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Clinical Trials/NCT06525376
NCT06525376CompletedNot Applicable

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

Deraya University1 site in 1 country150 target enrollmentStarted: July 1, 2024Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
150
Locations
1
Primary Endpoint
Cervical range of motion device (CROM)

Study Overview

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Investigator)

Eligibility Criteria

Ages
18 Years to 30 Years (Adult)
Sex
All
Accepts 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.

Outcomes

Primary Outcomes

Cervical range of motion device (CROM)

Time Frame: 6 weeks

The cervical range of motion (ROM) serves as a functional measure of one's capacity for head and neck movement

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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