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Massage Therapy for Breast Cancer Treatment-Related Swelling of the Arms - Article


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Clinical Trial: Massage Therapy for Breast Cancer Treatment-Related Swelling of the Arms

This study is currently recruiting patients.

Sponsored by: National Center for Complementary and Alternative Medicine (NCCAM)
Information provided by: National Center for Complementary and Alternative Medicine (NCCAM)

Purpose

The purpose of this study is to examine the short-term and long-term efficacy of massage therapy alone compared to massage therapy plus compression bandaging in the treatment of breast cancer treatment-related swelling of the arms and legs.

Condition Treatment or Intervention
Lymphedema
 Procedure: Manual lymph drainage
 Procedure: Combined physiotherapy
 Procedure: Compression bandaging

MedlinePlus related topics:  Lymphatic Diseases

Study Type: Interventional
Study Design: Treatment, Randomized, Single Blind, Active Control, Parallel Assignment, Efficacy Study

Official Title: Massage Therapy for Breast Cancer-Related Lymphedema

Further Study Details: 

Expected Total Enrollment:  88

Study start: January 2003

Massage therapy (in the form of manual lymph drainage [MLD]) and compression bandaging (CB) are integral components of combined physical therapy (CPT), the recommended treatment for peripheral lymphedema (LE). According to the World Health Organization, LE afflicts hundreds of millions worldwide and probably millions in the United States. Effects of various forms of massage on lymph circulation have been postulated for more than a century, but the efficacy of MLD alone without CB has not been demonstrated. New data suggest that MLD alone reduces established LE volume as effectively as CB in combination with CPT and minimizes LE development.

Patients will be randomly assigned to either treatment with MLD alone or a combination of MLD and CB. Patients will be treated in 10 one-hour sessions over 2 weeks. They will also undergo lymphangioscintigraphy (a nuclear medicine test) to depict the function of their lymphatic system. Patients will continue self treatment at home and will be followed for 6 months.

Eligibility

Genders Eligible for Study:  Both

Criteria

Inclusion Criteria:

  • Lymphedema (5% to 20% increase in volume) after breast cancer treatment

Exclusion Criteria:

  • Physically unable to perform massage or bandaging during home program

Location and Contact Information


Arizona
      University of Arizona, Tucson,  Arizona,  85724,  United States; Recruiting
Michael J. Bernas, MS  520-626-6118    michaelb@u.arizona.edu 
Marlys H. Witte, MD  520-626-6118    lymph@u.arizona.edu 

More Information

Study ID Numbers:  1 R21 AT01326-01
Record last reviewed:  September 2004
Last Updated:  October 13, 2004
Record first received:  April 14, 2003
ClinicalTrials.gov Identifier:  NCT00058851
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005

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December 2, 2009



Page Updated: September 6, 2005
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