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NCT00935714 Clinical Trial

Exercise and Breast Cancer Related Lymphedema: Influence of Muscle Group and Sequence on Volume Change in Swollen and Normal Arms

Breast Cancer Clinical Trial

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT00935714
Other study ID # 0023-09-HYMC
Secondary ID
Status Recruiting
Phase N/A
First received July 8, 2009
Last updated August 18, 2009
Start date August 2009

Study information
Verified date August 2009
Source Hillel Yaffe Medical Center
Contact Jillian H Bracha, BSc
Phone 972-523784551
Email gillianb@hy.health.gov.il
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Interventional

Clinical Trial Summary

Arm exercise influences arm volume and symptoms in breast cancer related lymphedema.

Recruitment information / eligibility
Status Recruiting
Enrollment 18
Est. completion date
Est. primary completion date January 2010
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- unilateral arm lymphedema as a result of breast cancer treatment

- completion of breast cancer treatments

- arm lymphedema onset 3 months or more after surgery and persistent for at least 6 months

- in the maintenance phase of lymphedema treatment

Exclusion Criteria:

- women with recurrent cancer

- intercurrent diseases affecting the swollen arm

- lack of understanding of the Hebrew language

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Factorial Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Other:
• Exercise

• Exercise

Locations
Country Name City State
Israel Hillel Yaffe Medical Center Hadera

Sponsors (2)
Lead Sponsor Collaborator
Hillel Yaffe Medical Center Tel Aviv University

Country where clinical trial is conducted

Israel, 

Outcome
Type Measure Description Time frame Safety issue
Primary Improved arm volume measurement Weekly for five weeks No
Secondary Quality of Life Weekly for 5 weeks No
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