Effects of Forward Head Posture Correction on Visual Acuity in Low Level Visually Impaired University Students

May 19, 2024 updated by: Riphah International University

Effects of Forward Head Posture Correction on Visual Acuity and Fatigue in Low Level Visually Impaired University Students

The aim of this research is to find the effect of forward head posture correction on visual acuity and fatigue in low level visually impaired university students. Randomized controlled trials at Cecos University of IT and Emerging Sciences would be done. The sample size would be 48. The subjects would be divided in two groups, 24 subjects Intervention group and 24 in control group. Study duration would be 6 months. Sampling technique applied would be a non-probability convenience sampling technique. Only 18-25 years low level visually impaired university students with forward head posture would be included. Tools used in the study would be asthenopia questionnaire, Snellen chart and CVA angle photogrammetry

Study Overview

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

Interventional

Enrollment (Actual)

48

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • KPK
      • Peshawar, KPK, Pakistan
        • Cecos University of IT and Emerging Scienecs

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult

Accepts Healthy Volunteers

No

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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
  1. Chin tuck (deep cervical flexor)
  2. Strengthening shoulder retractors
  3. Sternocleidomastoid muscle stretch
  4. Pectoralis stretch

The program will involve four exercises, including two strengthening exercises and two stretching exercises.

  1. Chin tuck (deep cervical flexor)
  2. Strengthening shoulder retractors
  3. Sternocleidomastoid muscle stretch
  4. Pectoralis stretch Participants will be instructed to perform three sets of 12 repetitions for the strengthening exercises, with a 30-second rest period allotted between each set. For the stretching exercises, participants will be instructed to hold each stretch for 30 seconds, with a 30-second rest period allotted between each exercise The experimental group will also receive postural Correction education
Active Comparator: Control group B
postural Correction education
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

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Aisha Razzaq, MSPT-OMPT, Riphah International University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 6, 2023

Primary Completion (Actual)

January 30, 2024

Study Completion (Actual)

February 15, 2024

Study Registration Dates

First Submitted

August 26, 2023

First Submitted That Met QC Criteria

August 30, 2023

First Posted (Actual)

August 31, 2023

Study Record Updates

Last Update Posted (Actual)

May 21, 2024

Last Update Submitted That Met QC Criteria

May 19, 2024

Last Verified

May 1, 2024

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)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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