Breast Cancer Clinical Trial

Cancer and Mindfulness-Based Cancer Recovery After Chemotherapy

Summary

Upon the completion of aggressive chemotherapy and radiation for curative intent cancers, many cancer survivors suffer from a myriad of symptoms ranging from physical symptoms such as hot flashes, insomnia, and fatigue to psychosocial symptoms including depression and anxiety. Mindfulness Based Cancer Recovery (MBCR) is a type of mind-body intervention. Mind-body interventions are defined as practices or interventions that focus on the connection and integration of the mind and body and the ability for these connections to effect changes on physical, emotional and spiritual levels for the purpose of promoting health and well being.

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Full Description

MBCR is a step wise standardized behavioral intervention of MBSR. The program is usually conducted in eight weekly class sessions that are 2-2.5 hours in length. During class sessions, participants are presented with mindfulness meditation techniques and share their experiences related to these meditation practices. There is a home practice component with an expectation of regular home meditation practice of 45 minutes per day. In addition to home meditation practice there are often reading assignments and reflective exercises that relate to mindfulness. A full day retreat generally occurs in the second half of the course, providing an opportunity for class participants to gain extended experience with mindfulness techniques.

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Eligibility Criteria

Inclusion Criteria:

Stage I-III breast cancer, gynecologic cancer or colorectal cancer
Cancer survivor at least 18 years of age at the time of study enrollment
Completed chemotherapy within the past six months at the time of consent (adjuvant hormone therapy is allowed)

Exclusion Criteria:

Psychologic disease in which informed consent cannot be obtained from the subject
Need for ongoing chemotherapy and/or radiation therapy

Study is for people with:

Breast Cancer

Estimated Enrollment:

45

Study ID:

NCT01601548

Recruitment Status:

Completed

Sponsor:

Masonic Cancer Center, University of Minnesota

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There is 1 Location for this study

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Masonic Cancer Center, University of Minnesota
Minneapolis Minnesota, 55455, United States

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Study is for people with:

Breast Cancer

Estimated Enrollment:

45

Study ID:

NCT01601548

Recruitment Status:

Completed

Sponsor:


Masonic Cancer Center, University of Minnesota

How clear is this clinincal trial information?

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