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Trial of Combined Aerobic and Resistance Exercise in Breast Cancer Survivors - Article


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Exercise/Physical Fitness

 




Clinical Trial: Trial of Combined Aerobic and Resistance Exercise in Breast Cancer Survivors

This study is not yet open for patient recruitment.
Verified by Alberta Cancer Board November 2005

Sponsored by: Alberta Cancer Board
Information provided by: Alberta Cancer Board
ClinicalTrials.gov Identifier: NCT00249015

Purpose

Endurance exercise such as walking has been shown to help breast cancer survivors maintain their energy and quality of life while they are receiving chemotherapy, but there have not been any studies on weight training. In this study, the researchers want to determine if a combined program of endurance and weight training exercises is better than a standard amount of endurance exercise or even a higher amount of endurance exercise in breast cancer survivors receiving chemotherapy. The study will be an experimental design in which the researchers have breast cancer survivors participate in each of the three different exercise programs. The researchers'''' main interest is in quality of life, which they will measure before and after the exercise programs by asking participants how they feel on various rating scales. The researchers will also measure their aerobic fitness on a treadmill and how strong they are by having them lift weights.
Condition Intervention Phase
Breast Cancer
 Behavior: Physical exercise
Phase III

MedlinePlus related topics:  Breast Cancer
Genetics Home Reference related topics:  breast cancer

Study Type: Interventional
Study Design: Educational/Counseling/Training, Randomized, Single Blind, Dose Comparison, Single Group Assignment, Safety/Efficacy Study

Official Title: Randomized Controlled Trial of Combined Aerobic and Resistance Exercise in Breast Cancer Survivors

Further study details as provided by Alberta Cancer Board:
Primary Outcomes: Quality of life
Secondary Outcomes: Cardiovascular fitness; Muscular strength; Body composition; Treatment completion rates; Adverse events
Expected Total Enrollment:  240

Study start: January 2006

Eligibility

Ages Eligible for Study:  18 Years and above,  Genders Eligible for Study:  Female
Criteria

Inclusion Criteria:

  • Are diagnosed with stage I-IIIA breast cancer
  • Are scheduled to receive neoadjuvant or adjuvant chemotherapy
  • Have not received previous chemotherapy
  • Did not receive transabdominal rectus abdominis muscle (TRAM) reconstructive therapy
  • Are 18 years or older
  • Received approval from their treating oncologist
  • Do not have uncontrolled hypertension, cardiac illness or psychiatric condition
  • Are not pregnant
  • Are able to understand and provide written consent in English or French
  • Have no major contraindications to exercise based on maximal aerobic and strength tests

Location and Contact Information

Please refer to this study by ClinicalTrials.gov identifier  NCT00249015

Kerry Courneya, PhD      780-432-2829    kerry.courneya@ualberta.ca

Canada, Alberta
      Cross Cancer Institute, Edmonton,  Alberta,  T6G 1Z2,  Canada
Paula Langenhoff, B.H.A  780-432-8909    paulalan@cancerboard.ab.ca 
Kerry Courneya, PhD,  Principal Investigator

Study chairs or principal investigators

Kerry Courneya, PhD,  Principal Investigator,  Alberta Cancer Board   

More Information

Study ID Numbers:  BR-01-0080
Last Updated:  December 8, 2005
Record first received:  November 4, 2005
ClinicalTrials.gov Identifier:  NCT00249015
Health Authority: Canada: Health Canada
ClinicalTrials.gov processed this record on 2006-01-10

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Page Updated: September 6, 2005
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