Actively Recruiting

Phase Not Applicable
Age: 13Years - 18Years
All Genders
Healthy Volunteers
ID06582290

Investigating the Clinical Utility of the Oxford Virtual Autism Assessment Tool (OVAAT)

Led by Oxford Health NHS Foundation Trust · Updated on 2024-09-03

60

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the Oxford Virtual Autism Assessment Tool (OVAAT), a new online diagnostic tool for Autism Spectrum Disorder (ASD). The study aims to see if the OVAAT can identify autistic traits, distinguish between autistic and non-autistic young people, and compare its performance to the existing ADOS-2 observational tool. This research addresses the need for a standardised virtual assessment that captures both observable and self-reported ASD features, especially for young people who prefer online assessments. Participants are divided into two groups: Group 1 includes 13 to 18 year olds awaiting an autism assessment within the Oxfordshire CAMHS Neurodevelopmental Conditions pathway, who will complete both the OVAAT and the ADOS-2 assessments. Group 2 consists of neurotypical young people aged 13 to 18 with no neurodevelopmental or mental health conditions, who will complete screening questionnaires and the OVAAT only. The OVAAT assessments are video and audio recorded via Microsoft Teams to allow a second clinical researcher to verify the findings. Throughout the study, participants will complete questionnaires that assess features of autism, ADHD, and common mental health conditions. The recordings from the OVAAT will be kept only until reviewed by a second researcher. Participants may receive a £10 Amazon voucher after completing the required assessments. The primary outcome is the evaluation of the OVAAT up to three weeks after recruitment. Secondary measures include established scales like the Revised Children's Anxiety and Depression Scale and the Autism Diagnostic Observation Schedule (ADOS-2). Safety monitoring includes confidentiality protections and pathways for further support if mental health concerns arise.

CONDITIONS

Brief Title

Investigating the Clinical Utility of the Oxford Virtual Autism Assessment Tool (OVAAT)

Who Can Participate

Age: 13Years - 18Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Group 1: Young people aged 13 to 18 waiting for an autism assessment in the Oxfordshire CAMHS Neurodevelopmental Conditions pathway
  • Group 2: Young people aged 13 to 18 with no neurodevelopmental or mental health conditions
  • Access to and ability to use a laptop or desktop computer in a quiet place to complete assessments
  • Ability to speak English fluently
Not Eligible

You will not qualify if you...

  • Group 1: Young people aged 13 to 18 waiting for autism assessment who have an existing or suspected neurodevelopmental diagnosis other than autism (e.g., ADHD, Learning Disability) or significant mental health problems (e.g., major depression, psychosis, eating disorder)
  • Group 1: Unable to speak English fluently
  • Group 2: Young people aged 13 to 18 with any suspected or current neurodevelopmental or mental health conditions
  • Group 2: Unable to speak English fluently

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - Up to 3 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (online or in-person) for screening measures

Diagnostic Evaluation

Duration - Within 2 to 3 months after screening

Participants complete the Oxford Virtual Autism Assessment Tool (OVAAT) and for some participants, the standard ADOS-2 autism assessment as part of the diagnostic process. The OVAAT assessment is video and audio recorded for reliability checks.

1 to 2 visits (online or in-person) depending on participant group and assessments

Trial Site Locations

Total: 1 location

1

Oxford Health NHS Foundation Trust

Oxford, United Kingdom, OX3 7JH

Actively Recruiting

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Research Team

S

Sophie Chalker

J

James Stacey

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

NON_RANDOMIZED

Model

CROSSOVER

Primary Purpose

DIAGNOSTIC

Number of Arms

2

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Published Research Related To This Trial

Usability and reliability of a remotely administered adult autism assessment, the autism diagnostic observation schedule (ADOS) module 4.

Jamie L Schutte, Michael P McCue, Bambang Parmanto...

https://pubmed.ncbi.nlm.nih.gov/25569603