N/A
N=90
Social Virtual-reality on Enhancing Social Interaction Skills in Children With Attention-deficit/Hyperactivity Disorder
Virtual Reality · Social Interaction · Attention-deficit/Hyperactivity Disorder
Bottom Line
View on ClinicalTrials.gov: NCT05778526 ↗Enrolled (actual)
90
Serious AEs
0.0%
Results posted
Mar 2025
Primary outcome: Primary: Acceptability and Compliance — 100; 96.6; 63.3 Percentage of sessions attended
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Virtual reality (Behavioral); Traditional social skills training (Behavioral)
- Age
- Pediatric · 6+ yrs
- Sex
- All
- Sponsor
- The Hong Kong Polytechnic University
- Primary completion
- Aug 2024
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Acceptability and Compliance |
100; 96.6; 63.3 | — |
| SECONDARY Riggio Social Skills Inventory Assessment |
38.20; 30.63; 24.50 | — |
| SECONDARY Social Skills Rating System - Parent Version (SSRS-P) |
33.33; 31.93; 31.50 | — |
| SECONDARY Behaviour Rating Inventory of Executive Function |
16.83; 17.98; 19.63 | — |
| SECONDARY Satisfaction of the Intervention |
6.8; 6.7 | — |
| SECONDARY Simulator Sickness Questionnaire |
0; 0; 0 | — |
Summary
The study targets children with diagnosed ADHD and aims to (1) develop a social virtual reality-based intervention, (2) investigate its effects on improving the social skills and executive functioning of inhibitions, emotional control and attention of the children compared to traditional social skills training and (3) evaluate the subjects acceptability and compliance with social VR training for enhancing social interaction skills. It is hypothesised that the social interaction skills of the participants in the social VR training group are likely to perform better than those in the traditional social skills training group. Participants in the waitlist control group will receive no change in social interaction skills compared with the two intervention groups.
Eligibility Criteria
Inclusion Criteria
- aged between 6 and 12 years
- ethnic Chinese
- residing in Hong Kong
- having received a diagnosis of ADHD by Child Assessment Service in Hong Kong or via private practice
- stable on pharmacological and/or psychological treatment for ADHD 8 weeks before baseline (determined by health care professionals on the basis of medication data and behavioural observation)
- no initiation or change of pharmacological treatment for ADHD during the intervention period
- the ability to read Chinese, and speak and listen to Cantonese by the child and by at least one of their parents or legal guardian
- willing to provide informed consent by both participants and one of their parents or legal guardian
Exclusion Criteria
- comorbid autism
- mental retardation
- an estimated IQ lower than 85 (using the Wechsler Intelligence Scale for Children - Fourth Edition (Hong Kong) (WISC-IV(HK)))
- autism spectrum disorder (previously diagnosed by health care professionals)
- comorbid acute psychiatric disorder (previously diagnosed by health care professionals)
- with a severe physical disability (e.g., blindness, deafness) or learning disability (e.g., dyslexia).
Data sourced from ClinicalTrials.gov (NCT05778526). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.