AzTrials
AzTrials

Neck PainNCT07484984

Scapular Depression at Rest: Implications for Cervical Pain and Functional Outcomes

An observational study of Neck Pain and Neck Disability, run by Cairo University at 1 site in Egypt.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

The purpose of this study is to explore whether depressed scapular alignment is associated with increased neck pain and decreased cervical functional capacity, and to investigate the correlation between the mean vertical scapular distance of both scapulae at rest, neck pain intensity, and cervical function. Read more about this study

Who is it for?
Ages 18 to 30 years, men onlyHealthy volunteers can take part
Conditions the study is for
Neck Pain, Neck Disability
What is being tested?
Assessment of the Vertical Scapular Position at Rest, Measurement of the Mean Vertical Scapular Distance at Rest and The Arabic version of Bournemouth questionnaire for neck pain (BQN)
How many people
128 participants
Where
1 siteEgypt
Study dates
20 Dec 2023to 10 Feb 2025
How long will I take part?
1 Day
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 30 years
  • Men only
  • Healthy volunteers accepted
  • Adult

Study population: The Faculty of Physical Therapy at Cairo University

Who may be able to join

  • - Young adults with age from 18 to 30 years old.
  • - Subjects with Body Mass Index less than 30

Who cannot join

  • - Cervical spine surgeries, fractures or pathologic trauma, Subjects with cervical or shoulder neurological movement disorder, Tempromandibular surgery, psychosocial problem.
  • - A documented diagnosis of scoliosis or a posterior rib hump greater than five degrees on forward bending as measured with the scoliometer (ATR ≥ 5°).
  • - Known or measured Leg Length Discrepancy (LLD) greater than 1 cm.

Trial locations and contacts

1 site in 1 country.

Egypt1 site
  • The Faculty of Physical Therapy at Cairo University

    Cairo, Giza Governorate, 11251

Other trials in Egypt

About this study

Official title: The Effect of Depressed Scapular Position at Rest on the Neck Pain and Function

The purpose of this study is to explore whether depressed scapular alignment is associated with increased neck pain and decreased cervical functional capacity, and to investigate the correlation between the mean vertical scapular distance of both scapulae at rest, neck pain intensity, and cervical function.

Read the detailed description

Introduction Neck pain is a major global health problem affecting a large portion of the adult population, with a worldwide prevalence ranging from 16.7% to 75.1%. The economic burden associated with neck pain is substantial, manifested through job-related issues, absenteeism, reduced productivity, and elevated treatment costs. In the United States alone, approximately 25.5 million individuals missed an average of 11.4 working days due to neck pain in 2012, and in 2016, healthcare expenditures related to neck pain reached approximately $134.5 billion, making it one of the most costly health conditions in the country.

While pain intensity has its socioeconomic consequences, also neck dysfunction constitutes an equally important dimension of this condition. Impaired neck function has been linked to deficits in cervical range of motion, proprioception, and muscular endurance, all of which can compromise daily activities, work performance, and overall quality of life. Among the multiple biomechanical factors influencing neck pain and function, the scapular position has gained growing attention. The scapula plays a critical role in maintaining postural alignment and providing a stable base for neck and shoulder movement.

Studies have shown initial evidence that individuals with neck pain may demonstrate altered scapular alignment when compared with healthy controls, though the limited sample sizes in such studies constrain the strength of these conclusions and warrant further investigation.

Also altered scapular alignment has been associated with decreased pressure pain thresholds (PPT) in the upper trapezius region, indicating heightened sensitivity to pain. Moreover, it may alter the length-tension relationship of the upper trapezius and levator scapulae muscles, potentially compromising cervical stability and movement efficiency. Such biomechanical alterations may manifest as reduced neck functional capacity, including limited range of motion and diminished performance in daily activities.

Assessment of scapular position and its influence on the cervical region has been carried out through several approaches, including comparisons of scapular resting alignment in individuals with and without neck pain, the analysis of how altering scapular positioning affects both pain and neck function, and the evaluation of pressure pain threshold in the upper trapezius as an indicator of sensitization. Despite these efforts, the relationship between depressed scapular position at rest, neck pain, and cervical function remains insufficiently explored, highlighting the need for further research to clarify this interaction. To our knowledge, the correlation between the mean vertical scapular distance of both scapulae at rest, neck pain and cervical function is not yet investigated or studied.

In this study, the investigator tried to shed some light on the effect of the depressed scapular position at rest on the neck region in terms of pain intensity, cervical function and to understand the correlation between the mean vertical scapular distance of both scapulae at rest, neck pain and cervical function which will help us to explore new measurements to be used in the diagnosis and the prognosis of patients with neck pain and cervical dysfunction.

Study Design: Cross-Sectional Observational study

Study groups

Included subjects were divided according to the vertical scapular position at rest into two groups:

  1. - Control group (A): 64 subjects with normal scapular position at rest.
  2. - Study group (B): 64 subjects with depressed Scapular position at rest.

