- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06019806
Effects of Forward Head Posture Correction on Visual Acuity in Low Level Visually Impaired University Students
Effects of Forward Head Posture Correction on Visual Acuity and Fatigue in Low Level Visually Impaired University Students
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
In recent years, the increasing use of modern technology has raised concerns about its potential impact on our visual health. However, research suggests that in addition to these factors environmental factors such as near work, visual stress, educational stress and acquired false head posture may have a greater impact on visual health of young adult population. Prolonged use of digital devices can cause digital eye strain, leading to symptoms such as headaches and blurred vision. However, poor posture can also cause strain on the eyes, leading to decreased visual acuity and compromised performance. It is essential to consider factors such as posture when assessing visual performance in university students, in addition to the impact of modern technology. The forward head posture (FHP) is the head movement that occurs from poor postural awareness and frequently leads to muscle imbalance and discomfort.
University students frequently experience a forward head position, especially those who spend a lot of time studying or using computers. Both forward head posture and visual impairment are more prevalent among university students. It has been found that 63.96% of university students, including both genders, exhibit a prevalence of forward head posture. . A 2019 study in America found that 67.8% of university students experience visual fatigue, with blurred vision being the most commonly reported symptom (27%). This suggests many students may have mild visual impairments, impacting their academic performance and quality of life. The existing research has mainly concentrated on studying visual impairment by defining specific levels of impairment such as 'moderate' and 'severe.' However, it is plausible that even a minor reduction in visual acuity, also known as 'mild' visual impairment (ranging from 20/30 to 20/70), could have a subtle but significant impact on an individual's ability to cope with activities of daily life. The position and movement of the head play a crucial role in visual perception, as the somatosensory system of the neck is intricately connected to the visual system. Spending most of the time using computers, mobile phones and reading can cause biomechanical alterations that make it difficult to keep a neutral head position and compromise the structural integrity .The Centre of Gravity (COG) of the head moves in anterosuperior direction as a result of this structural integrity compromise, increasing the stress on the neck. Each inch that the head is moved forward or anteriorly from its neutral position adds approximately 10 pounds (4.5 kilograms) of extra weight to the cervical spine.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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KPK
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Peshawar, KPK, Pakistan
- Cecos University of IT and Emerging Scienecs
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Both male and female
- Mild visual impairment, visual acuity of 20/30 to 20/70 and with symptoms of visual fatigue
- Forward head posture (FHP)
- Craniovertebral Angle less than 48-50
- Able to understand and provide informed consent
- Able to participate in the intervention and attend all the required
Exclusion Criteria:
- Visual impairment other than mild visual impairment (e.g., legal blindness)
- Pre-existing medical conditions or injuries that may affect the posture or visual function
- Any previous neck and Eye surgery.
- Previous history of treatment for FHP or visual impairment in the past six months(23)
- Any physical, neurological or cognitive disability that may affect the ability to participate in the intervention or the assessments
- Use of medication or treatments that may affect the posture or visual function
- Psychological conditions
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: postural correction group A
|
The program will involve four exercises, including two strengthening exercises and two stretching exercises.
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Active Comparator: Control group B
postural Correction education
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The control group would receive postural Correction education and they would be provided with a manuscript.
They would be then guided to follow these guidelines as a home plan for four weeks.
At the end of the Fourth week, they would be assessed.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Snellen Chart
Time Frame: 4 weeks
|
Universally used for measuring visual acuity.
|
4 weeks
|
|
Asthenopia Questionnaire
Time Frame: 4 weeks
|
Used for measuring Visual fatigue.
|
4 weeks
|
|
Craniovertebral Angle
Time Frame: 4 weeks
|
Craniovertebral angle is measured by taking 2 lateral photographs of the subject in a relaxed seated position without a back support.
Spinous process of C7 and the tragus of ear are marked with a body marker.
A horizontal line is drawn passing through C7 making a right angle with the vertical.
|
4 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Aisha Razzaq, MSPT-OMPT, Riphah International University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
- RiphahIU Shabi ul Hassan
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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