The Relationship Between Cervical Hypolordosis and Pain, Phone Addiction, and Nomophobia

September 28, 2022 updated by: Yasemin Şahbaz, University of Beykent

Examining the Relationship Between Cervical Hypolordosis and Pain, Phone Addiction, and Nomophobia in Young Adults

The aim of this study is to reveal the relationship between the degree of neck straightening and pain, phone addiction and nomophobia in young adult patients who applied to the clinic with the complaint of neck pain and were diagnosed with neck straightening as a result of radiological examinations.

120 patients who applied to the clinic with the complaint of neck pain and were diagnosed with cervical hypolordosis by radiological examination will be included in the study. After giving the necessary verbal and written information about the study, a link will be sent to the phones of the patients whose informed consent was obtained. Patients will access evaluation questions and survey questions via this link. Personal information with the Sociodemographic Data Form prepared by us; pain severity by Visual Analogue Scale (VAS); phone addiction level with the Smartphone Addiction Questionnaire (Young Population); nomophobia levels will be evaluated with the Nomophobia Scale.

Study Overview

Status

Completed

Conditions

Detailed Description

Indication or complications Patients between the ages of 18-35, diagnosed with neck flattening and who agreed to participate in the study will be included in the study. Patients under the age of 18 and older than 35, who cannot cooperate verbally and/or auditory, and who cannot cooperate psychologically and/or perceptually will be excluded from the study.

120 patients who applied to the clinic with the complaint of neck pain and were diagnosed with cervical hypolordosis by radiological examination will be included in the study. After giving the necessary verbal and written information about the study, a link will be sent to the phones of the patients whose informed consent was obtained. Patients will access evaluation questions and survey questions via this link. Personal information with the Sociodemographic Data Form prepared by us; pain severity by Visual Analogue Scale (VAS); phone addiction level with the Smartphone Addiction Questionnaire (Young Population); nomophobia levels will be evaluated with the Nomophobia Scale.

Sociodemographic Data Form: With the form, participants' name, surname, gender, age, height, weight, education status, marital status, smoking, alcohol, exercise habits, average daily sleep and smartphone usage time, screen usage time in the last 7 days, how many years smart phone usage information and contact information will be recorded.

Visual Analog Scale (VAS): participants are asked to select the point where they feel pain on a 10-centimeter (cm) horizontal line. 0 - no pain, 10 - unbearable pain. Pain conditions are evaluated separately at night, during activity and at rest.

Smartphone Addiction Questionnaire (Young Population): The scale consists of 33 questions and 7 sub-parameters. Sub-parameters Functioning Impairment, Withdrawal Symptom, Positive Expectation, Virtual Directed Relationship, Overuse, Social Network Addiction, and Physical are symptoms. As the score increases, the level of addiction increases. Nomophobia Scale: It has 20 items and 4 dimensions in total. These four dimensions, in order, are not being online, losing communication, not feeling comfortable, and not being able to access information. Each of the 20 questions in the 5-point Likert-type scale is scored by the participants as 1 point-strongly disagree, 7 points-strongly agree. If the total score is 20, it is graded as no nomophobia, 21-59 as mild nomophobia, 60-99 as moderate nomophobia, and 100-140 as extreme nomophobia.

Statistical analysis SPSS version 25 will be used in the analysis of the data. It will be evaluated whether the data are suitable for normal distribution. Descriptive statistics will be shown as mean ± standard deviation for variables with normal distribution, and median (min - max) for variables with non-normal distribution. Correlation tests will be used to check whether there is a relationship between the data.

For the relationship between independent variables, Spearman Correlation test or Pearson Correlation analysis will be performed according to the normal distribution and the level of significance will be accepted as p<0.05. If the correlation coefficient is r<0.2, it will be interpreted as very weak correlation or no correlation, between 0.2-0.4 as weak correlation, between 0.4-0.6 as moderate correlation, between 0.6-0.8 as high correlation and 0.8> as very high correlation.

Chronic neck pain is one of the most common musculoskeletal disorders. The cervical region contains many structures that can cause pain when damaged, such as muscles, ligaments, vertebrae, facet joints, intervertebral discs, spinal nerves. In addition, being the most mobile region of the vertebral column makes the cervical region vulnerable to possible traumas.

