NCT03568487

Brief Summary

Previous studies have proposed various ways to assess scapular dyskinesis, but they were impractical in clinical setting or the validity was questioned. The novel scapulometer we developed can measure the prominence of scapular medial border and inferior angle. We would like to examine its reliability and validity in subjects with symptomatic scapular dyskinesis. The long-term, high-intensity, unilateral loading may cause overhead athletes to develop adaptive changes in shoulder kinematics, range of motion (ROM) and strength in the dominant arm. We hypothesized that these changes may be related to scapular dyskinesis. According to the previous studies, we expect electromyography (EMG) biofeedback training can help improve the ratio of muscle activation of scapular muscle.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
170

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Jan 2019

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 30, 2018

Completed
27 days until next milestone

First Posted

Study publicly available on registry

June 26, 2018

Completed
6 months until next milestone

Study Start

First participant enrolled

January 2, 2019

Completed
3.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 31, 2022

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 31, 2022

Completed
Last Updated

March 20, 2025

Status Verified

May 1, 2024

Enrollment Period

3.6 years

First QC Date

May 30, 2018

Last Update Submit

March 17, 2025

Conditions

Keywords

scapular dyskinesisEMG biofeedbackscapulometer

Outcome Measures

Primary Outcomes (4)

  • Change of range of motion after 4-week training

    Passive interior rotation ROM and exterior rotation ROM of the glenohumeral joint will be assessed bilaterally using a hand-held standard universal goniometer. The player will lay supine with the humerus abducted to 90 degrees and elbow flexed to 90 degrees. The fulcrum of the goniometer is set at the olecranon process.

    Baseline and after 4-week training

  • Change of muscle strength after 4-week training

    The maximal isometric strength of 8 shoulder-scapula complex muscles will be assessed bilaterally using a handheld dynamometer. Each test will be performed twice, with a 30-second rest period between tests. The largest strength value for each muscle will be used for statistical analyses, normalized to body weight (in kilograms), and expressed as a percentage for inter individual comparison.

    Baseline and after 4-week training

  • Change of shoulder complex kinematics after 4-week training

    The Polhemus 3Space FASTRAK system (Polhemus Inc., Colchester, VT, USA) will be used to record shoulder complex kinematics.

    Baseline and after 4-week training

  • Change of muscular activities after 4-week training

    Bipolar surface electromyographic (EMG) electrodes will be placed over the upper trapezius (UT), middle trapezius (MT), lower trapezius (LT), and serratus anterior (SA) of the dominant shoulder to record muscular activities.

    Baseline and after 4-week training

Secondary Outcomes (2)

  • Forward shoulder posture (acromial distance)

    Baseline and after 4-week training

  • Pectoralis minor muscle length

    Baseline and after 4-week training

Study Arms (2)

Intensive scapula-focused approach

EXPERIMENTAL
Other: Intensive scapula-focused approach

Control therapy

ACTIVE COMPARATOR
Other: Control Therapy

Interventions

scapula-focused approach with exercises, 3 x 20 min training per week for 4 weeks

Intensive scapula-focused approach

not have any physical training but is encouraged to stay active as usual.

Control therapy

Eligibility Criteria

Age12 Years - 50 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

  • (1) with scapular dyskinesis
  • (2) overhead players (baseball, basketball, tennis, volleyball, and so on) at high schools

You may not qualify if:

  • if they have a history of shoulder pain or injury

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

National Taiwan University

Taipei, Taiwan

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

May 30, 2018

First Posted

June 26, 2018

Study Start

January 2, 2019

Primary Completion

July 31, 2022

Study Completion

July 31, 2022

Last Updated

March 20, 2025

Record last verified: 2024-05

Locations