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Reliability Study of 3D Sensor-Based Mobility Test for Static and Dynamic Posture Evaluation in Humans

Reliability Study of 3D Sensor-Based Mobility Test for Static and Dynamic Posture Evaluation in Humans

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0010075
Enrollment
28
Registered
2024-12-20
Start date
2024-10-15
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

None listed

Interventions

Medical Device : Participants underwent a single-session assessment using the iBalance device, a 3D sensor-based motion evaluation system. During the assessment, both static and dynamic postures were

Sponsors

Kyung Hee University Oriental Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Healthy Individuals 1. Adults aged 19 years or older who voluntarily decide to participate in this clinical study and sign the informed consent form. 2. Individuals who can perform the required movements for the study without difficulty. Chronic Neck Pain 1. Individuals experiencing neck pain for 3 months or longer. 2. Individuals reporting an average neck pain score of 3 or higher on the Numerical Rating Scale (NRS) in the past week. 3. Adults aged 19 years or older who voluntarily decide to participate in this clinical study and sign the informed consent form. Chronic Low Back Pain 1. Individuals experiencing low back pain for 3 months or longer. 2. Individuals reporting an average low back pain score of 3 or higher on the Numerical Rating Scale (NRS) in the past week. 3. Adults aged 19 years or older who voluntarily decide to participate in this clinical study and sign the informed consent form. Degenerative Knee Osteoarthritis 1. Individuals experiencing knee pain for 3 months or longer. 2. Individuals meeting the diagnostic criteria for degenerative knee osteoarthritis according to the guidelines of the American College of Rheumatology (ACR). 3. Individuals with Kellgren-Lawrence grade ?-? findings confirmed by X-ray taken within the past year. 4. Individuals with ultrasound findings of degenerative changes in cartilage, osteophytes, or medial meniscal extrusion (MME), which are indicative of degenerative knee osteoarthritis. 5. Adults aged 19 years or older who voluntarily decide to participate in this clinical study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: Healthy Individuals 1. Individuals diagnosed with joint or spinal diseases and undergoing treatment, or those with pain and functional disabilities. 2. Individuals who are expected to have difficulty adhering to the clinical study schedule. 3. Other individuals deemed unsuitable for participation by the investigator. Chronic Neck Pain 1. Individuals who have experienced pain in areas other than the neck within the past 3 months, reporting an average NRS score of 3 or higher in the past week, or those receiving medical treatment for these areas. 2. Individuals who are expected to have difficulty adhering to the clinical study schedule. 3. Other individuals deemed unsuitable for participation by the investigator. Chronic Low Back Pain 1. Individuals who have experienced pain in areas other than the low back within the past 3 months, reporting an average NRS score of 3 or higher in the past week, or those receiving medical treatment for these areas. 2. Individuals who are expected to have difficulty adhering to the clinical study schedule. 3. Other individuals deemed unsuitable for participation by the investigator. Degenerative Knee Osteoarthritis 1. Individuals who have experienced pain in areas other than the knee within the past 3 months, reporting an average NRS score of 3 or higher in the past week, or those receiving medical treatment for these areas. 2. Individuals who are expected to have difficulty adhering to the clinical study schedule. 3. Other individuals deemed unsuitable for participation by the investigator.

Design outcomes

Primary

MeasureTime frame
Relative reliability (Intraclass Correlation Coefficient, ICC) of angles, lengths, angular velocities, and position values for each movement.

Secondary

MeasureTime frame
Absolute reliability (Standard Error of Measurement (SEM)) of angles, lengths, angular velocities, and position values for each movement.;Absolute reliability (Minimal Detectable Change (MDC)) of angles, lengths, angular velocities, and position values for each movement.;Absolute reliability (Limits of Agreement (LOA)) of angles, lengths, angular velocities, and position values for each movement.

Countries

Korea, Republic of

Contacts

Public ContactSuji Lee

Kyung Hee University Oriental Medical Center

sjstarry41@naver.com+82-2-958-9202

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026