U01CA294539
Cooperative Agreement
Overview
Grant Description
From perceptions to behaviors: A comprehensive approach to examine the impact of public health communication messaging about the continuum of risk for tobacco products - Project summary.
Effective communication strategies are urgently needed to convey the relative risks of tobacco products accurately among adults who currently use combustible tobacco while minimizing such appeal among youth populations.
There is a significant gap in research on the impacts of communicating the continuum of tobacco products risks to diverse audiences.
Current research has primarily been limited to cross-sectional studies of single message exposures among adults.
As such, there is insufficient evidence on how messaging about the continuum of risk of tobacco products would influence the message response, receptivity, behavioral precursors, and tobacco use behaviors among the diverse audiences that these messages must reach.
The long-term objective of this project is to optimize future public health communication on the continuum of risk for tobacco products to minimize tobacco use harms among adults who use tobacco products and prevent youth initiation and progression of tobacco product use.
Our proposed project, in direct response to RFA-OD-23-021, will assess the effects of FDA tobacco product risk continuum messaging on adult users of combustible tobacco products (including those who have not yet been able to quit) and youth/young adults using an integrated study design that captures the full range of relevant outcomes, from immediate message response and receptivity to longer-term behavior.
This project is guided by a theoretical framework integrating key constructs in health communication (Message Impact Framework), persuasion (McGuire's Persuasion Framework), behavioral economics, and behavioral change theories (Reasoned Action).
Our specific aims are to:
(1) Generate rankings of messages and identify effective message features based on perceived message effectiveness and message comprehension;
(2) Characterize effects of messages and message features on response and receptivity, and precursors to behavior, including behavioral intentions; and
(3) Specify immediate and long-term behavioral effects of tobacco product risk continuum messages.
Approach: We will deploy a nimble framework to: refine messaging and develop control messages (message rating survey, cognitive interviews); formally test message response, receptivity, and effects on behavioral precursors (online national experiments, eye-tracking and neuroimaging); and assess immediate and long-term effects on behavior (mobile device-based message delivery and laboratory smoking topography studies) among samples of adults who use combustible tobacco, youth/young adults who use non-combustible tobacco, and youth/young adults who do not use tobacco.
Impact: The successful completion of this project will provide FDA with clear, rigorous, and comprehensive evidence regarding the effectiveness of the specific messages provided for this study, as well as theory-informed insights regarding broader message strategies to optimize future public health communication on the continuum of risk for tobacco products to diverse audiences.
Effective communication strategies are urgently needed to convey the relative risks of tobacco products accurately among adults who currently use combustible tobacco while minimizing such appeal among youth populations.
There is a significant gap in research on the impacts of communicating the continuum of tobacco products risks to diverse audiences.
Current research has primarily been limited to cross-sectional studies of single message exposures among adults.
As such, there is insufficient evidence on how messaging about the continuum of risk of tobacco products would influence the message response, receptivity, behavioral precursors, and tobacco use behaviors among the diverse audiences that these messages must reach.
The long-term objective of this project is to optimize future public health communication on the continuum of risk for tobacco products to minimize tobacco use harms among adults who use tobacco products and prevent youth initiation and progression of tobacco product use.
Our proposed project, in direct response to RFA-OD-23-021, will assess the effects of FDA tobacco product risk continuum messaging on adult users of combustible tobacco products (including those who have not yet been able to quit) and youth/young adults using an integrated study design that captures the full range of relevant outcomes, from immediate message response and receptivity to longer-term behavior.
This project is guided by a theoretical framework integrating key constructs in health communication (Message Impact Framework), persuasion (McGuire's Persuasion Framework), behavioral economics, and behavioral change theories (Reasoned Action).
Our specific aims are to:
(1) Generate rankings of messages and identify effective message features based on perceived message effectiveness and message comprehension;
(2) Characterize effects of messages and message features on response and receptivity, and precursors to behavior, including behavioral intentions; and
(3) Specify immediate and long-term behavioral effects of tobacco product risk continuum messages.
