Breast Cancer Clinical Trial

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Avon Foundation Program to Improve Quality of Life in Breast Cancer Survivors

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Summary

Women with breast cancer often suffer significant distress and disability from their disease. A practice of meditation-based stress reduction and cognitive-affective-behavioral learning may help women with breast cancer decrease their suffering and improve their quality of life.

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Full Description

The objective of this study in women recently treated for breast cancer is to determine whether an intervention program consisting of group and individual instruction in a meditation-based practice of stress-reduction and cognitive-affective-behavioral learning has the potential for reducing disabling distress and improving quality of life in a population vulnerable to the progression or recurrence of disease. Quality of life will be assessed at 12 months.

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Eligibility Criteria

Inclusion Criteria:

All women with stage I-III breast cancer who have received treatment within the preceding year will be eligible for inclusion in the study.

Exclusion Criteria:

Patients who refuse to participate will be excluded
Patients with metastatic (stage IV) cancer are excluded.

Study is for people with:

Breast Cancer

Estimated Enrollment:

94

Study ID:

NCT00278837

Recruitment Status:

Completed

Sponsor:

Weill Medical College of Cornell University

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There is 1 Location for this study

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The New York Presbyterian Hospital-Weill Medical Center
New York New York, 10021, United States

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Estimated Enrollment:

94

Study ID:

NCT00278837

Recruitment Status:

Completed

Sponsor:


Weill Medical College of Cornell University

How clear is this clinincal trial information?

Clinical Trial Resources

SurvivorNet’s Guide To Clinical Trials: What Are They And Are They Right for You?
Clinical Trials for Breast Cancer
Have You Been Diagnosed With Late-Stage Breast Cancer? Know That You Have Treatment Options.
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