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Validity and Reliability of Smartphone Inclinometer Application for Measurement of Cervical Range of Motion

Validity and Reliability of Smartphone Inclinometer Application for Measurement of Cervical Range of Motion: a Cross-sectional Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06525376
Enrollment
150
Registered
2024-07-29
Start date
2024-07-01
Completion date
2024-12-01
Last updated
2025-06-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Joint Function Disorder

Brief summary

Nowadays, smartphone technology provides opportunities for assessing and treating patients in clinical facilities and during the follow-up of the patient's progress. To date, many studies have assessed the validity and reliability of the smartphone application against universal goniometer for various joint motions, for instance, the spinal column, knee, and ankle. This study aims to determine the validity and reliability of smartphone inclinometer application for measurement of cervical region range of motion.

Interventions

DIAGNOSTIC_TESTsmartphone inclinometer application

an instrument for measuring angles of slope (or tilt), elevation, or depression of an object with respect to gravity.

Sponsors

Deraya University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

* Adults aged 18 to 33 years. * Both genders. * Subjects that are cooperative to follow my instructions

Exclusion criteria

* Subjects with severe spinal pathology. * Pregnancy and lactation. * Any musculoskeletal diseases that affect the cervical spine. * Any neurological diseases that affect the cervical spine. * History of trauma in the cervical spine. * Signs of cervical radiculopathy. * Signs of cervical myelopathy. * Signs of serious pathology. * subjects have a pacemaker or any other medical equipment that the magnet might have compromised.

Design outcomes

Primary

MeasureTime frameDescription
Cervical range of motion device (CROM)6 weeksThe cervical range of motion (ROM) serves as a functional measure of one's capacity for head and neck movement

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026