The Effects of Eccentric-focused Exercise on Posterior Shoulder Tightness in Symptomatic Overhead Athletes

Sponsor
National Yang Ming University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05305196
Collaborator
(none)
40
2
12

Study Details

Study Description

Brief Summary

The aim of this study is to investigate the effects of shoulder eccentric exercise training on shoulder mobility, rotator cuff strength, pain and dysfunction, scapular kinematics and muscle activation in symptomatic overhead athletes with posterior shoulder tightness.

Condition or Disease Intervention/Treatment Phase
  • Other: Eccentric-focused exercises
  • Other: Stretching exercises
  • Other: Hot pack
  • Other: Massage
N/A

Detailed Description

Overhead athletes commonly have posterior shoulder tightness due to repetitively high tensile loading during overhead throwing. However, intervention studies focused on posterior shoulder tightness in people with subacromial pain are still limited. Additionally, eccentric exercise was thought to improve the eccentric strength and neuromuscular control of posterior shoulder muscles to endure repetitively eccentric loading, which may improve posterior shoulder tightness and decrease the risk of subacromial pain. Nevertheless, no previous study investigated the influence of eccentric exercise on posterior shoulder tightness in overhead athletes. The aim of this study is to investigate the effects of shoulder eccentric exercise training on shoulder mobility, rotator cuff strength, pain and dysfunction, scapular kinematics and muscle activation in symptomatic overhead athletes with posterior shoulder tightness.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
The Effects of Eccentric-focused Exercise on Shoulder Mobility, Rotator Cuff Strength, Pain and Dysfunction, Scapular Kinematics and Muscle Activation in Symptomatic Overhead Athletes With Posterior Shoulder Tightness
Anticipated Study Start Date :
Aug 1, 2022
Anticipated Primary Completion Date :
Jul 31, 2023
Anticipated Study Completion Date :
Jul 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Eccentric-focused exercise group

Three eccentric-focused exercises addition to the general treatment group

Other: Eccentric-focused exercises
Three eccentric-focused exercises: Shoulder external rotator eccentric contraction in shoulder abduction 90 degree Shoulder external rotator eccentric contraction in shoulder abduction 0 degree Shoulder abductor eccentric contraction in shoulder abduction 90 degree

Other: Stretching exercises
Modified sleeper stretch Modified cross-body stretch

Other: Hot pack
Hot pack application on shoulder region

Other: Massage
Massage for upper trapezius

Active Comparator: General treatment group

hot pack application on shoulder region upper trapezius massage two stretching exercises (modified sleeper stretch and modified cross-body stretch)

Other: Stretching exercises
Modified sleeper stretch Modified cross-body stretch

Other: Hot pack
Hot pack application on shoulder region

Other: Massage
Massage for upper trapezius

Outcome Measures

Primary Outcome Measures

  1. Shoulder range of motion (measured with goniometer) [4 weeks]

    Shoulder external rotation, internal rotation, horizontal adduction range of motion in shoulder flexion 90 degrees

  2. Rotator cuff functional strength ratio (Pro 4, Biodex Medical Systems, Inc., Shirley, NY, USA) [4 weeks]

    Eccentric strength of shoulder external rotator and concentric strength of shoulder internal rotator are measured with isokinetic

  3. Shoulder pain [4 weeks]

    Pain is measured with Visual Analogue scale (VAS) Score range from 0 to 10. Scoring of 0 represents no pain and scoring of 10 represents pain as bad as it could possibly be.

  4. Shoulder function [4 weeks]

    Shoulder function is measured with Disability of the Arm, Shoulder and Hand questionnaire (DASH) Score range from 0 to 100. The higher of the score, the more disability.

  5. Shoulder endurance test [4 weeks]

    Participants will be instructed to execute a shoulder endurance test with the theraband®. Participants are asked to place their tested arm in a shoulder forward flexion 90-degree position, holding a 1-m long theraband® fixed at shoulder height on a graduated stick. Then, they are asked to pull the theraband® from the starting position to a 90-90 ending position at an alternated cadence given by a metronome. Males were asked to pull a green theraband® (2.1 kg) and females a red theraband ® (1.7 kg).

Secondary Outcome Measures

  1. Electromagnetic tracking system (Liberty electromagnetic tracking system, Polhemus , Colchester, VT,) [4 weeks]

    Scapular kinematics during shoulder elevation task in scapular plane

  2. Surface electromyography (TeleMyo 2400T G2, Noraxon USA Inc., Scottsdale, AZ, USA) [4 weeks]

    Muscle activation of infraspinatus, upper trapezius, lower trapezius and serratus anterior during shoulder elevation task in scapular plane

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years to 50 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Participate in overhead sports over 4 hours per week

  • Age between 20 to 50 years old

  • Glenohumeral joint range of motion deficit: Shoulder internal rotation loss more than 15 degrees compared to the non-dominant side and total arc of motion loss more than 5 degrees or/and horizontal adduction range of motion lo more than 15 degrees compared to the non-dominant side

  • Shoulder impingement syndrome criteria

Exclusion Criteria:
  • History of shoulder dislocation, fracture and operation

  • History of direct contact in upper extremities or cervical region in the past one month

  • Shoulder pain or neurological symptom caused by cervical problem

  • VAS more than 5 during shoulder elevation

  • Receive treatment for posterior shoulder tightness in the past 3 months

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • National Yang Ming University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
National Yang Ming University
ClinicalTrials.gov Identifier:
NCT05305196
Other Study ID Numbers:
  • YM110191F
First Posted:
Mar 31, 2022
Last Update Posted:
Jun 24, 2022
Last Verified:
Jan 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by National Yang Ming University

Study Results

No Results Posted as of Jun 24, 2022