- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02676193
Effect of Packaging on Smoking Perceptions and Behavior (CASA)
January 6, 2025 updated by: David Strong, University of California, San Diego
Effect of Packaging on Smoking Perceptions and Behavior: A Randomized Trial
The investigators are addressing two critical areas identified by the FDA: the impact of cigarette packaging and labeling on consumer perceptions and on smoking behavior; and the effectiveness of graphic warning labels on communicating risk of tobacco products.
In a randomized controlled trial (RCT), investigators will enroll committed smokers who have no intention of quitting in the next 6-months.
The three study arms will be: a) a blank pack with all marketing materials removed (PP); b) The Australian graphic warning images (Australian model-AM); or c) a standard pack with all marketing materials unaltered (ST).
The study includes a three month purchasing intervention and continued follow-up through 12 months.
Throughout the study interactive text messaging assessments will be used to measure acute and persistent impact of labeling and marketing on perceptions of tobacco products, subjective effects of consumption, awareness of tobacco-related harms, tobacco use behavior, and quitting motivation.
At three separate time points, participants will: a) complete a web-based questionnaire b) provide a saliva sample for cotinine analysis.
The rigorous design and extensive objective measurements are significant innovations on the currently published research in this field and should lead to significant advances in tobacco regulatory science.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Smokers handle their packs frequently.
Product packaging is a crucial medium by which the tobacco industry communicates product attributes, including reassurances about risk.
The industry uses branded imagery on packs to influence consumer perceptions of their product, while at the same time the tobacco control community uses health warning labels to communicate harmful and potentially harmful constituents and risks of tobacco products.
The World Health Organization Framework Convention on Tobacco Control (WHO FCTC) is a treaty enacted to ensure that every person is informed of the health consequences and addictive nature of tobacco consumption.
Article 11 of the treaty requires Parties to implement large, rotating health warnings and urges governments to restrict or prohibit the use of Industry logos, colors, brand images or promotional information on packaging other than brand names and product names displayed in a standard color and font style.
Study Objective: To conduct a randomized trial of the effect of cigarette pack design on 450 smokers of popular cigarette brands aged 21-65, who are committed to continue smoking (no intention to quit in the next 6-months).
These committed smokers will be randomized to have their cigarettes packaged in one of 3 study arms: a) blank pack design with all marketing materials removed (BP), b) blank pack with a large graphic warning label (AM: Australian model) and c) standard pack with marketing materials intact (ST: US model).
Study Type
Interventional
Enrollment (Actual)
359
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
California
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La Jolla, California, United States, 92093
- University of California, San Diego
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
21 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- 21-65 years of age
- A current resident of San Diego County
- Daily smokers of at least 5 cigarettes/day who are classified as in the pre-contemplator stage of change (i.e. do not intend to quit smoking in the next 6-months)
- Regular smokers of popular U.S. cigarette brands
- Have a cell phone with a text messaging service plan
Exclusion Criteria:
- Non-Daily cigarette smokers and daily smokers of alternative brand cigarettes
- Marked organic impairment or unstable medical problems (such as a seizure disorder)
- Current pregnancy or intent to become pregnant during the next 12 weeks
- Prisoners, incarcerated or institutionalized individuals
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Australian Packs
The intervention to be administered to participants randomized to this group is the purchase of their US brand of cigarettes packaged using standard Australian marketing for three months.
|
The intervention is the use of the assigned pack design.
|
|
Experimental: Blank Packs
The intervention to be administered to participants randomized to this group is the purchase of their US brand of cigarettes packaged using blank packaging for three months.
Blank packaging will indicate participants brand and will not have any brand-related images or labels.
|
The intervention is the use of the assigned pack design.
|
|
No Intervention: American Packs
Participants assigned the nonintervention group will purchase their US brand of cigarettes in the standard American packaging for three months.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Perceptions of Risk From Tobacco Use and Perceptions of Pack Appeal
Time Frame: Assessed over 4-months and 12-months
|
Changes in perceptions of risk from tobacco use and appeal of tobacco packs
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Assessed over 4-months and 12-months
|
|
Changes in Awareness and Concern about Health Hazards
Time Frame: Assessed over 4-months and 12-months
|
Changes in perceptions of harm and potential risks
|
Assessed over 4-months and 12-months
|
|
Changes in routinized behavior and persistence over time.
Time Frame: Assessed over 4-months and 12-months
|
Decreased willingness to display the pack in public.
|
Assessed over 4-months and 12-months
|
|
Changes in cigarette smoking behaviors.
Time Frame: Assessed over 4-months and 12-months
|
Changes in the percent smokers, consumption per smoker, and recent quit attempts validated with saliva cotinine.
|
Assessed over 4-months and 12-months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Pierce JP, Kealey S, Leas EC, Pulvers K, Stone MD, Oratowski J, Brighton E, Villasenor A, Strong DR. Effect of Graphic Warning Labels on Cigarette Pack-Hiding Behavior Among Smokers: The CASA Randomized Clinical Trial. JAMA Netw Open. 2022 Jun 1;5(6):e2214242. doi: 10.1001/jamanetworkopen.2022.14242.
- Strong DR, Pierce JP, Pulvers K, Stone MD, Villasenor A, Pu M, Dimofte CV, Leas EC, Oratowski J, Brighton E, Hurst S, Kealey S, Chen R, Messer K. Effect of Graphic Warning Labels on Cigarette Packs on US Smokers' Cognitions and Smoking Behavior After 3 Months: A Randomized Clinical Trial. JAMA Netw Open. 2021 Aug 2;4(8):e2121387. doi: 10.1001/jamanetworkopen.2021.21387. Erratum In: JAMA Netw Open. 2022 Nov 1;5(11):e2245981. doi: 10.1001/jamanetworkopen.2022.45981.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 1, 2016
Primary Completion (Actual)
September 1, 2022
Study Completion (Actual)
September 1, 2022
Study Registration Dates
First Submitted
January 28, 2016
First Submitted That Met QC Criteria
February 3, 2016
First Posted (Estimated)
February 8, 2016
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
January 6, 2025
Last Verified
January 1, 2025
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- R01CA190347 (U.S. NIH Grant/Contract)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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