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NCT01238250 · ClinicalTrials.gov registry record
Online Study of People Who Have Genetic Changes and Features of Autism: Simons Searchlight
A clinical trial of 16P11.2 Deletion Syndrome and ADNP, sponsored by Simons Searchlight.
- Recruiting
- Registry status
- 100,000
- Enrollment target
- 2
- Study locations
NCT01238250: Recruiting study of 16P11.2 Deletion Syndrome and ADNP, sponsored by Simons Searchlight.
NCT01238250 is a study of 16P11.2 Deletion Syndrome and ADNP that is actively recruiting participants, run by Simons Searchlight. The registered enrollment target is 100,000 participants. The trial reports 2 study locations across 2 states. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01238250, a study of 16P11.2 Deletion Syndrome and ADNP, is actively recruiting participants, sponsored by Simons Searchlight.
- RECRUITING
- Registry status
- 100,000 participants
- Enrollment target
- 2
- Study locations
Study 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.
Primary Outcome
Families with people who have specific documented gene changes that are associated with features of autism and other neurodevelopmental disorders will report detailed medical and family history information by phone. Online research surveys will be used to collect information about behavioral and learning characteristics, with the goal of improving clinical care and treatment for these people.
Conditions Studied
Study Locations (2)
Massachusetts
- Boston Children's Hospital - Boston
Pennsylvania
- Geisinger Health System - Lewisburg
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100,000 participants |
| Start Date | 2010-10 |
| Est. Completion | 2050-10 |
What NCT01238250 shows while recruiting
NCT01238250 is an observational study that tracks outcomes without assigning an intervention. Its 100,000 participants enrollment target places it among the larger protocols in the corpus.
The record links to 10 conditions, with 16P11.2 Deletion Syndrome appearing as the primary indexed condition, and to 0 interventions.
NCT01238250 reports a single indexed study location in Massachusetts, Pennsylvania.
Frequently Asked Questions
What is clinical trial NCT01238250 about?
NCT01238250 is a clinical study titled "Online Study of People Who Have Genetic Changes and Features of Autism: Simons Searchlight". 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 h...
What is the current status of trial NCT01238250?
This trial is currently recruiting. The enrollment target is 100,000 participants. The study started on 2010-10. Estimated completion is 2050-10.
What conditions does trial NCT01238250 study?
This clinical trial studies the following conditions: 16P11.2 Deletion Syndrome, ADNP, 16p11.2 Duplications, 1Q21.1 Deletion, 1Q21.1 Microduplication Syndrome (Disorder).
Who is sponsoring clinical trial NCT01238250?
This trial is sponsored by Simons Searchlight, which has 1 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01238250 being conducted?
This trial has 2 study locations across Massachusetts, Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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