Documenting outcomes associated with Persistent Tic Disorders (including Tourette Syndrome) in Children, Adolescents, and Young Adults through Surveillance
Closed Posted
- Opportunity number
- CDC-RFA-DD-24-0083
- Agency
-
Centers for Disease Control and Prevention
Department of Health and Human Services
- Applications due
- Award size
- $150,000 to $750,000
Opportunity facts
- Assistance listings
- Funding instrument
- Cooperative Agreement
- Category
-
- Health
- Eligible applicants
-
- Non-501(c)(3) Nonprofits
- City/Township Governments
- Independent School Districts
- State Governments
- County Governments
- Tribal Governments (Federally Recognized)
- 501(c)(3) Nonprofits
- Special District Governments
- Unrestricted
- For Profit Organizations
- Small Businesses
- Higher Education Inst. (Private)
- Higher Education Inst. (Public)
Opportunity details come from Grants.gov. Updated .
About this opportunity
This federal grant opportunity from the Centers for Disease Control and Prevention (CDC) seeks applications for a cooperative agreement to conduct surveillance of persistent tic disorders, including Tourette syndrome, among children, adolescents, and young adults. Eligible applicants must have the infrastructure and capacity to identify, collect, and disseminate information on outcomes associated with these disorders, such as expertise in disorder identification and the ability to collect and analyze survey data. The purpose is to document the public health burden of persistent tic disorders and generate data to inform education and outreach activities. Key requirements include collaborating with the CDC and other recipients to finalize measures, develop a standard data collection protocol, establish a data sharing approach, and analyze and disseminate the findings.
The total period of performance is five years, with individual awards up to $250,000 per year and a total of approximately $3,750,000 available under the Birth Defects and Developmental Disabilities - Prevention and Surveillance program (CFDA 93.073). Applications are due on April 15, 2024.
Synopsis
Eligible applicants should have the infrastructure and capacity to identify, collect, and disseminate information on outcomes associated with persistent tic disorders (PTD) including Tourette syndrome (TS) among children, adolescents, and young adults. Specifically, this entails: 1) access to a population of children, adolescents, and young adults with PTD/TS; 2) expertise in identification of PTD/TS; and 3) capacity to collect and analyze survey data and summarize and disseminate findings.CDC proposes to allocate funds to implement a Notice of Funding Opportunity (NOFO), Surveillance of Public Health Burden of Persistent Tic Disorders including Tourette Syndrome in Children, Adolescents, and Young Adults. The purpose of the NOFO is to conduct surveillance of persistent tic disorders (PTD) including Tourette syndrome (TS) among children, adolescents, and young adults to: • Document the public health burden (i.e., outcomes) of these disorders • Generate data that can be used to inform education and outreach activities to improve the health and well-being of individuals with tic disorders and their families. Proposed activities for this NOFO include the following: • Collaborate with CDC and other NOFO recipients to identify measures for priority areas of burden including cost, healthcare transition, suicidality, and co-occurring disorders. • Collaborate with CDC and other recipients to determine a standard survey and surveillance protocol across sites and shared data approach. • Collect and share de-identified data with CDC. • Collaborate with CDC and other NOFO recipients to analyze, summarize, and disseminate multi-site findings.
Files
| File | Type | Posted |
|---|---|---|
| CDC-RFA-DD-24-0083_NOFO_Questions_and_Answers_April 12_2024_Final.docx | DOCX document | |
| CDC-RFA-DD-24-0083.pdf |
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