Artificial Intelligence-Based Postural Feedback for Scoliosis
22 juni 2026 bijgewerkt door: 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.
Studie Overzicht
Toestand
Nog niet aan het werven
Interventie / Behandeling
Studietype
Ingrijpend
Inschrijving (Geschat)
30
Fase
- Niet toepasbaar
Contacten en locaties
In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.
Studiecontact
- Naam: Rommanee Rojasavastera, M.Sc.
- Telefoonnummer: +66837830777
- E-mail: rommanee.roj@mahidol.ac.th
Studie Locaties
-
-
Changwat Nakhon Pathom
-
Salaya, Changwat Nakhon Pathom, Thailand, 73170
- Faculty of Physical Therapy, Mahidol University
-
Contact:
- Rommanee Rojasavastera, M.Sc.
- Telefoonnummer: +66837830777
- E-mail: rommanee.roj@mahidol.ac.th
-
-
Deelname Criteria
Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Kind
- Volwassen
Accepteert gezonde vrijwilligers
Nee
Beschrijving
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.
Studie plan
Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Enkel
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Experimenteel: 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.
|
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).
|
|
Actieve vergelijker: 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.
|
The physical therapist conducted 60-minute sessions.
These sessions were grounded in the principles of the Schroth Method and Physiotherapeutic Scoliosis-Specific Exercises (PSSE).
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
REEDCO postural score
Tijdsspanne: before and immediately after intervention
|
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
Tijdsspanne: 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
Tijdsspanne: 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
|
|
Postural Variables Derived from a PAViR System
Tijdsspanne: 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
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Illness Perception
Tijdsspanne: 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.
|
before and immediately after intervention
|
|
Exercise Motivation
Tijdsspanne: 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.
|
before and immediately after intervention
|
Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Sponsor
Studie record data
Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.
Bestudeer belangrijke data
Studie start (Geschat)
1 juli 2026
Primaire voltooiing (Geschat)
1 juli 2027
Studie voltooiing (Geschat)
1 juli 2027
Studieregistratiedata
Eerst ingediend
17 juni 2026
Eerst ingediend dat voldeed aan de QC-criteria
22 juni 2026
Eerst geplaatst (Werkelijk)
25 juni 2026
Updates van studierecords
Laatste update geplaatst (Werkelijk)
25 juni 2026
Laatste update ingediend die voldeed aan QC-criteria
22 juni 2026
Laatst geverifieerd
1 juni 2026
Meer informatie
Termen gerelateerd aan deze studie
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- MU-CIRB 2026/171.2603
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
JA
Beschrijving IPD-plan
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.
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Nee
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
Nee
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .