Validation of Modified AST

Strength Clinical Trial

Official title:

Validity and Reliability of the Modified Athletic Shoulder Test

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05146115
• Other study ID #: modified AST
• Status: Completed
• Start date: December 1, 2021
• Est. completion date: March 1, 2022

Study information

• Verified date: May 2022
• Source: University of Liege
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial 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.

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)

Recruitment information / eligibility

• Status: Completed
• Enrollment: 20
• Est. completion date: March 1, 2022
• Est. primary completion date: February 15, 2022
• Gender: Male
• Age group: 18 Years to 35 Years

Eligibility

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

Related Conditions & MeSH terms

• Strength

Intervention

Other:
• Realization 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

Locations

Country	Name	City	State
Belgium	Laboratoire d'Analyse du Mouvement Humain	Liège

Sponsors (1)

Lead Sponsor	Collaborator
University of Liege

Country where clinical trial is conducted

Belgium, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Strength of anteflexors in "I" position	The strength developped in the "I" position will be assessed with a force plateform and a handheld dynamometer	Change from baseline to 10 days
Primary	Strength of anteflexors in "Y" position	The strength developped in the "Y" position will be assessed with a force plateform and a handheld dynamometer	Change from baseline to 10 days
Primary	Strength of anteflexors in "T" position	The strength developped in "T" position will be assessed with a force plateform and a handheld dynamometer	Change from baseline to 10 days
Primary	EMG activity of upper trapezius	EMG activity of upper trapezius will be measured with surface electrodes (Delsys Trigno)	during the first session
Primary	EMG activity of lower trapezius	EMG activity of lower trapezius will be measured with surface electrodes (Delsys Trigno)	during the first session
Primary	EMG activity of serratus anterior	EMG activity of serratus anterior will be measured with surface electrodes (Delsys Trigno)	during the first session