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Shoulder pain relief without the waiting room? a trial tests remote rehab

NCT ID NCT04322864

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Aug 03, 2026 · Last updated Aug 04, 2026 · Updated 1 time

Summary

This trial asks whether a telerehabilitation program—guided exercises done at home—can reduce shoulder pain and disability as effectively as traditional in-person physiotherapy. Adults aged 18 to 60 with persistent shoulder pain lasting at least three months are randomly assigned to either remote or in-person sessions, both focusing on strengthening key shoulder muscles. Over 12 weeks, researchers measure changes in pain, function, and confidence in managing symptoms. The goal is to see if remote care can expand access to effective treatment for those who face barriers like travel or long wait times.

What this could mean

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

Active substance
Telerehabilitation program of therapeutic strengthening exercises
What this could lead to
If effective, this could offer a convenient, low-cost alternative to in-person physiotherapy for people with persistent shoulder pain, improving access to care.
What could go wrong
The trial is relatively small and results may not apply to all shoulder conditions. Telerehabilitation may not suit everyone, and some patients may prefer or need hands-on guidance.

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

184 people

The number who actually took part.

Started

Oct 2021

Finished

Oct 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

18 to 60 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: * Age 18-60; * Self-reported pain of intensity equal to or greater than 3 points on the numerical pain scale (NDT) at rest or arm movement in the anterolateral region of the shoulder; * Duration of at least 3 months of shoulder pain; Exclusion Criteria: * History of trauma related to the onset of symptoms; * History of clavicle, scapula or humerus fracture; * History of surgical stabilization or rotator cuff repair; * History of shoulder dislocation; * Pain related to the cervical spine; * Adhesive capsulitis; * Systemic disease involving the joints and cognitive alteration that makes it impossible to carry out questionnaires or use the mobile application.

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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

  • Universidade Federal de São Carlos

    São Carlos, São Paulo, 13565-905, Brazil

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