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Validation and Inverse Analysis of The Athletic Shoulder Test (ASH).

Validation and Inverse Analysis of The Athletic Shoulder Test (ASH): Reliability of a Novel Upper Body Isometric Strength Test

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06763107
Enrollment
21
Registered
2025-01-08
Start date
2025-01-10
Completion date
2025-01-30
Last updated
2025-03-28

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

Conditions

Shoulder Pain, Sports Physical Therapy

Keywords

Shoulder Pain; Isometric Strength; Muscle Strength Imbalance; Sports Medicine; Rehabilitation

Brief summary

To validate both the Athletic Shoulder (ASH) test, conducted on rugby players, and its inverse, the Inverse Athletic Shoulder (IASH) test, for swimmers. This involves assessing the strength relationship between shoulder flexion and extension at three different adduction angles (180º, 135º, 90º) to identify potential injuries associated with these imbalances.

Interventions

PROCEDUREAthletic Shoulder (ASH) and Inverse Athletic Shoulder (IASH) Tests

Participants perform the Athletic Shoulder (ASH) test and Inverse Athletic Shoulder (IASH) test to measure maximal isometric shoulder strength in three positions (180º, 135º, 90º) during two separate sessions. Data is used to assess test reliability and validity for high-performance swimmers.

Sponsors

University of Vigo
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Intervention model description

Validation of isometric shoulder strength tests (ASH and IASH) in high-performance swimmers.

Eligibility

Sex/Gender
ALL
Age
14 Years to 18 Years
Healthy volunteers
Yes

Inclusion criteria

* High-performance swimmers. * Aged between 14 and 18 years. * No acute injuries in the cervical or scapular region. * Ability to perform the ASH and IASH tests without compensatory movements.

Exclusion criteria

* Acute injuries in the cervical or scapular region. * Inability to maintain proper positioning during the tests due to lack of adequate mobility or strength. * Refusal to sign informed consent (or legal guardian's consent for minors).

Design outcomes

Primary

MeasureTime frameDescription
Intraclass Correlation Coefficient (ICC) for ASH TestMeasured at two time points: baseline (Day 0) and follow-up (Day 2).Assessment of between-day reliability of the ASH test using intraclass correlation coefficients (ICC) for shoulder extension at three adduction angles (180º, 135º, 90º).
Intraclass Correlation Coefficient (ICC) for IASH TestMeasured at two time points: baseline (Day 0) and follow-up (Day 2).Assessment of between-day reliability of the IASH test using intraclass correlation coefficients (ICC) for shoulder flexion at three adduction angles (180º, 135º, 90º).
Coefficient of Variation (CV) for ASH and IASH TestsMeasured at two time points: baseline (Day 0) and follow-up (Day 2).Analysis of the coefficient of variation (CV) to evaluate data dispersion and consistency for both ASH and IASH tests.
Minimum Detectable Change (MDC) for ASH and IASH TestsMeasured at two time points: baseline (Day 0) and follow-up (Day 2).Calculation of the minimum detectable change (MDC) to identify the smallest significant change in performance beyond measurement error for both ASH and IASH tests.
Force Ratios Between ASH and IASH TestsMeasured at two time points: baseline (Day 0) and follow-up (Day 2).Evaluation of the agonist-antagonist strength ratios between ASH (extension) and IASH (flexion) tests across three adduction angles (180º, 135º, 90º).
Comparison of Shoulder Strength Between Preferred and Non-Preferred Breathing SidesMeasured at two time points: baseline (Day 0) and follow-up (Day 2).Analysis of differences in isometric shoulder strength between the preferred and non-preferred breathing sides in ASH and IASH tests across three adduction angles.
Evaluation of Test Fatigue and Its Impact on ReliabilityMeasured at two time points: baseline (Day 0) and follow-up (Day 2).Assessment of fatigue effects during ASH and IASH tests, considering the 20-second rest period and total number of efforts (36 per participant), and their potential impact on test reliability and strength measurements.

Countries

Spain

Outcome results

None listed

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