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NCT Number: NCT06473142

RELATION BETWEEN BODY POSTURE AND SHOULDER DYSFUNCTION

The purpose of this study will be to investigate if there is any correlation between shoulder dysfunction and the lateral alignment of the spine, scapular dyskinesia, pelvic tilting angle, Shoulder height angle, and trunk side bending (strength and mobility) in the frontal plane in patients with unilateral SIS.

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Key information

Age range

20 year–40 year

Sex eligibility

All sexes

Study type

Observational

Primary location

About this study

This study will be conducted to answer the following question:

Is there any correlation between shoulder dysfunction and the lateral alignment of the spine, scapular dyskinesia, pelvic tilting angle, Shoulder height angle, and trunk side bending (strength and mobility) in the frontal plane in patients with unilateral SIS?

This study will be limited to:

  • Thirty four (34) patients with unilateral SIS.
  • Male and female subjects will be included between 20 and 40 years of age .
  • Shoulder pain and disability level will be measured using the Arabic version of shoulder pain and disability index (SPADI).
  • Thoracolumbar lateral deviation will be measured using a scoliometer.
  • Scapular dyskinesia will be measured using lateral scapular slide test (LSST).
  • The pelvic tilting angle and shoulder height angle will be evaluated using Kinovea software.
  • Trunk side bending ROM will be evaluated using a bubble inclinometer .
  • Trunk side bending strength will be evaluated using a handheld dynamometer.

Assumptions:

It will be assumed that:

  • The instructions given to all individuals will be clear with satisfying explanations for all assessment methods.
  • All individuals will follow the instructions.

Hypotheses:

It will be hypothesized that:

  • There will be no significant correlation between pain score and measured variables in patients with unilateral SIS:
  • lateral spinal deviation
  • scapular dyskinesia
  • pelvic tilting angle in the frontal plane
  • shoulder height angle in the frontal plane
  • ipsilateral trunk lateral side bending ROM
  • contralateral trunk lateral side bending ROM
  • ipsilateral trunk lateral side bending strength
  • contralateral trunk lateral side bending strength
  • There will be no significant correlation between disability score and measured variables in patients with unilateral SIS:
  • lateral spinal deviation
  • scapular dyskinesia
  • pelvic tilting angle in the frontal plane
  • shoulder height angle in the frontal plane
  • ipsilateral trunk lateral side bending ROM
  • contralateral trunk lateral side bending ROM
  • ipsilateral trunk lateral side bending strength
  • contralateral trunk lateral side bending strength

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Non-athletic patients of both sexes.
  • referred by an orthopedic surgeon with a diagnosis of unilateral SIS (Stage I, or II).
  • Patients aged between 20 to 40 years.
  • BMI between 18.5 to 29.9 kg/m2.
  • having four or more of the following findings:
  • Shoulder pain that is located either anteriorly or laterally to the acromion process
  • Pain worsening by shoulder flexion and/or abduction
  • A painful movement arc ranging from 60° to 120°
  • A palpably painful greater tuberosity of the humerus
  • The pain is replicated using the supraspinatus empty-can test, A positive Neer impingement sign, external rotation resistance test, and a positive Hawkins sign.

Exclusion criteria

  • Systematic illnesses
  • Pregnancy
  • Any degenerative disorder or disc lesion affection of the spine
  • A history of upper limb or spinal surgery
  • Previous upper limb or spinal fractures
  • Post-traumatic shoulder pain
  • History of shoulder instability (positive Sulcus sign, positive apprehension test, and history of shoulder dislocation)
  • Clinical signs of cervical radiculopathy (pain related to cervical movements)
  • Adhesive capsulitis
  • Tumors
  • Shoulder labral or cartilage lesions
  • Capsular or ligamentous tears or avulsions
  • any apparent deformity in the lower limbs including leg length discrepancy.

Treatment and study plan

Primary outcomes

  1. Thoracolumbar lateral deviation

    Time frame: 2 MONTHES

    will be measured using a scoliometer

  2. Scapular dyskinesia

    Time frame: 2 monthes

    will be measured using lateral scapular slide test (LSST)

  3. The pelvic tilting angle and shoulder height angle

    Time frame: 2 monthes

    will be evaluated using Kinovea software

  4. Trunk side bending ROM

    Time frame: 2 Monthes

    will be evaluated using a bubble inclinometer

  5. Trunk side bending strength

    Time frame: 2 monthes

    will be evaluated using a handheld dynamometer

  6. Shoulder pain and disability level

    Time frame: 2 monthes

    will be measured using the Arabic version of shoulder pain and disability index (SPADI)

Study contacts

Contact information is provided by the study sponsor or research team.

AMR SAAD TAWFIK SOLIMAN, demonstrator

CONTACT

[email protected]

+201002043808 ext. 00201002043808

enas fawzy youssf, professor

CONTACT

[email protected]

00201127867507 ext. 00201145300981

Sponsors and collaborators

Lead sponsor

Cairo University

Other

Registry information

Official study title

CORRELATION BETWEEN SHOULDER DYSFUNCTION AND FRONTAL PLANE POSTURE IN SUBACROMIAL IMPINGEMENT SYNDROME

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Jun 25, 2024
Registry last updated
Sep 4, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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