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

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

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05128448
Enrollment
22
Registered
2021-11-22
Start date
2021-10-17
Completion date
2022-02-28
Last updated
2021-11-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Posterior Shoulder Tightness

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.

Interventions

OTHERCross-body stretch (CBS)

CBS is a self administered stretch that aims to stretch posterior shoulder structures

OTHERMobilisation with movement (MWM)

WMW is a musculoskeletal procedure that aims to improve restricted and/or painful range of movement

Sponsors

Federal University of Health Science of Porto Alegre
Lead SponsorOTHER

Study design

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

Sex/Gender
ALL
Age
18 Years to 45 Years
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.

Design outcomes

Primary

MeasureTime frameDescription
Horizontal adductionchange immediately after the interventionHorizontal adduction in 90 degrees of shoulder flexion
Internal rotationchange immediately after the interventionInternal rotation at 90 degrees of shoulder abduction

Secondary

MeasureTime frameDescription
Mechanical sensitivitychange immediately after the interventionPain pressure threshold with an algometer (Wagner instruments, FPX 25)

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026