Treatment of Lymphedema: Application of the Kinesio Taping
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|ClinicalTrials.gov Identifier: NCT00155220|
Recruitment Status : Unknown
Verified August 2004 by National Taiwan University Hospital.
Recruitment status was: Recruiting
First Posted : September 12, 2005
Last Update Posted : January 27, 2006
There are 2 parts to this study.
- Reliability of water displacement, circumference, tonometer.
- Effect of taping: lifting effect measured with sonography
- Effect of taping: peripheral circulation measured with DRT4
- Effects of different intervention models including decongestive lymphatic therapy (DLT) and modified DLT
|Condition or disease||Intervention/treatment||Phase|
|Lymphedema||Device: Low Stretch Bandage and Kinesio Tape||Phase 2|
To investigate the reliability study of water displacement and circumference measurement and the change in thickness of subcutaneous space measured by sonography and blood flow measured by DRT4 in normal subjects after applying K-tape.
The incidence of breast carcinoma is in the second place in women in Taiwan. Lymphedema is a common complication after treatment of breast carcinoma; it will lead not only to cosmetic problems but is also uncomfortable, and causes functional limitation for patients. The common management for lymphedema is decongestive lymphatic therapy (DLT) including skin care, manual lymph drainage, remedial exercises and compression therapies. At present, all possible compression therapies for lymphedema have limitations. Patients have poor compliance in using short-stretch bandage and compression garments due to the climate in Taiwan. Applying kinesio tape (K-tape) became a new treatment method in physical therapy; the inventor Dr. Kase claimed that the K-tape can improve circulation and remove congestion. Besides, it demonstrated good therapeutic effects in clinical application. However, there are few studies to show the clinical effects of K-tape. This restricts the further application of K-tape. Following the previous study, the purpose is to compare the effects among traditional DLT, modified DLT which replaces bandage with K-tape, and DLT combined K-tape in patients with lymphedema.
A randomized control study will be executed. Sixty patients with post-mastectomy lymphedema will be randomly grouped into taping, bandage and mixed groups. Each subject will go through 4 weeks of a control period, 4 weeks of an intervention period, and followed by 3 months of an observation period. The evaluation items include physical therapy assessment, the severity of swelling, such as arm circumference, volume of water displacement, related symptoms, the upper extremity function and quality of life. The evaluation will be executed 4 weeks before the interventions (start of control period), before the intervention (start of intervention period), after a 4 week intervention and 3 months after the intervention to compare the effects among 3 kinds of treatment. Subjects in each group will receive treatments including skin care, manual lymphatic drainage, pneumatic compression therapy and exercise during the intervention period; the taping group’s patients will receive additional K-tape treatment; the mixed group’s patients will receive K-tape combined bandage treatment. Each group will be treated 2 hours/time, 5 times/week; the entire course will take 4 weeks.
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||60 participants|
|Intervention Model:||Parallel Assignment|
|Official Title:||Treatment of Lymphedema- Application of the Kinesio Taping|
|Study Start Date :||August 2004|
|Estimated Study Completion Date :||March 2006|
- The severity of swelling, such as arm circumference, volume of water displacement
- The evaluation will be executed 4 weeks before the interventions, before the intervention, after 4 week intervention and 3 months after intervention.
- Related symptoms, the upper extremity function and quality of life
- The evaluation time the same as primary outcomes
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00155220
|School and Graduate Institute of Physical Therapy College of Medicine, National Taiwan University||Recruiting|
|Contact: Jau-Yih Tsauo, PhD 88623123456 ext 7320 firstname.lastname@example.org|
|Principal Investigator: Jau-Yih Tsauo, PhD|
|Study Chair:||Jau-Yih Tsauo, PhD||NTUH|