Smartphone Addiction and Temporomandibular Joint Dysfunction in Individuals With Nonspecific Neck Pain

April 24, 2023 updated by: Ayşe Abit Kocaman, Kırıkkale University
It has been reported that excessive use of smartphones increases the stress on the cervical spine, and changes in cervical curvature and pain in the muscles around the neck are associated with the increase in stress. Studies have reported that smartphone users with addictions have neck pain (68%), upper back pain (62%), right shoulder pain (52%), left shoulder pain (46%), and right hand pain (46%). As a result of our study, the frequency of smartphone addiction and temporomandibular joint dysfunction and related factors in individuals with nonspecific neck pain were examined and the results we obtained will contribute to the literature.

Study Overview

Study Type

Observational

Enrollment (Actual)

60

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

      • Kırıkkale, Turkey, 7110
        • Ayşe Abit Kocaman

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

18 years to 45 years (Adult)

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Individuals with nonspecific neck pain, individuals who voluntarily agreed to participate in our study and signed the consent form

Description

Inclusion Criteria:

  • Presence of neck pain lasting at least 6 months
  • Being between the ages of 18-45
  • Individuals with a score between 10-40 points according to the Neck Disability Index
  • Individuals who have never had a history of shoulder or neck surgery

Exclusion Criteria:

  • Individuals with signs of radicular pain (positive neck distraction test, Spurling's neck compression test, and Adson's test)
  • Individuals who get less than 10 points or more than 40 points according to the Neck Disability Index
  • Those with a previous history of shoulder and neck surgery
  • Individuals with accompanying shoulder pain
  • Individuals with spinal cord tumors
  • Individuals with meningeal tumors
  • Individuals who do not want to participate in the study

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
patient group,healthy group
Cranio- Cervical Flexion Test, cervical mobility, Pressure Pain Threshold,Functional evaluation of the temporomandibular joint,Pittsburg Sleep Quality Index
Cranio- Cervical Flexion Test, cervical mobility, Pressure Pain Threshold,Functional evaluation of the temporomandibular joint,Pittsburg Sleep Quality Index

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Cranio- Cervical Flexion Test
Time Frame: Day 1
An inflatable pressure unit (StabilizerTM, Chattanooga Group, Inc., Hixson, TN) will be used during testing.
Day 1
Evaluation of cervical mobility
Time Frame: Day 1
Cervical region flexion, extension, lateral flexion and rotation movements will be evaluated with Baseline Bubble Inclinometer.
Day 1
Evaluation of Pressure Pain Threshold
Time Frame: Day 1
Pressure pain threshold assessment will be performed with an algometer, which is an objective assessment method.Measurements will be made from three different regions: anterior temporal muscle body, masseter muscle body and TMJ (lateral to the mandibular condyle).
Day 1
Functional evaluation of the temporomandibular joint
Time Frame: Day 1
The Helkimo Clinic Craniomandibular Index will be used in the evaluation of TMJ (5). This index consists of 5 subsections: pain on muscle palpation, pain on TMJ palpation, pain on mandible functions, TMJ functions (sound, gliding at maximum opening, luxation and/or locking) and mandible movement capacity.
Day 1
Smartphone Addiction Scale Short Form
Time Frame: Day 1
Each item is scored between 1-6. The high score informs about the severity of smartphone addiction. Those who have a total score above 29.50 are considered as smartphone addiction.
Day 1

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pittsburgh Sleep Quality Index
Time Frame: Day 1
It is a reliable, valid and standardized scale that measures sleep quality over a one-month period and provides clinical evaluation of various sleep disorders that may affect sleep quality.
Day 1

Collaborators and Investigators

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

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the 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 (Actual)

April 15, 2022

Primary Completion (Actual)

March 15, 2023

Study Completion (Actual)

April 1, 2023

Study Registration Dates

First Submitted

April 10, 2022

First Submitted That Met QC Criteria

April 10, 2022

First Posted (Actual)

April 18, 2022

Study Record Updates

Last Update Posted (Actual)

April 26, 2023

Last Update Submitted That Met QC Criteria

April 24, 2023

Last Verified

April 1, 2023

More Information

Terms related to this study

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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