- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05892250
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
Status
Recruiting
Conditions
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:
- Juan Guerrero, MSc
- Phone Number: 7067 56957601527
- Email: juan.guerrero@uantof.cl
-
-
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.
Sponsor
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- 17798315
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.
Clinical Trials on Shoulder Impingement Syndrome
-
Mahidol UniversityCompletedSubacromial Impingement Syndrome | Shoulder Impingement Syndrome | Subacromial Pain Syndrome | Subacromial Impingement | Impingement Syndrome, ShoulderIndonesia
-
Copenhagen University Hospital, HvidovreUniversity of Copenhagen; Aalborg University; Metropolitan University CollegeCompletedSubacromial Impingement SyndromeDenmark
-
Uskudar State HospitalNot yet recruitingSubacromial Impingement Syndrome | Shoulder Impingement Syndrome | Shoulder Pain | Subacromial Impingement | Shoulder Impingement
-
Hadassah Medical OrganizationUnknownShoulder Impingement Syndrome.
-
King Saud UniversityUnknownImpingement Syndrome, ShoulderSaudi Arabia
-
National Taiwan University HospitalCompletedShoulder Impingement Syndrome (SIS); Round Shoulder Posture (RSP)Taiwan
-
Central Finland Hospital DistrictOulu University Hospital; Academy of FinlandActive, not recruitingSubacromial Impingement SyndromeFinland
-
Linkoeping UniversityCompletedSubacromial Impingement SyndromeSweden
-
Cairo UniversityCompletedImpingement Syndrome, ShoulderEgypt
-
Sevgi Medical CenterCompletedSubacromial Impingement Syndrome | Subacromial ImpingementTurkey
Clinical Trials on Conventional physical therapy
-
Riphah International UniversityCompletedAdhesive Capsulitis of ShoulderPakistan
-
Federal University of BahiaFundação de Amparo à Pesquisa do Estado da BahiaUnknown
-
University of ValenciaCompleted
-
University of LahoreCompletedLow Back Pain, MechanicalPakistan
-
Kars State HospitalCompletedShoulder Pain | Myofascial Pain | HemiplegiaTurkey
-
Ragaee Saeed MahmoudRecruiting
-
University of LahoreCompletedDiabetic NeuropathiesPakistan
-
St George's, University of LondonThe Health FoundationCompleted
-
Riphah International UniversityCompleted
-
South Valley UniversityRecruiting