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Study on analgesic efficacy of virtual reality (VR) during venipentesis in patients of PICU

Study on analgesic efficacy of virtual reality (VR) during venipentesis in patients of PICU

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300073767
Enrollment
Unknown
Registered
2023-07-20
Start date
2023-08-01
Completion date
Unknown
Last updated
2023-07-30

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

Conditions

Pediatric acute pain

Interventions

group A:VR is given according to different age groups: 5 to 8 years old, 8 to 12 years old, and 12 to 15 years old, each group of ages corresponds to 3 health animation or entertainment programs of th
group B:ipad is given according to different age groups: 5 to 8 years old, 8 to 12 years old, and 12 to 15 years old, each group of ages corresponds to 3 health animation or entertainment programs of
Group C:N/A

Sponsors

Children's Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
5 Years to 15 Years

Inclusion criteria

Inclusion criteria: ? Age range: 5 years =y=15 years; ? In medical need for venipuncture, clear mind and can communicate; ? With informed consent and complete data.

Exclusion criteria

Exclusion criteria: 1. Using of analgesic and sedative drugs, 2. Children who are critically ill and need emergency venipuncture; 3. Children with multi-drug resistance and/or infectious diseases.

Design outcomes

Primary

MeasureTime frame
Two pain scores: FLACC and vNRS-11;

Secondary

MeasureTime frame
respiratory rate(RR);heart rate(HR);blood pressure(BP);temporary anagesia and sedation drugs(dosage and frequency);

Countries

China

Contacts

Public ContactDandan Pi

Children's Hospital of Chongqing Medical University

pdd133@hospital.cqmu.edu.cn+86 134 3615 3657

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026