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Virtual reality distraction for needle-related pain and distress in children and adolescents with autism spectrum disorder (ASD)

A comparison of virtual reality distraction and treatment as usual for needle-related pain and distress in children and adolescents with autism spectrum disorder (ASD): a feasibility study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN14514643
Enrollment
30
Registered
2023-07-12
Start date
2023-07-13
Completion date
Unknown
Last updated
2025-09-08

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

Conditions

Children and adolescents with a diagnosis of Autism Spectrum Disorder (ASD) with or without a co-occurring Intellectual Disability (ID). Mental and Behavioural Disorders

Interventions

Intervention Condition: Participants in the intervention condition will receive access to Virtual Reality (an Oculus Rift 2 and the VR app Ocean Rift) for the duration of their venipuncture procedure.

Sponsors

Ollscoil na Gaillimhe – University of Galway
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Children and adolescents with a diagnosis of Autism Spectrum Disorder (ASD) with or without a co-occurring Intellectual Disability (ID), and their parents/legal caregivers 2. Have a venipuncture scheduled or attend the day ward and require a venipuncture.

Exclusion criteria

Exclusion criteria: 1. Children under the age of 5 years and over the age of 18 years 2. Have not been clinically diagnosed as having ASD/ASD-ID 3. Children/adolescents with medical conditions that preclude virtual reality use such as epileptic seizures and vision problems 4. The inability to obtain consent from a parent/legal caregiver, and assent from a child

Design outcomes

Primary

MeasureTime frame
1. A task analysis of the venipuncture is gathered during the procedure 2. Pain is measured using a visual analogue scale (VAS) after the procedure 3. Feasibility data related to wearing the VR headset will be gathered after the procedure

Secondary

MeasureTime frame
Parent and Nurse/Phlebotomist Measures: 1. Behaviour measured by Behaviour Observation Checklist during the venipuncture. 2. Pain measured by visual analogue scale (VAS) during the procedure 3. Satisfaction with VR and venipuncture measured using Likert rating scales after the procedure

Countries

Ireland

Outcome results

None listed

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