- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06525376
Validity and Reliability of Smartphone Inclinometer Application for Measurement of Cervical Range of Motion
June 24, 2025 updated by: Deraya University
Validity and Reliability of Smartphone Inclinometer Application for Measurement of Cervical Range of Motion: a Cross-sectional Study
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 Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
150
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Minya, Egypt, 05673
- Deraya university
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Description
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.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
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
|
6 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
July 1, 2024
Primary Completion (Actual)
October 1, 2024
Study Completion (Actual)
December 1, 2024
Study Registration Dates
First Submitted
July 24, 2024
First Submitted That Met QC Criteria
July 24, 2024
First Posted (Actual)
July 29, 2024
Study Record Updates
Last Update Posted (Actual)
June 26, 2025
Last Update Submitted That Met QC Criteria
June 24, 2025
Last Verified
June 1, 2025
More Information
Terms related to this study
Other Study ID Numbers
- Physical Therapy 2
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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