Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Can video games help breast cancer survivors recover arm function?

NCT ID NCT07068347

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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tests whether virtual reality (VR) games, combined with lifestyle changes like walking and better sleep, can improve arm function in women who had breast cancer surgery. Sixty female survivors aged 30-60 will be randomly assigned to VR therapy or conventional physical therapy, with or without lifestyle advice. The goal is to see which approach reduces pain, improves movement, and boosts quality of life.

What this could mean

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

Active substance
Virtual reality (VR) therapy and lifestyle modification (walking, diet, sleep habits)
What this could lead to
If successful, this could offer a more engaging and effective way to improve arm function and quality of life for breast cancer survivors after surgery.
What could go wrong
This is a small, early-stage trial with only 60 participants, so results may not apply to everyone. The VR approach is still experimental and may not prove better than standard physical therapy.

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

60 people

The number who actually took part.

Started

Apr 2025

Expected to finish

Jun 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

30 to 60 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: * Female breast cancer survivors aged 30-60 years. * Women with breast cancer who have undergone any type of breast cancer surgery (e.g., mastectomy, lumpectomy, or breast reconstruction), regardless of the specific surgical procedure will be included. * Participants able to carry on upper limb and whole-body physical activity will be included. * Participants able to use smart devices such as mobile phones and computers will be included. * Patients obtaining a physician's clearance for fitness testing and exercise will be included. * Patients having no physical limitations prohibiting exercise will be included. * Patients diagnosed with grade 0-3 of breast cancer who had undergone surgery will be included. * who were currently in the 2nd \~ 4th months after cancer surgery. * Presence of upper limb dysfunction (e.g., pain, reduced range of motion and weakness). Exclusion Criteria: * Subjects suffering from active malignant tumors or bilateral breast cancer. * Participants disabling physical or psychological ailments not allowing them to participate in the intervention . * Patients who had lymphedema will be excluded. * Participants with visual disorders that interfered with a video game- based exercise. * Subjects with cognitive disorders, mental disorders, or cooperation issues will be excluded.Subjects with vascular or cardiopulmonary disorders. * Subjects with previous breast cancer surgery on the present or contralateral side. * Participants having upper extremity ROM limitation before the surgery will be excluded. * Participants with presence of pace-maker, infection, open wounds, or wound drains will be excluded.

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Breast cancer are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

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.

Contacts and locations

Locations

  • District Head Quarters Hospital

    Rawalpindi, Punjab Province, Pakistan

  • Holy Family Hospital

    Rawalpindi, Punjab Province, Pakistan

  • Kinifit Physiotherapy Center

    Islamabad, Pakistan

More trials for these conditions

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