- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07031310
- Original Trial
Correlation Between Forward Head Posture and Cervical Radiculopathy
Correlation Between Forward Head Posture and Cervical Radiculopathy in Smart Phone Users
Study Overview
Status
Conditions
Detailed Description
Cross-sectional observational study . 120 Participants will be recruited from students and employees of Nahda university (smart phone users) from both genders with age ranged between (18-35) years old.
outcomes measurement
- Photogrammetric method to assess CVA by smart phone application FHP
- Smartphone application for measuring cervical range of motion
- Numerical Pain Rating Scale to assess pain intensity
- Arabic neck disability index for measuring cervical function
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Locations
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Bani-Suef, Egypt
- Faculty of Physical Therapy, Nahda University.
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- 1. Adult subjects aged from 18-35 years old, with FHP using smart phone more than 4 hours per day.
2. Subjects with FHP (craniovertebral angle) [CVA] < 49° 3. Normal body mass index (BMI <25).
Exclusion Criteria:
- 1- Signs of serious pathology (e.g., malignancy, inflammatory disorders, infection).
2- History of cervical spine surgery. 3- History of trauma or fractures in cervical spine. 4- Vascular syndrome such as vertebrobasilar insufficiency.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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smart phone users
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
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Somatosensory evoked potential of median nerve
Time Frame: at the time of enrollment
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at the time of enrollment
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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change in Craniovertebral angle
Time Frame: At the time of enrollment
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At the time of enrollment
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Change in cervical range of motion
Time Frame: At the time of enrollment
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At the time of enrollment
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|
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Change in pain intensity
Time Frame: At the time of enrollment
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At the time of enrollment
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Assessment of cervical function
Time Frame: At the time of enrollment
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for assessment of cervical function.
we will use Neck disability index which is a 10-items questionnaire that measures a patient's self-reported neck pain related disability.
Questions include activities of daily living, such as: personal care, lifting, reading, work, driving, sleeping, recreational activities, pain intensity, concentration and headache.
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At the time of enrollment
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Collaborators and Investigators
Sponsor
Investigators
- Study Chair: Soheir Shehata Rizkalla, Professor, Department of Basic sciences for physical therapy, Faculty of Physical Therapy , Cairo university, Cairo, Egypt
Study record dates
Study Major Dates
Study Start (Actual)
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/025/00087
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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