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Validation of Modified AST

Validity and Reliability of the Modified Athletic Shoulder Test

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05146115
Enrollment
20
Registered
2021-12-06
Start date
2021-12-01
Completion date
2022-03-01
Last updated
2022-05-17

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

Conditions

Strength

Brief summary

The objective of the study is the validate and to assess the reliability of a modified version of the Athetic Shoulder Test. The activity of peri-scapular muscles during the realization of the test will be assessed too.

Detailed description

The study will be divided into two sessions. A time of 7-10 days will be provided between the two sessions of tests to limit the influence of sport and training on the results. Session 1: * Warm-up * Realization of the Athletic Shoulder Test (with EMG captors on upper trapezius, lower trapezius and serratus anterior) * Realization of the modified Athletic Shoulder Test (with EMG captors on upper trapezius, lower trapezius and serratus anterior) Session 2: * Warm-up * Realization of the Athletic Shoulder Test (with EMG captors on upper trapezius, lower trapezius and serratus anterior) * Realization of the modified Athletic Shoulder Test (with EMG captors on upper trapezius, lower trapezius and serratus anterior)

Interventions

OTHERRealization of the Athletic Shoulder Test and the Modified Athletic Shoulder Test

The participants will have to perform both tests two times, with a 7-10 days rest period between the two sessions

Sponsors

University of Liege
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
MALE
Age
18 Years to 35 Years

Inclusion criteria

* to practice an overhead sport at least 5 hours a week

Exclusion criteria

* no shoulder pain * no history of shoulder pain * no history of shoulder surgery * no scoliosis or lower limb lengths differences

Design outcomes

Primary

MeasureTime frameDescription
Strength of anteflexors in I positionChange from baseline to 10 daysThe strength developped in the I position will be assessed with a force plateform and a handheld dynamometer
Strength of anteflexors in Y positionChange from baseline to 10 daysThe strength developped in the Y position will be assessed with a force plateform and a handheld dynamometer
Strength of anteflexors in T positionChange from baseline to 10 daysThe strength developped in T position will be assessed with a force plateform and a handheld dynamometer
EMG activity of upper trapeziusduring the first sessionEMG activity of upper trapezius will be measured with surface electrodes (Delsys Trigno)
EMG activity of lower trapeziusduring the first sessionEMG activity of lower trapezius will be measured with surface electrodes (Delsys Trigno)
EMG activity of serratus anteriorduring the first sessionEMG activity of serratus anterior will be measured with surface electrodes (Delsys Trigno)

Countries

Belgium

Outcome results

None listed

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