NCT05857540

Brief 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.

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
64

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started May 2023

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

April 11, 2023

Completed
1 month until next milestone

First Posted

Study publicly available on registry

May 12, 2023

Completed
8 days until next milestone

Study Start

First participant enrolled

May 20, 2023

Completed
1.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2025

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 30, 2025

Completed
Last Updated

May 22, 2025

Status Verified

May 1, 2025

Enrollment Period

1.9 years

First QC Date

April 11, 2023

Last Update Submit

May 19, 2025

Conditions

Keywords

PlyometricStrengtheningOverhead athleteShoulder instability

Outcome Measures

Primary Outcomes (4)

  • 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).

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

  • 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).

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

  • 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.

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

  • 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.

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

Secondary Outcomes (3)

  • Shoulder function

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

  • Visual analogue scale (VAS) of shoulder pain and instability

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

  • Global rating of change (GRC)

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

Study Arms (2)

Plyometric training group

EXPERIMENTAL

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

Strengthening training group

ACTIVE COMPARATOR

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

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.

Plyometric training group

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.

Strengthening training group

Eligibility Criteria

Age20 Years - 40 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • 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.
  • Self-reported decreased performance or feeling fear to perform shoulder movements during sports or daily activities
  • Positive findings on ≥ 1 of the following 5 tests: load and shift test, apprehension, relocation, \& surprise tests, Gagey hyperabduction test, sulcus sign, Feagin test
  • Recreational overhead athletes who keep practicing ≥ 4 hours/week in the recent 1 month and with ≥ 1 year overhead sports experience

You may not qualify if:

  • Full contact sport athletes
  • Severe shoulder instability with \> 5 shoulder dislocations history
  • Obvious shoulder bony/labrum lesion in the dominant side warranted for surgery first as decided by the orthopedic surgeon
  • Previous surgery or fracture in the shoulder area on the dominant side within 1 year
  • Voluntary instability (the ability to deliberately dislocate one's shoulder)
  • During acute phase after shoulder dislocation event
  • 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
  • Pregnancy
  • Cancer, neck pain, brain \& neurological impairment
  • Ehlers-Danlos syndrome or Marfan syndrome
  • Unable to attend 6 weeks supervised training

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

National Yang Ming Chiao Tung University

Taipei, Taipei, 112, Taiwan

Location

MeSH Terms

Conditions

Shoulder Dislocation

Condition Hierarchy (Ancestors)

Joint DislocationsJoint DiseasesMusculoskeletal DiseasesWounds and InjuriesShoulder Injuries

Study Officials

  • Yin-Liang Lin, PhD

    National Yang Ming Chiao Tung University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

April 11, 2023

First Posted

May 12, 2023

Study Start

May 20, 2023

Primary Completion

April 1, 2025

Study Completion

June 30, 2025

Last Updated

May 22, 2025

Record last verified: 2025-05

Locations