The Effect of Exercise Intervention on Forward Head Posture and Round Shoulder Posture in Symptomatic Competitive Swimmer

February 4, 2026 updated by: Fu-Jie Kang, Fooyin University

Competitive Swimmer, Swimmer's Shoulder, Forward Head Posture, Round Shoulder Posture

This study is an exercise intervention study, and its findings will help to clarify the effects of exercise on forward head posture and rounded shoulder posture in competitive swimmers. It is expected that the results of this study will assist in ensuring that forward head posture and rounded shoulder posture are taken into consideration when competitive swimmers undergo related exercise training in the future. The purpose of this experiment is purely for academic research and does not constitute a physical examination or a medical diagnosis.

Study Overview

Study Type

Interventional

Enrollment (Actual)

42

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Taiwan
      • Kaohsiung, Taiwan, Taiwan, 831301
        • Department of physical therapy, Fooyin university

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  1. High school competitive swimmers
  2. With shoulder pain: unilateral or bilateral shoulder pain who had a self-reported shoulder pain score of ≥ 40 points for at least one month, measured using a visual analogue scale (VAS). VAS scores range from 0 to 100, with higher scores indicating greater pain.
  3. With round shoulder posture (RSP): Forward shoulder angle (FSA) ≥ 52°.
  4. With forward head posture (FHP): forward head angle (FHA) ≥ 46°.

Exclusion Criteria:

  1. A history of fractures
  2. Previous surgery to the upper extremity or shoulder joint
  3. Full-thickness rotator cuff tears
  4. Cervical radiculopathy
  5. Shoulder dislocation
  6. Structural deformities of the cervical or thoracic spine
  7. Any neurological disorder

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: intervention group
The intervention group performed an exercise program targeting RSP and FHP, which included three strengthening exercises and two stretching exercises. Each session lasted approximately 50 minutes and was conducted three times per week for a total of eight weeks.

Strengthening exercises: Based on the relevant literature review, the primary aim of the strengthening exercises was to enhance the strength of the middle trapezius, lower trapezius, and serratus anterior muscles, including: Y to W exercise, L to Y exercise and Scapular protraction exercise.

Stretching exercises: Based on a review of the relevant literature, stretching exercises primarily target the pectoralis minor and the cervical extensor muscles, including: Pectoralis flexibility and Chin tucks exercise.

No Intervention: non-intervention group
The non-intervention group did not receive the above exercise training during the eight-week intervention period; however, the relevant exercise training was provided after the completion of the eight-week experiment.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
forward head angle (FHA)
Time Frame: Both groups underwent baseline posture assessments prior to the intervention and post-intervention posture assessments at the end of the 8-week training period.
The forward head angle (FHA) (Degree): The FHA is defined as the angle formed by the intersection of two lines: one vertical line passing through the spinous process of the seventh cervical vertebra (C7), and a second line connecting the C7 spinous process to the tragus of the ear. A larger FHA value indicates a more severe FHP. The examiner photographed the standing posture. The photograph was then analyzed using AutoCAD software (AutoDesk Inc., Sausalito, CA) to calculate the FHA (forward head angle) value.
Both groups underwent baseline posture assessments prior to the intervention and post-intervention posture assessments at the end of the 8-week training period.
forward shoulder angle (FSA)
Time Frame: Both groups underwent baseline posture assessments prior to the intervention and post-intervention posture assessments at the end of the 8-week training period.
The FSA (forward shoulder angle) (Degree): The FSA is defined as the angle formed by the intersection of two lines: one vertical line passing through the spinous process of the seventh cervical vertebra (C7), and a second line connecting the C7 spinous process to the center of the humerus. A larger FSA value indicates a more severe RSP. The examiner photographed the standing posture. The photograph was then analyzed using AutoCAD software (AutoDesk Inc., Sausalito, CA) to calculate the FSA (forward shoulder angle) value.
Both groups underwent baseline posture assessments prior to the intervention and post-intervention posture assessments at the end of the 8-week training period.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pectoralis minor index (PMI)
Time Frame: Both groups underwent baseline assessments prior to the intervention and post-intervention assessments at the end of the 8-week training period.
PMI (cm/cm): The examiner used a digital caliper to measure the distance between the inferomedial border of the coracoid process and the fourth rib-sternal junction. This measured distance (cm) was then divided by the participant's height (cm) and multiplied by 100 to obtain the PMI.
Both groups underwent baseline assessments prior to the intervention and post-intervention assessments at the end of the 8-week training period.
Shoulder pain and disability index (SPADI)
Time Frame: Both groups underwent baseline assessments prior to the intervention and post-intervention assessments at the end of the 8-week training period.
SPADI: Shoulder pain and disability index (SPADI) was selected for assessment of shoulder pain and disability. Score from 0 to 10. Higher scores indicate greater pain and disability.
Both groups underwent baseline assessments prior to the intervention and post-intervention assessments at the end of the 8-week training period.
Scapular upward rotation (SUR) angle
Time Frame: Both groups underwent baseline assessments prior to the intervention and post-intervention assessments at the end of the 8-week training period.
SUR (degree): Measurements were obtained using an ACUMAR™ digital inclinometer. Measurements were taken in three positions: with the arms resting at the sides, with the arms elevated to 60°, and with the arms elevated to 120° . SUR (°) was defined as the angle between the scapular spine and the horizontal reference line.
Both groups underwent baseline assessments prior to the intervention and post-intervention assessments at the end of the 8-week training period.
Scapular anterior tilt index (SATI)
Time Frame: Both groups underwent baseline assessments prior to the intervention and post-intervention assessments at the end of the 8-week training period.
SATI: The participant lay supine on a bed in a relaxed position. The distance (cm) between the posterior border of the acromion and the bed surface was measured, and this value was then divided by 100 to obtain the SATI.
Both groups underwent baseline assessments prior to the intervention and post-intervention assessments at the end of the 8-week training period.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 27, 2023

Primary Completion (Actual)

March 23, 2024

Study Completion (Actual)

October 31, 2024

Study Registration Dates

First Submitted

January 20, 2026

First Submitted That Met QC Criteria

February 4, 2026

First Posted (Actual)

February 11, 2026

Study Record Updates

Last Update Posted (Actual)

February 11, 2026

Last Update Submitted That Met QC Criteria

February 4, 2026

Last Verified

February 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • NCKU HREC-E-112-082-2

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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