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New combo therapy offers hope for seniors with stubborn shoulder pain

NCT ID NCT07184242

Symptom relief Sponsor: University of Jaén 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026

Summary

This study tested a 12-week program combining multi-joint strength exercises and sensory stimulation for 80 adults over 60 with chronic rotator cuff-related shoulder pain. The experimental group received the combo plus standard care, while the control group got standard care alone. Researchers measured pain, function, sleep, and emotional factors to see if the combined approach leads to better 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

80 people

The number who actually took part.

Started

Sep 2025

Finished

Dec 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

60 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 60 years of age. * Be able to understand the instructions and answer the questionnaires designed for this study, as well as participate in the established physical tests. * People with rotator cuff-related shoulder pain (RCSRP) of at least 3 months' duration. * Sign informed consent to participate in the study. * Possible medical diagnoses to categorize you as RCSRP: * Subacromial syndrome or subacromial pain syndrome. * Subacromial impingement. * Rotator cuff tendinopathy/tendinitis/tendinosis. * Subdeltoid/subacromial bursitis. * Non-traumatic partial tears of a rotator cuff tendon affecting less than 50% of the tendon thickness. * Mild/moderate intrasubstance rotator cuff tears. Exclusion Criteria: * Complete/massive rotator cuff tears. * Corticosteroid injections within the last 6 weeks. * Recent surgery on that shoulder or planned surgery within the next 3 months. * Bilateral shoulder pain. * Presence of glenohumeral fractures or osteoarthritis confirmed by radiographic examination. * Psychiatric illnesses or central or peripheral neurological disorders that make it difficult to grasp, cooperate, or follow instructions during the procedure. * Individuals with an absolute contraindication to moderate-to-high-intensity physical exercise based on prior medical testing. * Presence of severe difficulties with gait, balance, or functional activity, or hearing or vestibular disorders that prevent the performance of the prescribed exercises. * Visual disturbances that cannot be corrected with glasses, contact lenses, or surgery. * Being enrolled in another physical exercise or treatment program during the study.

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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.

Shoulder pain

Contacts and locations

Locations

  • ICOT rehabilitation centers

    Las Palmas de Gran Canaria, Spain

More trials for these conditions

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