Meditation and Cognitive Function in Women With Breast Cancer



Status:Active, not recruiting
Conditions:Breast Cancer, Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:18 - Any
Updated:12/1/2018
Start Date:October 2007
End Date:October 2019

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Feasibility Study of Meditation, Cognitive Function, and Quality of Life in Women With Breast Cancer

The goal of this behavioral research study is to learn if participating in a Tibetan
meditation program helps to improve quality of life for women after chemotherapy and during
recovery from breast cancer. Whether the meditation program helps to improve brain function
and sleep quality will also be studied.

Screening Tests:

During the "screening" visit, you will be asked 4 questions about your memory and
concentration abilities. Based on how you score on this screening questionnaire, you may not
be eligible to participate in the study even if you have already signed the informed consent
form.

If you are found to be eligible for the study based on the screening questionnaire, you will
complete some tests during the screening visit to check your memory and concentration. For
example, you will be asked to remember a list of words and then be asked to recall them
later. You will also complete questionnaires asking about your mood, quality of life, and
other things like sleep, nervousness, and your experience with cancer. All together, the
tests and questionnaires should take about 90 minutes to complete.

Study Groups:

You will be randomly assigned (as in the toss of a coin) to 1 of 2 groups. People in Group 1
will take part in a Tibetan meditation program. People in Group 2 will be placed on a waiting
list. They may participate in the meditation program 3 months after being enrolled in the
study (when Group 1 has finished the follow-up visit).

Meditation Sessions:

If you are Group 1, you have 12 sessions of Tibetan meditation (2 times a week), over a
6-week period. You will be asked to complete a form asking about your satisfaction with the
program at the start of each week. The form will take 1-2 minutes to complete.

The meditation sessions will take place at M. D. Anderson. During the meditation sessions,
you will do deep breathing and visualization exercises and produce some sounds like "Ah."
Each session will last about 60 minutes. One (1) or more of these meditation sessions may be
videotaped by the study staff for check the quality of the sessions. Only the study staff
will be able to view this videotape. All videos will be destroyed after the data is
collected.

Participants in both groups will be mailed a questionnaire packet to fill out and send back
(return postage will be included in the packets) at 1 month and then at the end of the
meditation sessions (2 months). The questionnaires will ask about your mood, quality of life,
and other things like sleeping habits and nervousness. The packet will take about 45 minutes
to fill out. If you are in Group 2, you will receive packets at about the same time.

Your responses on these questionnaires will not be shared with your doctor. If you feel you
need a doctor's opinion about anything that is asked in these questionnaires (for example, if
you feel depressed or distressed), please contact your doctor.

Follow-up Visit:

One (1) month after the last meditation session (or at a similar time, for participants in
Group 2), you will be asked to return to the clinic. You will take some tests to check your
memory and concentration, similar to the tests you took at your screening visit. You will
complete questionnaires asking about your mood, quality of life, and other things like sleep,
nervousness, and your experience with cancer. All together, the questionnaires and tests
should take about 90 minutes to complete.

Once the follow-up visit is complete, the study is over. After Group 1 has completed the
follow-up visit, Group 2 will be given the option to take the meditation classes.

This is an investigational study. Up to 60 participants will be enrolled in this study. All
will be enrolled at M. D. Anderson.

Inclusion Criteria:

1. Women with stage I - III breast cancer who have undergone chemotherapy (either
neoadjuvant or adjuvant) 6 - 60 months prior to recruitment.

2. Women who report cognitive impairment since starting chemotherapy as assessed by four
questions from the FACT-Cog.

3. Women must be 18 years or older.

4. Women must be able to read, write and speak English.

5. Women must be currently undergoing hormone therapy (e.g., Tamoxifen or AIs)

6. Willing to come to MDACC for the meditation sessions and assessment sessions.

7. Women must be within 2 hours driving distance of MDACC.

Exclusion Criteria:

1. Women who have a documented diagnosis of a formal thought disorder (e.g.,
schizophrenia) will be excluded from the study.

2. Women with metastatic disease to the brain or any past neurologic injury.

3. Women with a Mini-Mental State Examination score of 23 or below.

4. Women with recurrent cancer
We found this trial at
1
site
1515 Holcombe Blvd
Houston, Texas 77030
 713-792-2121
University of Texas M.D. Anderson Cancer Center The mission of The University of Texas MD...
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