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Neck Discomfort During Smartphone UseNCT07907549

Content Interest, Neck Posture, and Discomfort During Smartphone Use

A study testing Preferred/High-Interest Smartphone Video Viewing and Neutral/Lower-Interest Smartphone Video Viewing in people with Neck Discomfort During Smartphone Use, run by Karabuk University at 1 site in Turkey (Türkiye).

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

This study will examine whether personal interest in smartphone video content changes neck discomfort, posture, and pressure pain sensitivity in young adults. One hundred regular smartphone users aged 18 to 30 years will complete two 30-minute video-viewing sessions, separated by 48 to 72 hours. Read more about this study

Who is it for?
Ages 18 to 30 yearsHealthy volunteers can take part
Conditions the study is for
Neck Discomfort During Smartphone Use
What is being tested?
Preferred/High-Interest Smartphone Video Viewing and Neutral/Lower-Interest Smartphone Video Viewing
Could I receive a placebo?
No, everyone receives an active treatment
How many people
100 participants
Where
1 siteTurkey (Türkiye)
Study dates
15 Nov 2026to 31 Mar 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

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

Who may be able to join

  • Aged 18-30 years.
  • Regular smartphone user and willing to attend both experimental sessions.
  • Able to understand and follow study instructions and provide written informed consent.
  • No diagnosed serious cervical pathology. Occasional mild, transient neck or shoulder discomfort after prolonged smartphone use does not preclude participation.

Who cannot join

  • Serious cervical spine or shoulder trauma or surgery within the previous six months.
  • Active neurological, rheumatological, or serious musculoskeletal disease.
  • Acute neck/shoulder pain on the assessment day or baseline neck discomfort greater than 2 on a 0-10 scale.
  • Recent analgesic use that could affect measurement, or an acute health condition preventing safe participation.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Ece Acar, PhD, PT contact

+905457925035

eceacar@karabuk.edu.tr

Turkey (Türkiye)1 site
  • Karabuk University, Faculty of Health Sciences, Department of Physiotherapy and Rehabilitation

    Karabük, Karabük Province

    Ece Acar, PhD, PT, +905457925035, eceacar@karabuk.edu.tr

Other trials in Turkey (Türkiye)

About this study

Official title: Content Interest Level, Neck Posture, and Perceived Discomfort During Smartphone Use: A Randomized Crossover Study

This study will examine whether personal interest in smartphone video content changes neck discomfort, posture, and pressure pain sensitivity in young adults. One hundred regular smartphone users aged 18 to 30 years will complete two 30-minute video-viewing sessions, separated by 48 to 72 hours. One session will use personally preferred, high-interest content and the other neutral, lower-interest content. The order will be randomly assigned. The same study phone, stand, seating, and viewing setup will be used in both sessions. Neck and shoulder discomfort will be recorded during viewing, neck and trunk posture will be measured from video, and pressure pain threshold will be assessed before and after viewing. Engagement, enjoyment, and emotional responses will also be measured. The main comparison is neck discomfort at minute 30 between the two content conditions.

Read the detailed description

This is a single-center, two-condition, two-period randomized crossover experiment at Karabuk University, Faculty of Health Sciences, Department of Physiotherapy and Rehabilitation. One hundred participants will be allocated 1:1 to sequence AB or BA. A is preferred/high-interest video content; B is neutral/lower-interest content. Sequence allocation will be computer-generated by a researcher not involved in measurement and concealed in numbered sealed envelopes. Sessions will be separated by 48-72 hours and scheduled at similar times of day where possible.

A separate preparatory pilot involving up to 12 volunteers will test workflow and technical procedures. Pilot observations will not enter the main hypothesis analyses or the main enrollment target of 100. Substantial protocol changes after the pilot will require an ethics amendment before the main study.

Videos will be selected from a standardized pool matched as closely as possible for duration, resolution, volume, subtitles, and presentation. After short previews, interest/enjoyment ratings will identify preferred/high-interest and lower-interest content that does not evoke negative emotion. Violent, frightening, sexual, or strongly negative material will not be used. Both conditions involve video viewing only.

