Adjustable Compression Wrap Versus Compression Bandage Reduce to Breast Cancer-related Lymphedema

Instituto Nacional de Cancer, Brazil

Status: Completed

Conditions: Lymphedema of Upper Arm; Breast Cancer Related Lymphedema; Lymphedema, Secondary; Breast Neoplasms

Treatments: Device: Compression Bandage; Device: Adjustable Compression Wrap

Study type: Interventional

Funder types: Other

Identifiers

NCT04934098

Stage 1 Compression Therapy

Details and patient eligibility

About

This is a randomized clinical trial with women with lymphedema secondary to breast cancer. The intervention will consist of the use of self-adjusting clothing versus compressive bandaging (routine treatment of the institution). Self-adjusting clothing is expected to be more effective for the treatment of lymphedema reduction, when compared to standard treatment, in addition to promoting a better quality of life and functionality.

Full description

This is a randomized clinical trial, simple blind, which aims to evaluate the effectiveness of the use of self-adjusting compression garments (Read Wrap®) in reducing the volume of the upper limb of women with lymphedema secondary to breast cancer. It will be carried out in a referral hospital for the treatment of breast cancer in Brazil, with inclusion scheduled for June 2021 and follow-up of up to 1 year. All volunteers must have lymphedema in the upper limb after surgical treatment for breast cancer for more than 6 months, indicating phase 1 of compressive therapy. According to the sample calculation, 72 women will be needed to be randomly randomized in a 1: 1 ratio among the experimental intervention group (n = 36) and the standard intervention group (n = 36). The intervention consists of compressive therapy in the volume reduction phase for lymphedema secondary to breast cancer. The Experimental Intervention Group will receive an adjustable compaction wrap (Read Wrap®) while the standard Intervention Group will be submitted to compressive bandaging and will be followed up on an outpatient basis, as per institutional routine, twice a week, for 30 days. The institutional protocol for the lymphedema reduction phase will be respected, in which the orthosis is used at home for as long as possible, with time off just for bathing and sleeping, in addition, skincare and therapeutic exercises for upper limbs must be performed daily. An orientation booklet and home exercises of the institutional routine will be delivered. During the first 30 days of treatment, all study participants will be accompanied by a telephone channel that will be made available for questions, guidance, and communications of adverse events, in addition to a therapeutic diary that will be delivered at the first consultation and collected after this period, destined to notify relevant information that considers the use of compressive therapy, such as facilities, difficulties and time of use, symptoms related to the arm and adverse effects that may arise, and to monitor adherence to exercises. The suspension of treatment before the anticipated end of therapy will occur when adverse effects are observed, such as an increase in limb volume greater than 10% from the last measurement, signs of dermatitis, associated skin, or allergy. The case will be evaluated by the physiotherapy team and, when necessary, by the medical team and the treated procedures will be adopted.

Data collection will take place through the analysis of physical and electronic data, medical records, interviews, and physical examination. The interviews will be conducted through questionnaires produced by the researchers, in addition to validated questionnaires for the Brazilian population. The evaluations will take place in the outpatient clinic of the physiotherapy service of the hospital on the 1st, 7th, and 30th day of the intervention for immediate evaluation, and will be followed up to 1 year later, to verify the measures of long-term results. The analysis of the data will be descriptive and comparative of the intervention groups, about the selected variables and the main results, through the analysis of measures of central tendency, dispersion, and frequency distribution. The evaluation of the result will be carried out by intention of treatment, using linear and simple, and multiple logistic regression. For all analyzes, a 95% confidence interval will be considered.

Enrollment: 72 patients

Sex: Female

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Women

  1. Age over 18 years
  2. Undergo surgical treatment for breast cancer
  3. Diagnosed with lymphedema in the upper limb stabilized for a period ≥6 months
  4. Indicated the second phase of compressive therapy / treatment of lymphedema

Exclusion criteria

• Women with:

  1. Bilateral lymphedema;
  2. Lymphedema since the preoperative period;
  3. Presence of phlogistic signs in the limb with lymphedema;
  4. Treatment of lymphedema (phase 1) in the last three months;
  5. Previous history of allergic reaction to the material used for compressive therapy;
  6. Active regional or remote disease;
  7. In chemotherapy or radiation therapy;
  8. Functional changes in the upper limbs prior to the diagnosis of breast cancer;
  9. Heart disease and decompensated systemic arterial hypertension; psychiatric, mental, neurological disorders or cognitive deficits that make it impossible to answer the questionnaires.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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72 participants in 2 patient groups

Adjustable compression wrap

Experimental group

Description:

Daily use of the Adjustable Compression Wrap on the upper limb with breast cancer-related lymphedema during phase 1 compression therapy.

Treatment:

Device: Adjustable Compression Wrap

Compression Bandage

Active Comparator group

Description:

Daily use of compression bandage on the upper limb with breast cancer-related lymphedema during phase 1 compression therapy.

Treatment:

Device: Compression Bandage