Viewing Study NCT01238250



Ignite Creation Date: 2024-05-05 @ 11:02 PM
Last Modification Date: 2024-10-26 @ 10:27 AM
Study NCT ID: NCT01238250
Status: RECRUITING
Last Update Posted: 2024-01-16
First Post: 2010-11-09

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

Study Overview

Official Title: Online Study of People Who Have Genetic Changes and Features of Autism Simons Searchlight
Status: RECRUITING
Status Verified Date: 2024-01
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: None
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?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
Simons VIP Connect OTHER Simons Foundation None
Simons Searchlight OTHER None None
Simons VIP OTHER None None