Combine Effect Of Myofascial Release Technique and Ocular Muscle Exercise Among University Students

December 20, 2024 updated by: Riphah International University

Combine Effect of Myofascial Release Technique and Ocular Muscle Exercise in Myopia With Eye Strain Headache Among University Students

The current study aim to determine the effect of myofascial release technique and ocular muscle exercise to release eye strain headache in myopic students.

This study aim to reduce eye strain headache to improve quality of life and student academic performance. This study will enable the students to to work on digital device for a long period of time without any discomfort.

Study Overview

Status

Completed

Conditions

Detailed Description

According to recent researches MFR technique used to relax the muscles tension in muscles and fascia. This technique also enhance ROM. In this technique Apply gentle and sustain pressure on muscle start with light pressure gradually increase as it tolerated move the fingers along the length of muscle during apply pressure to take deep breath to help relax and facilitate the release.

Previous study showed a significant improvement in reduction of the number of headache days (p < 0.001) and the headache pain level (p < 0.001) following treatment.

The other intervention of this study is the ocular muscle exercise. Previous study showed that strengthening neck exercises like isometric neck exercise improve muscular strength and it is also delivering long term treatment effect on cervical pain.

This study divide in to two groups. Group A (experimental group) and Group B (control group)Patient in group A will receive ocular muscle exercise which is consist of three exercise like palm exercise, blinking exercise, pencil pushup exercise This group will also receive myofascial release technique on sternocleidomastoid muscle and upper trapezius muscles. Patient in group B will receive ocular muscle exercise and neck isometric exercise.

This study will manage the musculoskeletal and visual aspects of headaches and eye strain by combining myofascial release treatments with eye exercises. This study will contribute to reduce the eye strain headache and improve their quality of life and improve students' academic performance during class room and online learning.

Study Type

Interventional

Enrollment (Actual)

36

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

    • Khyber Pakhtunkhawa
      • Peshawar, Khyber Pakhtunkhawa, Pakistan
        • Abasyn University Peshawar

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

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Age = 20- 30 years old
  • Gender= male / female
  • Diagnosed of Mild (-0.50 to -3.0 D) and moderate ( -3.0 to -6.0 D) myopia
  • Unilateral or bilateral headache with mild or medium intensity
  • Pain around eyes, forehead and temples
  • Headache with neck stiffness or pain
  • Headache increase with visual activity such as reading, using computer or cell phone.
  • Headache associate with triggers in sternocleidomastoid, upper trapezius
  • Positive convergent test (13)

Exclusion Criteria:

  • History of genetic disease
  • History of refractive surgery
  • Wear contact lenses
  • Headache associate with photophobia
  • Headache associate with phonophobia
  • History of neck trauma
  • Cervical radiculopathy, herniated disc, arthritis
  • Pain aggravated by movements of head

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
Active Comparator: manual therapy
ocular muscle exercise like palm , blinking and pencil pushups neck isometric exercise

Ocular muscle exercise which is consist of three exercise like palm exercise, blinking exercise, pencil pushup exercise.

3 sets of 10 repetition 5 days a week. As well as strengthening exercise the neck isometric exercise. each exercise consist of 3 sets of 5 repetition 5 days a week.

Total of three sessions .

Experimental: myofascial release therapy
myofascial release technique along with ocular and neck isometric exercise.

Ocular muscle exercise which is consist of three exercise like palm exercise, blinking exercise, pencil pushup exercise.

3 sets of 10 repetition 5 days a week. As well as strengthening exercise the neck isometric exercise. each exercise consist of 3 sets of 5 repetition 5 days a week.

Total of three sessions .

Experimental group given MFR along with neck isometric and ocular muscle exercise.

myofascial release technique on sternocleidomastoid muscle and upper trapezius muscles. Patients will be treated 3 seconds to 2 minutes, three days in a week.

Ocular muscle exercise will perform 3 sets of 10 repetition 5 days a week. As well as strengthening exercise the neck isometric exercise. This exercise will performed 3 sets of 5 repetition 5 days a week.

Total of three sessions .

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Computer vision syndrome questionnaire
Time Frame: 5 days
CVS is consist of 13 sections its scoring in the form of mild, moderate severe,
5 days

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
tape measure method
Time Frame: 5 days
Tape used to measure the length of muscle ( SCM, upper trapezius ) measurement from the baseline to third week.
5 days

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Sidra Ghias, MS, 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)

March 1, 2024

Primary Completion (Actual)

June 1, 2024

Study Completion (Actual)

June 1, 2024

Study Registration Dates

First Submitted

May 6, 2024

First Submitted That Met QC Criteria

May 6, 2024

First Posted (Actual)

May 9, 2024

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

December 20, 2024

Last Verified

December 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • REC/MS-PT/01796

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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