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Smartphone rehab after breast cancer surgery shows promise

NCT ID NCT06156397

Symptom relief Sponsor: Medipol University 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 30, 2026 · Updated 2 times

Summary

This study tested whether technology-based rehabilitation (telerehabilitation or a mobile app) could improve arm and shoulder function after breast cancer surgery, compared to standard physiotherapy. 45 women who had surgery with lymph node removal participated. The goal was to see if remote or app-based exercise programs could help recovery just as well as in-person sessions.

What this could mean

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

Active substance
Technological based rehabilitation (telerehabilitation and mobile application supported exercise program)
What this could lead to
If successful, this could show that remote or app-based rehab is as effective as in-person physiotherapy for recovery after breast cancer surgery.
What could go wrong
This is a small, completed study with only 45 participants, so results may not apply to everyone. The interventions are compared to standard care, not a placebo, and the primary outcome is range of motion, not long-term function.

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

45 people

The number who actually took part.

Started

Nov 2023

Finished

Feb 2024

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

30 to 65 years

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: * Being diagnosed with breast cancer and undergoing surgery and having axillary lymph node dissection performed during surgery * Finding the cases in the post-operative (post-op) 2nd week * Age range between 30 and 65 years * Limited shoulder ROM in preoperative evaluations absence * No speech or hearing problems * Patients included in the study are volunteers Exclusion Criteria: * Previous ipsilateral or contralateral breast cancer surgery * Presence of active or metastatic cancer focus * A neurological disease that affects upper extremity functionality or * Finding orthopedic surgery * Having hearing or visual impairment * Carrying a pacemaker * Presence of infection and open wound * Finding a drain after surgery * Cases with mental and cooperation problems

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Conditions

The condition(s) this trial relates to.

breast cancer breast neoplasm

As listed by the trial registrant

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

Breast cancer

Contacts and locations

Locations

  • The University of Health Sciences Haydarpaşa Numune Hospital

    Istanbul, Üsküdar, 34668, Turkey (Türkiye)

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