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Recruiting NCT07543484

Kinematics and Muscle Activity During the Tennis Serve and Musculoskeletal Characteristics in Tennis Players With Subacromial Pain Syndrome or History of Shoulder Pain

Observational Shoulder Pain

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Shoulder Pain. Basic parameters: 18 years — 40 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Taiwan
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Tennis players often suffer from shoulder pain due to the repetitive high-loaded overhead movements during serving, and subacromial pain syndrome is one of the main types of shoulder pain. Previous shoulder injury has been identified as one of the risk factors for shoulder overuse injuries in overhead sports. No research has explored differences in trunk kinematics and shoulder muscle activities among tennis players with and without subacromial pain syndrome or a history of shoulder pain. Furthermore, limited studies have examined shoulder kinematics during tennis serve and musculoskeletal characteristics in tennis players with subacromial pain syndrome or a history of shoulder pain. Therefore, this study aims to investigate shoulder and trunk kinematics and shoulder muscle activity during the tennis serve and musculoskeletal characteristics in tennis players with subacromial pain syndrome or a history of shoulder pain. This study will recruit sixty tennis players with subacromial pain syndrome, a history of shoulder pain, and healthy players. The electromagnetic tracking system will be applied to collect shoulder and trunk kinematics during the tennis serve, and surface electromyography will be simultaneously used for recording shoulder muscle activities. Moreover, we will collect shoulder and trunk rotational joint range of motion, isometric strength and rate of force development of shoulder internal and external rotation, scapulothoracic and glenohumeral joint control capability, upper quarter Y-balance test performance, and posterior shoulder endurance. This study will compare the difference of these measures in tennis players with subacromial pain syndrome or a history of shoulder pain to healthy players.

Primary outcome measures

  • Degree of the glenohumeral and scapulothoracic joint during serving [Time frame: Day 1]
  • Amplitude of the activation of glenohumeral and periscapular muscles [Time frame: Day 1]
  • Shoulder active range of motion [Time frame: Day 2]
  • Shoulder passive range of motion [Time frame: Day 2]
  • Trunk rotational range of motion [Time frame: Day 2]
  • Isometric strength and rate of force development of shoulder internal and external rotation [Time frame: Day 2]
  • Scapulothoracic and glenohumeral joint control ability [Time frame: Day 2]
  • Upper quarter Y-balance test performance [Time frame: Day 2]
  • Posterior shoulder endurance [Time frame: Day 2]
Secondary outcome measures (2)
  • Degree of shoulder and scapular kinematics during arm elevation [Time frame: Day 1]
  • Amplitude of the activation of glenohumeral and periscapular muscles during arm elevation [Time frame: Day 1]

Eligibility criteria

Inclusion criteria

  • Amateur tennis players
  • National Tennis Rating Program (NTRP) should level ≥ 3.5
  • Training experience: ≥ 3 years, current or former school team players
  • Training volume: ≥ 4 hours/week

Exclusion criteria

  • Any current musculoskeletal injuries preventing maximum skill execution at the time of testing
  • Previously had any form of surgery or trauma
  • Patient-reported pain that will inhibit participation in this study

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Case-control

Study locations

Taiwan · 1 center
  • No. 155, Sec. 2, Linong St. Beitou Dist., Taipei City 112304, Taiwan — Taipei

Identifiers

NCT: NCT07543484 · NYCU114005AF

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