Joint Function DisorderNCT06525376
Validity and Reliability of Smartphone Inclinometer Application for Measurement of Cervical Range of Motion
A study testing smartphone inclinometer application in people with Joint Function Disorder, run by Deraya University at 1 site in Egypt.
Trial 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… Read more about this study
- Who is it for?
- Ages 18 to 30 yearsHealthy volunteers can take part
- Conditions the study is for
- Joint Function Disorder
- What is being tested?
- smartphone inclinometer application
- How many people
- 150 participants
- Where
- 1 siteEgypt
- Study dates
- 1 Jul 2024to 1 Dec 2024
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 30 years
- All sexes
- Healthy volunteers accepted
- Adult
Who may be able to join
- Adults aged 18 to 33 years.
- Both genders.
- Subjects that are cooperative to follow my instructions
Who cannot join
- 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.
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- Signs of cervical myelopathy.
- Signs of serious pathology.
- subjects have a pacemaker or any other medical equipment that the magnet might have compromised.
Trial locations and contacts
1 site in 1 country.
About this study
Official title: 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.
- Conditions
- Joint Function Disorder
- Being tested
- smartphone inclinometer application
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
smartphone inclinometer applicationDiagnostic test
an instrument for measuring angles of slope (or tilt), elevation, or depression of an object with respect to gravity.
What is being measured
The primary outcome is the main question the study is designed to answer.
Cervical range of motion device (CROM)
The cervical range of motion (ROM) serves as a functional measure of one's capacity for head and neck movement
Measured: 6 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted29 Jul 2024
- Study start1 Jul 2024
- Primary completion1 Oct 2024
- Study completion1 Dec 2024
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Joint Function DisorderStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind
- Who is masked
- Participant, Investigator
- Enrolment
- 150 participants (actual)
Sponsor and investigators
- Lead sponsor
- Deraya University
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06525376
- Sponsor's protocol ID
- Physical Therapy 2
- Status last verified
- Jun 2025
- First submitted
- 24 Jul 2024
- Last updated
- 26 Jun 2025
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 26 Jun 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Validity and Reliability of Smartphone Inclinometer Application for Measurement of Cervical Range of Motion: a Cross-sectional Study
- ClinicalTrials.gov ID
- NCT06525376
- Acronym / sponsor ID
- Physical Therapy 2
- Conditions
- Joint Function Disorder
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 150 participants (actual)
- Lead sponsor
- Deraya UniversityUniversity, hospital or other
- Study start
- 1 Jul 2024 (actual)
- Primary completion
- 1 Oct 2024 (actual)
- Study completion
- 1 Dec 2024 (actual)
- First posted
- 29 Jul 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (participant, investigator)
Who may qualify
- Ages
- 18 to 30 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (3 listed)
- Adults aged 18 to 33 years.
- Both genders.
- Subjects that are cooperative to follow my instructions
Key exclusion criteria (9 listed)
- 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.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| smartphone inclinometer applicationan instrument for measuring angles of slope (or tilt), elevation, or depression of an object with respect to gravity. | Diagnostic test | – |
Primary outcome
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
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 26 Jun 2025.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing smartphone inclinometer application in people with Joint Function Disorder, run by Deraya University at 1 site in Egypt.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 26 Jun 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Cervical range of motion device (CROM) (time frame: 6 weeks). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 Jun 2025.