Are Axioscapular Muscles Activity and Cervical Curvature Associated With Disability in Neck Pain

March 7, 2024 updated by: Omar Mohamed Ali Elabd, Delta University for Science and Technology

Are Axioscapular Muscles Activity and Cervical Curvature Associated With Disability in Patients With Chronic Nonspecific Neck Pain? - A Cross Sectional Exploratory Study

Despite the important role of axioscapular muscles electromyography and cervical posture as outcomes for the management of chronic neck non specific pain , there is gab of evidence that highlight their association to the commonly used neck disability index. The quest to improve outcomes for individuals suffering from chronic nonspecific neck pain is underscored by the need to identify key prognostic variables that can guide clinical decision-making and intervention strategies. This study seeks to bridge the gap in research by examining the association between neck disability index score, cervical sagittal curvature, and axioscapular muscles electromyography in forms of both trapezius and levator scapula root mean squares to indicate muscular activities and median frequencies to indicate muscular fatigue.

Study Overview

Status

Active, not recruiting

Intervention / Treatment

Study Type

Observational

Enrollment (Actual)

60

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

    • Dakahleya
      • Gamasa, Dakahleya, Egypt, 7731168
        • Delta University For Science and Technology

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

  • Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

patients with chronic nonspecific neck pain lasting longer than three months

Description

Inclusion Criteria:

  • chronic nonspecific neck pain
  • age between 20 and 40 years,
  • either sex
  • symptoms lasting longer than three months

Exclusion Criteria:

  • Pregnancy
  • Spinal surgeries
  • spinal deformities
  • visual or auditory issues
  • ongoing physical or medical treatment for cervical or low back pain

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Neck disability
Time Frame: at the enrollment
Neck disability will be measured using the neck disability index. It is a 10-item questionnaire. The patient will be asked to respond by selecting the checkbox next to each statement that most accurately reflect him/her.
at the enrollment
Curvature angle of the cervical spine
Time Frame: at the enrollment

A flexible ruler (ati, FC-700R, Taiwan) will be used to measure the cervical spine curve. To calculate the angle, the patient's elbows will be resting on the armrest directly below the acromion as the patient sat in a chair with his feet flat on the floor, and the ruler will firmly press against the patient's upright cervical spine between the occiput and the seventh cervical spinous process. A mathematical equation will be used: angle (Q)

=arc tan (2b / a). whereas: a, Length between the two endpoints of the cervical curve; b, Length of the perpendicular from the midpoint of line a to the curve

at the enrollment
root-mean-square value (RMS) of Surface electromyography for both upper trapezius and levator scapula
Time Frame: at the enrollment

electromyography (MyoSystemTM 1400A, Noraxon Inc, 15770 N) will be used to measure:

  • the maximum voluntary isometric contraction of both upper trapezius and levator scapula for 3 trials.
  • Writing task electromyography amplitude for 15 minutes, a semistatic load, after the MVIC evaluation

Finally, root-mean-square value (%) of both upper trapezius and levator scapula will be calculated as : Writing task electromyography amplitude divided by the average of the three maximum voluntary isometric contraction trials.

at the enrollment

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)

December 17, 2023

Primary Completion (Estimated)

March 10, 2024

Study Completion (Estimated)

March 20, 2024

Study Registration Dates

First Submitted

March 3, 2024

First Submitted That Met QC Criteria

March 7, 2024

First Posted (Actual)

March 8, 2024

Study Record Updates

Last Update Posted (Actual)

March 8, 2024

Last Update Submitted That Met QC Criteria

March 7, 2024

Last Verified

March 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • NO: PT. BU. EC. 7

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Personal preference

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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