Image

Effect of Preoperative Exercise on the Prevention of Secondary Lymphedema in Breast Cancer Patients

Effect of Preoperative Exercise on the Prevention of Secondary Lymphedema in Breast Cancer Patients

Recruiting
20-80 years
Female
Phase N/A

Powered by AI

Overview

Research purpose: Lymphedema is a very common complication in breast cancer patients. However, since there is currently no curable treatment, it is important to prevent and reduce the severity of lymphedema. The purpose of this study is to evaluate whether preoperative exercise is effective in preventing lymphedema after surgery. For secondary outcome, the preventive effects of exercise on other upper extremity dysfunctions (eg. pectoralis tightness, Axillary web syndrome, Adhesive capsulitis), which are common in breast cancer patients, were assessed.

Description

Study subjects:

  • Patients aged 20 or older who were first diagnosed with breast cancer
  • Patients scheduled to undergo neoadjuvant chemotherapy before surgery Study design: Prospective randomized controlled comparative clinical study
  • Intervention is performed for at least 3 months during the neoadjuvant chemotherapy period before surgery.
  • Treatment group: Individually tailored exercise consisting of aerobic, strength, and flexibility exercises is prescribed, self-exercise compliance monitoring through an application, and diet management education through nutritional counseling.
  • Control group: One session of flexibility exercise training, diet management education through nutritional counseling

Result variable:

  • Primary outcome variable:
    1. Incidence and severity of postoperative lymphedema: bilateral upper limb volume, ICG lymphography
  • Secondary outcome variables:
    1. Clinical information: Demographic, disease and treatment-related data
    2. Physical-related: height/weight/waist circumference measurement, body composition test, physical examination (axillary membrane evaluation)
    3. Upper extremity function (shortening of the pectoralis major muscle, adhesive capsulitis): evaluation of shoulder range of motion, upper extremity muscle strength/grip strength
    4. Quality of life assessment: European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire-Core 30(EORTC QLQ-C30), European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire-Breast cancer module 23(EORTC QLQ-BR23)

Assessment Schedule:

  • Initial treatment and evaluation: Immediately after breast cancer diagnosis
  • Follow-up evaluation: Immediately after completion of exercise intervention (preoperatively), and at 1, 3, and 6 months postoperatively.

Number of study subjects:

  • This study will be conducted as a preliminary study for future research, and will be conducted on a total of 60 patients (30 in the experimental group and 30 in the control group) with an allocation ratio between groups of 1:1.

Eligibility

Inclusion Criteria:

  • Patients aged 20 or older and younger than 80 who were first diagnosed with breast cancer
  • Patients scheduled for surgery and starting neoadjuvant chemotherapy before surgery

Exclusion Criteria:

  • Patients with medical contraindications to exercise intervention or pain or musculoskeletal conditions that may limit active exercise intervention

Study details
    Breast Neoplasms

NCT06421285

Asan Medical Center

15 October 2025

Step 1 Get in touch with the nearest study center
We have submitted the contact information you provided to the research team at {{SITE_NAME}}. A copy of the message has been sent to your email for your records.
Would you like to be notified about other trials? Sign up for Patient Notification Services.
Sign up

Send a message

Enter your contact details to connect with study team

Investigator Avatar

Primary Contact

  Other languages supported:

First name*
Last name*
Email*
Phone number*
Other language

FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

How safe are clinical trials?

Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.