Effect of Cervical Stability Training on Somatosensory Evoked Potential and Cervical Spine in Forward Head Posture (FHP)

November 25, 2021 updated by: Al Shaymaa Shaaban Abd El Azeim, Cairo University
to investigate the effect of cervical stability training on somatosensory evoked potential and cervical spine in forward head posture

Study Overview

Status

Not yet recruiting

Detailed Description

The use of electronic tools is increasing in worldwide varieties and the attractiveness of these tools lead to variety of groups of people, especially teenagers, using them for prolonged period of time leading to increased musculoskeletal problems. Excessive use of smartphones for long period of time can lead to decreased postural control and forward head postur (FHP) as phone users maintain an abnormal alignment of the head and neck. The habit of repetitive use of computers, TV, mobile phones, and video games and even back packs forces the body to exhibit bad posture. The overall prevalence of FHP was reported to be 66% in computer based workers.

cervical stability training play a major role in treatment of forward head posture so this study will be conducted to investigate its role on craniovertebral angle, cervical range of motion, pain intensity level, functional disability, neck flexor and extensor muscles endurance, lordotic cervical curvature, somatosensory evoked potential in forward head patient.

Study Type

Interventional

Enrollment (Anticipated)

40

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

      • Giza, Egypt, 11251
        • Salah Eid Ahmed Ali

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

18 years to 40 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

Adult participant (18-to-40years old) with forward head posture, BMI 20-to-25 kg/m², The area of mechanical neck pain will defined to the cervical region, possibly with referred pain into the occipit, nuchal muscles, and shoulders, All patients will have chronic neck pain for more than 3 months, Craniovertebral angle of ˂ 49.

Exclusion Criteria:

Signs of serious pathology (e.g., rheumatoid diseases, ankylosing spondylitis), History of cervical spine surgery, History of trauma or fractures in cervical spine, Signs of cervical radiculopathy or myelopathy, Vascular syndrome such as vertebrobasilar insufficiency.

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

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: cervical stability training
cervical stability training will be received three times a week for eight weeks
cervical stability training will be contain three phases, each phase has six positions ( supine, forearms, sidelying, four point kneeling, sitting and standing position)
TENS, hot packs, stretching exercise of superficial neck muscles, and postural advice.
Active Comparator: traditional treatment
traditional treatment will be received three times a week for eight weeks
TENS, hot packs, stretching exercise of superficial neck muscles, and postural advice.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
somatosensory evoked potential
Time Frame: up to eight weeks
somatosensory evoked potential will be measured by electromyograph device
up to eight weeks
craniovertebral angle
Time Frame: up to eight weeks
craniovertebral angle will be measured photographically by surgimap program
up to eight weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
pain intensity level
Time Frame: up to eight weeks
pain will be measured by visual analogue scale
up to eight weeks
functional disability
Time Frame: up to eight weeks
disability will be measured by arabic neck disability index
up to eight weeks
cervical range of motion
Time Frame: up to eight weeks
Phone application (clinometer) will used to measure cervical range of motion using smartphone (Infinix Note 5)
up to eight weeks
endurance test
Time Frame: up to eight weeks
flexion and extension endurance will be measured using pressure biofeedback unit
up to eight weeks
cervical curvature
Time Frame: up to eight weeks
digital x ray will be used to measure cervical curvature
up to eight weeks

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 (Anticipated)

December 15, 2021

Primary Completion (Anticipated)

March 1, 2022

Study Completion (Anticipated)

March 1, 2022

Study Registration Dates

First Submitted

November 25, 2021

First Submitted That Met QC Criteria

November 25, 2021

First Posted (Actual)

December 8, 2021

Study Record Updates

Last Update Posted (Actual)

December 8, 2021

Last Update Submitted That Met QC Criteria

November 25, 2021

Last Verified

November 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • P.T.REC/012/003459

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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