- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05149183
Effect of Cervical Stability Training on Somatosensory Evoked Potential and Cervical Spine in Forward Head Posture (FHP)
Study Overview
Status
Conditions
Intervention / Treatment
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
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: salah E Ahmed, master
- Phone Number: 01158125773
- Email: salaheid07@gmail.com
Study Locations
-
-
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Giza, Egypt, 11251
- Salah Eid Ahmed Ali
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
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
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
Sponsor
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
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
Studies a U.S. FDA-regulated device product
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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