Each participant was assessed once on the same day of enrollment. No follow-up assessments will be performed.

Statistical Analysis Statistical analysis was performed through the statistical package for social sciences (SPSS) version 20 for windows.

Statistical Procedures

The following statistical procedures were conducted:

  1. Descriptive statistics was used to summarize and describe the main features of a dataset and conducted in terms of mean and standard deviation.
  2. Unpaired t test was conducted for comparison of the subject characteristics between groups.
  3. Shapiro Wilktest was conducted for testing normality of data.
  4. One way MANOVA was used for comparison of the Mean Vertical Scapular Distance of both scapulae at rest (Z), Non-Derangement Mechanical Neck Pain, and Cervical Function between groups.
  5. Spearman correlation coefficient was conducted to investigate the correlation between the Mean Vertical Scapular Distance of both scapulae at rest (Z), Non-Derangement Mechanical Neck Pain, and Cervical Function.
  6. The level of significance for all statistical tests was set at p < 0.05.
Being tested
Assessment of the Vertical Scapular Position at Rest, Measurement of the Mean Vertical Scapular Distance at Rest, The Arabic version of Bournemouth questionnaire for neck pain (BQN), The Arabic Version of Copenhagen Neck Functional Disability Scale (CNFDS)
Keywords
Depressed scapular position at rest, The Protractor T8-method, Bournemouth questionnaire for neck pain (BQN), Copenhagen Neck Functional Disability Scale (CNFDS)
Medical subject headings
Neck Pain

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Assessment of the Vertical Scapular Position at RestOther

    Assessment of the Vertical Scapular Position at Rest using a Laser level meter, a tripod head, a camera and adhesive round stickers.

  • Measurement of the Mean Vertical Scapular Distance at RestOther

    Measurement of the Mean Vertical Scapular Distance at Rest of both Scapulae using the Protractor - T8 method

  • The Arabic version of Bournemouth questionnaire for neck pain (BQN)Other

    The Arabic version of Bournemouth questionnaire for neck pain (BQN) to measure Non Derangement Mechanical Neck Pain

  • The Arabic Version of Copenhagen Neck Functional Disability Scale (CNFDS)Other

    The Arabic Version of Copenhagen Neck Functional Disability Scale (CNFDS) to measure cervical function

Study groups in NCT07484984
Study groupRoleWhat they receive
Control GroupSubjects with Normal Scapular Position at Rest
Receives: Other: Assessment of the Vertical Scapular Position at Rest; Other: Measurement of the Mean Vertical Scapular Distance at Rest; Other: The Arabic version of Bournemouth questionnaire for neck pain (BQN); Other: The Arabic Version of Copenhagen Neck Functional Disability Scale (CNFDS)
Study GroupSubjects with Depressed Scapular Position at Rest
Receives: Other: Assessment of the Vertical Scapular Position at Rest; Other: Measurement of the Mean Vertical Scapular Distance at Rest; Other: The Arabic version of Bournemouth questionnaire for neck pain (BQN); Other: The Arabic Version of Copenhagen Neck Functional Disability Scale (CNFDS)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Neck Pain

    The Arabic version of Bournemouth questionnaire for neck pain (BQN) will be used to measure Neck Pain.

    The lowest score is 0 and the highest score is 70. High scores reflect severe pain and lower life quality.

    Measured: Baseline

  2. Cervical Function

    The Arabic Version of Copenhagen Neck Functional Disability Scale (CNFDS) will be used to measure cervical function. The lowest score is 0 and the highest score is 30. Worse disability is indicated by higher scores.

    Measured: Baseline

  3. The Vertical Scapular Distance at Rest for both Scapulae

    The Vertical Scapular Distance at Rest will be measured using a Protractor (the Protractor - T8 method). The spinous process of T8 (SPT8) and the inferior angle of the scapula (IAS) serving as the primary anatomical landmarks of interest. Two horizontal lines are drawn at these two anatomical landmarks representing their horizontal levels, then the vertical distance between these two levels is measured three times, then their mean was recorded, the spirit level of the protractor ensures that the level of the measurement was the same at all times. this process was done for the right and the left scapulae, and the mean of the two scapulae measurements was calculated.

    Measured: Baseline

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted20 Mar 2026
  2. Study start20 Dec 2023
  3. Primary completion23 Dec 2024
  4. Study completion10 Feb 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case-control
Time perspective
Cross-sectional
Enrolment
128 participants (actual)
Target duration
1 Day
IDs, dates and publications
ClinicalTrials.gov ID
NCT07484984
Sponsor's protocol ID
P.T.REC/012/006018
Status last verified
Mar 2026
First submitted
17 Mar 2026
Last updated
23 Mar 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Neck Pain and Neck Disability, run by Cairo University at 1 site in Egypt.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 23 Mar 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Neck Pain (time frame: Baseline). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 23 Mar 2026.

Free account

Keep searching with a free account

You’ve used your 3 free searches for this session. Log in or create a free AzTrials account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in