy at least three months but no more than two years prior;
be physically able to exercise as measured by the Physical Activity Readiness Questionnaire-Revised (Thomas, Reading, & Shephard, 1992) ;
be currently physically inactive as measured by the Godin Leisure Time Exercise Questionnaire (Godin & Shepard, 1985); and
be contemplating increasing physical activity as measured by the Exercise Stages of Change - Short Form (Marcus, Selby, Niaura, & Rossi, 1992).

Study is for people with:

Breast Cancer

Estimated Enrollment:

68

Study ID:

NCT01419613

Recruitment Status:

Completed

Sponsor:

H. Lee Moffitt Cancer Center and Research Institute

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There is 1 Location for this study

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H. Lee Moffitt Cancer Center and Research Institute
Tampa Florida, 33612, United States

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Estimated Enrollment:

68

Study ID:

NCT01419613

Recruitment Status:

Completed

Sponsor:


H. Lee Moffitt Cancer Center and Research Institute

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