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Effects of Yoga in Breast Cancer Patients

Primary Purpose

Breast Cancer

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Yoga Group
Stretching Control Group
Waitlist Control Group
Questionnaire
Sponsored by
M.D. Anderson Cancer Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Breast Cancer focused on measuring Breast Cancer, Tibetan Yoga, Stretching Program, Yoga, Quality of Life, Questionnaire, Survey

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  1. Women with Stage 0 - III breast cancer, undergoing daily adjuvant radiation for 6 weeks in the Department of Radiation Oncology at the M. D. Anderson
  2. The participants will need to be 18 years of age or older.
  3. Patients should be able to read, write, and speak English or Spanish.

Exclusion Criteria:

  1. Patients who have a documented diagnosis of a formal thought disorder (e.g., schizophrenia) will be excluded from the study.
  2. Patients with metastatic disease of the bone will be excluded to avoid any bone fractures that may result from yoga movements.
  3. Patients with active/non-canalized deep vein thrombosis will be excluded from the study.
  4. Patients who have not undergone any surgical treatment for their cancer will be excluded to ensure a more homogeneous sample.
  5. Patients with extreme mobility issues (e.g., unable to get in and out of a chair unassisted) will be excluded.
  6. Patients who have practiced yoga or taken yoga classes in the year prior to diagnosis will be excluded.
  7. Patients diagnosed with lymphedema at baseline will be excluded.

Sites / Locations

  • University of Texas MD Anderson Cancer Center

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Other

Arm Label

Group 1 Yoga Program

Group 2 Stretching Program

Group 3 Waitlist Control Group

Arm Description

3 sessions of yoga each week for 6 weeks. Questionnaire evaluating treatment-related symptoms during the middle of radiotherapy.

3 sessions of stretching each week for 6 weeks. Questionnaire evaluating treatment-related symptoms during the middle of radiotherapy.

Option of participating in the yoga or stretching program after the study has ended. Questionnaire evaluating treatment-related symptoms during the middle of radiotherapy.

Outcomes

Primary Outcome Measures

Fatigue and sleep assessed with self-report measures and actigraphy.

Secondary Outcome Measures

To see if yoga will help to improve patients' quality of life (QOL) during treatment for cancer and during recovery from the effects of cancer treatment.
To learn if a yoga program is effective in helping to decrease emotional distress and improve physiological functioning.

Full Information

First Posted
July 27, 2007
Last Updated
August 30, 2022
Sponsor
M.D. Anderson Cancer Center
Collaborators
National Institutes of Health (NIH), National Cancer Institute (NCI)
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1. Study Identification

Unique Protocol Identification Number
NCT00508794
Brief Title
Effects of Yoga in Breast Cancer Patients
Official Title
Biobehavioral Effects of Yoga During Breast Cancer Treatment
Study Type
Interventional

2. Study Status

Record Verification Date
August 2022
Overall Recruitment Status
Completed
Study Start Date
March 9, 2006 (Actual)
Primary Completion Date
August 11, 2022 (Actual)
Study Completion Date
August 11, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
M.D. Anderson Cancer Center
Collaborators
National Institutes of Health (NIH), National Cancer Institute (NCI)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
In this study researchers will examine the initial efficacy of implementing a yoga program for patients with breast cancer as an adjuvant to their radiotherapy. Patients with breast cancer who are undergoing radiotherapy will be randomly assigned to either a yoga group (YG), or a stretching (ST) control group, or a waitlist control (WL) group. Participants in YG and ST groups will attend three sessions each week throughout their 6-week radiotherapy schedule. The sessions will be coordinated with the treatment schedule and conducted adjacent to the treatment facility. Measures will be obtained prior to randomization, a brief assessment during the middle of radiation therapy, during the last week of radiation therapy, and 1, 3 and 6 months after the last radiation session. With the inclusion of two control groups in this randomized trial researchers will attempt to validate the benefits of yoga as an adjuvant to radiotherapy in patients with breast cancer wherein researchers will control for specific components of the yoga program and also examine some of the mechanisms that are necessary for the program to be effective. Our specific aims in the proposed study are to: Conduct an initial evaluation of whether participation in the yoga program improves patients' fatigue and sleep disturbances. Fatigue and sleep will be assessed with self-report measures and the use of actigraphy for a more objective measure of sleep quality. Secondary end points will include examining QOL, mental health and objective physiological outcomes (blood samples for immune measures, saliva samples for cortisol levels, and heart rate variability). Exploratory analyses will examine some plausible mediators of the yoga program including cognitive processing, spirituality, and finding meaning in the cancer experience.
Detailed Description
If you choose to take part in this study, you will come to M. D. Anderson for your first visit. If this is not convenient, a researcher can visit you at your home. At this time, you will be asked to complete several questionnaires. The questions will ask about your sleeping habits, how you have been feeling, and your general QOL. This will take about 45-60 minutes to complete. Researchers, will then ask you to complete a daily sleep diary for the next 7 days. During this time, you will be given an actigraph watch to wear that will collect data about your day-time activity and sleeping habits. The watch should be worn 24 hours a day for 7 days a week. You will have an electrocardiogram (ECG - a test to measure the electrical activity of your heart) and your breathing rate will be measured. After your first visit to M. D. Anderson or after a researcher has visited you at home, you will be randomly assigned (as in the toss of a coin) to one of 3 groups. Participants in the first group will take part in a yoga program. If you are assigned to the yoga group, you will take part in 3 sessions of yoga each week for 6 weeks. You may take part in the yoga sessions any 3 days of the week. Each yoga session will last around 60 minutes. During the yoga sessions, you will also be asked to do breathing exercises and to perform different movements and meditation. None of the movements are difficult. You will be able to follow this program at your own pace. Participants in the second group will take part in a stretching program. If you are assigned to the stretching group, you will take part in 3 sessions of stretching each week for 6 weeks. You may take part in the stretching sessions any 3 days of the week. Each stretching session will last around 60 minutes. During these stretching sessions you will be asked to do simple stretching exercises. None of the movements are difficult. You will be able to follow this program at your own pace. Beginning with the second week, participants in the first and second groups will be asked to complete a brief questionnaire, about the yoga or stretching program, before the first class each week. The questionnaire will take about 1 to 2 minutes to complete. You will also have an ECG and your breathing rate will be measured before and after one of the classes during the third or fourth week and again during the last week. Each stretching and yoga session will be audio and video taped for the purpose of quality control. Participants in the third group will not take part in the yoga or stretching program during this study. However, if you are assigned to this group, you will be given the option of participating in the yoga or stretching program after the study has ended. This will be after you have finished your last assessment. All participants will complete a brief questionnaire during the middle of radiotherapy. The questionnaire will evaluate your treatment-related symptoms and will take about 15 minutes to complete. During the last week of radiotherapy, and at 1, 3, and 6 months after the end of radiation treatment, all participants will be asked to fill out a packet of questionnaires (similar to those taken at the first visit). It should take about 45 minutes to complete all of the questionnaires. If it is not convenient for you to come to M. D. Anderson, a researcher can visit you at home to help with the questionnaires. You will then be asked to complete another daily sleep diary for another 7 days. During this time, you will wear an actigraph watch 24 hours a day for 7 days a week to collect the same data as before. During this time, you will have an ECG and your breathing rate will be measured. All participants will be asked to refrain from participating in any other yoga classes for the duration of the study. Your participation in this study will be over after your 6-month assessment. This is an investigational study. Up to 180 patients will take part in this study. All will be enrolled at M. D. Anderson.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer
Keywords
Breast Cancer, Tibetan Yoga, Stretching Program, Yoga, Quality of Life, Questionnaire, Survey

