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Stress Reduction in Older Women With Stage II, Stage III, or Stage IV Breast Cancer

Primary Purpose

Breast Cancer, Psychosocial Effects of Cancer and Its Treatment

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
psychosocial assessment and care
quality-of-life assessment
Sponsored by
Unity Health Toronto
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional trial for Breast Cancer focused on measuring stage II breast cancer, stage IV breast cancer, stage IIIA breast cancer, stage IIIB breast cancer, psychosocial effects of cancer and its treatment

Eligibility Criteria

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

DISEASE CHARACTERISTICS: Diagnosis of stage II, III, or IV breast cancer No brain or CNS metastases Hormone receptor status: Not specified PATIENT CHARACTERISTICS: Age: 55 and over Sex: Female Menopausal status: Not specified Performance status: ECOG 0-2 Life expectancy: More than 3 months Hematopoietic: Not specified Hepatic: Not specified Renal: Not specified Other: No non-cancer life-threatening illness No history of major psychiatric disorders No drug abuse dependency disorder PRIOR CONCURRENT THERAPY: Biologic therapy: Not specified Chemotherapy: Not specified Endocrine therapy: Not specified Radiotherapy: Not specified Surgery: Not specified

Sites / Locations

  • St. Joseph Hospital
  • Hope Center
  • Maharishi International University

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
October 4, 2000
Last Updated
July 9, 2013
Sponsor
Unity Health Toronto
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1. Study Identification

Unique Protocol Identification Number
NCT00006346
Brief Title
Stress Reduction in Older Women With Stage II, Stage III, or Stage IV Breast Cancer
Official Title
Stress Reduction For Breast Cancer in Women 55 Years of Age or Older: Enhancing Quality of Life and Survival
Study Type
Interventional

2. Study Status

Record Verification Date
March 2010
Overall Recruitment Status
Completed
Study Start Date
August 2000 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
September 2003 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Unity Health Toronto

4. Oversight

5. Study Description

Brief Summary
RATIONALE: Transcendental meditation may be an effective way to decrease the amount of stress in older women with breast cancer. It is not yet known if transcendental meditation is more effective than basic breast cancer education in improving quality of life. PURPOSE: This randomized clinical trialstudies stress reduction in improvingquality of life in older women with stage II, stage III, or stage IV breast cancer.
Detailed Description
OBJECTIVES: Compare the effects of active stress reduction with transcendental meditation vs basic breast cancer education on quality of life and survival time in older women with stage II, III, or IV breast cancer. Determine behavioral mechanisms that may mediate the effects of stress reduction on survival in these patients. Determine baseline variables that contribute to predicting survival time in these patients. OUTLINE: This is a randomized, single blind (to medical staff), multicenter study. Patients are stratified according to age and participation in support groups. Patients with stage IV disease are also stratified according to type of metastases (visceral vs non-visceral) and timing of metastases (first diagnosis vs recurrence). Patients are randomized to 1 of 2 treatment arms. Arm I: Patients receive usual medical care and instruction on stress reduction using transcendental meditation (TM), which involves a standard 7-step course. Patients attend training for approximately 1-1.5 hours per session for a total of 6 sessions over 1 week, while receiving usual medical care. Patients then practice TM twice a day for 20 minutes. Patients attend group meetings for approximately 90 minutes once or twice monthly for 6 months to ensure proper technique and understanding. Arm II: Patients receive usual medical care and basic literature on breast cancer. Quality of life is assessed at baseline and then every 6 months for up to 3 years. Patients are followed monthly for up to 2.5 years. PROJECTED ACCRUAL: Approximately 166 patients (83 per treatment arm) will be accrued for this study within 6 months.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer, Psychosocial Effects of Cancer and Its Treatment
Keywords
stage II breast cancer, stage IV breast cancer, stage IIIA breast cancer, stage IIIB breast cancer, psychosocial effects of cancer and its treatment

7. Study Design

Study Phase
Not Applicable

8. Arms, Groups, and Interventions

Intervention Type
Procedure
Intervention Name(s)
psychosocial assessment and care
Intervention Type
Procedure
Intervention Name(s)
quality-of-life assessment

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
DISEASE CHARACTERISTICS: Diagnosis of stage II, III, or IV breast cancer No brain or CNS metastases Hormone receptor status: Not specified PATIENT CHARACTERISTICS: Age: 55 and over Sex: Female Menopausal status: Not specified Performance status: ECOG 0-2 Life expectancy: More than 3 months Hematopoietic: Not specified Hepatic: Not specified Renal: Not specified Other: No non-cancer life-threatening illness No history of major psychiatric disorders No drug abuse dependency disorder PRIOR CONCURRENT THERAPY: Biologic therapy: Not specified Chemotherapy: Not specified Endocrine therapy: Not specified Radiotherapy: Not specified Surgery: Not specified
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rhoda S. Pomerantz, MD, MPH
Organizational Affiliation
Unity Health Toronto
Official's Role
Study Chair
Facility Information:
Facility Name
St. Joseph Hospital
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60657
Country
United States
Facility Name
Hope Center
City
Terre Haute
State/Province
Indiana
ZIP/Postal Code
47809
Country
United States
Facility Name
Maharishi International University
City
Fairfield
State/Province
Iowa
ZIP/Postal Code
52557
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
19815592
Citation
Nidich SI, Fields JZ, Rainforth MV, Pomerantz R, Cella D, Kristeller J, Salerno JW, Schneider RH. A randomized controlled trial of the effects of transcendental meditation on quality of life in older breast cancer patients. Integr Cancer Ther. 2009 Sep;8(3):228-34. doi: 10.1177/1534735409343000.
Results Reference
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Stress Reduction in Older Women With Stage II, Stage III, or Stage IV Breast Cancer

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