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Pre-Surgery workouts may stop arm swelling in breast cancer patients

NCT ID NCT07301580

Prevention Sponsor: University of Health Sciences Balikesir Hospital Eduation and Research Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at whether a personalized exercise program, started before breast cancer surgery and continued for 12 months after, could prevent lymphedema (arm swelling) and improve recovery. Forty women scheduled for breast cancer surgery took part. They received structured exercise instructions and were monitored regularly. The goal was to see if this approach could reduce the chance of developing lymphedema and help with pain, movement, and quality of life.

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

40 people

The number who actually took part.

Started

Oct 2024

Finished

Oct 2025

Lead sponsor

A government agency

The lead sponsor is a government body.

Who can take part

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

Ages

18 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: * Women aged 18 years or older * Diagnosed with breast cancer and scheduled for surgical treatment * Able to perform prescribed upper-extremity exercises * Able to provide informed consent and complete follow-up assessments. Exclusion Criteria: * Presence of metastatic disease at baseline * Neurological, orthopedic, or systemic conditions limiting upper-extremity mobility * Prior breast or axillary surgery on the same side * Planned neoadjuvant chemotherapy that would delay the initiation of the exercise program * Inability to comply with the exercise instruction or follow-up schedule

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Conditions

The condition(s) this trial relates to.

breast cancer Breast Cancer Lymphedema myalgic encephalomeyelitis/chronic fatigue syndrome

As listed by the trial registrant

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

Breast cancer-related arm lymphedema Fatigue syndrome, chronic Prehabilitation Quality of life impairment

Contacts and locations

Locations

  • UHS Balikesir Ataturk Health and Application Center

    Balıkesir, Turkey (Türkiye)

More trials for these conditions

Other studies related to the condition(s) this trial covers.