Dynamic Humeral Centering Exercises in Subacromial Pain Syndrome

January 12, 2024 updated by: Juan Guerrero Henriquez, Universidad de Antofagasta

Effects of Dynamic Humeral Centering Exercises on Functionality and Disability in Subacromial Pain Syndrome

Subacromial pain syndrome is one of the most common musculoskeletal health conditions, causing decreased of range of motion, loss of muscle strength and disability in the shoulder region. It has been proposed that dynamic humeral centering exercises could contribute to overcome these disorders, through the modification of the dimensions of the subacromial space, however, there is no consensus on its effectiveness nor direct variables that account for its efficacy. Therefore, the aim of this research is to determine the effects of a dynamic humeral centering exercise program on the functionality and disability of patients with subacromial pain syndrome.The effects of the dynamic humeral head exercises program, as well as the objective description of factors and variables associated with subacromial pain syndrome, will also allow rehabilitation science professionals to aim their interventions according to the knowledge of direct variables, which will allow objective follow-up of interventions on subacromial pain syndrome diagnosed patients.

Study Overview

Study Type

Interventional

Enrollment (Estimated)

84

Phase

  • Not Applicable

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

      • Antofagasta, Chile, 1240000
        • Recruiting
        • Universidad de Antofagasta
        • Contact:

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

No

Description

Inclusion Criteria:

  • Older than 18 years old and less than 60 years old.
  • Pain in the lateral and upper arm region for more than two weeks of evolution.
  • At least three positive tests in the following: Neer's impingement sign, Hawkins-Kennedy impingement sign, Pattes' maneuver, Jobe's test or painful arch.

Exclusion Criteria:

  • Having any of the following diagnoses: frozen shoulder, shoulder girdle joint instability, cancer, glenohumeral arthrosis, symptomatic acromioclavicular arthritis, glenohumeral arthritis, rheumatoid arthritis, or fibromyalgia.
  • Cervical or thoracic pain.
  • Fracture or surgery in the shoulder region or in the last 6 months.

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

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Control group
Intervention will consist of a conventional physical therapy treatment program that includes manual therapy techniques and exercise
Manual techniques and therapeutic exercise
Experimental: Experimental group
Intervention will consist of a conventional physical therapy treatment program that includes manual therapy techniques and exercise plus Dynamic Humeral Centering exercises
Manual techniques and therapeutic exercise and active dynamic humeral centering exercises

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Subacromial space dimensions
Time Frame: baseline
Ultrasonography measure of coracohumeral and acromiohumeral distances
baseline

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pain intensity
Time Frame: baseline
Participants' self-reported pain intensity during activities of daily living, night pain, and pain at rest
baseline
Range of motion
Time Frame: baseline
Active and passive range of motion in coronal, sagital and transverse planes
baseline
Muscular endurance
Time Frame: baseline
Time (in seconds) it takes for the participant to become fatigued when performing repetitive movements with the upper extremity in the frontal plane
baseline
Muscular endurance
Time Frame: baseline
Number of repetitions performed by the subject until fatigue occurs when performing repetitive movements with the upper limb in the frontal plane
baseline
Shoulder Pain and Disability Index
Time Frame: baseline
Measures the percentage of disability in a person, with a minimum value of 0 (best) and a maximum of 100 percent.(worse)
baseline

Collaborators and Investigators

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

March 6, 2023

Primary Completion (Estimated)

July 24, 2025

Study Completion (Estimated)

December 18, 2025

Study Registration Dates

First Submitted

May 18, 2023

First Submitted That Met QC Criteria

May 27, 2023

First Posted (Actual)

June 7, 2023

Study Record Updates

Last Update Posted (Estimated)

January 15, 2024

Last Update Submitted That Met QC Criteria

January 12, 2024

Last Verified

January 1, 2024

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

The information will be provided to other researchers upon request to the principal investigator of the project.

IPD Sharing Time Frame

Data will be available once there are publications associated with the clinical trial. These data will be available for 4 years.

IPD Sharing Access Criteria

By e-mail request

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP
  • ICF
  • ANALYTIC_CODE
  • CSR

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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