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Validation of Modified AST

Sponsor
University of Liege (Other)
Overall Status
Completed
CT.gov ID
NCT05146115
Collaborator
(none)
20
Enrollment
1
Location
3
Actual Duration (Months)
6.8
Patients Per Site Per Month

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Realization of the Athletic Shoulder Test and the Modified Athletic Shoulder Test

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)

Study Design

Study Type:
Observational
Actual Enrollment :
20 participants
Observational Model:
Cohort
Time Perspective:
Other
Official Title:
Validity and Reliability of the Modified Athletic Shoulder Test
Actual Study Start Date :
Dec 1, 2021
Actual Primary Completion Date :
Feb 15, 2022
Actual Study Completion Date :
Mar 1, 2022

Outcome Measures

Primary Outcome Measures

  1. Strength of anteflexors in "I" position [Change from baseline to 10 days]

    The strength developped in the "I" position will be assessed with a force plateform and a handheld dynamometer

  2. Strength of anteflexors in "Y" position [Change from baseline to 10 days]

    The strength developped in the "Y" position will be assessed with a force plateform and a handheld dynamometer

  3. Strength of anteflexors in "T" position [Change from baseline to 10 days]

    The strength developped in "T" position will be assessed with a force plateform and a handheld dynamometer

  4. EMG activity of upper trapezius [during the first session]

    EMG activity of upper trapezius will be measured with surface electrodes (Delsys Trigno)

  5. EMG activity of lower trapezius [during the first session]

    EMG activity of lower trapezius will be measured with surface electrodes (Delsys Trigno)

  6. EMG activity of serratus anterior [during the first session]

    EMG activity of serratus anterior will be measured with surface electrodes (Delsys Trigno)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 35 Years
Sexes Eligible for Study:
Male
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Laboratoire d'Analyse du Mouvement Humain Liège Belgium 4000

Sponsors and Collaborators

  • University of Liege

Investigators

  • Principal Investigator: Camille Tooth, ULiège

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Camille Tooth, Physiotherapist, University of Liege
ClinicalTrials.gov Identifier:
NCT05146115
Other Study ID Numbers:
  • modified AST
First Posted:
Dec 6, 2021
Last Update Posted:
May 17, 2022
Last Verified:
May 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of May 17, 2022