ClinicalTrials.gg
CompletedNCT05241743Updated Sep 29, 2022

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

An observational study in Neck Pain, sponsored by University of Beykent. Completed at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 35 Years. Per ClinicalTrials.gov, last updated 2022-09-29.

Sponsored by University of Beykent · Observational

Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
120
Ages
18 Years to 35 Years
Sex
All
01

Study summary

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.

Read the 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.

02

Conditions studied

  • Neck Pain

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Keywords

  • neck pain
  • Nomophobia
  • phone addiction
03

In context

Neck Pain

1,259 studies on the registry are indexed under Neck Pain; 256 are open to participants now.

This study's enrollment of 120 is above the median of 93 across 218 observational studies indexed under Neck Pain.

Browse Neck Pain studies →

Lead sponsor

University of Beykent is the lead sponsor of 56 studies on the registry; 15 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 35 Years
Sexes eligible
All
Accepts healthy volunteers
No
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.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

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

Exclusion criteria

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
05

Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
120 participants (actual)
Patient registry
No

Interventions

  • Otherradiological examination, pain, nomophobia, phone addiction

    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.

06

What researchers measure

Primary outcomes

  1. Visual Analog Scale

    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.

    Time frame: through study completion, an average of 1 year

  2. Nomophobia

    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.

    Time frame: through study completion, an average of 1 year

  3. Smartphone Addiction Survey (Young Population)

    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.

    Time frame: through study completion, an average of 1 year

Secondary outcomes

  1. Cervical Radiography

    C2-7 Cobb Angle

    Time frame: through study completion, an average of 1 year

07

Study locations

1 site
  • Yasemin ŞAHBAZ
    Beylikduzu, Istanbul 34500, Turkey (Türkiye)
08

References and documents

Publications

  • Reed MD, Van Nostran W. Assessing pain intensity with the visual analog scale: a plea for uniformity. J Clin Pharmacol. 2014 Mar;54(3):241-4. doi: 10.1002/jcph.250. Epub 2014 Jan 23. No abstract available. PubMed 24374753 ↗
  • Kwon M, Lee JY, Won WY, Park JW, Min JA, Hahn C, Gu X, Choi JH, Kim DJ. Development and validation of a smartphone addiction scale (SAS). PLoS One. 2013;8(2):e56936. doi: 10.1371/journal.pone.0056936. Epub 2013 Feb 27. PubMed 23468893 ↗
  • Lee S, Kang H, Shin G. Head flexion angle while using a smartphone. Ergonomics. 2015;58(2):220-6. doi: 10.1080/00140139.2014.967311. Epub 2014 Oct 17. PubMed 25323467 ↗
  • Eitivipart AC, Viriyarojanakul S, Redhead L. Musculoskeletal disorder and pain associated with smartphone use: A systematic review of biomechanical evidence. Hong Kong Physiother J. 2018 Dec;38(2):77-90. doi: 10.1142/S1013702518300010. Epub 2018 Aug 14. PubMed 30930581 ↗

Individual participant data

Plan to share: No

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Apr 2021 to primary completion in Jul 2022, 15 months.

How these figures are worked out, and which studies are left out of them.

Registered
Nov 1, 2021
First posted
Feb 16, 2022
StartActual
Apr 1, 2021
Primary completionActual
Jul 1, 2022
CompletionActual
Aug 1, 2022
Last update
Sep 29, 2022
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 29, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05241743
Lead sponsor
University of Beykent
Collaborators
Beylikduzu State Hospital, Bakirkoy Dr. Sadi Konuk Research and Training Hospital
Responsible party
Yasemin Şahbaz (doctoral lecturer, University of Beykent) — Principal investigator
First posted
Feb 16, 2022
Start date
Apr 1, 2021
Primary completion
Jul 1, 2022
Completion
Aug 1, 2022
Last update
Sep 29, 2022

Study contacts

Yasemin ŞAHBAZ, Asis.Prof
study director · University Beykent

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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