Effect of Virtual Reality in Adolescents With Thoracic Hyperkyphosis
Effect of Virtual Reality on Kyphotic Angle and Quality of Life in Adolescents With Thoracic Hyperkyphosis
1 other identifier
interventional
46
1 country
1
Brief Summary
The study aims to:
- 1.Investigate the effect of virtual reality on kyphotic angle in adolescents with thoracic hyperkyphosis.
- 2.Investigate the effect of virtual reality on quality of life in adolescents with thoracic hyperkyphosis.
- 3.Investigate the effect of virtual reality on the enjoyment level in adolescents with thoracic hyperkyphosis.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jan 2026
Shorter than P25 for not_applicable
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
Study Start
First participant enrolled
January 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2026
CompletedFirst Submitted
Initial submission to the registry
July 28, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
July 30, 2026
CompletedFirst Posted
Study publicly available on registry
July 31, 2026
CompletedJuly 31, 2026
July 1, 2026
6 months
July 28, 2026
July 28, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
assessment of Kyphotic Angle
Kyphotic angle assessment using a bubble inclinometer involves the following steps: firstly, zero the inclinometer on a vertical wall. Next, identify the spinous processes of C7, T1, T12, and L1. Place the cephalic foot of the inclinometer on the C7 spinous process, then repeat for the lower thoracic spine with the caudal foot on T12. The kyphosis angle is calculated by adding the angles from both inclinometer placements.
At baseline and after 12 weeks
Secondary Outcomes (2)
assessment of Quality of Life
At baseline and after 12 weeks
assessment of Participant Enjoyment
At baseline and after 12 weeks
Study Arms (2)
conventional exercise program
ACTIVE COMPARATORThe control group included 23 patients and received a comprehensive corrective exercise program for thoracic hyperkyphosis
Virtual reality-based posture training
EXPERIMENTALThe experimental group will receive the same program as the control group in addition to virtual reality-based posture training using Meta Quest 3 - a virtual reality headset with the Totally Basketball game.
Interventions
treatment will last for 40-50 minutes, 3 days a week for 12 weeks Exercises will include: * Chin tuck * Stretching of neck extensor muscles * Stretching of pectoral muscle groups in standing and supine positions * T, Y, W and I exercises in a prone position. * Postural perception training (PPT) * Thoracic self-mobilization
Meta Quest 3 is an Mixed Reality headset providing augmented reality and virtual reality capabilities, allowing users to engage in both physical and virtual environments. Participants will play the "Totally Basketball" game, which promotes upper body engagement and postural correction through movements focusing on cervical retraction, scapular stabilization, and thoracic extension. The virtual reality sessions will last 20 minutes, scheduled after 30 to 45 minutes of conventional exercises, three times a week for eight weeks. Each session includes an introduction to the headset, a safety briefing, supervised trials, and active gameplay aimed at addressing thoracic hyperkyphosis with physiotherapist oversight to ensure safety and proper technique.
Eligibility Criteria
You may qualify if:
- Participants must meet all the following conditions:
- Adolescents with a kyphosis angle \>40°.
- Aged 13 to 18 years.
- Normal body mass index range
You may not qualify if:
- Participants who met one of the following criteria will be excluded:
- Adolescents who cannot understand or follow instructions.
- Congenital spinal deformities.
- Developmental disorders.
- Adolescent athletes.
- Neurological, musculoskeletal, and cardiopulmonary diseases.
- Vision or hearing impairments.
- Medical conditions hindering physical activity
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Cairo Universitylead
Study Sites (1)
out-patient clinic, faculty of physical therapy, Cairo university
Cairo, Egypt
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
July 28, 2026
First Posted
July 31, 2026
Study Start
January 1, 2026
Primary Completion
July 1, 2026
Study Completion
July 30, 2026
Last Updated
July 31, 2026
Record last verified: 2026-07