Exercise in Women at Risk for Breast Cancer
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|ClinicalTrials.gov Identifier: NCT00092950|
Recruitment Status : Completed
First Posted : September 27, 2004
Last Update Posted : July 2, 2017
This 2-part study will examine how much exercise people usually do in the course of their daily lives and how two different types of exercise-stretching and walking-affect the amount of fat in the body and certain hormones in the blood. It will also examine whether exercise can be increased by physician counseling with and without the use of a pedometer, and if exercising changes levels of stress, anxiety, and depression.
Breast cancer survivors and women at high risk for breast cancer who are between 18 and 75 years of age and who exercise less than 3 times per week may be eligible for this study. Candidates are screened with a medical history and physical examination, and their endurance and flexibility are tested by stretching exercises and by a 6-minute walk or run.
All participants complete study Part 1. Those who are eligible may also participate in Part 2.
- Part 1: Subjects wear a pedometer (a small device that measures the number of steps taken) on their waistband during all waking hours for 1 week without changing their usual level of activity. Depending on their level of activity, subjects may be invited to participate in Part 2 of the study.
- Part 2: Subjects are placed in either a walking group or a stretching group for 12 weeks. At the end of the 12-week period, those in the walking group are offered participation in the stretching group, and those in the stretching group are offered participation in the walking group.
Walking group participants wear a pedometer every day for 12 weeks. They are asked to gradually increase the number of steps they take each day, to keep a record of their daily step count, and to report periodically to the study staff on their progress. For 1 week during the study, participants also wear a device called an accelerometer that is used to verify the accuracy of the pedometer step counts.
Stretching group participants follow a program of stretching exercises for 12 weeks, with their progress monitored periodically by staff. During week 12, participants wear a pedometer and accelerometer.
All Part 2 participants also have the following tests and procedures:
- Blood draw: collected at the beginning and end of the study to test for certain hormones and HDL cholesterol levels.
- Questionnaires: about stress, anxiety, and depression levels; these are completed at the beginning and end of the study, and a detailed questionnaire about diet is completed at home or during a clinic visit.
- Body composition measurement: A "bioelectrical impedance" test, which measures body fat, is done at the beginning and end of the study. For this test, the subject lies on an examining table and a small electrical current is passed through electrodes placed on one hand and one foot. Although a small electrical current is used, this test is not painful.
- Endurance and flexibility testing: At the end of the study, participants repeat the 6-minute walk or run endurance test and the stretching flexibility test performed at screening.
|Condition or disease||Intervention/treatment||Phase|
|Breast Neoplasms||Behavioral: Physical activity||Phase 2|
Hide Detailed Description
Evidence suggests that high levels of physical activity can decrease breast cancer risk.
Physical activity could therefore represent a viable breast cancer prevention strategy.
In order to study the effect of physical activity on breast cancer risk, we must first develop feasible and efficacious physical activity interventions.
To determine the rate of compliance with a physical activity intervention using a pedometer, a physician prescription, and a motivational booklet.
To determine whether this intervention is more effective than a control of stretching exercises at increasing physical activity.
To determine whether physical activity as measured by a pedometer correlates with other measures of physical activity.
To assess the effect of the physical activity intervention on serum biomarkers, quality of life, functional capacity and body composition.
To examine long-term compliance with a program of increased physical activity and assess post program exercise motivation and adherence.
Eligible patients are women age 18-75 who meet one of the following criteria:
History of breast cancer without evidence of recurrent disease.
Gail model 5 year risk greater than 1.7%.
Claus model lifetime risk greater than 20%.
History of appropriately treated DCIS.
History of high risk lesion on breast biopsy (ADH, ALH, LCIS).
Known or suspected BRCA1 or BRCA2 mutation.
Patients must be sedentary at baseline and must be medically fit to exercise.
This is a randomized pilot study designed to assess the feasibility of a physical activity intervention in breast cancer survivors and women at high risk for breast cancer.
Stage I: Patients undergo a baseline activity evaluation for one week which involves wearing a sealed pedometer - those that have an average daily step count of less than 5,000 steps are eligible for randomization.
Stage II: Patients are assigned to either a walking intervention, (including a pedometer, a physician exercise prescription with a final goal of walking 10,000 steps per day, and a motivational booklet) or a control of stretching exercise for a period of 12 weeks.
Biomarkers, functional capacity, body composition and diet are assessed at the beginning and end of study.
This study plans to randomize 80 subjects, and has a greater than 90% power to detect a mean increase of 3,000 steps per day in intervention subjects.
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||88 participants|
|Official Title:||A Pilot Study of a Three Month Intervention for Increasing Physical Activity in Sedentary Women at Risk for Breast Cancer|
|Study Start Date :||September 23, 2004|
|Actual Primary Completion Date :||December 7, 2009|
|Actual Study Completion Date :||December 7, 2009|
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00092950
|United States, Maryland|
|National Institutes of Health Clinical Center, 9000 Rockville Pike|
|Bethesda, Maryland, United States, 20892|