ClinicalTrials.gg
Active, not recruitingNCT05857540Updated May 22, 2025

The Effects of Upper-Extremity Plyometric Combined Strength Training in Overhead Athletes With Shoulder Instability

An interventional study of Plyometric and strengthening exercises and Strengthening exercise in Glenohumeral Subluxation, Shoulder Subluxation and Shoulder Instability Subluxation Bilateral, sponsored by National Yang Ming Chiao Tung University. Active, not recruiting at 1 site in Taiwan. Open to participants aged 20 Years to 40 Years. Per ClinicalTrials.gov, last updated 2025-05-22.

Sponsored by National Yang Ming Chiao Tung University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
64
Allocation
Randomized
Ages
20 Years to 40 Years
Sex
All
01

Study summary

The purpose of this randomized controlled trial is to investigate the additional effects of upper extremity plyometric training versus strength training alone in recreational overhead athletes with shoulder instability. The investigators hypothesis that compared to strengthening training alone, plyometric training combined with strengthening training will significantly improve shoulder isokinetic strength, proprioception, scapular kinematics, symptoms of shoulder instability, and shoulder function.

Read the detailed description

Background: Shoulder instability is a common problem in active young adults with a wide spectrum ranging from microinstability, subluxation to dislocation. In patients with instability of Stanmore polar type 2 or 3, recurrent shoulder instability may be related to abnormal movement patterns but not result from trauma. Non-operative management is suggested to this subgroup as the first-line treatment. Previous rehabilitation protocols including progressive shoulder muscles strengthening and neuromuscular control training have shown positive effects on functional outcomes in individuals with shoulder instability. Recent protocols for shoulder instability usually include various types of plyometric training to prepare injured athletes to return to sports. Plyometric training in lower extremity has been wildly used for knee injury prevention. In upper extremity, plyometrics also has been shown to improve isokinetic strength, throwing performance, and proprioception in healthy subjects and healthy overhead athletes. However, it is still not well-understood that whether a strengthening training combined with plyometrics would be more effective to improve shoulder neuromuscular control and shoulder function in subjects with instability. The purpose of this study is to investigate the additional effects of upper extremity plyometric training in recreational overhead athletes with anterior shoulder instability. The investigators hypothesis that compared to strengthening training alone, plyometric training combined with strengthening training will significantly improve strength, proprioception, shoulder kinematic and muscle activity, shoulder pain and shoulder function.

Methods: A total of 64 participants with anterior shoulder instability will be randomized to either an experimental group (plyometric and strengthening training) or a control group (strengthening training). Both groups will receive a 50-minute supervised training protocol twice a week for 6 weeks. The primary outcomes include (1) isokinetic assessment of internal and external rotation (peak torque, time to peak torque, and amortization time); (2) proprioception (active and passive joint position sense); (3) seated medicine ball throw test (distance in cm). The secondary outcomes include (1) shoulder pain and instability with 10-cm visual analogue scale (VAS); (2) shoulder function assessed with the Disability of Arm, Shoulder and Hand (DASH) questionnaire; (3) Global rating of change (GRC). GRC will be measured after the end of 12 session of intervention, and all the other outcomes will be measured at baseline and following 12 sessions of exercise training. The two-way repeated measures ANOVAs will be used to compare primary and secondary outcome variables between groups. The significant level was set at 0.05.

02

Conditions studied

  • Glenohumeral Subluxation
  • Shoulder Subluxation
  • Shoulder Instability Subluxation Bilateral

Browse trials for

Keywords

  • Plyometric
  • Strengthening
  • Overhead athlete
  • Shoulder instability
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 64 is close to the median of 60 across 71 interventional studies indexed under Shoulder Dislocation.

Browse Shoulder Dislocation studies →

Lead sponsor

National Yang Ming Chiao Tung University is the lead sponsor of 208 studies on the registry; 60 are open to participants now.

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

04

Who can participate

Ages eligible
20 Years to 40 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

  1. Have experience of at least 1 of the following symptoms of shoulder instability during upper extremity movement: (a) pain, clicking, a sense of the shoulder coming apart, (b) dead-arm syndrome, or (c) subluxation of the joint.
  2. Self-reported decreased performance or feeling fear to perform shoulder movements during sports or daily activities
  3. Positive findings on ≥ 1 of the following 5 tests: load and shift test, apprehension, relocation, \& surprise tests, Gagey hyperabduction test, sulcus sign, Feagin test
  4. Recreational overhead athletes who keep practicing ≥ 4 hours/week in the recent 1 month and with ≥ 1 year overhead sports experience

Exclusion criteria

Exclusion Criteria:

  1. Full contact sport athletes
  2. Severe shoulder instability with > 5 shoulder dislocations history
  3. Obvious shoulder bony/labrum lesion in the dominant side warranted for surgery first as decided by the orthopedic surgeon
  4. Previous surgery or fracture in the shoulder area on the dominant side within 1 year
  5. Voluntary instability (the ability to deliberately dislocate one's shoulder)
  6. During acute phase after shoulder dislocation event
  7. Not suitable to start plyometric training yet: Shoulder muscle weakness (manual muscle test \<3) or range of motion limitation (\<90 abduction, \<70 external rotation) in the dominant side
  8. Pregnancy
  9. Cancer, neck pain, brain \& neurological impairment
  10. Ehlers-Danlos syndrome or Marfan syndrome
  11. Unable to attend 6 weeks supervised training
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
64 participants (estimated)

Study arms

  • Experimental
    Plyometric training group

    Participants in this group will receive upper extremity plyometric training in body weight or with weight ball and strengthening exercises with band, dumbbell and barbell. The difficulty and intensity of the movement protocol will increase weekly. They will be trained 2 times per week for 6 weeks with an average duration of 50 min per session.

