Correlation Between BMI and Craniovertebral Angle and Their Impact on Hand Grip Strength and Neck Functional Disability in Egyptian University Student

June 25, 2024 updated by: Mohamed Ababa, Ahram Canadian University

Objective: To find the relation between cranio-vertebral angle and hand grip strength in university student mobile users.

Design: cross sectional study. Setting: Ahram Candian University Subjects:100 male and female university students with age ranged from 20 to 30 years old will participate in this study.

Intervention: cross sectional study to detect the relation between cranio-vertebral angle and hand grip strength in university student mobile users.

Main measures:

  • FHP app (Pyeongtaek, South Korea) mobile application
  • Hand dynamometer (the JAMAR® Hydraulic Hand) (Lupton-Smith et al.,2022)
  • Mechanical height and weight scale
  • Visual Analogue Scale
  • Arabic Neck Disability Index Results: The results will be obtained via one-way analyses of variance (ANOVA).

Study Overview

Status

Not yet recruiting

Conditions

Study Type

Observational

Enrollment (Estimated)

100

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

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

No

Sampling Method

Probability Sample

Study Population

100 male and female patients Their ages will range from 20-30 years old. Their BMI will be between than 20- 30kg/m2, All of them suffer from mild degree of neck pain and They complain from neck pain for 1 month ago

Description

Inclusion Criteria:

  • • Their ages will range from 20-30 years old.

    • Their BMI will be between than 20- 30kg/m2.
    • All of them suffer from mild degree of neck pain.
    • The subjects complain from neck pain for 1 month ago
  • Exclusion criteria:

Exclusion criteria were a history of any of the following condition:

  • inflammatory diseases or any rheumatic disorders,
  • a history of vertebral fractures
  • surgical spinal fixation.
  • •any neurological disorders like MS

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
Group (A):
Body mass index < 25
FHP app (Pyeongtaek, South Korea) mobile application ,is mobile application to asses cranio vertebral angle
Other Names:
  • • Hand dynamometer
  • • Visual Analogue Scale
  • • Arabic Neck Disability Index
Group (B):
Body mass index > 25
FHP app (Pyeongtaek, South Korea) mobile application ,is mobile application to asses cranio vertebral angle
Other Names:
  • • Hand dynamometer
  • • Visual Analogue Scale
  • • Arabic Neck Disability Index

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
craniovertebral angle will measured by FHP (Forward Head Posture ) mobile application
Time Frame: baseline
It is a mobile application which is objective to detect the cervical posture by measuring the CV angle. It is an application that requires an Android version 4.0 or higher installed on a smartphone
baseline
Hand grip strength will measured by Hand dynamometer (the JAMAR® Hydraulic Hand)
Time Frame: baseline
it is tool used to asses hand grip strength
baseline
Pain level will measured by Visual Analogue Scale
Time Frame: base line
VAS is a line with a length of 10 where one end (right) means no pain and the other means severe unbearable pain. Each patient was asked to put a mark on the line that mostly describe his or her pain intensity.
base line
Neck functional disability will assess by Arabic Neck Disability Index
Time Frame: baseline
it consist of 10 questions in total, including ones about pain intensity, personal care, lifting, reading, headaches, driving, concentration, work, sleeping, and recreation Each item is scored from 0 (no disability) to 5 (total disability)
baseline

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)

June 26, 2024

Primary Completion (Estimated)

June 30, 2024

Study Completion (Estimated)

July 1, 2024

Study Registration Dates

First Submitted

June 12, 2024

First Submitted That Met QC Criteria

June 25, 2024

First Posted (Actual)

June 26, 2024

Study Record Updates

Last Update Posted (Actual)

June 26, 2024

Last Update Submitted That Met QC Criteria

June 25, 2024

Last Verified

June 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • P.T - ORT- 4/2024-540

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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