Plain-English translation of NCT06871696 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
This is a research study that invites families to share medical and family information through easy-to-answer online questionnaires. Researchers are building a database of people with intellectual disability or autism spectrum disorder that is caused by a specific genetic change. By collecting this information from many families with the same genetic mutation, scientists hope to better understand how these conditions affect people over time and develop more personalized care plans.
Currently, doctors know little about how genetic mutations cause intellectual disability and autism in different people—why some people have more severe symptoms than others, what health complications to watch for, and how treatments might affect each person differently. This study exists to fill those gaps so doctors can provide better, more targeted care based on each person's unique genetic situation.
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If you join, you would fill out online questionnaires developed by medical professionals but written in simple, family-friendly language. These questionnaires ask about your or your family member's medical history, symptoms, treatments, and how the condition affects daily life. There are no clinic visits or medical procedures—everything happens online at your own pace. Participation is part of an ongoing study, so your information helps build a growing database that researchers use to understand genetic intellectual disabilities and autism better.
AI-generated summary from trial data · Jun 14, 2026 · Not medical advice
France