Viewing Study NCT01238250


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Ignite Modification Date: 2025-12-27 @ 4:33 PM
Study NCT ID: NCT01238250
Status: RECRUITING
Last Update Posted: 2025-06-06
First Post: 2010-11-09
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Online Study of People Who Have Genetic Changes and Features of Autism: Simons Searchlight
Sponsor: Simons Searchlight
Organization:

Study Overview

Official Title: Online Study of People Who Have Genetic Changes and Features of Autism: Simons Searchlight
Status: RECRUITING
Status Verified Date: 2025-06
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Simons Searchlight is an observational, online, international research program for families with rare genetic variants that cause neurodevelopmental disorders and may be associated with autism. Simons Searchlight collects medical, behavioral, learning, and developmental information from people who have these rare genetic changes. The goal of this study is to improve the clinical care and treatment for these people. Simons Searchlight partners with families to collect data and distribute it to qualified researchers.
Detailed Description: Simons Searchlight has expanded over the last several years to include additional gene changes and participation through remote formats, either online or by phone. This allows English and Spanish-speaking families from across the world to participate at times that are convenient to their schedule. Participants can donate blood, saliva, or both. These samples are then linked to medical, behavioral, learning, and developmental data in order to understand the effects of specific gene changes.

Information provided by participants will be stripped of any personal identifying information and made available to qualified scientists around the world.

The Simons Foundation, a New York-based private foundation, is committed to finding science-based solutions and working towards the development of targeted treatments to improve the lives of people who have genetic and developmental differences.

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: False
Is an FDA AA801 Violation?:

Secondary ID Infos

Secondary ID Type Domain Link View
Simons Searchlight OTHER Simons Foundation View
Simons VIP OTHER Simons Foundation View
Simons VIP Connect OTHER Simons Foundation View