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Recruiting NCT06737627

Development and Validation of the Observatory Battery of Common Eye Disorders for Adults With Intellectual Disability

Observational Intellectual Disability

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: no intervention.
Who it may be relevant to
Registry conditions: Intellectual Disability. Basic parameters: from 20 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Taiwan
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Background: Around 15% of the global population has some form of disability. Rights to obtain proper health care is an emphasis in the United Nationals Convention on the Right of People with Disability. Due to the importance of improving vision health for people with disabilities, studies on how to identify vision problems becomes extremely important in policy formulation for all countries. Among all types of disabilities, people with intellectual disability (ID) are among the ones where vision problems are the hardest to detect. Currently, no caregiver assessable scales are available, as a result, adults with ID are at high risk of delayed diagnose for common ocular conditions. Objectives: This is a one-year project. The objective of this study is two folds: 1. To develop an item bank of ocular conditions of adults with ID; 2. To develop a scale for caregivers to detect ocular conditions for adults with ID, and to validate the reliability, construct validity and responsiveness of the scale.

Interventions

  • Other no intervention
    no intervention

Primary outcome measures

  • Collection of Socioeconomic Data for Individuals with Disabilities [Time frame: 1-3 months]
  • Assessment Scales for Individuals with Disabilities [Time frame: 1-3 months]
  • Ophthalmologic Examination Form [Time frame: 1-3 months]

Eligibility criteria

Inclusion criteria

  • Age 20 and above
  • Primary caregivers for at least one adult with ID (have disability identification or (and) certification).

Exclusion criteria

  • Unable to communicate in Mandarin or Taiwanese.(Primarycaregivers)
  • Unable to cooperate with eye examination.(ID)

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Other

Study locations

Taiwan · 2 centers
  • Care facility — New Taipei City
  • Care facility — Taipei

Identifiers

NCT: NCT06737627 · 202212036RINA

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