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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05149183
Other study ID # P.T.REC/012/003459
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date December 15, 2021
Est. completion date March 1, 2022

Study information

Verified date November 2021
Source Cairo University
Contact salah E Ahmed, master
Phone 01158125773
Email salaheid07@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

to investigate the effect of cervical stability training on somatosensory evoked potential and cervical spine in forward head posture


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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 40
Est. completion date March 1, 2022
Est. primary completion date March 1, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 40 Years
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

Other:
cervical stability training
cervical stability training will be contain three phases, each phase has six positions ( supine, forearms, sidelying, four point kneeling, sitting and standing position)
traditional treatment
TENS, hot packs, stretching exercise of superficial neck muscles, and postural advice.

Locations

Country Name City State
Egypt Salah Eid Ahmed Ali Giza

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary somatosensory evoked potential somatosensory evoked potential will be measured by electromyograph device up to eight weeks
Primary craniovertebral angle craniovertebral angle will be measured photographically by surgimap program up to eight weeks
Secondary pain intensity level pain will be measured by visual analogue scale up to eight weeks
Secondary functional disability disability will be measured by arabic neck disability index up to eight weeks
Secondary cervical range of motion Phone application (clinometer) will used to measure cervical range of motion using smartphone (Infinix Note 5) up to eight weeks
Secondary endurance test flexion and extension endurance will be measured using pressure biofeedback unit up to eight weeks
Secondary cervical curvature digital x ray will be used to measure cervical curvature up to eight weeks
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