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Pilates vs mirror therapy: which eases shoulder pain after neck surgery?

NCT ID NCT07297706

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 tested whether Pilates exercises or mirror therapy works better for shoulder pain and stiffness after neck dissection surgery. Fifty-two adults aged 35 to 55 took part. Both treatments aim to improve movement and reduce pain without medication.

What this could mean

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

Active substance
Pilates exercises and mirror therapy
What this could lead to
If one approach works better, it could offer a simple, drug-free way to improve shoulder function and reduce pain after neck surgery.
What could go wrong
This is a small, completed trial with only 52 people, so results may not apply to everyone. Both therapies are low-risk, but individual results can vary.

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

52 people

The number who actually took part.

Started

Apr 2025

Finished

Oct 2025

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

35 to 55 years

Sex

Anyone

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: 1. Patient's age ranged between 35-55 years. 2. Both genders will participate in the study. 3. All patients suffering from shoulder dysfunction post-unilateral neck dissection surgeries ( modified radical and selective neck dissection surgeries). 4. All patients will have shoulder pain, limited ROM (flexion, abduction, external rotation) and limited shoulder function. 5. All patients will begin the treatment program 1-3 months after neck dissection surgeries. 6. All patients enrolled in the study will have their informed consent. Exclusion Criteria: 1. Subjects suffering from active malignant tumors. 2. Subjects with rotator cuff tears or other shoulder ligaments injuries. 3. A history of neck or ipsilateral shoulder injuries, pain in the last 6-month prior neck dissection surgeries. 4. Adhesive capsulitis secondary to diabetes mellitus or fractures. 5. Recurrent shoulder dislocation. 6. Recent fractures or surgeries in the shoulder. 7. Neurological disorder 8. The presence of residual local regional cancer or distant metastases to other regions. 9. Comorbid medical illness or psychiatric illness and visual disturbance that would prevent completion of treatment.

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Conditions

The condition(s) this trial relates to.

Shoulder Pain

As listed by the trial registrant

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

Contacts and locations

Locations

  • Kasr El Ainy Learning Hospital and National Cancer Institute

    Cairo, Egypt

More trials for these conditions

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