Approach: We will deploy a nimble framework to: refine messaging and develop control messages (message rating survey, cognitive interviews); formally test message response, receptivity, and effects on behavioral precursors (online national experiments, eye-tracking and neuroimaging); and assess immediate and long-term effects on behavior (mobile device-based message delivery and laboratory smoking topography studies) among samples of adults who use combustible tobacco, youth/young adults who use non-combustible tobacco, and youth/young adults who do not use tobacco.
Impact: The successful completion of this project will provide FDA with clear, rigorous, and comprehensive evidence regarding the effectiveness of the specific messages provided for this study, as well as theory-informed insights regarding broader message strategies to optimize future public health communication on the continuum of risk for tobacco products to diverse audiences.
Awardee
Funding Goals
THE FAMILY SMOKING PREVENTION AND TOBACCO CONTROL ACT (TCA) PROVIDES THE AUTHORITY TO REGULATE TOBACCO PRODUCT MANUFACTURING, DISTRIBUTION AND MARKETING. REGULATORY RESEARCH WILL PROVIDE THE SCIENTIFIC EVIDENCE TO GUIDE THE IMPLEMENTATION OF THIS AUTHORITY. RESEARCH AREAS INCLUDE: 1) TOBACCO PRODUCT COMPOSITION AND DESIGN 2), THE TOXICITY OF TOBACCO PRODUCTS, 3) ADDICTION AND ABUSE LIABILITY OF TOBACCO PRODUCTS, 4) THE SHORT- AND LONG-TERM HEALTH EFFECTS OF TOBACCO PRODUCTS, 5) PEOPLE'S BEHAVIORS RELATED TO TOBACCO PRODUCT USE AND CHARACTERISTICS, 6) COMMUNICATING TO THE PUBLIC REGARDING NICOTINE AND THE HEALTH EFFECTS OF TOBACCO PRODUCTS, 7) THE INFLUENCES OF TOBACCO MARKETING ON SUSCEPTIBILITY AND TOBACCO PRODUCT USE, AND 8) THE POTENTIAL OR ACTUAL IMPACT OF FDA REGULATORY ACTIONS. THE STRATEGIC PRIORITIES FOR THESE RESEARCH AREAS CAN BE FOUND AT HTTPS://WWW.FDA.GOV/TOBACCOPRODUCTS/RESEARCH/RESEARCH-PRIORITIES
Grant Program (CFDA)
Awarding Agency
Place of Performance
Baltimore,
Maryland
212182608
United States
Geographic Scope
Single Zip Code
Related Opportunity
Analysis Notes
Amendment Since initial award the total obligations have increased 95% from $2,490,060 to $4,855,315.
The Johns Hopkins University was awarded
Optimizing Tobacco Risk Communication: Impactful Messaging Public Health
Cooperative Agreement U01CA294539
worth $4,855,315
from the National Institute of Allergy and Infectious Diseases in August 2024 with work to be completed primarily in Baltimore Maryland United States.
The grant
has a duration of 4 years and
was awarded through assistance program 93.077 Family Smoking Prevention and Tobacco Control Act Regulatory Research.
The Cooperative Agreement was awarded through grant opportunity Public Health Communication Messaging about the Continuum of Risk for Tobacco Products (U01 Clinical Trial Required).
Status
(Ongoing)
Last Modified 9/24/25
Period of Performance
8/16/24
Start Date
7/31/28
End Date
Funding Split
$4.9M
Federal Obligation
$0.0
Non-Federal Obligation
$4.9M
Total Obligated
Activity Timeline
Subgrant Awards
Disclosed subgrants for U01CA294539
Transaction History
Modifications to U01CA294539
Additional Detail
Award ID FAIN
U01CA294539
SAI Number
U01CA294539-4016811793
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Private Institution Of Higher Education
Awarding Office
75NC00 NIH National Cancer Institute
Funding Office
75NA00 NIH OFFICE OF THE DIRECTOR
Awardee UEI
FTMTDMBR29C7
Awardee CAGE
5L406
Performance District
MD-07
Senators
Benjamin Cardin
Chris Van Hollen
Chris Van Hollen
Modified: 9/24/25