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.
Not Applicable
- Registration Number
- CTRI/2024/04/066300
- Lead Sponsor
- Teena Ajit Paul
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
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
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.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 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 Outcome Measures
Name Time Method The secondary outcome will be the safety of the device used by recording any negative outcomes.Timepoint: 1 hour from test.