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CompletedNCT07403123Updated Feb 11, 2026

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

An interventional study of exercise intervention: included three strengthening exercises and two stretching exercises. in Swimmer Shoulder, Forward Head Posture and Posture and Mobility of the Upper Quadrant, sponsored by Fooyin University. Completed at 1 site in Taiwan. Open to participants aged 16 Years to 18 Years. Per ClinicalTrials.gov, last updated 2026-02-11.

Sponsored by Fooyin University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 2 years 3 months after the study started (first participant enrolled Sep 2023, registered Jan 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
42
Allocation
Randomized
Ages
16 Years to 18 Years
Sex
All
01

Study summary

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.

02

Conditions studied

  • Swimmer Shoulder
  • Forward Head Posture
  • Posture and Mobility of the Upper Quadrant

Keywords

  • swimmer shoulder
  • forward head posture
  • round shoulder posture
03

In context

Lead sponsor

Fooyin University is the lead sponsor of 16 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
16 Years to 18 Years
Sexes eligible
All
Accepts healthy volunteers
No

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

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
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
42 participants (actual)

Study arms

  • 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.

    Other: exercise intervention: included three strengthening exercises and two stretching exercises.

  • 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.

Interventions

  • Otherexercise intervention: included three strengthening exercises and two stretching exercises.

    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.

06

What researchers measure

Primary outcomes

  1. forward head angle (FHA)

    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.

    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.

  2. forward shoulder angle (FSA)

    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.

    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.

Secondary outcomes

  1. Pectoralis minor index (PMI)

    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.

    Time frame: Both groups underwent baseline assessments prior to the intervention and post-intervention assessments at the end of the 8-week training period.

  2. Shoulder pain and disability index (SPADI)

    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.

    Time frame: Both groups underwent baseline assessments prior to the intervention and post-intervention assessments at the end of the 8-week training period.

  3. Scapular upward rotation (SUR) angle

    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.

    Time frame: Both groups underwent baseline assessments prior to the intervention and post-intervention assessments at the end of the 8-week training period.

  4. Scapular anterior tilt index (SATI)

    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.

    Time frame: Both groups underwent baseline assessments prior to the intervention and post-intervention assessments at the end of the 8-week training period.

07

Study locations

1 site
  • Department of physical therapy, Fooyin university
    Kaohsiung, Taiwan 831301, Taiwan
08

References and documents

Individual participant data

Plan to share: Yes

Supporting information: Study protocol

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 11, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07403123
Lead sponsor
Fooyin University
Collaborators
National Science and Technology Council, Taiwan
Responsible party
Fu-Jie Kang (Assistant professor, Fooyin University) — Principal investigator
First posted
Feb 11, 2026
Start date
Sep 27, 2023
Primary completion
Mar 23, 2024
Completion
Oct 31, 2024
Last update
Feb 11, 2026

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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