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RecruitingNCT07115225VAL_PPT_PUpdated Sep 17, 2026

Validation of an Upper Extremity Physical Performance Test Battery in Patients After Shoulder Dislocation

An interventional study of Analytical test - Shoulder Range of Motion (ROM) and Analytical test - Shoulder Strength in Return to Sport and Shoulder Dislocation or Subluxation, sponsored by University Ghent. Recruiting at 2 sites in Belgium. Open to participants aged 16 Years to 55 Years. Per ClinicalTrials.gov, last updated 2026-09-17.

Sponsored by University Ghent · Not applicable, Interventional, and Other

From the registry’s dates

  • Started Jul 2025; still recruiting 1 year 4 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
129
Allocation
Not applicable
Ages
16 Years to 55 Years
Sex
All
01

Study summary

The goal of this exploratory prospective study is to determine if an upper extremity test battery, comprised of physical performance tests, analytical tests and patient-reported outcome measures, can predict successful return to sports and quality of life in athletes (age 16-55) after shoulder dislocation.

The main research questions are:

  • Can an Upper Extremity Physical Performance Test Battery predict successful return to sports (= return to pre-injury sports level) in athletes after shoulder stabilization procedure
  • Can an Upper Extremity Physical Performance Test Battery predict the quality of life in athletes after shoulder stabilization procedure

Participants will:

  • Fill out questionnaires pre-operatively
  • Fill out the SIRSI questionnaire throughout the rehabilitation
  • Undergo a testing battery in the return to sport phase, including physical performance tests, analytical tests and patient-reported outcome measures
  • Fill out questionnaires every 3 months after return to sports, up to 1 year.
Read the detailed description

After enrollment, athletes will be asked about their injury history, and demographic information will also be collected, including gender, age, athlete experience, and sports level. During rehabilitation (duration: typically between 3 and 6 months), the participant will be given a monthly questionnaire that surveys their rehabilitation progress. At the time they return to sport (after green light by orthopaedic surgeon and physiotherapist), they are tested once with the test battery (physical performance tests, analytical tests and patient-reported outcome measures). Patients will be tested as close as possible to the actual return to sport timing. Following, they are monitored for another year with questionnaires, every 3 months, that survey their pain, current level of competition, quality of life, confidence in the shoulder and possible re-injuries. This way, the included participants will be monitored for +- 18 months (duration of rehabilitation + 1 year follow-up after return to sport).

02

Conditions studied

  • Return to Sport
  • Shoulder Dislocation or Subluxation
03

In context

Shoulder Dislocation

105 studies on the registry are indexed under Shoulder Dislocation; 22 are open to participants now.

This study's planned enrollment of 129 is above the median of 60 across 71 interventional studies indexed under Shoulder Dislocation.

Browse Shoulder Dislocation studies →

Lead sponsor

University Ghent is the lead sponsor of 350 studies on the registry; 86 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
16 Years to 55 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Practising sports with moderate to high demand on the shoulder (based on Degree of Shoulder Involvement in Sport (DOSIS) scale), minimal weekly 3 hours
  • Shoulder instability event (anterior direction)
  • Healthy contralateral shoulder
  • Completion of the postoperative rehabilitation protocol

Exclusion criteria

Exclusion Criteria:

  • Other upper limb pathologies/ associated injuries: e.g. posterior instability, or rotator cuff tear,...
  • Being pregnant
  • No intention to return to pre-injury sport
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
129 participants (estimated)

Study arms

  • Experimental
    Patients after shoulder stabilization procedure (Latarjet or Bankart procedure)

    Patients who underwent shoulder stabilization surgery (Latarjet or Bankart procedure) between the ages of 16 and 55 years old

    Other: Analytical test - Shoulder Range of Motion (ROM) · Other: Analytical test - Shoulder Strength · Other: Modified-Athletic Shoulder Test (M-AST) · Other: Physical performance test - Unilateral Seated Shot-Put Test (USSPT) · Other: Physical performance test - modified-Closed Kinetic Chain Upper Extremity Stability Test (m-CKCUEST) · Other: Supine moving apprehension test (SMAT) · Other: Physical performance test - Posterior shoulder endurance test (PSET) · Other: Patient-reported outcome measure - The Shoulder Instability-Return to Sport after Injury (SIRSI) · Other: Patient-reported outcome measure - Numeric Pain Rating Scale (NPRS) · Other: Modified Tampa-Scale of Kinesiophobia for Anterior Shoulder Instability (TSK-SI)

Interventions

  • OtherAnalytical test - Shoulder Range of Motion (ROM)

    Passive external rotation in supine position with arm in 90° abduction - passive internal rotation in supine position with arm in 90° abduction.

