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New rehab protocol aims to improve sleep and pain after rotator cuff surgery

NCT ID NCT07135375

Knowledge-focused Sponsor: LAURA CASTILLO VEJAR 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 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 26, 2026 · Last updated Aug 07, 2026 · Updated 1 time

Summary

This study is testing a new physical therapy protocol for people over 50 who have had arthroscopic rotator cuff surgery. Researchers will track shoulder function, pain levels, and sleep quality over the recovery period. The goal is to gather better evidence on what helps patients heal more effectively.

What this could mean

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

Active substance
Rehabilitation protocol
What this could lead to
If successful, this could help create clearer rehab guidelines for better recovery after rotator cuff surgery.
What could go wrong
This is a small, early observational study with no control group, so results may not apply to everyone. It only measures short-term 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 50 people

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

Started

Jul 2025

Expected to finish

Sep 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

50 years and older

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: * People over 50 years of age * People have undergone arthroscopic rotator cuff of one or more tendons. * Patients must sign informed consent and undergo physical therapy center (up to week 12 postoperatively). Exclusion Criteria: * Patients who develop postoperative stiffness or adhesive capsulitis during the rehabilitation process. * Patients with symptoms of cervical radiculopathy or previously diagnosed sleep disorders. * Patients with neurological or cognitive disorders who have difficulty following instructions

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Conditions

The condition(s) this trial relates to.

Pain Rotator Cuff Injuries rotator cuff syndrome sleep disorder

As listed by the trial registrant

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

Functionality Pain Rehabilitation Rotator cuff Rotator cuff injuries Sleep

Contacts and locations

Locations

  • Temuco, senador estebanez 779

    Temuco, Chile

  • Trimedkine

    Temuco, Chile

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