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
191 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Group 1 Yoga Program
Arm Type
Experimental
Arm Description
3 sessions of yoga each week for 6 weeks. Questionnaire evaluating treatment-related symptoms during the middle of radiotherapy.
Arm Title
Group 2 Stretching Program
Arm Type
Experimental
Arm Description
3 sessions of stretching each week for 6 weeks. Questionnaire evaluating treatment-related symptoms during the middle of radiotherapy.
Arm Title
Group 3 Waitlist Control Group
Arm Type
Other
Arm Description
Option of participating in the yoga or stretching program after the study has ended. Questionnaire evaluating treatment-related symptoms during the middle of radiotherapy.
Intervention Type
Behavioral
Intervention Name(s)
Yoga Group
Intervention Description
3 sessions of yoga each week for 6 weeks.
Intervention Type
Behavioral
Intervention Name(s)
Stretching Control Group
Intervention Description
3 sessions of stretching each week for 6 weeks
Intervention Type
Behavioral
Intervention Name(s)
Waitlist Control Group
Intervention Description
Option of participating in the yoga or stretching program after the study has ended.
Intervention Type
Other
Intervention Name(s)
Questionnaire
Other Intervention Name(s)
Survey
Intervention Description
Questionnaire evaluating treatment-related symptoms during the middle of radiotherapy.
Primary Outcome Measure Information:
Title
Fatigue and sleep assessed with self-report measures and actigraphy.
Time Frame
Measures will be obtained prior to randomization, a brief assessment during the middle of radiation therapy, during the last week of radiation therapy, and 1, 3 and 6 months after the last radiation session.
Secondary Outcome Measure Information:
Title
To see if yoga will help to improve patients' quality of life (QOL) during treatment for cancer and during recovery from the effects of cancer treatment.
Time Frame
4 Years
Title
To learn if a yoga program is effective in helping to decrease emotional distress and improve physiological functioning.
Time Frame
4 Years

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Women with Stage 0 - III breast cancer, undergoing daily adjuvant radiation for 6 weeks in the Department of Radiation Oncology at the M. D. Anderson The participants will need to be 18 years of age or older. Patients should be able to read, write, and speak English or Spanish. Exclusion Criteria: Patients who have a documented diagnosis of a formal thought disorder (e.g., schizophrenia) will be excluded from the study. Patients with metastatic disease of the bone will be excluded to avoid any bone fractures that may result from yoga movements. Patients with active/non-canalized deep vein thrombosis will be excluded from the study. Patients who have not undergone any surgical treatment for their cancer will be excluded to ensure a more homogeneous sample. Patients with extreme mobility issues (e.g., unable to get in and out of a chair unassisted) will be excluded. Patients who have practiced yoga or taken yoga classes in the year prior to diagnosis will be excluded. Patients diagnosed with lymphedema at baseline will be excluded.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lorenzo Cohen, PhD
Organizational Affiliation
M.D. Anderson Cancer Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Texas MD Anderson Cancer Center
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States

12. IPD Sharing Statement

Links:
URL
http://www.mdanderson.org
Description
University of Texas MD Anderson Cancer Center Website

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Effects of Yoga in Breast Cancer Patients

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