In the literature, it has been shown that long-term and repeated use of a smartphone while the neck is flexed causes neck pain. When using a smartphone, the device is usually held below eye level, one or both hands grasp the device, and the thumb is actively used to tap the screen and switch between apps. Prolonged protraction and flexion posture of the neck causes a spatial change between the spine and the line of gravity, causing overload in the muscles and connective tissues, leading to many problems such as discomfort, pain, reduction in cervical lordosis in smartphone users.

Technological developments in the last year have led to a significant increase in the use of mobile technology. According to the Household Information Technologies Usage Survey of the Turkish Statistical Institute, it was revealed that 96.9% of the households have mobile phones and smart phones in 2016. Especially the easy portability of smart phones, the increase in internet networks, and the easy access to information and entertainment content have increased the usage rates even more. Along with the Covid-19 Pandemic, young people, like all individuals in the society, had to stay away from their school, work and social circles within the scope of quarantine measures and have to stay at home. The use of on-line methods has increased in education and training activities, in the working system of many workplaces, in communication with family relatives and social environment. Whether this level of use has reached the level of addiction should be investigated. In addition to all these, the investigators observe that neck pain complaints increase due to the decrease in physical activity, the increase in the time spent with a smartphone, and the lack of attention to ergonomic principles during smartphone use. As far as the investigators know, there is no study in the literature examining the relationship between neck straightening, pain, phone addiction and nomophobia. Therefore, the investigators think that study will contribute to the literature.

Study Type

Observational

Enrollment (Actual)

120

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

    • Istanbul
      • Beylikdüzü, Istanbul, Turkey, 34500
        • Yasemin ŞAHBAZ

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 35 years (ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Patients who applied to the Department of Orthopedics and Traumatology of Beylikdüzü State Hospital with the complaint of neck pain and were diagnosed with cervical hypolordosis by radiological examination.

Description

Inclusion Criteria:

  • Patients between the ages of 18-35
  • Diagnosed with neck flattening
  • Patients who agreed to participate in the study

Exclusion Criteria:

  • Patients under the age of 18 and older than 35,
  • Who cannot cooperate verbally and/or auditory,
  • Who cannot cooperate psychologically and/or perceptually

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
Visual Analog Scale
Time Frame: through study completion, an average of 1 year
Participants are asked to select the point where they feel their pain on a 10-centimeter (cm) horizontal line. 0 - no pain, 10 - unbearable pain. Pain conditions are evaluated separately at night, during activity and at rest.
through study completion, an average of 1 year
Nomophobia
Time Frame: through study completion, an average of 1 year
It has 20 items and 4 dimensions in total. These four dimensions, in order, are not being online, losing communication, not feeling comfortable, and not being able to access information. Each of the 20 questions in the 5-point Likert-type scale is scored by the participants as 1 point - strongly disagree, 7 points - strongly agree. If the total score is 20, it is graded as no nomophobia, 21-59 as mild nomophobia, 60-99 as moderate nomophobia, 100-140 as extreme nomophobia.
through study completion, an average of 1 year
Smartphone Addiction Survey (Young Population)
Time Frame: through study completion, an average of 1 year
The scale consists of 33 questions and 7 sub-parameters in total. Sub-parameters Functioning Impairment, Withdrawal Symptom, Positive Expectation, Virtual Directed Relationship, Overuse, Social Network Addiction, and Physical are symptoms. As the score increases, the level of addiction increases.
through study completion, an average of 1 year

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Cervical Radiography
Time Frame: through study completion, an average of 1 year
C2-7 Cobb Angle
through study completion, an average of 1 year

Collaborators and Investigators

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

Investigators

  • Study Director: Yasemin ŞAHBAZ, Asis.Prof, University Beykent

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 1, 2021

Primary Completion (ACTUAL)

July 1, 2022

Study Completion (ACTUAL)

August 1, 2022

Study Registration Dates

First Submitted

November 1, 2021

First Submitted That Met QC Criteria

February 14, 2022

First Posted (ACTUAL)

February 16, 2022

Study Record Updates

Last Update Posted (ACTUAL)

September 29, 2022

Last Update Submitted That Met QC Criteria

September 28, 2022

Last Verified

September 1, 2022

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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