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Clinical Trials in Taiwan / NCT07459881
Starting soon Not applicable

Effects of Combined Upper Extremity Exercise and Pneumatic Compression Therapy on Breast Cancer-Related Lymphedema

NCT07459881 · tracked via the Priya Life Science Taiwan tracker
Phase
Not applicable
Started
2026-03
Last updated
2026-03-10

Condition(s) studied

Breast Cancer Lymphedema

Investigational drug(s) / intervention(s)

Combined Upper Extremity ExercisePneumatic Compression Therapy

Combined Upper Extremity Exercise: Warm-up (5 min): shoulder flexion, abduction, circular motion Active and resistance training (20 min): using elastic bands or 0.5 kg weights: Seated rowing/Chest press/Lat pulldown/Single-arm row/Biceps curl/Triceps extension Two sets of 10 repetitions (or up to 3 sets depending on tolerance) Stretching (5 min): overhead stretch, lateral flexion, biceps/triceps stretch

Pneumatic Compression Therapy: duration:20 minutes Multi-chamber upper limb sleeve Sequential distal-to-proximal inflation Pressure range: 20-40 mmHg (adjusted according to tolerance and safety limits) Monitoring for pain, numbness, pallor, or circulatory compromise

Study summary

Breast cancer is one of the most common cancers among women worldwide. With advances in treatment, survival rates have steadily increased; however, postoperative complications continue to affect patients' quality of life, with upper extremity lymphedema being among the most prevalent. Breast cancer related lymphedema (BCRL) can result in arm swelling, pain, restricted mobility, and psychological distress, all of which negatively impact daily functioning and social partici pation .

Previous studies have demonstrated that regular and moderate upper extremity exercise does not exacerbate lymphedema; instead, it may improve shoulder mobility, muscular strength, and contribute to edema control. In addition, therapeutic modalities such as pneumatic compression pumps and manual lymphatic drainage have been proven effective in reducing swelling and enhancing patient comfort . Recent systema tic reviews further support the beneficial effects of exercise interventions on upper limb function and quality of life in breast cancer survivors.

Therefore, combining upper extremity exercise with pneumatic compression therapy may re present a promising integrative intervention to improve lymphedema and related functional limitations. This study aims to investigate the effects of such a combined approach on breast cancer patients with lymphedema by comparing outcomes across multiple ti me points, including arm circumference measurements, shoulder range of motion, upper extremity function (DASH), and quality of life (FACT B), with the goal of establishing a more comprehensive rehabilitation model.

Eligibility

Sex
FEMALE
Min age
20 Years
Max age
70 Years
Healthy volunteers
No
Inclusion Criteria: 1. Female breast cancer patients aged 20-70 years 2. Postoperative unilateral breast cancer surgery with a clinical diagnosis of lymphedema (stage I or II breast cancer treatment, with unilateral lymphedema greater than 2 cm and less than 8 cm at least one measurement point) 3. Completion of subsequent chemotherapy/radiotherapy or other treatments at least 3 months postoperatively 4. Ability to cooperate with 12 treatments and all assessments and sign a consent form Exclusion Criteria: 1. Breast cancer with a tendency for recurrence or metastasis 2. Severe infection of the upper limb (cellulitis) 3. Uncontrolled heart failure, deep vein thrombosis (DVT), severe peripheral vascular disease 4. Stage III lymphedema, bilateral lymphedema, or need to take medications that may affect sweat glands in the upper limbs 5. Other musculoskeletal disorders of the upper limbs, joint deformities, or a history of surgery 6. Pregnancy or other conditions unsuitable for participation

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Far Eastern Memorial Hospital New Taipei City Taiwan

More Far Eastern Memorial Hospital trials in Taiwan

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07459881 on ClinicalTrials.gov ↗ ← All trials in Taiwan