Shoulder Tendinopathy Clinical Trial
Official title:
Efficacy of Therapeutic Exercise vs. Treatment of Myofascial Trigger Points in Shoulder Tendinopathies: Randomised Clinical Trial
NCT number | NCT06241404 |
Other study ID # | 250124 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | October 1, 2023 |
Est. completion date | January 15, 2024 |
Verified date | February 2024 |
Source | Universidad Católica de Ávila |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Background: Shoulder pain commonly affects the general population, with rotator cuff tendinopathy being the most common cause. the most common cause, with rotator cuff tendinopathy diminishing function and quality of life, leading to a major socio-economic impact. quality of life, leading to a major socio-economic impact. As a result, there are two treatment approaches with potential effectiveness: therapeutic exercise (TE) and myofascial trigger point treatment (TMT). trigger point treatment (TTP). Objective: The main objective of this randomised clinical trial is to determine the efficacy of ET versus treatment of MTPs in shoulder tendinopathies. Methods: For this study, 20 participants were randomly divided into two groups: a ET group, with which a 10-exercise programme was initiated (n = 10), and a PGM group which was given an intervention protocol (n = 10). intervention protocol (n = 10). Both received a total of 10 sessions. Pain intensity pain intensity, pressure pain threshold (PPT) and range of motion (ROM) were assessed before starting and after 10 sessions. and after 10 sessions.
Status | Completed |
Enrollment | 80 |
Est. completion date | January 15, 2024 |
Est. primary completion date | November 1, 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 75 Years |
Eligibility | Inclusion Criteria: - Signed informed consent form. - Patients diagnosed by an orthopaedic surgeon with shoulder tendinopathy. tendinopathy. - Symptoms of shoulder pain lasting more than 3 months. - Pain on Jobe, Patte and infraspinatus assessment manoeuvres (highlighting abduction and abduction and external rotation). Exclusion Criteria: - Previous shoulder surgery. - Radiating (non-referred) pain from cervical radiculopathy. - Shoulder pain associated with other diagnoses (Examples: retractile capsulitis, subacromial syndrome, tendon rupture, posterosuperior conflict, etc.). subacromial syndrome, tendon rupture, posterosuperior conflict, etc). - Patients with multiple pathologies. - Patients with neurological disorders. |
Country | Name | City | State |
---|---|---|---|
Spain | Jorge Velázquez Saornil | Ávila |
Lead Sponsor | Collaborator |
---|---|
Universidad Católica de Ávila |
Spain,
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Range of motion | measurement of shoulder range of motion | At the end of Session 10 (each Session is 7 days) | |
Primary | pain intensity | measured on a VAS scale where 0 is the minimum and 10 is the maximum. | At the end of Session 10 (each Session is 7 days) | |
Secondary | pressure pain threshold | measured by algometer | At the end of Session 10 (each Session is 7 days) |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT04636528 -
Digital Versus Conventional Physical Therapy for Chronic Shoulder Tendinopathy
|
N/A |