Participants will sit comfortably in an adjustable chair with back support and use the same study smartphone and adjustable stand. Screen position, distance, brightness, sound, room lighting, seating, and camera setup will be reproduced across sessions. Natural head and trunk movements will be allowed during each 30-minute session.

Neck and bilateral shoulder discomfort will be recorded at baseline and minutes 10, 20, and 30 using the 0-10 Borg CR-10 discomfort scale. The primary endpoint is neck discomfort at minute 30. Sagittal video-photogrammetry will assess neck and trunk angles at minutes 0, 5, 10, 15, 20, 25, and 30. Markers will be placed at the tragus, C7, T12, and greater trochanter. Neck flexion is defined by the tragus-C7 line relative to vertical; trunk angle is formed by the C7-T12 and T12-greater trochanter lines. Kinovea will be used for coded-image analysis by a trained assessor who will be unaware of the content condition where possible. Participants cannot be blinded to their own preferences.

Digital algometry will measure pressure pain threshold bilaterally at the upper trapezius and at the dominant tibialis anterior before and immediately after viewing. A 1 cm2 probe will apply pressure at approximately 30 kPa/s, stopping at first pain. Three measurements per site will be averaged, with 30-60 seconds between measurements. Measurement order will be maintained across sessions.

The Turkish Extended Nordic Musculoskeletal Questionnaire will describe baseline symptoms. End-of-session assessments will include the Turkish Flow Short Scale, interest/enjoyment subscale of the Turkish Intrinsic Motivation Inventory, and Self-Assessment Manikin valence and arousal ratings. Baseline sleep, recent intense physical activity, caffeine, analgesic use, and discomfort will be recorded to assess session comparability and deviations.

Mixed-effects models will include condition, time, condition-by-time, period, and sequence, with participant as a random effect. The primary analysis compares minute-30 neck discomfort within participants. Additional models will include neck and trunk angles to explore the relationship independent of measured postural exposure. Pressure pain threshold will be examined with condition-by-time (pre/post) interaction. Effect sizes and 95% confidence intervals will be reported with two-sided alpha 0.05.

Participants may stop at any time. Marked pain, dizziness, numbness/tingling, visual discomfort, or unwillingness to continue will end the task immediately. All data and images will be coded. Identifiable images will not be published or presented without separate explicit written permission.

Being tested
Preferred/High-Interest Smartphone Video Viewing, Neutral/Lower-Interest Smartphone Video Viewing

What participants receive

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

  • Preferred/High-Interest Smartphone Video ViewingBehavioural

    Thirty minutes of seated viewing on a standardized study smartphone and adjustable stand. Content is selected from a standardized pool after preview-based interest/enjoyment ratings, choosing personally preferred/high-interest material without strongly negative emotional content. Device, sound, screen brightness, seating, viewing position, and environment are matched to the neutral condition.

  • Neutral/Lower-Interest Smartphone Video ViewingBehavioural

    Thirty minutes of seated video viewing using lower-interest content from the same standardized pool, selected to avoid negative emotion. Duration, resolution, volume, subtitles, presentation, smartphone, stand, seating, viewing position, brightness, and room setup are matched as closely as possible to the preferred/high-interest condition.

Study groups in NCT07907549
Study groupRoleWhat they receive
Sequence AB: High-Interest Then Neutral ContentExperimentalParticipants first view preferred/high-interest video content for 30 minutes, then neutral/lower-interest content for 30 minutes in the second session after a 48-72-hour interval. Both sessions use the same study smartphone, stand, chair, and viewing setup.
Receives: Behavioral: Preferred/High-Interest Smartphone Video Viewing; Behavioral: Neutral/Lower-Interest Smartphone Video Viewing
Sequence BA: Neutral Then High-Interest ContentExperimentalParticipants first view neutral/lower-interest video content for 30 minutes, then preferred/high-interest content for 30 minutes in the second session after a 48-72-hour interval. Both sessions use the same study smartphone, stand, chair, and viewing setup.
Receives: Behavioral: Preferred/High-Interest Smartphone Video Viewing; Behavioral: Neutral/Lower-Interest Smartphone Video Viewing

What is being measured

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

  1. Neck Discomfort at Minute 30

    Perceived neck discomfort measured with the 0-10 Borg CR-10 discomfort scale, where 0 indicates no discomfort and higher scores indicate greater discomfort. The primary endpoint is the within-participant difference between preferred/high-interest and neutral/lower-interest content conditions at minute 30.

