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A simple Pre-Surgery exercise routine may curb Post-Breast-Cancer arm swelling

NCT ID NCT07743294

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Aug 03, 2026 · Last updated Aug 04, 2026 · Updated 1 time

Summary

This trial tests whether starting upper limb rehabilitation exercises one day before breast cancer surgery can reduce the risk and severity of arm lymphedema (swelling) after surgery. Half of the participants will receive individualized exercise instruction, while the other half gets standard nursing education. Researchers will track arm circumference, physical function, quality of life, and care needs over a year to see if the pre-surgery exercise makes a difference.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Preoperative upper limb rehabilitation exercise
What this could lead to
If effective, this simple exercise program could become a standard pre-surgery practice to reduce arm swelling and improve recovery and quality of life for breast cancer patients.
What could go wrong
This is a single-center trial with 105 participants, so results may not apply broadly. The exercise may not significantly reduce lymphedema, and adherence or individual variation could affect outcomes.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 105 people

The number the study aims to enrol. It can still change while the study runs.

Started

Jun 2024

Expected to finish

Dec 2026

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

20 years and older

Sex

Female participants only

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Diagnosed with malignant breast cancer confirmed by post-surgical tissue examination. * Receiving primary surgery, including tumor resection combined with axillary lymph node dissection. * Age 20 years or older. * Conscious, able to communicate in Mandarin or Taiwanese, aware of diagnosis, capable of completing questionnaires and participating in interventions, and signed informed consent. Exclusion Criteria: * Severe cognitive impairment or unaware of diagnosis, unable to complete questionnaires or correctly execute intervention measures. * Patients in the control group who independently schedule outpatient rehabilitation after returning home. * Unable to communicate in Mandarin or Taiwanese. * Undergoing breast reconstruction surgery.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    2 sites. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • National Taiwan University Hospital

    RECRUITING

    Taipei, Taiwan

  • National Taiwan University Hospital Cancer Center

    RECRUITING

    Taipei, 106, Taiwan

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