  • OtherAnalytical test - Shoulder Strength

    Shoulder external rotation and internal rotation measured with a hand held dynanometer in supine lying

  • OtherModified-Athletic Shoulder Test (M-AST)

    Shoulder strength in the antero-posterior plane measured with a hand held dynanometer in prone lying

  • OtherPhysical performance test - Unilateral Seated Shot-Put Test (USSPT)

    Set up requires that the subject is placed in a seated position (knees bent at 90° degrees) with their back against the wall, and a 3 kg medicine ball held at height of the shoulder. When ready, the subject will perform a shot put motion to push the medicine ball as far as possible in a horizontal direction. The average of three trials is recorded for each arm.

  • OtherPhysical performance test - modified-Closed Kinetic Chain Upper Extremity Stability Test (m-CKCUEST)

    The test is performed in a push-up position with the hands one half-arm span apart on strips of athletic tape. The person reaches with alternating hands across the body to touch the piece of tape under the opposing hand. The number of cross-body touches performed in 15 seconds is recorded. In total, three 15-s test trials were performed, with 45 s rest between each trial.

  • OtherSupine moving apprehension test (SMAT)

    The beginning position of the participant is lying in a supine position while holding the weight just over their chest. Participants move their shoulder to 135° of abduction with the elbow extended, then returning to the starting position, and immediately move their shoulder to 180° of abduction with the elbow fully extended and finally return to the starting position. This cycle is repeated as much as possible for 1 minute.

  • OtherPhysical performance test - Posterior shoulder endurance test (PSET)

    The participant is positioned prone, with the test shoulder off the table and the arm in 90° of horizontal abduction, the point at which the participant is to hold the arm as long as possible until fatigue. The participant holds a weight equal to 2% of his body weight (rounded to the nearest 0.5 kg).

  • OtherPatient-reported outcome measure - The Shoulder Instability-Return to Sport after Injury (SIRSI)

    Psycho-social questionnaire assessing the psychological readiness of athletes to return to sport following traumatic shoulder instability and conservative or surgical management. The SIRSI includes 12 questions with an 11-point Likert scale in the form of blocks to be ticked from 0 to 10. The total score is equal to the sum of the values of the 12 responses then determined in relation to 100 to obtain a percentage. High scores correspond to a positive psychological response.

  • OtherPatient-reported outcome measure - Numeric Pain Rating Scale (NPRS)

    Patient's shoulder pain will be measured using an 11-point NRS, with a minimum value of zero ("no pain") and a maximum score of 10 ("the worst pain possible")

  • OtherModified Tampa-Scale of Kinesiophobia for Anterior Shoulder Instability (TSK-SI)

    modified Tampa Scale of Kinesiophobia (TSK) to make it suitable for application in patients with anterior shoulder instability. The TSK-SI contains 18 items and the total score can range from 18 to 72, with 18 being the "best" score (no fear of movement/kinesiophobia) and 72 being the "worst" score (severe fear of movement/kinesiophobia)

06

What researchers measure

Primary outcomes

  1. Subjective Patient Outcome for Return to Sports (SPORTS) score

    Subjective Patient Outcome for Return to Sports (SPORTS) score is a single-item scale that measures athletes' ability to return to their preinjury sport based on effort and performance. It is scored on a 10-point scale with 0 points allocated to the patient who does not resume the same sport and 10 points to the patient who is able to perform, without pain, the same sport, at same level of effort and performance as before the onset of his/her impairment.

    Time frame: 3 months, 6 months, 9 months, 12 months post-return to sport

  2. Western Ontario Shoulder Instability Index (WOSI)

    The WOSI score questionnaire is a tool designed for self-assessment of shoulder function for patients with shoulder instability. It consists of four subscales with a total of 21 items. Each question in this version is scaled on a Numerical Rating Scale from 0 (best) to 10 (worst), with the WOSI score ranging from 0 (highest shoulder-related quality of life) to 210 (worst shoulder-related quality of life).

    Time frame: pre-operatively; in return to sport phase; 3 months, 6 months, 9 months, 12 months post-return to sport

Secondary outcomes

  1. Re-injury

    The questionnaire will capture re-injuries and subsequent injuries within 12 months after return to sport

    Time frame: 3 months, 6 months, 9 months, 12 months post-return to sport

07

Study locations

2 of 2 sites recruiting
  • AZ Monica, Deurne - Orthopedie
    Antwerp, Belgium
    Recruiting
  • Department of rehabilitation sciences, Ghent university
    Ghent, 9000, Belgium
    Recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 17, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07115225
Lead sponsor
University Ghent
Collaborators
AZ Monica Campus Antwerpen
Responsible party
Sponsor
First posted
Aug 11, 2025
Start date
Jul 3, 2025
Primary completion
Jan 1, 2029 (estimated)
Completion
Jan 1, 2029 (estimated)
Last update
Sep 17, 2026

Study contacts

Jasper Stubbe
Contact
jasper.stubbe@ugent.be
+32 9 332 26 33
Ann Cools
principal investigator · University Ghent

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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