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Virtual Reality Immersive Intervention for Preoperative Anxiety Relief, Perioperative Stress Response Modulation, and Its Physiological Mechanisms in Children with Bone Trauma

Virtual Reality Immersive Intervention for Preoperative Anxiety Relief, Perioperative Stress Response Modulation, and Its Physiological Mechanisms in Children with Bone Trauma

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600126802
Enrollment
Unknown
Registered
2026-06-16
Start date
2026-06-20
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Bone Trauma (Pediatric)

Interventions

VR group:In the recovery room (approximately 30 minutes before anesthesia induction), after being fitted with physiological monitoring devices, the child experiences customized VR content lasting abou
Control group: In the same area, the child receives routine preoperative care, including verbal comfort from nurses and parents, reading picture books, playing with toys, etc., with a duration matched

Sponsors

Affiliated Chenggong Hospital of Xiamen University (73rd Army Group Hospital)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to 12 Years

Inclusion criteria

Inclusion criteria: 1. Children aged 2 to 12 years, either gender, diagnosed with bone trauma and scheduled for elective or sub-emergency orthopedic surgery in our hospital; 2. Surgery performed under general anesthesia, with anesthetic protocols standardized by the department of anesthesiology; 3. American Society of Anesthesiologists (ASA) physical status I or II; 4. The legal guardian of the child is fully informed about the study, volunteers to participate, and signs the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Contraindications to VR device use, including: severe visual or auditory impairment; facial or cranial deformity/unhealed wounds; active skin infection on the face or head; history of epilepsy; severe motion sickness; 2. History of psychiatric or neurological disorders (e.g., autism, intellectual disability, attention-deficit/hyperactivity disorder) that may interfere with VR experience or outcome assessment; 3. Long-term use (>2 weeks) of sedatives, anxiolytics, antidepressants, or antipsychotics before surgery; 4. Emergency surgery (interval from admission to operation 38.0?), active infection, or systemic inflammatory response; 6. Severe dysfunction of vital organs (heart, lungs, liver, kidneys, brain), ASA physical status >= III; 7. Previous participation in any interventional study related to VR or biofeedback.

Design outcomes

Primary

MeasureTime frame
Modified Yale Preoperative Anxiety Scale Score;

Secondary

MeasureTime frame
Stress-related hormones;Postoperative pain score;Postoperative sleep quality;Postoperative delirium;Health indicators;

Countries

China

Contacts

Public ContactLai Yanfang

Affiliated Chenggong Hospital of Xiamen University (73rd Army Group Hospital)

1277218567@qq.com+86 135 9954 3966

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 29, 2026