NCT06019806

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
48

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Sep 2023

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
5 days until next milestone

First Posted

Study publicly available on registry

August 31, 2023

Completed
6 days until next milestone

Study Start

First participant enrolled

September 6, 2023

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 30, 2024

Completed
16 days until next milestone

Study Completion

Last participant's last visit for all outcomes

February 15, 2024

Completed
Last Updated

May 21, 2024

Status Verified

May 1, 2024

Enrollment Period

5 months

First QC Date

August 26, 2023

Last Update Submit

May 19, 2024

Conditions

Keywords

forward head posturevisual fatiguecraniovertebral anglepostural correction exercises

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

EXPERIMENTAL

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

Other: POSTURAL CORRECTION four exercises

Control group B

ACTIVE COMPARATOR

postural Correction education

Other: postural Correction education with a manuscript

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

postural correction group A

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.

Control group B

Eligibility Criteria

Age15 Years - 28 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64)

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

Location

MeSH Terms

Conditions

Asthenopia

Condition Hierarchy (Ancestors)

Eye Diseases

Study Officials

  • Aisha Razzaq, MSPT-OMPT

    Riphah International University

    PRINCIPAL INVESTIGATOR

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

Locations