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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00877188
Other study ID # 200808034R
Secondary ID NTUH98-M1178
Status Completed
Phase N/A
First received March 22, 2009
Last updated December 20, 2012
Start date January 2009
Est. completion date December 2010

Study information

Verified date November 2012
Source National Taiwan University Hospital
Contact n/a
Is FDA regulated No
Health authority Taiwan: Department of Health
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the effects of a combined aerobic and resistance exercise program in breast cancer survivors.


Description:

Cancer and cancer treatment side effects are associated with fatigue, pain, decreased cardiovascular fitness and muscle strength, and overall quality of life. Furthermore, cancer survivors are at increased risk for cancer recurrence and for secondary effect such as cardiovascular disease, diabetes, obesity, osteoporosis, and functional decline. Increase physical activity or exercise is proposed to overcome the negative psychological and physiological effects. Preliminary research evidence shows that exercise in cancer survivors improves quality of life, cardiorespiratory fitness, physical functioning, and decrease of fatigue. However, the best exercise mode and intensity has not been well established. Little is known regarding the long term effect. No study investigated impact of exercise for breast cancer survivors on upper extremity function, and correlation between fitness, upper extremity function and quality of life.


Recruitment information / eligibility

Status Completed
Enrollment 34
Est. completion date December 2010
Est. primary completion date October 2010
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- stage 0 to II breast cancer diagnosed within 5 years

- complete adjuvant therapy > 2 months, except hormone therapy

- > 18 years

Exclusion Criteria:

- disease in progress, recurrent, or metastasis

- medical or musculoskeletal condition which resistance exercise is contraindicated

- medication which may alter exercise response

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Other:
exercise
supervised combined aerobic and progressive resistance training for 12 weeks

Locations

Country Name City State
Taiwan Graduate School of Physical Therapy, College of Medicine, NTU Taipei

Sponsors (1)

Lead Sponsor Collaborator
National Taiwan University Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary muscle fitness, quality of life, upper extremity function baseline, 12 weeks post exercise training and follow up 12 weeks Yes
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