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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03757520
Other study ID # 0018827704
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 11, 2019
Est. completion date October 18, 2020

Study information

Verified date November 2020
Source University of Jazan
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will be conducted in the Department of physical therapy, College of Applied Medical Sciences,Jazan University, to investigate text neck syndrome and hand grip force in smart phone addiction among students of jazan university


Description:

Four hundreds students with age 19 to 26 years old, and right dominant hand, will be recruited from the College of Applied Medical Sciences, Jazan University. Subjects will be randomly assigned to into a heavy user group (n=300; female and male students) and a control or regular use group (n=300; female and male students) according to their smartphone addiction proneness scale. Baseline hydraulic hand dynamometer: (Fabrication Enterprises Incorporated, White Plains,New York, USA) is used to measure the hand grip strength and pinch strength. Algometer Commander (JTech Medical Company) is used on the location of the trigger point to assess the amount of pressure the patient could sustain before the patient registered the pressure as being painful for upper fiber of trapezius muscle and sternocleidomastoid muscle


Recruitment information / eligibility

Status Completed
Enrollment 600
Est. completion date October 18, 2020
Est. primary completion date August 16, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 19 Years to 26 Years
Eligibility Inclusion Criteria: 1. The participant will be right-handed. 2. No abnormal findings confirmed through physical and neurological examination. 3. No congenital abnormalities in either the cervical or the lumbar spine. 4. No history of severe surgical procedures ( Park et al., 2015) . Exclusion Criteria: 1. History of a neurological disease. 2. History of musculoskeletal injury of neck and lumbar region. 3. Unstable medical condition.

Study Design


Intervention

Diagnostic Test:
Pain Pressure Threshold
The pain pressure thresholds (PPTs) will be measured using an pressure algometer commander over potential trigger points (TrPs) on the body for upper fiber of trapezius, and sternocleidomastoid muscle.
Hand Grip Force
For measuring the grip strength, the subjects will be asked to sit on a chair with their hip joint flexed at 90 degree, and shoulder joint in a neutral position. The elbow is fixed at 90 degree flexion, forearm in a neutral position, and wrist at 0 to 15 degree radial deviation The test will be performed twice, and the higher value between the two measurements will be selected.

Locations

Country Name City State
Saudi Arabia Jazan University Riyadh Jazan

Sponsors (1)

Lead Sponsor Collaborator
Wafaa Mahmoud Amin

Country where clinical trial is conducted

Saudi Arabia, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain pressure threshold for upper fiber of trapezius muscle Using Algometer to measure pain pressure for upper trapezius trigger point which lies in the more horizontal fibers of the upper trapezius on the back of the shoulder, about halfway between spine and the acromion on right and left side for 3 repetition for each 3 minutes
Primary Pain pressure threshold for sternocleidomastoid muscle Using Algometer to measure pain pressure for sternocleidomastoid muscle on right and left side for 3 repetition for each. Measurement will includes three sites on each side:
1. upper part of the sternal division of the muscle near to its insertion into the mastoid process. 2. he mid-part of the sternal division of the muscle. 3. lower end of this division near to its attachment to the sternum.
9 minutes
Primary Hand Grip Force For measuring the grip strength, the subjects will be asked to sit on a chair with their hip joint flexed at 90 degree, and shoulder joint in a neutral position.
The elbow is fixed at 90 degree flexion, forearm in a neutral position, and wrist at 0 to 15 degree radial deviation.The test will be performed twice, and the higher value between the two measurements will be selected.
The subjects are allowed a rest time of more than 5 minutes after the first measurement to avoid examiner bias and to decrease physical stress
15 minutes
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