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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05892250
Other study ID # 17798315
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date March 6, 2023
Est. completion date December 18, 2025

Study information

Verified date January 2024
Source Universidad de Antofagasta
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Recruiting
Enrollment 84
Est. completion date December 18, 2025
Est. primary completion date July 24, 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Conventional physical therapy
Manual techniques and therapeutic exercise
Conventional physical therapy + Dynamic Humeral Centering exercises
Manual techniques and therapeutic exercise and active dynamic humeral centering exercises

Locations

Country Name City State
Chile Universidad de Antofagasta Antofagasta

Sponsors (1)

Lead Sponsor Collaborator
Universidad de Antofagasta

Country where clinical trial is conducted

Chile, 

Outcome

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