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Frozen shoulder study reveals muscle weakness patterns

NCT ID NCT07520604

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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 Results may not be published yet.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)

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Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
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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

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Status unknown
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First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study compared shoulder muscle strength and fatigue between 60 people with frozen shoulder (adhesive capsulitis) in the recovery phase and healthy individuals. Researchers used a special machine to measure peak torque and fatigue index of shoulder muscles. The goal was to understand how frozen shoulder affects muscle function, not to test a treatment.

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Study facts

What this study's own registry entry says, in plain language.

Participants

60 people

The number who actually took part.

Started

Feb 2015

Finished

Dec 2016

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.

Who is studied

In the present study, 60 participants between 40 and 60 years were recruited. They were enrolled in the experimental group, which included 30 typical subjects with unilateral AC and the control group (dominant shoulder) that included 30 healthy individuals of the same age and sex. Individuals were recruited from the outpatient clinics and respective orthopedic centers. They were informed through an advertisement poster placed on the bulletin of the mentioned locations and referred from a physician.

Ages

40 to 60 years

Sex

Anyone

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: The AC group included participants that met the following criteria, based on a previous study conducted by Ramirez \[2\] : 1. clinical diagnosis of unilateral AC by an orthopedic specialist, with the limitation of both active and passive glenohumeral ROM, exceeding 25% in at least two of the following planes: flexion, abduction, and external rotation 2. symptom duration between 3 and 12 months 3. no prior surgery to the involved shoulder 4. age between 40 and 60 years. -The control group consisted of healthy individuals of comparable age and sex distribution with no history of shoulder pain, injury, or pathology Exclusion Criteria: 1. history of shoulder fracture, dislocation, or surgery; 2. corticosteroid or muscle relaxant use within the previous three months 3. cardiovascular or respiratory conditions that could limit physical testing 4. concurrent participation in structured shoulder strengthening programs 5. inability to perform the isokinetic assessment protocol safely 6. systemic musculoskeletal, neurological or rheumatologic disorders, such as diabetes mellitus, rheumatoid arthritis and cervical radiculopathy. Individuals with diabetes mellitus were excluded due to its well-established association with AC.

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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

  • Faculty of Physical Therapy, Cairo University

    Giza, Giza Governorate, 12511, Egypt

More trials for these conditions

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