- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07669428
Artificial Intelligence-Based Postural Feedback for Scoliosis
June 22, 2026 updated by: Rommanee Rojasavastera, Mahidol University
The Effect of Artificial Intelligence-Based Postural Feedback on Posture Correction in Idiopathic Scoliosis Patients
Due to advancements in technology, Posture-Analyzing and Virtual Reconstructing (PAViR) systems were developed.
They used Red-Green-Blue-Depth camera sensors and artificial intelligence to evaluate human posture alignment, muscle balance, and movement without the use of radiation or physical markers.
This technology served as a portable, X-ray-like device that was safe and user-friendly, providing detailed views of bone and muscle models alongside easy-to-understand 3D visualizations.
However, how to utilize the data obtained from PAViR to support traditional treatment remained unclear.
To fill this gap, this study aimed to investigate the effects of AI-based postural feedback on posture correction in patients with idiopathic scoliosis.
Study Overview
Status
Not yet recruiting
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
30
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 Contact
- Name: Rommanee Rojasavastera, M.Sc.
- Phone Number: +66837830777
- Email: rommanee.roj@mahidol.ac.th
Study Locations
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Changwat Nakhon Pathom
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Salaya, Changwat Nakhon Pathom, Thailand, 73170
- Faculty of Physical Therapy, Mahidol University
-
Contact:
- Rommanee Rojasavastera, M.Sc.
- Phone Number: +66837830777
- Email: rommanee.roj@mahidol.ac.th
-
-
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
- Child
- Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Diagnosis of adolescent idiopathic scoliosis (AIS) by a physician.
- Aged between 10 and 18 years.
- Cobb angle between 10 and 40 degrees.
Exclusion Criteria:
- Leg length discrepancy greater than 2 cm, measured from the anterior superior iliac spine (ASIS) to the lateral malleolus.
- Previous history of spinal surgery.
- Musculoskeletal or neurological injuries that affect balance and gait.
- Inability to follow the research procedures.
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: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: AI-Based Postural Feedback Group
Participants in the experimental group received postural feedback via the PAViR system, integrated with posture correction exercises and physical therapy for scoliosis.
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The physical therapist reported the findings from the PAViR system to the participants during a 10-minute session.
Data regarding skeletal alignment and muscle imbalances were provided to enhance participants' self-awareness of their specific postural issues.
Furthermore, these insights were integrated into the subsequent training sessions for the experimental group.
The physical therapist conducted 60-minute sessions.
These sessions were grounded in the principles of the Schroth Method and Physiotherapeutic Scoliosis-Specific Exercises (PSSE).
|
|
Active Comparator: Conventional Postural Feedback Group
Participants in the control group received the same exercise and therapy sessions, but without the postural feedback provided by the PAViR system.
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The physical therapist conducted 60-minute sessions.
These sessions were grounded in the principles of the Schroth Method and Physiotherapeutic Scoliosis-Specific Exercises (PSSE).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
REEDCO postural score
Time Frame: before and immediately after intervention
|
The REEDCO Posture Assessment was used to evaluate postural scores during comfortable standing and postural self-correction.
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before and immediately after intervention
|
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Angle of trunk rotation
Time Frame: before and immediately after intervention
|
A scoliometer was used to evaluate the angle of trunk rotation during Adam's Forward Bend Test.
|
before and immediately after intervention
|
|
Postural Variables Derived from a 3D Motion Analysis System
Time Frame: before and immediately after intervention
|
A 3D motion analysis system (VICON Motion Systems Ltd., Oxford, UK) was used to evaluate postural variables during comfortable standing, postural self-correction, and the Adam's Forward Bend Test.
|
before and immediately after intervention
|
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Postural Variables Derived from a PAViR System
Time Frame: before and immediately after intervention
|
A PAViR system (MGsolutions Inc., Seoul, South Korea) was used to evaluate postural variables during comfortable standing, postural self-correction, and the Adam's Forward Bend Test.
|
before and immediately after intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Illness Perception
Time Frame: before and immediately after intervention
|
The Brief Illness Perception Questionnaire (IPQ-B) was an accurate and valid assessment tool to measure and monitor illness perceptions.
It consisted of nine items rated on a scale from 0 (minimum) to 10 (maximum).
The first five assessed cognitive perceptions such as the effect on life (item 1); duration of illness (item 2); control over illness (item 3); beliefs about the effectiveness of treatment (item 4); and experience of symptoms (item 5).
Items 6 and 8 assessed emotional aspects, which included concern about the illness and a multifaceted question about mood.
Item 7 assessed the degree of understanding of the illness.
The final item was open-ended, asking respondents to rank the three most important factors causing their illness.
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before and immediately after intervention
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Exercise Motivation
Time Frame: before and immediately after intervention
|
The Behavioral Regulation in Exercise Questionnaire-2 (BREQ-2) was a 19-item questionnaire that measured the stages of the self-determination continuum with respect to motivation to exercise using a 5-point Likert scale (0 = not true for me, 4 = very true for me) and was modified by Markland and Tobin.
The version by Markland and Tobin added an amotivation factor to the original external, introjected, identified, and intrinsic regulation factors.
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before and immediately after intervention
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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 (Estimated)
July 1, 2026
Primary Completion (Estimated)
July 1, 2027
Study Completion (Estimated)
July 1, 2027
Study Registration Dates
First Submitted
June 17, 2026
First Submitted That Met QC Criteria
June 22, 2026
First Posted (Actual)
June 25, 2026
Study Record Updates
Last Update Posted (Actual)
June 25, 2026
Last Update Submitted That Met QC Criteria
June 22, 2026
Last Verified
June 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- MU-CIRB 2026/171.2603
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
Research data will be shared in a de-identified format only; for instance, participant names will be replaced with codes, and faces will be blurred in all images.
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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