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A clinical trial to study the accuracy of a novel technology-enabled tool to identify the risk of dyslexia in children aged 6 to 10 years.

Gaze Pattern Based Screening For Early Identification Of Risk Of Dyslexia In School Children. - Not applicable

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/04/066300
Enrollment
140
Registered
2024-04-25
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

None listed

Interventions

Intervention1: AI-DST: The screening involves use of a wearable eye tracking device with infrared cameras that track the gaze pattern while children read grade appropriate text on a screen. We use an
Attention
Executive functions
Visuospatial functions
and Comprehension, learning, and memory. All of the tests included in the battery were either originally developed for or standardized on children in the West
there are norms for each test at each age level. In their India-based study with normal school-going children in the age range of 5–15 years, Kar et al. (2011) report that the test–retest reliability

Sponsors

Teena Ajit Paul
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. As participants are underaged, guardian consent and verbal consent from participant will be primary criteria for inclusion. 2.Participants should demonstrate a basic level of reading comprehension in the language the screening is conducted.

Exclusion criteria

Exclusion criteria: The following individual will be excluded: 1. non-consenting children. 2. Children with visual impairment. 3. Children with significantly below average intelligence. 4. Children with reading comprehension below the test threshold.

Design outcomes

Primary

MeasureTime frame
The primary outcome will be measured as percent accuracy of the tool determined by comparison with an assessment tool, the NIMHANS Neuropsychological Battery for Children.Timepoint: 4 weeks

Secondary

MeasureTime frame
The secondary outcome will be the safety of the device used by recording any negative outcomes.Timepoint: 1 hour from test.

Countries

India

Contacts

Public ContactTeena Ajit Paul

JSS Medical College, Mysuru

nayanabaishabadi@jssuni.edu.in8105828888

Outcome results

None listed

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