Neck Joint Position Error Among Taibah Students University; Saudi Arabia; Cross Section Design

May 13, 2023 updated by: walaa M Ragab, Taibah University
this study was done to answer the following: Is there a difference between students without and with varying degrees of text neck in cervical proprioception defect? Is there a correlation between JPE and severity of text neck among Taibah students University?

Study Overview

Status

Completed

Conditions

Study Type

Observational

Enrollment (Actual)

68

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

      • Medina, Saudi Arabia, 42353
        • Taibah University

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

Non-Probability Sample

Study Population

All four groups were recruited from the college of medical rehabilitation sciences, Applied Medical Sciences, and Business administration faculty through posters, word of mouth, and by WhatsApp groups.

Description

Inclusion Criteria:

  • A convenient sample of 68 female students
  • the age was between 18-25 years

Exclusion Criteria:

  • Any students with neck pain or previous neck or back surgery or a history of a previous accident were excluded
  • Also, we excluded any student with a history of fracture injury of the cervical column, scoliosis, severe thoracic kyphosis, rheumatic disease, torticollis, loss of standing balance, use of hearing aid, and persistent respiratory problems.

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
normal group
no text neck
devices to objectively assess proprioception of the neck
mild text neck
devices to objectively assess proprioception of the neck
moderate text neck
devices to objectively assess proprioception of the neck
severe text neck
devices to objectively assess proprioception of the neck

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
neck proprioception error
Time Frame: one day
we measured joint position error for all students from sitting and standing using laser beam detection error
one day

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
joint position error
Time Frame: one day
we measured joint position error of cervical spine by measuring neck motion by phone goniometer and inclinometer.
one day

Collaborators and Investigators

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

Investigators

  • Principal Investigator: walaa ragab, phd, Taibah 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)

January 31, 2022

Primary Completion (Actual)

April 18, 2022

Study Completion (Actual)

April 18, 2022

Study Registration Dates

First Submitted

April 29, 2023

First Submitted That Met QC Criteria

May 13, 2023

First Posted (Actual)

May 16, 2023

Study Record Updates

Last Update Posted (Actual)

May 16, 2023

Last Update Submitted That Met QC Criteria

May 13, 2023

Last Verified

May 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • taibah

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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