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Neck PainNCT04730960

Comparison of Cervical Region Characteristics of People With Smartphone Addiction

An observational study of Neck Pain and Postural; Defect, run by Hacettepe University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

In healthy participantsng adults, the anterior tilt position of the head and consequently flattening of the cervical lordosis may results in impaired neutral posture of the spine during daily long-term computer etc. use with today's technology. Read more about this study

Who is it for?
Ages 18 to 30 years
Conditions the study is for
Neck Pain, Postural; Defect, Young Adult
How many people
86 participants
Where
1 siteTurkey (Türkiye)
Study dates
15 Jul 2021to 5 Jan 2022
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 30 years
  • All sexes
  • Adult

Study population: Healthy patients between the ages of 18 and 30 without neck problems will be included in the study.

Who may be able to join

  • Being in the age range of 18-30,
  • Not having mental - cognitive problems,
  • Being a volunteer participant.

Who cannot join

  • Having any surgery on the vertebral column,
  • Having an inflammatory disease,
  • Having a rheumatological disease,
  • Having a history of malignancy,
  • Having congenital spinal cord anomalies, congenital and / or subsequent spinal deformities,
  • Having radiculopathy, myelopathy and / or other neurological disorders, vestibular disorders,
  • Having a history of acute trauma.

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Hacettepe University

    Ankara

Other trials in Turkey (Türkiye)

About this study

Official title: Comparison of Cervical Region Characteristics of People With Smartphone Addiction According to Gender

In healthy participantsng adults, the anterior tilt position of the head and consequently flattening of the cervical lordosis may results in impaired neutral posture of the spine during daily long-term computer etc. use with today's technology. In addition, the increasing use of smart phones may also promote this negative results. According to a study, the estimated total smartphone sales for 2012 was 660 million, but as of 2015, it is estimated that a total of one billion units worldwide. It is also thought that phone sales will continue to increase over the years, as it facilitates daily life activities.

As a result of our literature review, the investigators have not come across a study that evaluates demographic information such as the duration of using smartphones or computers, cervical position sense, neck muscle strength, physical activity and general psychological status, which the investigators think may affect the performance of deep cervical flexor muscles in healthy participantsng adults. With this study, it will be ensured that more information about the factors affecting the performance of deep cervical flexor muscles will be determined in advance and necessary steps will be taken to prevent the factors that may cause neck problems in the future.

Medical subject headings
Neck Pain

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT04730960
Study groupRoleWhat they receive
Study GroupHealthy patients between the ages of 18 and 30 without neck problems will be included in the study.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Muscle Strength Assessment

    The strength of the cervical flexor and extensor muscles will be measured with a digital hand dynamometer. While measuring with a dynamometer, the positions and methods of the fine muscle test defined by Lovett will be based on. Each muscle test with the dynamometer will be done three times. The subject will be given a break of at least one minute to rest between repetitions. The highest 3-repetitive results obtained as a result of these measurements will be recorded as the maximum power and in Newton (N) to be used in statistical analysis.

    Measured: 10-15 minutes

  2. Cervical Joint Range of Movement Assessment

    Cervical Range of Motion (CROM 3) device will be used for active evaluation of cervical range of motion. CROM 3 is a valid and reliable device . The CROM 3 instrument is a special version of the universal goniometer adapted to the cervical region, developed to evaluate cervical joint motion in 3 planes. Flexion and extension range of motion is measured on the first gravity-dependent quadrant on the side of the CROM 3 device. The gravity-dependent second quadrant CROM 3 device is located on the anterior surface and measures the degree of lateral flexion. The third quadrant is a compass dial on the upper surface of the CROM 3 device and measures the right and left rotation. In order for the compass dial to measure the degree of rotation accurately, magnetic field reinforcement, which is a part of the device, was applied to the shoulders of the subject. Flexion, extension, lateral flexion and rotation movements will be measured with the CROM 3 device.

    Measured: 10-15 minutes

  3. Cervical Joint Position Sense Assessment

    When evaluating joint position sense, 6 positions will be evaluated including flexion, extension, right and left lateral flexion, right and left rotation. CROM 3 device will be used while making measurements. When the subject starts the test, he will be told to sit upright in a comfortable position with the arms at the sides and look forward. The head of the subject will be brought to the targeted point, slowly and passively, up to 65 percent of the maximum range of motion he has, which was previously determined by the physiotherapist. The case will be passively held at the point reached for three seconds and will be told to feel position. Then the head of the subject will be brought back to the neutral position. Then he will be told to remember the phenomenon and passively come to the point brought. The degree of error between the point and the previously determined reference point will be recorded. This process will be repeated three times and the average value will be calculated.

    Measured: 10-15 minutes

  4. Smartphone Addiction Assessment

    Individuals' smartphone use will be evaluated with the Smartphone Addiction Scale. Kwon et al. The "Smartphone Usage Scale" developed by "Smartphone Usage Scale" is a 6 point Likert type scoring scale consisting of 33 items. Each item is evaluated as "1: Absolutely no" and "6: Absolutely yes". The total score in the scale, which was validated in Turkish, varies between 33-198, and as the score increases, it means increase in smartphone addiction. Daily life disorders consist of 6 subtitles: positive expectation, feeling of deprivation, virtual oriented relationship, overuse and endurance.

    Measured: 10-15 minutes

  5. Posture Assessment

    Individuals' head and shoulder posture will be evaluated by taking sagittal plan photographs; shoulder and head angles will be calculated. In previous studies, anterior tilt was defined as the angle between the line between the tragus and C7 and the line drawn in the vertical direction from C7 equal to or greater than 46 °. Shoulder protraction is defined as the angle between the line between the acromion and the line C7 and the line drawn vertically from C7 is equal to or greater than 52 °.Reflective markers will be placed on the dominant side ear (tragus), acromion and C7 spinous process; their places will be marked on the skin and in the photo. Individuals will be taught to position them with their feet shoulder-width apart, standing 40 cm in front of the wall, and moving their upper and lower extremities, in their own resting positions. In the sagittal plane, a high resolution digital camera will be placed on a tripod three meters away.

    Measured: 10-15 minutes

  6. Physical Activity Assessment

    Physical activity levels of individuals will be evaluated with IPAQ - short form. IPAQ - short form consists of 4 separate parts and 7 questions in total. This form contains questions about physical activities performed for at least 10 minutes in the last 7 days. The questionnaire determines how many days in the last week and how long for each day heavy physical activities, moderate intensity physical activities, walking and the time spent during the day without moving (sitting, lying, etc.). It is done by MET method to determine the level of physical activity. The IPAQ - short form has been validated in Turkish.

    Measured: 10-15 minutes

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted29 Jan 2021
  2. Study start15 Jul 2021
  3. Primary completion5 Dec 2021
  4. Study completion5 Jan 2022

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case crossover
Time perspective
Prospective
Enrolment
86 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04730960
Sponsor's protocol ID
SP123
Status last verified
May 2021
First submitted
26 Jan 2021
Last updated
26 Nov 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Neck Pain and Postural; Defect, run by Hacettepe University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 26 Nov 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Muscle Strength Assessment (time frame: 10-15 minutes). The study lists 6 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 Nov 2025.

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