Effects of Forward Head Posture Correction on Visual Acuity in Low Level Visually Impaired University Students
1 other identifier
interventional
48
1 country
1
Brief Summary
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
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Sep 2023
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 26, 2023
CompletedFirst Posted
Study publicly available on registry
August 31, 2023
CompletedStudy Start
First participant enrolled
September 6, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 30, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
February 15, 2024
CompletedMay 21, 2024
May 1, 2024
5 months
August 26, 2023
May 19, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Snellen Chart
Universally used for measuring visual acuity.
4 weeks
Asthenopia Questionnaire
Used for measuring Visual fatigue.
4 weeks
Craniovertebral Angle
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
Study Arms (2)
postural correction group A
EXPERIMENTAL1. Chin tuck (deep cervical flexor) 2. Strengthening shoulder retractors 3. Sternocleidomastoid muscle stretch 4. Pectoralis stretch
Control group B
ACTIVE COMPARATORpostural Correction education
Interventions
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
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.
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Cecos University of IT and Emerging Scienecs
Peshawar, KPK, Pakistan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Aisha Razzaq, MSPT-OMPT
Riphah International University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 26, 2023
First Posted
August 31, 2023
Study Start
September 6, 2023
Primary Completion
January 30, 2024
Study Completion
February 15, 2024
Last Updated
May 21, 2024
Record last verified: 2024-05
Data Sharing
- IPD Sharing
- Will not share