Actively Recruiting
Augmented Reality-Assisted Physiotherapy for Adolescents With Idiopathic Scoliosis: A Qualitative Study
Led by Hasan Kalyoncu University · Updated on 2025-07-16
15
Participants Needed
1
Research Sites
8 weeks
Total Duration
On this page
Sponsors
H
Hasan Kalyoncu University
Lead Sponsor
T
The Scientific and Technological Research Council of Turkey
Collaborating Sponsor
AI-Summary
What this Trial Is About
This study aims to explore the effects of augmented reality (AR)-supported physiotherapy on body awareness, motivation, and exercise adherence in adolescents diagnosed with Adolescent Idiopathic Scoliosis (AIS). Using a qualitative phenomenological approach, the study will involve semi-structured interviews with adolescents who have completed at least four weeks of AR-based physiotherapeutic scoliosis-specific exercises. The goal is to understand participants' lived experiences with AR-enhanced rehabilitation and to inform the development of adolescent-centered, technology-integrated physiotherapy strategies in conservative scoliosis care.
CONDITIONS
Official Title
Augmented Reality-Assisted Physiotherapy for Adolescents With Idiopathic Scoliosis: A Qualitative Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Aged between 10 and 18 years
- Diagnosed with adolescent idiopathic scoliosis (AIS)
- Completed at least 4 weeks of AR-based physiotherapy
- Sufficient Turkish language proficiency to participate in interviews
- Provided written informed consent (adolescent and guardian)
You will not qualify if you...
- Presence of neurological or cognitive conditions interfering with communication
- Withdrew before completing the intervention program
- Declined audio recording of interviews
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Hasan Kalyoncu University
Gaziantep, Turkey (Türkiye)
Actively Recruiting
Research Team
A
ADNAN BATUHAN COŞKUN, PhD
CONTACT
M
MERVE KARATEL, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
1
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