- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06012292
Effect of Mobile Phone Addiction With Forward Head Posture on Pain and Cervical Functions (FHP)
Study Overview
Status
Conditions
Detailed Description
Nowadays, the mobile phone has become an important requirement. The number of mobile phone users and the duration of mobile phone use are increasing rapidly, and the side effects can be detrimental one of them is forward head posture.
Prolonged use of the mobile phone has also affected posture, resulting in many musculoskeletal disorders or improper posture. Neck posture, particularly in a sitting position, is regarded an essential contributing factor to the development and long-term maintenance of cervical pain and headache. Neck flexed posture increased due to the frequent use of the relatively small screen of a mobile phone compared to that of a desktop computer. Constant use may also have unexpected consequences: increased stress on the cervical spine.
Forward head posture (FHP) is the most common side effect of prolonged, sustained mobile and tablet use. This leads to extension at atlantooccipital (C1 to C2) joints with flexion of lower cervical spine (C4 to C7) and flattening of mid cervical lordosis which cause joint dysfunction associated with negative affection of lung function, abnormal afferent information affecting the tonic neck reflex and encourages the gradual adaptation of FHP.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: AMal M Fayed, Master
- Phone Number: 01029299592
- Email: amalbahgat076@gmail.com
Study Locations
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-
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Beheira, Egypt, 22744
- Amal Mohammed Bahgat Fayed
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Forward head with craniovertebral angle less than 50 degree.
- Both sexes will participate in this study.
- Their age will be ranging from 18-40years (Molaeifar et al., 2021).
- Body mass index is ranged from 18-25 kg /m2 (Molaeifar et al., 2021).
- Area of mobile phone is 17 × 8cm.
- Participants will be randomly allocated into 2 groups, group (A) should not have addicted to mobile phone and group (B) should have addicted to mobile phone.
Exclusion Criteria:
- Previous cervical operation.
- Musculoskeletal disorders such as cervical spine fracture, myelopathy, spinal cord tumor.
- Neurological conditions that affected head, neck, and upper limbs.
- Cervical disc or spondylosis.
- Respiratory diseases such as Restrictions in lung function.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
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Group A Not addicted to mobile phone
Addicted to mobile phone less than four hours per day.
|
|
Group B addicted to mobile phone
Addicted to mobile phone more than four hours per day.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain pressure threshold
Time Frame: one week
|
Pain pressure threshold will be measured by pressure algometer
|
one week
|
|
Respiratory functions
Time Frame: one week
|
Respiratory functions including tidal volume and total lung capacity will be measured by incentive spirometer
|
one week
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Endurance of deep neck flexor muscles
Time Frame: one week
|
Endurance of deep neck flexor muscles will be measured by pressure biofeedback unit stabilizer
|
one week
|
|
Neck functional disability level
Time Frame: one week
|
Neck functional disability level will be measure by Copenhagen Neck Functional Disability scale Arabic version
|
one week
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- P.T.REC/012/004269
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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