Artificial Intelligence-Based Postural Feedback for Scoliosis
The Effect of Artificial Intelligence-Based Postural Feedback on Posture Correction in Idiopathic Scoliosis Patients
1 other identifier
interventional
30
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Jul 2026
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 17, 2026
CompletedFirst Posted
Study publicly available on registry
June 25, 2026
CompletedStudy Start
First participant enrolled
July 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
July 1, 2027
June 25, 2026
June 1, 2026
1 year
June 17, 2026
June 22, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (4)
REEDCO postural score
The REEDCO Posture Assessment was used to evaluate postural scores during comfortable standing and postural self-correction.
before and immediately after intervention
Angle of trunk rotation
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
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
Postural Variables Derived from a PAViR System
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 Outcomes (2)
Illness Perception
before and immediately after intervention
Exercise Motivation
before and immediately after intervention
Study Arms (2)
AI-Based Postural Feedback Group
EXPERIMENTALParticipants in the experimental group received postural feedback via the PAViR system, integrated with posture correction exercises and physical therapy for scoliosis.
Conventional Postural Feedback Group
ACTIVE COMPARATORParticipants in the control group received the same exercise and therapy sessions, but without the postural feedback provided by the PAViR system.
Interventions
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).
Eligibility Criteria
You may qualify if:
- Diagnosis of adolescent idiopathic scoliosis (AIS) by a physician.
- Aged between 10 and 18 years.
- Cobb angle between 10 and 40 degrees.
You may not qualify if:
- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Faculty of Physical Therapy, Mahidol University
Salaya, Changwat Nakhon Pathom, 73170, Thailand
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Masking Details
- The assessor was blinded to the participant groups and operated independently from the intervention provider.
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Researcher
Study Record Dates
First Submitted
June 17, 2026
First Posted
June 25, 2026
Study Start
July 1, 2026
Primary Completion (Estimated)
July 1, 2027
Study Completion (Estimated)
July 1, 2027
Last Updated
June 25, 2026
Record last verified: 2026-06
Data Sharing
- IPD Sharing
- Will share
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.