Strategic Plan Objective Detail
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Question 7: Objective C  

$2,785,368.00
Fiscal Year: 2010

Green dot: Objective has greater than or equal to the recommended funding.7C. Develop and have available to the research community means by which to merge or link databases that allow for tracking the involvement of people in ASD research by 2010. IACC Recommended Budget: $1,300,000 over 2 years.

Download 2010 Question 7: Objective C projects (EXCEL)
Note: Initial Sort is by Principal Investigator. Sorting by other columns is available by clicking on the desired column header.
Project Title Principal Investigator Institution
Autism Registry Simon, Gregory Group Health Cooperative
Accelerating autism research through the Interactive Autism Network Law, Paul Kennedy Krieger Institute
Interactive Autism Network (IAN) Law, Paul Kennedy Krieger Institute
A centralized standard database for the Baby Siblings Research Consortium Young, Gregory University of California, Davis
Pilot project to assess web-based family recruitment for autism genetics studies Nelson, Stan; Constantino, John; Law, Paul University of California, Los Angeles; Washington University in St. Louis; Kennedy Krieger Institute

Objective Cumulative Funding Table

IACC Strategic Plan Objective 2008 2009 2010 2011 2012 Total
Develop and have available to the research community means by which to merge or link databases that allow for tracking the involvement of people in ASD research by 2010.

IACC Recommended Budget: $1,300,000 over 2 years
6.1
$6,767,808
4 projects

7.C
$1,665,180
2 projects

7.C
$2,785,368
5 projects

7.C
$1,387,146
7 projects

7.C
$985,158
6 projects

$13,590,660
7.C. Funding: The recommended budget was met. Significantly more than the recommended minimum budget was allocated to projects specific to this objective.

Progress: IAN and Group Health Cooperative Autism Registry are two examples of projects that are responsive to this objective. This objective should be considered to be met, with funding exceeding the recommended budget and a large number of diverse projects addressing this issue. NDAR, IAN and AGRE are all publicly available databases.

Remaining Gaps, Needs and Opportunities: To advance this objective we need to encourage patients and families to join the registry. Compared to registry numbers for cystic fibrosis (100%), autism is behind at ~4% of patients enrolled in a registry. A table of the numbers of registrants by year would be an informative figure. We need more organized systems to improve participation.