HOME  | CONTACT  | PATIENT LOGIN  | CLINIC LOGIN  | FAQ
  • PATIENTS &
    HEALTHY VOLUNTEERS
  • INVESTIGATORS
  • CROS / SPONSORS
  • CAREERS
  • TRIAL ALERTS

TRIALS SEARCH
      
  • HEALTH NEWS

  • RSS FEEDS

  • ABOUT TRIALS

  • LINK TO US


View Clinical Trial (Medical Research Study)


Effects of Tibetan Yoga on Fatigue and Sleep in Cancer

This study is not currently recruiting Study Participants on ClinicalConnection.com. If you would like to find active studies please search for clinical trials

Signup
Browse Studies

City:   Houston
State:   Texas
Zip Code:   77030
Conditions:   Breast Cancer
Purpose:   The goal of this behavioral research study is to learn if participating in a Tibetan yoga program helps to improve quality of life for women during treatment for or recovery from breast cancer. Researchers are also interested in whether the yoga program helps to improve sleep, lung function, and physical therapy, based on outcomes.
Study Summary:   You will come to M. D. Anderson for an initial meeting. You will complete several questionnaires asking about mood, quality of life, and other things like sleep, fatigue, anxiety, and coping skills. You will also have an electrocardiogram (ECG - a test to measure the electrical activity of your heart). Both the questionnaires and the ECG test should take about 60 minutes, total, to complete. You will also wear an actigraph (a watch-like instrument that records arm movements) for 7 days. The actigraph records information about your physical activity, rest, and sleep. You will be asked to complete daily sleep diary forms that ask about some behaviors, your sleep, and sleep quality for the 7 days. At the end of the 7 days, you will return the actigraph and sleep diaries to the research staff, or a member of the research staff can go to your home to pick them up. You will then be randomly assigned (as in the toss of a coin) to one of three groups. People in the first group will take part in a Tibetan yoga program. People in another group will take part in stretching program. People in the third group will get usual care. People in the stretching and usual care groups will be given the opportunity to take part in the Tibetan yoga program, after the end of the study. If you are assigned to the yoga group, you will take part in 4 weekly sessions of Tibetan yoga. If you are not able to attend 4 weekly sessions, you can attend 1 session every 3 weeks, for a total of 4 sessions over 12 weeks, of Tibetan yoga. You will be asked to complete a brief form at the start of each session that will take 1-2 minutes to complete. During the yoga sessions, you will be asked to do deep breathing exercises and perform different stretching and movement exercises. You will be able to move through the exercises at your own pace. Sessions occurring weekly will last 90 minutes. Sessions occurring once every 3 weeks will last 90 minutes. All sessions will be provided free of charge. One or more of these yoga sessions may be videotaped by the study staff for quality assurance purposes. Only the study staff will be able to view this videotape. If you are assigned to the stretching group, you will take part in 4 weekly sessions in which you will be asked to do simple stretching exercises. If you are not able to attend 4 weekly sessions, you can attend 1 session every 3 weeks, for a total of 4 sessions over 12 weeks. Sessions occurring weekly will last 90 minutes. Sessions occurring once every 3 weeks will last 90 minutes. All sessions will be provided free of charge. None of the movements are difficult. You will be able to follow this program at your own pace. If you are assigned to the yoga or stretching group, you will take part in 3 "booster" sessions consisting of a review and practice of the entire program. If you are in the 4 weekly sessions, your booster sessions will take place 1 and 2 months after your last yoga or stretch class and again around the time of your 6-month assessment. If you are in the classes that meet every 3 weeks over a 12-week period, your booster sessions will take place 3 and 6 weeks after your last yoga or stretch class and again around the time of your 6-month assessment. If a need for counseling/therapy arises, your primary care physician will be notified and can refer you to the Section of Psychiatry, Department of Neuro-Oncology. One week, 3 months, 6 months, and 12 months after the end of the yoga or stretching sessions (or similar time for the usual care group), you will be asked to return to the clinic. You will fill out a packet of questionnaires and complete an ECG evaluation again. The questionnaires and tests should take about 60 minutes to complete. You will also be asked to wear the actigraph and complete daily sleep diary forms for another 7 days. At the end of the 7 days, you will return the actigraph and sleep diaries to the research staff, or a member of the research staff can go to your home to pick them up. This will be your last participation in the study. After the study is over, if you took part in the stretching or were in the usual care group, you will be given the option to take the yoga classes. This is an investigational study. As many as 480 patients could take part in this study. All will be enrolled at M. D. Anderson.
Criteria:   Inclusion Criteria: 1. Women with stage I-III breast cancer who are undergoing neoadjuvant or adjuvant chemotherapy weekly for 12 weeks followed by four cycles of an anthracycline-based treatment every 21 days or six to eight cycles of chemotherapy every 21 days or are within 24 months post-treatment (surgery and/or chemotherapy and/or radiotherapy - patients can still be taking hormonal treatment). 2. 18 years of age or older. 3. Able to read, write and speak English 4. Able to come to UTMDACC for intervention and assessment sessions. Exclusion Criteria: 1. Metastatic disease of the bone. 2. Documented diagnosis of a formal thought disorder (e.g., schizophrenia). 3. Engaged in psychiatric or psychological counseling or support groups. 4. Reports the need for psychological services. 5. Score of 23 or below on the Mini-Mental State Examination. 6. Presence of lymphedema at the start of the study.
NCT ID:   NCT00507923
Primary Contact:   Principal Investigator
Lorenzo Cohen, PhD
M.D. Anderson Cancer Center

