Skip to content

Virtual Reality-based Schroth Exercise Versus Traditional Schroth Exercise on Trunk Kinematics in Scoliosis

Virtual Reality-based Schroth Exercise Versus Traditional Schroth Exercise on Trunk Kinematics and Quality of Life in Scoliosis

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07794020
Enrollment
54
Registered
2026-08-31
Start date
2026-09-01
Completion date
2027-02-28
Last updated
2026-08-31

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

Conditions

Scoliosis, Scoliosis Idiopathic

Keywords

virtual reality, Scoliosis

Brief summary

The study will be conducted to compare three-dimensional trunk kinematics (rotation, tilt, and flexion/extension) and quality of life among adolescents with idiopathic scoliosis receiving traditional Schroth physiotherapeutic scoliosis-specific exercises, Schroth exercises combined with immersive virtual reality using Meta Quest 2 (OhShape), and Schroth exercises combined with low-cost mobile virtual reality using Google Cardboard with a gaze-controlled game.

Detailed description

Physiotherapeutic scoliosis-specific exercises (PSSE), particularly the Schroth method, are widely recommended as a first-line conservative treatment for adolescent idiopathic scoliosis and have demonstrated effectiveness in reducing curve progression, improving posture, and enhancing quality of life. However, the long-term success of Schroth rehabilitation is highly dependent on patient adherence and the accurate execution of complex three-dimensional corrective postures, which remain challenging for adolescents to maintain outside supervised clinical settings. Poor adherence to traditional Schroth programs has been reported, with rates ranging between 30% and 50%, limiting the real-world effectiveness of conservative scoliosis management. Adolescents frequently report low motivation, boredom, and difficulty understanding or maintaining corrective postures without continuous feedback, which compromises motor learning and postural control. Digital rehabilitation technologies, particularly virtual reality (VR), have emerged as promising tools to enhance engagement, motivation, and motor learning in rehabilitation programs. VR-based exercise has demonstrated positive effects on adherence, movement accuracy, and postural awareness in neurological and musculoskeletal rehabilitation. Immersive VR platforms provide real-time visual and auditory feedback and promote task-oriented training in an engaging gaming environment, which is particularly suitable for adolescent populations. To date, no randomized controlled trial has directly compared immersive high-end VR platforms with low-cost mobile VR solutions for the delivery of scoliosis-specific exercises, nor has any study quantified real-time trunk kinematics during VR-guided Schroth rehabilitation using Wearable inertial measurement units (IMUs) technology. Evaluating these interventions may provide clinicians with valuable insight into cost-effective, scalable, and engaging rehabilitation strategies for adolescents with idiopathic scoliosis, particularly in resource-limited healthcare settings

Interventions

OTHERTraditional schroth supervised exercise

participants will perform traditional supervised Schroth physiotherapeutic scoliosis-specific exercises. The intervention consists of two supervised sessions per week, 45 minutes each, for 12 weeks

OTHEROhShape virtual reality gameplay environment

OhShape is a posture-matching rhythm-based VR game that requires users to perform precise trunk and body movements in response to visual and auditory cues, thereby promoting postural awareness, motor coordination, and movement accuracy. The Meta Quest 2 headset provides a fully immersive virtual reality experience with six degrees of freedom (6DOF) head and body tracking, allowing real-time spatial interaction and posture-based feedback during exercise execution.

OTHERGoogle Cardboard Mobile Virtual reality Zombie Shooter

It is a low-cost mobile virtual reality (VR) intervention delivered via Google Cardboard. A custom Unity-based zombie-shooting VR game will be used, in which participants are required to maintain the corrected Schroth posture while engaging in a gaze-controlled shooting task, using head and trunk alignment to aim and interact with virtual targets. Mobile VR platforms such as Google Cardboard provide three degrees of freedom (3DOF) tracking and represent an accessible, low-cost alternative to high-end immersive VR systems.

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
10 Years to 19 Years
Healthy volunteers
No

Inclusion criteria

* Age: 10-19 years. * Diagnosed adolescent idiopathic scoliosis (AIS) confirmed by spinal radiography . * Cobb angle between 20° and 35° (moderate curve, below surgical threshold). * No prior spinal surgery. * Ability to perform Schroth exercises independently. * Ability to use a virtual reality headset. * No prior virtual reality experience. * Free from pain or pain less than 8 on visual analogue scale. * Type of curve (thoracolumbar s scoliosis).

Exclusion criteria

* Secondary scoliosis (neuromuscular or post-surgical scoliosis). * Severe structural deformity (Cobb angle \>50° or severe vertebral rotation). * Neurological or neuromuscular disorders affecting balance or proprioception. * Active orthopedic injury or recent surgery (\<2 years) involving the spine or lower extremities. * Severe cardiopulmonary disease contraindicating exercise. * Uncontrolled pain (Visual Analog Scale \>8). * Current participation in another structured spinal rehabilitation program or participation within the last 6 months. * History of severe cybersickness or prior intolerance to virtual reality exposure. * Vision or hearing impairment preventing interaction with virtual reality--based games

Design outcomes

Primary

MeasureTime frameDescription
Trunk kinematics: Trunk rotation angle (Yaw)16 weeksDerived from gyroscope data(gyroZ) using wearable inertial measurement units (IMUs) to measure dynamic rotation toward midline during exercise execution.

Secondary

MeasureTime frameDescription
Trunk kinematics: trunk tilt angle (roll/ pitch)16 weeksderived from accelerometer data (accX, accY) using IMUs to assess frontal plane trunk asymmetry correction during exercise execution.
Trunk Kinematics: Trunk flexion/ extension angle16 weeksDerived from accelerometer data relative to gravity using wearable inertial measurement unit (IMUs) to monitor sagittal plane alignment during exercise execution.
Corrected posture holding time16 weeksThe cumulative duration (seconds ) and percentage of session time during which participants maintain the predefined curve specific corrected trunk posture within acceptable angular deviation threshold, quantified via real-time 50 Hz.
Health related quality of life (SRS-22r)16 weeksAssessed using the scoliosis research society-22r questionnaire mean domain scores evaluating pain, self image, function, mental health and satisfaction. The score is graded from 1 to 5; 1 means the worst and 5 means the best quality of life.
pediatric health utility (EQ-5D-Y and EQ-VAS)16 weeksAssessed using the EuroQol 5 dimention youth version utility scores and the self rated EuroQol visual analogue scale (0-100) to measure overall health status. 0 means the worst and 100 means the best health.
Trial retention rate16 weeksTo assess feasibility, calculated as the percentage of randomized participants who successfully complete post treatment assessment and follow-up periods.
intervention adherence rate16 weeksQuantified using clinic attendance logs calculated as (attended sessions / scheduled sessions)\*100 to categorize participants into high, moderate or low adherence.
Safety and incidence of adverse events16 weeksPercentage of participants experiencing treatment related adverse events such as muscle strain or safe withdrawals from the study.

Countries

Egypt

Contacts

CONTACTHend Saed, Master
hhend.samy@gmail.com01027722937
CONTACTAfaf Tahoon, PHD
afaf.Tahoon@pt.cu.edu.eg01015401783
STUDY_CHAIREnas youssef, professor

Cairo University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 1, 2026