Effects of Ai Chi on Scapular Muscle Activation in Overhead Athletes With Scapular Dyskinesis

Sponsor
National Taiwan University Hospital (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT05714163
Collaborator
(none)
25
1
9.5
2.6

Study Details

Study Description

Brief Summary

Scapular dyskinesis (SD) is common in overhead athletes and negatively influence the athletes' performance, increasing the risk of shoulder injury. The kinetic chain (KC) exercises for SD rehabilitation that emphasize importance of core strength and scapula stability during skillful performance. Ai Chi, the aquatic exercises performed in functional positions, which are adequate for power transfer of KC. This study will investigate the effect of KC-based water exercises, Ai Chi, on scapular muscles in overhead athletes with SD.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The purpose of this study is to investigate muscle activations of the upper trapezius (UT), lower trapezius (LT), serratus anterior (SA), latissimus dorsi (LD), and muscle balance ratios of UT/LT, UT/SA I in overhead athletes with SD via KC-based exercise in water and on land. KC-based exercises including the movement patterns of Ai Chi which consist of shoulder flexion/ extension, horizontal abduction/ adduction, internal and external rotation, scapular protraction/retraction combined with spinal rotation.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    25 participants
    Observational Model:
    Other
    Time Perspective:
    Cross-Sectional
    Official Title:
    Effects of Ai Chi on Scapular Muscle Activation in Overhead Athletes With Scapular Dyskinesis
    Actual Study Start Date :
    Oct 16, 2022
    Anticipated Primary Completion Date :
    Jul 31, 2023
    Anticipated Study Completion Date :
    Jul 31, 2023

    Outcome Measures

    Primary Outcome Measures

    1. Percentage of maximal voluntary isometric contraction of upper trapezius (UT), lower trapezius (LT), serratus anterior (SA), latissimus dorsi (LD) [Through study completion, an average of 10 months]

      The muscle activity of UT, LT, SA and LD of the dominant hand will be recorded for 3 trials of each exercises with 3-seconds concentric phase and 3-seconds eccentric phase. There is a 3-second rest between trails and one-minute rest between exercises.

    Secondary Outcome Measures

    1. Muscle balance ratio of UT/SA [Through study completion, an average of 10 months]

      The muscle balance ratio will be calculated to represent the conditions of these force couples in scapular region.

    2. Muscle balance ratio of UT/LT [Through study completion, an average of 10 months]

      The muscle balance ratio will be calculated to represent the conditions of these force couples in scapular region.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    20 Years to 99 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • The participants are overhead athletes with scapular dyskinesis (SD) who played overhead sports activities at least 3 hours/week.
    Exclusion Criteria:
    • the individuals who have shoulder/neck pain in recent 3 months (VAS >7/10)

    • severe shoulder trauma (the collision shoulder, shoulder sprains or strains)

    • severe scoliosis (Cobb angle > 25 degrees)

    • surgery of upper extremity (the shoulder, cervical spine and elbow) or cervical spine

    • peripheral nerve injury or neurological disease (impaired sensation or motor function: numbness, tingle, muscle weakness)

    • body mass index (BMI) >25

    • infectious disease (upper respiratory tract infection, skin infection, etc.)

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 National Taiwan University Hospital Taipei Taiwan

    Sponsors and Collaborators

    • National Taiwan University Hospital

    Investigators

    • Principal Investigator: Jiu-Jenq Lin, National Taiwan University Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    National Taiwan University Hospital
    ClinicalTrials.gov Identifier:
    NCT05714163
    Other Study ID Numbers:
    • 202208053RINA
    First Posted:
    Feb 6, 2023
    Last Update Posted:
    Feb 6, 2023
    Last Verified:
    Jan 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by National Taiwan University Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Feb 6, 2023