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HealthyNCT07190937

Evaluation of the Angle of Head and Neck Flexion Forward During Mobile Phone Use

An observational study of Healthy, run by Kutahya Health Sciences 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

The aim of this study is to investigate the effect of smartphone use on head and neck flexion angle during sitting and standing positions. Read more about this study

Who is it for?
Ages 18 to 30 yearsHealthy volunteers can take part
Conditions the study is for
Healthy
How many people
30 participants
Where
1 siteTurkey (Türkiye)
Study dates
15 Feb 2025to 15 Jul 2025
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
  • Healthy volunteers accepted
  • Adult

Study population: Kutahya Health Sciences University, Faculty of Health Sciences, Department of Physiotherapy and Rehabilitation students

Who may be able to join

  • Being between the ages of 18 and 30
  • Using a smartphone for more than one hour per day

Who cannot join

  • Having a musculoskeletal, neurological, or mental disorder
  • Having had trauma or surgery in the neck, upper, or lower extremities

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Kutahya Health Sciences University

    Kütahya, Merkez, 43000

Other trials in Turkey (Türkiye)

About this study

Official title: Evaluation of Head and Neck Flexion Angle While Using a Smartphone

The aim of this study is to investigate the effect of smartphone use on head and neck flexion angle during sitting and standing positions.

Read the detailed description

With the increasing duration of smartphone use, concerns about musculoskeletal problems related to intensive use have also increased. Studies have shown that smartphone users tend to report pain symptoms in the neck and shoulder girdle, and that the severity of symptoms increases with the duration of smartphone use. Smartphone users are exposed to prolonged head and neck flexion during activities such as watching videos and texting. Maintaining this static posture for extended periods of time results in changes in cervical flexion angles. Numerous studies in the literature have found that neck and head flexion angles increase with smartphone use, and these angles increase with the duration of smartphone use. Studies in the literature have reported that head flexion angles typically range from 33 to 45 degrees during smartphone use. Smartphones, with their smaller screens, cause greater flexion angles in the cervical region compared to computer and tablet use. Therefore, it is important to assess head and neck flexion angles during smartphone use. Based on these assessments, it should be recommended that individuals choose appropriate positions. The study will include 30 individuals between the ages of 18 and 30, who use smartphones for more than one hour per day and for at least one year, and who have no physical disabilities. Before data collection begins, each participant who agrees to participate will sign a voluntary consent form. After inquiring about their demographic characteristics, smartphone usage duration, and medical history, each participant will watch a video using a designated smartphone in a laboratory setting, while their head and neck flexion angle will be measured using Kinovea Software. A 6.67-inch Xiaomi Mi 10T Pro smartphone will be used to watch the videos. The video will be a 5-minute video on water consumption (https://www.youtube.com/watch?v=nqZ0b6X_6Vs), and the participants' entire video will be recorded. The video will be watched in two different postures: standing and sitting in a backless chair. To minimize the effects of fatigue, participants will be given a 5-minute rest period between the two postures. Assessments will be conducted first while sitting and then while standing. Reference points (right lateral canthus, right tragus, C7 spinous process) will be marked with an anti-allergic erasable board marker to determine head and neck flexion angles. The angle between the line between the tragus and C7 spinous process and the vertical line passing through the C7 spinous process will be determined as the neck flexion angle. The angle between the line between the canthus and tragus and the vertical line passing through the tragus will be determined as the head flexion angle. The camera will be placed on a tripod 80 cm away from the participant, perpendicular to the sagittal plane of the participant, at a height corresponding to the level of the C7 spinous process. Participants will be instructed not to make any upper extremity movements while sitting. While standing, participants will be instructed not to reveal any movement in their lower extremities. Participants will be instructed to hold the smartphone with both hands during both postures. Before starting the study, a pilot study with five participants will be conducted to validate and calibrate the procedure. The changes in head and neck flexion angles for each participant between seconds 0, 150, and 300, and the average head and neck angle over the 5-minute period will be calculated using Kinovea Software.

Conditions
Healthy
Keywords
kinovea, posture, smartphone use, cervical flexion angle, head flexion angle

What participants receive

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

Study groups in NCT07190937
Study groupRoleWhat they receive
individualsIndividuals between the ages of 18-30 who have used a smartphone for at least 1 year

What is being measured

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

  1. Kinovea Software

    Calculation of head and neck flexion angle using Kinovea Software

    Measured: Baseline (First assessment)

Timeline

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

  1. First posted24 Sep 2025
  2. Study start15 Feb 2025
  3. Primary completion15 Jun 2025
  4. Study completion15 Jul 2025

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
Other
Time perspective
Cross-sectional
Enrolment
30 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07190937
Sponsor's protocol ID
2024/11-06
Status last verified
Sep 2025
First submitted
15 Sep 2025
Last updated
30 Sep 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Healthy, run by Kutahya Health Sciences 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 2 inclusion and 2 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 30 Sep 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?

Kinovea Software (time frame: Baseline (First assessment)). 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 30 Sep 2025.

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