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CompletedNCT07806955Updated Sep 8, 2026

Correlation Between Scapular Dyskinesia and Thoracic Kyphosis

An observational study in Scapular Dyskinesia, sponsored by Cairo University. Completed at 1 site in Egypt. Open to participants aged 18 Years to 60 Years. Per ClinicalTrials.gov, last updated 2026-09-08.

Sponsored by Cairo University · Observational

Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
150
Ages
18 Years to 60 Years
Sex
All
01

Study summary

  • This study will be conducted to investigate:
  1. the correlation between scapular dyskinesis and thoracic kyphosis in patients with chronic nonspecific neck pain
  2. the correlation between scapular dyskinesis and shoulder functional disability in patients with chronic nonspecific neck pain
Read the detailed description

This study investigates the relationship between scapular dyskinesia, thoracic kyphosis, and shoulder functional disability in patients with chronic nonspecific neck pain. Chronic neck pain is commonly associated with postural abnormalities, altered cervical and thoracic alignment, and impaired scapular movement. Scapular dyskinesia may contribute to muscle imbalance, reduced shoulder stability, and functional limitations. Although previous studies examined scapular abnormalities in shoulder and neck disorders separately, limited research has explored their association with thoracic alignment in chronic neck pain patients. Therefore, this study aims to evaluate the correlation between scapular dyskinesia and thoracic kyphosis and assess shoulder functional disability associated with scapular dyskinesia in individuals with chronic nonspecific neck pain.

02

Conditions studied

  • Scapular Dyskinesia

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03

In context

Dyskinesias

179 studies on the registry are indexed under Dyskinesias; 24 are open to participants now.

This study's enrollment of 150 is above the median of 54 across 35 observational studies indexed under Dyskinesias.

Browse Dyskinesias studies →

Lead sponsor

Cairo University is the lead sponsor of 4,941 studies on the registry; 1,458 are open to participants now.

Of its 37 completed or terminated interventional studies of FDA-regulated products, 5 (14%) have results posted.

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

04

Who can participate

Ages eligible
18 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

The study population consisted of adults both male and female aged 18-60 years with non-specific chronic neck pain and scapular dyskinesia who attended the outpatient physical therapy clinic in Elsheikh Zayed specialized hospital

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • both male and female Patients diagnosed with scapular dyskinesia From 18 to 60 years old

Exclusion criteria

Exclusion Criteria:

-

05

Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
150 participants (actual)
Patient registry
No

Groups and cohorts

  • Only 1 group composed of 150 patient both male and female was recruited

    One group composed of 150 patient both male and female with chronic non-specific neck pain was recruited from the outpatient physical therapy clinic of Elsheikh Zayed specialized hospital and was assessed for presence of scapular dyskinesia

    Diagnostic Test: Lateral scapular slide test is used to asses scapular dyskinesia

Interventions

  • Diagnostic testLateral scapular slide test is used to asses scapular dyskinesia

    Lateral scapular slide test is used to asses scapular dyskinesia and Flexi curve ruler is used to assess thoracic kyphosis and DASH questionnaire is used to assess the functional disabilities of the shoulder joint

06

What researchers measure

Primary outcomes

  1. Degree of scapular dyskinesia Kyphotic index Degree of Shoulder functional disabilities

    Degree of scapular dyskinesia is detected by lateral scapular slide test Kyphotic index is measured by the Flexi curve ruler Degree of Shoulder functional disabilities is assessed by DASH questionnaire

    Time frame: The procedure is applied through 6 months

07

Study locations

1 site
  • Outpatient physical therapy clinic at Elsheikh Zayed specialized hospital
    Giza, Sheizh Zayed City, Egypt
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Oct 2025 to primary completion in Mar 2026, 5 months.

How these figures are worked out, and which studies are left out of them.

Registered
Sep 2, 2026
First posted
Sep 8, 2026
StartActual
Oct 1, 2025
Primary completionActual
Mar 8, 2026
CompletionActual
Mar 8, 2026
Last update
Sep 8, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 8, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07806955
Lead sponsor
Cairo University
Responsible party
Eman Gamal Elsherbiny Mohammed (Physical therapist, Cairo University) — Principal investigator
First posted
Sep 8, 2026
Start date
Oct 1, 2025
Primary completion
Mar 8, 2026
Completion
Mar 8, 2026
Last update
Sep 8, 2026
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Sep 2025. You cannot join it, but the record below documents what was studied.

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