    Procedure: Plyometric and strengthening exercises

  • Active comparator
    Strengthening training group

    Participants in this group will receive upper extremity strengthening exercises with band, dumbbell and barbell. The intensity of the movement protocol will increase weekly. They will be trained 2 times per week for 6 weeks with an average duration of 50 min per session.

    Procedure: Strengthening exercise

Interventions

  • ProcedurePlyometric and strengthening exercises

    Each session includes 2 upper-extremity plyometric exercises in bodyweight or with weight ball for 15-20 minutes and 4-5 strengthening exercises with band, dumbbell or barbell for 30-35 minutes. The difficulty of the movement protocol will increase weekly. They will be trained 2 times per week for 6 weeks with an average duration of 50 min per session.

  • ProcedureStrengthening exercise

    Each session includes 5 upper-extremity strengthening exercises with band, dumbbell or barbell for 50 minutes. The difficulty of the movement protocol will increase weekly. They will be trained 2 times per week for 6 weeks with an average duration of 50 min per session.

06

What researchers measure

Primary outcomes

  1. Shoulder isokinetic muscle strength

    Shoulder isokinetic muscle strength will be measured by dynamometer in 3 modes (concentric/concentric, concentric/eccentric, eccentric/concentric) at 3 angular velocities (90°/s, 180°/s, \& 240°/s), 1 set of 5 repetitions for each angular velocities. Shoulder isokinetic muscle strength will be normalized by body weight (BW) and described with peak torque/BW (N·m·kg-1).

    Time frame: Change from baseline shoulder isokinetic muscle strength through completion of 12-session intervention, an average of 6 weeks

  2. Shoulder acceleration time, deceleration time, and amortization time

    Shoulder acceleration time, deceleration time, and amortization time will be measured by dynamometer in concentric/concentric mode at 3 angular velocities (90°/s, 180°/s, \& 240°/s) and will be described with millisecond (ms).

    Time frame: Change from baseline shoulder isokinetic muscle strength through completion of 12-session intervention, an average of 6 weeks

  3. Shoulder proprioception

    Shoulder proprioception will be measured by dynamometer in 90° shoulder abduction and 90° elbow flexion position, including active joint position sense and passive joint position sense. The proprioception will be described with degree of error from target position.

    Time frame: Change from baseline shoulder external rotation joint position sense through completion of 12-session intervention, an average of 6 weeks

  4. Seated medicine ball throw distance

    Subjects will throw a 2kg soft weighted ball as far forward as possible with dominant arms while sitting with back against a wall and legs bending with feet flat on the floor. Outcomes include average throwing distance and maximal throwing distance (cm). The distances are measured with measure tape.

    Time frame: Change from baseline seated medicine ball throw distance through completion of 12-session intervention, an average of 6 weeks

Secondary outcomes

  1. Shoulder function

    Shoulder function will be measured by the disabilities of the arm, shoulder and hand (DASH) questionnaire, including the disability/symptom section (30 items, scored 1-5) and the optional high performance Sport/Music or Work section (4 items, scored 1-5). A higher score indicates greater disability.

    Time frame: Change from baseline DASH questionnaire through completion of 12-session intervention, an average of 6 weeks

  2. Visual analogue scale (VAS) of shoulder pain and instability

    Shoulder pain and instability will be measured by visual analogue scale (VAS). Subjects need to mark the point that they feel represent their perception of their current state on a 10-cm line. Scores range from 0 (no symptom) to 100 (maximum symptom).

    Time frame: Change from baseline VAS of shoulder pain and instability through completion of 12-session intervention, an average of 6 weeks

  3. Global rating of change (GRC)

    The improvements in a patient's condition will be measured with 15-point self-report GRC scale. Score ranges from -7 (lack of progress) to 7 (maximum of progress).

    Time frame: through completion of 12-session intervention, an average of 6 weeks

07

Study locations

1 site
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from May 2023 to primary completion in Apr 2025, 22 months.

Of 39 non-industry interventional studies with no phase under Shoulder Dislocation, half reached primary completion within 22 months of starting (the median), counting those still running; a quarter within 11 and three quarters within 39. This study's 22 months is close to that.

Counting every sponsor, half of 39 studies reached it within 22 months; a quarter within 11 and three quarters within 39.

How these figures are worked out, and which studies are left out of them.

Registered
Apr 11, 2023
First posted
May 12, 2023
StartActual
May 20, 2023
Primary completionActual
Apr 1, 2025
CompletionEst.
Jun 30, 2025
Last update
May 22, 2025
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on May 22, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05857540
Responsible party
Yin-Liang Lin (Assistant Professor, National Yang Ming Chiao Tung University) — Principal investigator
First posted
May 12, 2023
Start date
May 20, 2023
Primary completion
Apr 1, 2025
Completion
Jun 30, 2025 (estimated)
Last update
May 22, 2025

Study contacts

Yin-Liang Lin, PhD
principal investigator · National Yang Ming Chiao Tung University

Oversight

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

Not currently enrolling

This study is active, not recruiting, as verified in May 2025. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion