The Relationship Between Cervical Endurance Time and Eye Gaze

May 29, 2025 updated by: Atef Nadier, Al-Ahliyya Amman University

The Relationship Between Cervical Endurance Time and Eye Gaze Dual Time in University Students

46 normal students will participate at the study; they will be randomly divided (male and female) into 2 groups (23 for each group) The study will be conducted in physical therapy lab and Speech and hearing center at Allied medical school.

Study Overview

Study Type

Observational

Enrollment (Estimated)

46

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

Sampling Method

Probability Sample

Study Population

normal students at university, level 3

Description

Inclusion Criteria:

  • Normal students

Exclusion Criteria:

  • subjects achieving less than 20 mmHg in the CCFT test
  • Students with cervical pain within the last six months

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Endurance time during gazing
Time Frame: at base line
measured by seconds
at base line
Endurance time without gazing gazing
Time Frame: at base line
measured by seconds
at base line
Attention Span Scale for Students
Time Frame: at base line
Questionnaire
at base line
Cervical Vestibular-Evoked Myogenic Potential (cVEMP)
Time Frame: at base line
at base line

Collaborators and Investigators

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

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 (Estimated)

July 1, 2025

Primary Completion (Estimated)

September 28, 2025

Study Completion (Estimated)

March 28, 2026

Study Registration Dates

First Submitted

May 21, 2025

First Submitted That Met QC Criteria

May 29, 2025

First Posted (Actual)

May 30, 2025

Study Record Updates

Last Update Posted (Actual)

May 30, 2025

Last Update Submitted That Met QC Criteria

May 29, 2025

Last Verified

May 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • 1979

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

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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