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OpenTrials
Completed

NCT Number: NCT06598774

Cervical Parameters and Body Awareness in Relation to Smartphone Addiction

The study was planned as a observational, cross-sectional study

Completed

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Key information

Age range

18 year–25 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Atılım University

Ankara, Turkey (Türkiye)

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • being a smartphone user
  • being between the ages of 18 and 25

Exclusion criteria

  • neck pain
  • radicular pain
  • neurological symptoms
  • cervical surgery or cervical trauma

Treatment and study plan

Assessment of head posture:

Other

Head posture was assessed using photographic methods and craniovertebral angle

Assessment of Cervical Pain Pressure Threshold

Other

The cervical PPTs were assessed using a mechanical pressure algometer (Baseline Force Gauge Model 12-0304; Baseline, NY, USA).

Assessment of general cervical mobility

Other

Cervical mobility was assessed using the CROM (Cervical Range of Motion) deluxe device.

Assessment of upper cervical mobility

Other

It will be assessed using the CROM device and the flexion-rotation test.

Assessment of Body Awareness

Other

Body awareness will be assessed using a questionnaire designed to determine normal or abnormal sensitivity levels in body composition.

Primary outcomes

  1. Assessment of Body Awareness

    Time frame: Day 1

    Body awareness will be assessed using a questionnaire designed to determine normal or abnormal sensitivity levels in body composition. The questionnaire consists of four subgroups: 1) Changes in body processes, 2) Sleep-wake cycle, 3) Prediction of disease onset, and 4) Prediction of body responses, with a total of 18 items. Participants were asked to rate each item using a scale from 1 to 7. It has a minimum score of 18 and a maximum score of 126, with higher scores indicating greater body awareness. The validity and reliability of this questionnaire have been reported to be high.

  2. Assessment of head posture

    Time frame: Day 1

    Head posture will be assessed using photographic methods and craniovertebral angle. The craniovertebral angle is calculated as the angle between a horizontal line passing through C7 and a line extending from the tragus of the ear to C7 [23]. An angle less than 49 degrees indicates an anterior head position.

  3. Assessment of Cervical Pain Pressure Threshold (PPT)

    Time frame: Day 1

    The cervical PPTs will be assessed using a mechanical pressure algometer (Baseline Force Gauge Model 12-0304; Baseline, NY, USA). A force will be applied perpendicularly to a 0.5 cm² area at an approximate rate of 3 N/s. While the patient is seated, pressure is applied at the midpoint of the upper trapezius muscle, and 2 cm lateral to the C2 spinous process bilaterally [25]. For each area, two measurements are taken at intervals, and the average of these measurements is calculated to determine the final value.

  4. Assessment of general cervical mobility

    Time frame: Day 1

    Cervical mobility will assessed using the CROM (Cervical Range of Motion) deluxe device, developed by the University of Minnesota. The CROM is an inclinometer system that utilizes gravity and magnetic effects [26]. It is validated for accuracy and reliability. The device consists of two fixed inclinometers for the sagittal and frontal planes, a horizontal inclinometer with a magnetic needle mounted on the top of the device, a magnetic neck brace, a scale-equipped arm with a ruler mounted on the top, and a vertebra locator arm with a weighing system.

  5. Assessment of upper cervical mobility

    Time frame: Day 1

    The CROM device is securely attached to the participant's head while they lay supine on a treatment table. The evaluator asks the participant to relax while the neck is brought to its maximum cervical flexion. In the full flexion position, the head and neck are passively rotated as far as possible within the limits of comfortable pain or physiological stiffness. The procedure is repeated twice on each side with a 30-second rest between tests. The sensitivity of the flexion-rotation test was found to be 91%, its specificity 90%, and its overall diagnostic accuracy 91% . The cervical flexion-rotation test is an important tool in identifying movement impairment at the C1/2 segment and can be used accurately and reliably even by inexperienced examiners.

Sponsors and collaborators

Lead sponsor

Nagihan Acet

Other

Registry information

Official study title

Does Smartphone Addiction Affect Cervical Spine Mobility, Head Posture, Body Awareness, and Pain Pressure Threshold?

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Sep 19, 2024
Registry last updated
Nov 25, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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