    Measured: At minute 30 of each of two sessions, separated by 48-72 hours

Secondary outcomes (7)
  1. Neck Discomfort Over Time

    Repeated perceived neck discomfort on the 0-10 Borg CR-10 scale. Higher values indicate greater discomfort.

    Measured: Baseline and minutes 10, 20, and 30 in each session; sessions 48-72 hours apart

  2. Right and Left Shoulder Discomfort

    Right and left shoulder discomfort measured separately using the 0-10 Borg CR-10 scale. Higher values indicate greater discomfort; sides are analyzed separately.

    Measured: Baseline and minutes 10, 20, and 30 in each session; sessions 48-72 hours apart

  3. Neck Flexion Angle

    Sagittal neck flexion angle in degrees between the tragus-C7 line and vertical, measured from standardized video frames using Kinovea.

    Measured: Minutes 0, 5, 10, 15, 20, 25, and 30 of each session; sessions 48-72 hours apart

  4. Trunk Angle

    Sagittal trunk angle in degrees formed by the C7-T12 and T12-greater trochanter lines, measured using Kinovea from standardized video frames.

    Measured: Minutes 0, 5, 10, 15, 20, 25, and 30 of each session; sessions 48-72 hours apart

  5. Task Engagement and Flow

    Task engagement and flow assessed with the Turkish Flow Short Scale. The flow score reflects absorption and fluency during the video-viewing task; higher flow scores indicate greater flow experience.

    Measured: Immediately after each 30-minute session; sessions 48-72 hours apart

  6. Interest and Enjoyment

    Interest/enjoyment assessed with the interest/enjoyment subscale of the Turkish Intrinsic Motivation Inventory. Higher scores indicate greater intrinsic interest and enjoyment; used as a manipulation check.

    Measured: Immediately after each 30-minute session; sessions 48-72 hours apart

  7. Emotional Valence and Arousal

    Self-Assessment Manikin pictorial ratings of emotional valence and arousal, reported separately. Valence reflects unpleasant-to-pleasant affect; arousal reflects calm-to-excited activation. Used to characterize the emotional response to content.

    Measured: Immediately after each 30-minute session; sessions 48-72 hours apart

Timeline

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

  1. First posted30 Oct 2026
  2. Study start15 Nov 2026 (estimated)
  3. Primary completion31 Mar 2027 (estimated)
  4. Study completion31 Mar 2027 (estimated)

Resources

More details

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

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Basic science
Allocation
Randomised
Intervention model
Crossover
Model description
Two-condition, two-period AB/BA crossover. Participants are randomized 1:1 to preferred/high-interest then neutral/lower-interest content, or the reverse sequence. Each session lasts 30 minutes, separated by 48-72 hours. Each participant receives both conditions and serves as their own control.
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
100 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07907549
Sponsor's protocol ID
KBU-PHONE-INTEREST-2026
Status last verified
Oct 2026
First submitted
24 Oct 2026
Last updated
30 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A study testing Preferred/High-Interest Smartphone Video Viewing and Neutral/Lower-Interest Smartphone Video Viewing in people with Neck Discomfort During Smartphone Use, run by Karabuk 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 4 inclusion and 4 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: opening soon, as of the sponsor's last update on 30 Oct 2026. 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?

This study is still under way. Results are not available in the source record yet.

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

Contact Ece Acar, PhD, PT (+905457925035, eceacar@karabuk.edu.tr), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Neck Discomfort at Minute 30 (time frame: At minute 30 of each of two sessions, separated by 48-72 hours). 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 Oct 2026.

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