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Completed

NCT Number: NCT07680231

Smartphone Versus Back Range of Motion: Validity and Reliability in Lumbar Range of Motion Assessment

This study aims to investigate the clinimetric properties of the iPhone Level application as a suitable alternative to the Back Range of Motion device in assessing lumbar range of motion, including flexion, extension, and lateral flexion.

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Key information

Age range

18 year–25 year

Sex eligibility

Male

Study type

Observational

Primary location

Cairo University

Giza, 12613, Egypt

About this study

Range of motion measurement is vital in physiotherapy for assessing deficits, establishing diagnoses, and planning interventions. Digital advancements now allow Range of motion assessment through devices and applications, such as the back range of motion, which is a gold standard for measuring lateral flexion due to its validity. Furthermore, studies indicate that the iPhone Level app effectively measures Range of motion in various joints, demonstrating good reliability and validity. This study aims to evaluate the reliability and concurrent validity of the iPhone Level application specifically for measuring lumbar flexion, extension, and side bending Range of motion.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Age 18-25 years old
  • Healthy Male university students
  • All participants have normal BMI

Exclusion criteria

  • Recent back, pelvic, or abdominal surgeries, traumatic injury to the back .
  • Lower limb deformities, e.g., leg length discrepancy.
  • Adolescent idiopathic scoliosis
  • Any overweight or obese participants

Treatment and study plan

easement tool 1 - BROM device

Device

The BROM device consists of an inclinometer for measuring sagittal plane motions (flexion/extension) and a gravity goniometer/compass for lateral flexion. Participants stood upright with feet apart. Measurements were taken for flexion, extension, and bilateral lateral flexion. Three trials per movement were recorded and averaged.

Measurement tool 2 - iPhone level application

Device

The iPhone Level app was placed at T12-L1 and S1-S2 spinal levels. Lumbar flexion and extension ROM was calculated by subtracting S1-S2 angle from T12-L1 angle. For lateral flexion, the app was placed at T12 and S2 and the same subtraction method applied. Three trials per movement were recorded and averaged.

Primary outcomes

  1. assessment of flexion and extension range of motion using inclinometer

    Time frame: at baseline

    During lumbar flexion and extension measurements using the Back Range of Motion (BROM) device, patients stand upright with extended knees and feet approximately 17 centimeters apart. For flexion, they bend forward to touch the floor, while for extension, they bend backward with crossed arms. An inclinometer is secured over the sacrum, and its position is centered to record readings in degrees. An L-shaped slide arm measures the distance between the T12 and S1 spinous processes. The device isolates lumbar motion from pelvic motion, and the stationary flexion/extension unit minimizes errors, enhancing measurement accuracy.

  2. assessment of lateral flexion range of motion using inclinometer

    Time frame: at baseline

    For measuring lumbar lateral flexion, the subject's sides are parallel to a wall to prevent compensatory forward trunk flexion. An inclinometer is secured over the sacral region at S1, using a belt for stability. A gravity goniometer is placed on the upper thoracic region to capture trunk angular displacement during side bending. The inclinometer is levelled and zeroed before movement, allowing for precise measurement of lateral lumbar movement while reducing thoracic and pelvic compensations. Accurate placement of the device is essential for reliable results. The subject slides their hand down the thigh, keeping weight on the opposite leg to ensure the measurement reflects true lateral flexion.measures]

Secondary outcomes

  1. assessment of flexion and extension range of motion using smartphone

    Time frame: at baseline

    To measure lumbar flexion range of motion (ROM) using the iPhone Level app, participants are positioned standing upright with feet shoulder-width apart. T12-L1 and S1-S2 spinal levels are identified through palpation and marked on the skin. The iPhone is placed at these levels to record angles during maximum lumbar flexion. Total lumbar flexion ROM is calculated by subtracting the angle at S1-S2 from T12-L1. Subjects perform maximum lumbar flexion and extension with straight knees, and measurements are taken across three trials.

  2. assessment of lateral flexion range of motion using smartphone

    Time frame: at baseline

    During the measurement of lumbar side bending using the iPhone Level application, the subject will stand in a neutral upright position with feet shoulder-width apart and hands placed on the hips to prevent arm movement from influencing the measurement. The spinous processes of T12 and S2 are identified and marked on the skin. The iPhone is first placed and zeroed at the T12 level, and the subject is instructed to bend sideways (toward one side) as far as possible without lifting the heels or rotating the trunk. The device remains aligned at T12 to capture the angular displacement. The same procedure is repeated with the device positioned at S2, and the final lumbar side bending range of motion is calculated by subtracting the angle at S2 (pelvic movement) from that at T12 (trunk movement). This method isolates lumbar lateral flexion and has shown good reliability and validity in clinical settings

Sponsors and collaborators

Lead sponsor

Cairo University

Other

Collaborators

  • October University for Modern Sciences and Arts

Registry information

Official study title

Clinimetric Properties of Smartphone Application as a Suitable Alternative to Back Range of Motion Device in Assessing the Back Range of Motion

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Jul 2, 2026
Registry last updated
Jul 2, 2026

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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