Skip to main content
Clinical Trials/NCT05128448
NCT05128448UnknownNot Applicable

Comparative Effects of Two Procedures for the Management of Posterior Shoulder Tightness

Federal University of Health Science of Porto Alegre2 sites in 1 country22 target enrollmentStarted: October 17, 2021Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Sponsor
Enrollment
22
Locations
2
Primary Endpoint
Horizontal adduction

Study Overview

Brief Summary

This study aims to compare the effects of a self-stretch procedures versus a clinician applied musculoskeletal procedure in individuals with posterior shoulder tightness.

Detailed Description

Posterior shoulder mobility has been considered a contributing factor to shoulder related movement dysfunction. There is evidence indicating that posterior shoulder tightness (PST) might be present in individuals with impingement related symptoms, post-operative conditions and overhead athletes. Several studies have investigated the effects of musculoskeletal procedures (joint mobilisations and stretch) in subjects with posterior shoulder tightness (PST). This cross-over design aims to compare the differences between a well-established procedure - the crossbody stretch - versus mobilisation with movement, on range of motion and pain pressure threshold of asymptomatic individuals with unilateral PST.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Masking Description

All measurements will be conducted by research assistants unaware of the interventions applied. Statistical analyses will be performed by a blinded research assistant.

Eligibility Criteria

Ages
18 Years to 45 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Asymptomatic individuals without any history of shoulder pain necessitating medical attention.
  • Presence of unilateral restriction of at least 10 degrees of internal rotation deficit during the internal rotation mobility test in 90 degrees of shoulder abduction.

Exclusion Criteria

  • Asymptomatic individuals that present with shoulder pain on the assessment day.
  • Individuals with chronic conditions not affecting the shoulder.
  • Individuals with clinical depression.
  • Individuals that used analgesic and/or anti-inflammatory medication in the previous 24 hours of assessment.
  • Individuals with fibromialgia.
  • Individuals engaged in overhead sports.

Outcomes

Primary Outcomes

Horizontal adduction

Time Frame: change immediately after the intervention

Horizontal adduction in 90 degrees of shoulder flexion

Internal rotation

Time Frame: change immediately after the intervention

Internal rotation at 90 degrees of shoulder abduction

Secondary Outcomes

  • Mechanical sensitivity(change immediately after the intervention)

Investigators

Sponsor
Federal University of Health Science of Porto Alegre
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Rafael Baeske

Principal investigator

Federal University of Health Science of Porto Alegre

Study Sites (2)

Loading locations...

Similar Trials