Assessment of Shoulder Peak Torque and Fatigue Index in Individuals With Adhesive Capsulitis (AC)

April 2, 2026 updated by: Azza Mohammed, Cairo University

Biomechanical Assessment of Shoulder Peak Torque and Fatigue Index in Individuals With Adhesive Capsulitis: A Case-Control Study

Adhesive capsulitis (AC) is a common painful disorder associated with diminishing glenohumeral movement. This has led to the need for an evidence-based approach to assess the isokinetic strength and endurance of shoulder muscles in such disease conditions.The main aim of the current study was to determine whether isokinetic dynamometric values of peak torque (PT) and fatigue index of shoulder muscles are different between patients with AC in the recovery phase and the healthy subjects.

Study Overview

Detailed Description

Adhesive capsulitis (AC) is a common painful disorder associated with diminishing glenohumeral movement. This has led to the need for an evidence-based approach to assess the isokinetic strength and endurance of shoulder muscles in such disease conditions.The main aim of the current study was to determine whether isokinetic dynamometric values of peak torque (PT) and fatigue index of shoulder muscles are different between patients with AC in the recovery phase and the healthy subjects.The study involved a total of sixty subjects within the age group 40 and 60 years comprising thirty in the recovery phase of AC and thirty healthy controls. The Biodex System 3 Isokinetic dynamometer was used to measure shoulder abductor, internal rotator and external rotator peak torques and fatigue indices.

Study Type

Observational

Enrollment (Actual)

60

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Giza Governorate
      • Giza, Giza Governorate, Egypt, 12511
        • Faculty of physical therapy, Cairo University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

N/A

Sampling Method

Non-Probability Sample

Study Population

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.

Description

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.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
healthy control group
30 healthy controls participated in the study
The Biodex System 3 Isokinetic dynamometer was used to measure shoulder abductor, internal rotator and external rotator peak torques and fatigue indices
group of Adhesive capsulitis (AC)
30 patients with AC participated in the study
The Biodex System 3 Isokinetic dynamometer was used to measure shoulder abductor, internal rotator and external rotator peak torques and fatigue indices

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
shoulder abductor peak torque
Time Frame: one year
shoulder abductor isokinetic peak torque
one year
shoulder internal rotator peak torque
Time Frame: one year
shoulder internal rotator isokinetic peak torque
one year
shoulder external rotator peak torque
Time Frame: one year
shoulder external rotator isokinetic peak torque
one year
shoulder abductor fatigue index
Time Frame: one year
shoulder abductor isokinetic fatigue index
one year
shoulder internal rotator fatigue index
Time Frame: one year
shoulder internal rotator isokinetic fatigue index
one year
shoulder external rotator fatigue index
Time Frame: one year
shoulder external rotator isokinetic fatigue index
one year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Azza M, professor, Cairo university

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 20, 2015

Primary Completion (Actual)

November 10, 2016

Study Completion (Actual)

December 3, 2016

Study Registration Dates

First Submitted

March 27, 2026

First Submitted That Met QC Criteria

April 2, 2026

First Posted (Actual)

April 9, 2026

Study Record Updates

Last Update Posted (Actual)

April 9, 2026

Last Update Submitted That Met QC Criteria

April 2, 2026

Last Verified

April 1, 2026

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • P.T.REC/012/006256

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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