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Augmented Reality-Assisted Physiotherapy for Adolescents With Idiopathic Scoliosis: A Qualitative Study

A Qualitative Evaluation of the Effects of Augmented Reality-Supported Training Methods on Body Awareness and Exercise Adherence in Adolescents With Idiopathic Scoliosis

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07067125
Acronym
AR-AIS
Enrollment
15
Registered
2025-07-16
Start date
2025-06-01
Completion date
2025-07-31
Last updated
2025-07-16

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

Conditions

Scoliosis Idiopathic Adolescent, Scoliosis Idiopathic Adolescent Treatment

Keywords

Adolescent idiopathic scoliosis, augmented reality, qualitative research, psychosocial adjustment, physiotherapy

Brief summary

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.

Detailed description

This prospective qualitative study is designed to examine how adolescents with AIS experience AR supported physiotherapeutic scoliosis-specific exercises. A phenomenological design was selected to capture participants' lived experiences, perceptions of body awareness, and motivational responses to the intervention. The study will be conducted in a physiotherapy unit in Türkiye, with ethics approval obtained from the institutional review board. Eligible participants will include adolescents aged 10 to 18 years who are clinically diagnosed with AIS and have completed a minimum of four weeks of AR-based physiotherapy delivered by licensed physiotherapists. The AR intervention incorporates visual feedback, avatar-based motion monitoring, and gamified elements to support postural correction and therapeutic engagement. Data will be collected through face-to-face, semi-structured interviews using an interview guide informed by existing literature and expert consultation. Interviews will explore how participants perceive their postural awareness, exercise motivation, adherence challenges, and psychosocial adjustments within the AR-supported environment. All interviews will be audio-recorded and transcribed verbatim. Collected data will be analyzed using Braun and Clarke's thematic analysis framework, supported by NVivo software. Two independent researchers will code the transcripts to ensure analytical rigor and thematic validity. The study is expected to contribute to the refinement of conservative scoliosis rehabilitation practices by integrating adolescent perspectives and addressing the biopsychosocial dimensions of care enhanced through technology.

Interventions

BEHAVIORALAR-Supported Scoliosis-Specific Physiotherapy

This intervention consists of scoliosis-specific physiotherapy supported by AR technology. Participants will engage in postural correction exercises delivered by licensed physiotherapists using an AR system that provides real-time avatar feedback, movement guidance, and gamified motivation. The intervention aims to improve body awareness, adherence, and motivation among adolescents diagnosed with AIS. Each participant will complete at least four weeks of structured AR-supported sessions.

Sponsors

The Scientific and Technological Research Council of Turkey
CollaboratorOTHER
Hasan Kalyoncu University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Masking description

This is an open-label single-group study; no parties will be masked during the intervention or data collection processes.

Intervention model description

This study utilizes a single-group interventional design in which all participants will receive augmented reality-supported physiotherapeutic scoliosis-specific exercises for a minimum of four weeks. The intervention will be delivered by licensed physiotherapists using a standardized protocol that includes real-time visual feedback and interactive training components. No control or comparison group is included. This design was selected to qualitatively explore participants' individual experiences, perceptions of body awareness, motivational responses, and adherence behaviors during AR-based rehabilitation. Data will be collected through post-intervention interviews.

Eligibility

Sex/Gender
ALL
Age
10 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* 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)

Exclusion criteria

* Presence of neurological or cognitive conditions interfering with communication * Withdrew before completing the intervention program * Declined audio recording of interviews

Design outcomes

Primary

MeasureTime frameDescription
Change in Body Awareness Following AR-Supported PhysiotherapyWithin 1 week after completing the 4-week interventionThis outcome will assess adolescents' subjective body awareness, including their perception of postural alignment, movement control, and physical self-understanding, after completing AR-supported scoliosis-specific physiotherapy. Data will be collected through semi-structured interviews and analyzed thematically to evaluate perceived changes in awareness.

Countries

Turkey (Türkiye)

Contacts

Primary ContactADNAN BATUHAN COŞKUN, PhD
adnanbatuhan.coskun@hku.edu.tr+905323901464
Backup ContactMERVE KARATEL, PhD
kmerve.karatel@hku.edu.tr+905348293531

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026