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Not yet recruitingNCT07907549Updated Oct 30, 2026

Content Interest, Neck Posture, and Discomfort During Smartphone Use

An interventional study of Preferred/High-Interest Smartphone Video Viewing and Neutral/Lower-Interest Smartphone Video Viewing in Neck Discomfort During Smartphone Use, sponsored by Karabuk University. Not yet recruiting at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 30 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-30.

Sponsored by Karabuk University · Not applicable, Interventional, and Basic science

Updated Oct 30, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
100
Allocation
Randomized
Ages
18 Years to 30 Years
Sex
All
01

Study 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. 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.

02

Conditions studied

  • Neck Discomfort During Smartphone Use
03

In context

Lead sponsor

Karabuk University is the lead sponsor of 142 studies on the registry; 39 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 30 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

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

  • 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.

Exclusion criteria

Exclusion Criteria:

  • 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.
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Single (Outcomes assessor)
Enrollment
100 participants (estimated)

Study arms

  • Experimental
    Sequence AB: High-Interest Then Neutral Content

    Participants 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.

    Behavioral: Preferred/High-Interest Smartphone Video Viewing · Behavioral: Neutral/Lower-Interest Smartphone Video Viewing

  • Experimental
    Sequence BA: Neutral Then High-Interest Content

    Participants 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.

    Behavioral: Preferred/High-Interest Smartphone Video Viewing · Behavioral: Neutral/Lower-Interest Smartphone Video Viewing

Interventions

  • BehavioralPreferred/High-Interest Smartphone Video Viewing

    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.

  • BehavioralNeutral/Lower-Interest Smartphone Video Viewing

    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.

06

What researchers measure

Primary outcomes

  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.

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

Secondary outcomes

  1. Neck Discomfort Over Time

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

    Time frame: 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.

    Time frame: 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.

    Time frame: 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.

    Time frame: 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.

    Time frame: 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.

    Time frame: 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.

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

Other outcomes

  1. Pressure Pain Threshold

    Exploratory mechanistic outcome measured in kPa with calibrated digital algometry at the right and left upper trapezius and dominant tibialis anterior. A 1 cm2 probe is applied perpendicular to the skin at approximately 30 kPa/s until first pain. Three readings per site are averaged, with 30-60 seconds between readings. Higher values indicate lower pressure pain sensitivity. Sites are analyzed separately.

    Time frame: Before and immediately after each 30-minute session; sessions separated by 48-72 hours

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 30, 2026
Show all 1 update
  1. Oct 30, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07907549
Lead sponsor
Karabuk University
Responsible party
Ece ACAR (Assistant Professor, Principal Investigator, Karabuk University) — Principal investigator
First posted
Oct 30, 2026
Start date
Nov 15, 2026 (estimated)
Primary completion
Mar 31, 2027 (estimated)
Completion
Mar 31, 2027 (estimated)
Last update
Oct 30, 2026

Study contacts

Ece Acar, PhD, PT
Contact
eceacar@karabuk.edu.tr
+905457925035
Ece Acar, PhD, PT
principal investigator · Karabuk University

Oversight

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

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