NCT06885060Active, not recruiting
Exploring Eye Vergence Markers ADHD) and ASD
Exploring Eye Vergence Markers in Attention Deficit Hyperactivity Disorder (ADHD) and Autism Spectrum Disorder (ASD).
Source: ClinicalTrials.gov · Last updated 3 Feb 2026
Brief summary (registry, in English)
The investigators study aims to evaluate the utility of eye vergence, an eye-tracking measure, as an indicator of visuo-spatial attention in children aged 4-17 years and adults, using computer-based eye-tracking tasks. Eye vergence, a binocular movement crucial for depth perception, has recently been linked to attentional control and neurodevelopmental conditions (NDCs) like ADHD and ASD. The investigators will work with children and adults from the CAN and Beckenham clinical centres to explore the relationship between eye vergence and diagnostic categories, potentially identifying subgroups with specific or overlapping attentional differences. This research may aid in the early detection of attention deficits, informing targeted treatments. The investigators will compare neuropsychological and behavioural data from routine clinical sessions with neurophysiological data collected via eye-tracking in a large sample of children aged 7-17 and adults with ADHD and ASD. These clinical measures are well-validated. The study will assess the modulation of eye vergence, pupil size, and head movements across tasks that target different attentional processes, such as orienting, disengaging, inhibiting, and sustaining attention. These tasks will be adapted from both Braingaze's battery and other validated eye-tracking tasks. Additionally, the investigators will explore whether AI can enhance the accuracy of rating scales and questionnaires used to measure ADHD and ASD symptoms in children and adults. With consent, the investigators will use data from previously diagnosed patients collected during routine assessments at the CAN and Beckenham centres. The investigators will also test the accuracy of using a smartphone selfie camera as an eye tracker. In a subset of 50 children (25 clinical and 25 controls), the investigators will evaluate this technology for its ability to measure eye vergence and identify attentional differences. This study qualifies as basic science because it aims to explore fundamental mechanisms of eye vergence and its relationship with attention, rather than evaluating or marketing a medical device for diagnosis or treatment. The primary objective is to understand how eye vergence, as a neurophysiological measure, correlates with attentional processes in individuals with ADHD and ASD. Although the study utilizes an eye-tracking device, it does so as a research tool to collect data on visual and cognitive processes. The focus is on expanding the knowledge of cognitive function and attention regulation in neurodevelopmental conditions, not on testing or validating the device for clinical use. This distinction makes the study appropriate for review by the receiving REC as basic scientific research, rather than as a clinical trial of a medical device.
- Status (registry)
- Active, not recruiting
- Study type
- Observational
- Enrollment
- 200 (estimated)
- First submitted
- 7 Mar 2025
- Start date
- 1 Feb 2025
- Primary completion date
- 31 Jul 2026
- Lead sponsor
- Elizabeth Kilbey
- Diseases
- Autism
- NCT number
- NCT06885060
What you commit to
- Study type: Observational
- Planned participants: 200
- From 1 Feb 2025 to the primary completion date, 31 Jul 2026
- 3 sites in 2 countries
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other
- Those with non-corrected vision - e.g. near-sightedness, far-sightedness, strabismus or nystagmus
- Individuals with any other oculomotor deficiency, blindness or vision loss.
Who the study is looking for
- Clinical Groups: Patients currently undergoing or who have previously undergone an assessment for either ADHD and/or Autism at either the CAN centre or Dr Kilbey's private practice in Beckenham.
- Control Group: Subjects without a diagnosis of either ADHD nor Autism, who show no traits of these conditions.
- People of any gender/sex who are aged older than 6 years old.
Age in the registry: 6 years to - · Sex: All · Accepts healthy volunteers
Sites (3)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Braingaze SL Coordinator of this site? Confirm its status | Barcelona | Spain | Unknown status |
| The Dr Kilbey Practice Coordinator of this site? Confirm its status | Beckenham | United Kingdom | Unknown status |
| Child and Adult Neurodevelopment Assessment Ltd Coordinator of this site? Confirm its status | New Malden | United Kingdom | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.