Backup Contact:   N/A
Location Contact:   Houston, Texas 77030
United States



There is no listed contact information for this specific location.

Site Status: N/A

Click here to see:
  • Clinical trials for Breast Cancer in Houston, Texas

Data Source:   ClinicalTrials.gov
Date Processed:   May 22, 2013
Modifications to this listing:   Only selected fields are shown, please use the link below to view all information about this clinical trial.
Click to view Full Listing


  • NEARBY STUDIES

Within 25 Miles

Gout - Houston TX

Crohn's Disease - Sugar Land TX

Crohn's Disease - Pasadena TX

Crohn's Disease - Houston TX

COPD (Chronic Obstructive Pulmonary Disease) - Houston TX

Chronic Low Back Pain with Constipation - Houston TX

Asthma - Houston TX

Type 2 Diabetes - Houston TX

Asthma - Houston TX

Rheumatoid Arthritis - Sugar Land TX

Major Depression Disorder - Houston TX

Hepatitis C - Houston TX

Gout - Houston TX

Irritable Bowel Syndrome - Houston TX

Rheumatoid Arthritis - Houston TX

Crohn's Disease - Pasadena TX

Chronic Low Back Pain - Houston TX

Crohn's Disease - Houston TX

Type 2 Diabetes - Houston TX

Irritable Bowel Syndrome with Diarrhea - Houston TX

High Cholesterol - Houston TX

Constipation - Houston TX

Chest Pain - Houston TX

HIV - Houston TX

Stomach Problems - Houston TX

Diabetes - Houston TX

Breathing Problems - Houston TX

Gout - Houston TX

Gout - Houston TX

Psoriatic Arthritis - Houston TX

Excessive Daytime Sleepiness with Narcolepsy - Houston TX

High Potassium - Houston TX

Type 2 Diabetes - Houston TX

Ulcerative Colitis - Houston TX

Asthma (Ages 18-65) - Houston TX

Asthma (Ages 18-65) - Houston TX

Low Back Pain and Constipation - Houston TX

Low Back Pain and Constipation - Houston TX

Low Back Pain and Constipation - Houston TX

Irritable Bowel Syndrome - Houston TX

Irritable Bowel Syndrome (with diarrhea) - Houston TX

Irritable Bowel Syndrome (with diarrhea) - Pasadena TX

Irritable Bowel Syndrome (with diarrhea) - Houston TX

Irritable Bowel Syndrome (with diarrhea) - Houston TX

Irritable Bowel Syndrome (with diarrhea) - Sugar Land TX

Irritable Bowel Syndrome (with diarrhea) - Houston TX

Asthma - Houston TX

Uncontrolled Angina (Adult Stem Cell Research) - Houston TX

Dry Eye - League City TX

Emphysema/COPD (Chronic Obstructive Pulmonary Disease) - Houston TX

Within 50 Miles

Type 2 Diabetes - Tomball TX

Type 2 Diabetes and Recent Heart Hospitalization - Tomball TX

Type 2 Diabetes - Tomball TX

Gout - Tomball TX

Gout - Kingwood TX

Gout - Sealy TX

Asthma (Ages 18-65) - Dickinson TX

Within 100 Miles

 
Clinical Connections Home | Investigators | CROs / Sponsors | Clinical Trials Notification | Search Clinical Trials | About Clinical Trials | Links | Terms And Conditions | Sitemap | Suggestions / Feedback
© 1998-2013 | All trademarks are property of their legal owners. | All Rights Reserved

ClinicalConnection.com is a resource that provides individuals with information regarding clinical trials that are being conducted worldwide.

ClinicalConnection.com does not conduct these clinical trials nor endorse them. Please consult your doctor or physician before participating.