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NCT04777578 Clinical Trial

Effects of Dry Needling in Teres Major in Patients With Shoulder Pain

Shoulder Pain Clinical Trial

Official title:
Effects of Dry Needling in Teres Major in Patients With Shoulder Pain

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT04777578
Other study ID # CASVE-NM-21-504
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date February 25, 2021
Est. completion date January 5, 2022

Study information
Verified date March 2021
Source Universidad de Zaragoza
Contact Luis Ceballos Laita, PhD
Phone 975 12 91 00
Email luis.ceballos@uva.es
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of the study is to investigate the effects of the dry needling technique in teres major muscles on pain, range of motion, strength and extensibility of the posterior part of the tissues of the shoulder in athletes with shoulder pain.

Recruitment information / eligibility
Status Recruiting
Enrollment 40
Est. completion date January 5, 2022
Est. primary completion date December 20, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 30 Years
Eligibility Inclusion Criteria: - Athletes with Shoulder pain - Glenohumeral internal rotation deficit - Presence of active MTrP in the teres major muscle Exclusion Criteria: - Previous surgery in the upper limb - Previous physiotherapy treatments in the shoulder - Dry needling contraindications - Previous dry needling experience to mantain the blinding

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Dry needling
Dry needling based on fast-in fast-out technique in the teresa major muscle

Locations
Country Name City State
Spain Luis Ceballos Laita Soria

Sponsors (1)
Lead Sponsor Collaborator
Universidad de Zaragoza

Country where clinical trial is conducted

Spain, 

Outcome
Type Measure Description Time frame Safety issue
Primary Pain intensity the examiners assess the pain intensity using a visual analoigue scale Baseline
Primary Pain intensity the examiners assess the pain intensity using a visual analoigue scale immediately after the intervention
Secondary Range of motion the examiners assess the shoulder range of motion with an universal goniometer Baseline
Secondary Range of motion the examiners assess the shoulder range of motion with an universal goniometer immediately after the intervention
Secondary Strength the examiners assess the shoulder range of motion with a hand-held dynamometer Baseline
Secondary Strength the examiners assess the shoulder range of motion with a hand-held dynamometer immediately after the intervention
Secondary Extensibility the examiners assess the extensibility of the posterior part of the tissues of the shoulder using a digital inclinometer Baseline
Secondary Extensibility the examiners assess the extensibility of the posterior part of the tissues of the shoulder using a digital inclinometer immediately after the intervention
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