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Completed

NCT Number: NCT03051750

Comparison of Techniques for Breast Cancer-Related Lymphedema.

This crossover study compares two different treatment techniques for Breast Cancer-Related Lymphedema: 1. Complex Physical Therapy plus Pressotherapy.

2. Kinesio Taping.

Completed

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Hospital Universitario 12 de Octubre

Madrid, 28041, Spain

About this study

Breast Cancer-Related Lymphedema (BCRL) tends to progress in stage and grade if it is not treated.

Complex Physical Therapy (CPT), that includes Manual Lymph Drainage + Multilayer Bandage + Self-care, is the most used technique in order to join the benefits of each technique by the lack of great results with only one technique. The most volume reduction found in a study was achieved combining CPT and Pressotherapy(P). On the other hand, the use of Kinesio Taping (KT) for BCRL has been spreading lately although its clinical efficacy has not been determined by high quality studies.

GOALS:

Main objective: To analyze the effectiveness in the reduction of BCRL volume with KT versus CPT+P in patients attended at the rehabilitation service at HU12Octubre.

Secondary objectives:

To analyze possible changes after each therapy in:

  • DASH (Disability Arm, Shoulder and Hand) outcome measure score.
  • TTDL (textile therapeutic device for lymphedema) questionnaire score (a quality of life questionnaire for patients with breast cancer-related upper lymb lymphedema using textile therapeutic device that has been validated previously).
  • Symptoms associated with BCRL (pain, heaviness, pressure and hardness) using visual analogue scale (VAS).
  • Goniometry of Upper Limb.

METHODOLOGY OF THE STUDY:

Design: crossover trial, with a 3-month washout period between both treatment phases. Open design: it is impossible during the treatment to blind physiotherapists and patients, due to the observable differences between both therapies neither during their application nor in the hours after their removal, by the marks left in the skin. The statistical analysis will be supervised by staff of the Clinical Research Unit-Clinical Trials (i+12) of HU12Octubre with the variables coded to blind the analyst.

Interventions: The two therapies compared are:

  • CPT+ P.
  • KT. Sample size: a sample of 50 patients (25 in each group) was calculated. Subjects of study and randomization: An initial computerized randomized sample was generated among the patients who had attended the Breast Pathology Rehabilitation visit at HU12Octubre during the previous year and who met the eligibility criteria and they were randomly assigned to the groups.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Submit BCRL
  • Be a patient of the Breast Pathology Rehabilitation at Hospital Universitario 12 de Octubre.
  • Signing the informed consent.

Exclusion criteria

  • Breast Cancer metastasis or other active tumor. 2) Intravenous chemotherapy or radiotherapy actually. 3) Heart or kidney failure. 4) Use diuretics. 5) active infection (erysipelas) or any cutaneous disease in UL or back. 5) Bilateral lymphadenectomy. 6) present deterioration or cognitive delay that would prevent understanding instructions and purpose of the study.
  • Have performed treatment for BCRL during the 3 months prior to the start of the study (previous washing phase).

Treatment and study plan

Complex Physical Therapy plus Pressotherapy

Other

Kinesio Taping

Other

Primary outcomes

  1. Changes in the volume difference between the upper limb with lymphedema and the healthy upper limb before and after treatment.

    Time frame: Four weeks during each treatment phase

    Truncated Cone Formula for Volume from upper limb circumference.

Secondary outcomes

  1. Score on the DASH Outcome Measure.

    Time frame: Four weeks during each treatment phase

    Validated questionnaire about Disability of the Arm,Shoulder and Hand.

  2. Score of the TTDL questionnaire.

    Time frame: Four weeks during each treatment phase

    a quality of life questionnaire for patients with breast cancer-related upper lymphedema using textile therapeutic device validated previously (not yet published).

  3. Symptoms associated with BCRL (pain, heaviness, pressure and hardness) using modified visual analogue scale (VAS).

    Time frame: Four weeks during each treatment phase

    Wong-Baker faces pain rating scale.

  4. Stage of the lymphedema.

    Time frame: Four weeks during each treatment phase

    I, IIA, IIB III, IV.

  5. Goniometry of Upper Limb.

    Time frame: Four weeks during each treatment phase

    Goniometry of shoulder, elbow and wrist.

  6. Body Mass Index.

    Time frame: Four weeks during each treatment phase

    The weight in kilograms divided by the square of the height in metres (kg/m2).

Other outcomes

  1. Age.

    Time frame: First day of treatment of the first phase.

    Years old at the beginning of the study.

  2. Time since axillary surgery.

    Time frame: First day of treatment of the first phase.

    Time since axillary surgery in years at the beginning of the study.

  3. Type of axillary surgery.

    Time frame: First day of treatment of the first phase.

    Lymphadenectomy or Sentinel Lymph Node Biopsy.

  4. Type of breast surgery.

    Time frame: First day of treatment of the first phase.

    Lumpectomy or mastectomy.

  5. Radiotherapy for Breast Cancer.

    Time frame: First day of treatment of the first phase.

    Yes or not.

  6. Time since the appearance of the BCRL.

    Time frame: First day of treatment of the first phase.

    Years since the BCRL appeared.

Sponsors and collaborators

Lead sponsor

Violeta Pajero Otero

Other

Collaborators

  • Hospital Universitario 12 de Octubre
  • University of Castilla-La Mancha

Registry information

Official study title

Complex Physical Therapy Plus Pressotherapy Versus Kinesio Taping in Breast Cancer-Related Lymphedema. Randomized Crossover Trial.

Important dates

Study start
2016
Primary completion
2016
Study completion
2016
First posted
Feb 14, 2017
Registry last updated
Feb 15, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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