Perceptions of Tobacco ProductsUSC TCORS P4NCT07721883
Social Media Influences on Engagement and Susceptibility to Non-combustible Tobacco Product Use Among Youth and Young Adults (AYA)
A study testing Each intervention will be a picture of a social media post. The posts will vary (in a 3X2 factorial design) the type of flavor described and whether concealability is described. in people with Perceptions of Tobacco Products, run by University of Southern California at 1 site in United States.
Trial summary
The purpose of this study is to present social media posts with varying combinations of flavor types and mentions of stealth use, to adolescents and determine whether these message characteristics increase adolescents' perceptions of these products and susceptibility to using these products. Read more about this study
- Who is it for?
- Ages 14 to 17 yearsHealthy volunteers can take part
- Conditions the study is for
- Perceptions of Tobacco Products
- What is being tested?
- Each intervention will be a picture of a social media post. The posts will vary (in a 3X2 factorial design) the type of flavor described and whether concealability is described.
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 4,500 participants
- Where
- 1 siteUnited States
- Study dates
- 1 Jul 2025to 1 May 2028
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 14 to 17 years
- All sexes
- Healthy volunteers accepted
- Child
Who may be able to join
- High school student
- Provides parental consent and youth assent
Who cannot join
- No parental consent or youth assent
- Can't read or speak English
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
United States1 site, 1 recruiting
- Recruiting
University of Southern California
Los Angeles, California, 90032
Jennifer Unger, PhD, 3233330580, unger@usc.edu
About this study
Official title: USC Tobacco Center of Regulatory Science - Project 4: Social Media Influences on Engagement and Susceptibility to Non-combustible Tobacco Product Use Among Youth and Young Adults (AYA)
The purpose of this study is to present social media posts with varying combinations of flavor types and mentions of stealth use, to adolescents and determine whether these message characteristics increase adolescents' perceptions of these products and susceptibility to using these products.
Read the detailed description
University of Southern California Social Behavioral and/or Secondary Research Protocol Template
General Information Study Title: TCORS3 Project 4: Social media influences on engagement and susceptibility to non-combustible tobacco product use among youth and young adults (AYA)
PI Name: Jennifer Unger, Ph.D.
Study Information
- What is the general purpose of the study? What do the investigators hope to learn? (Maximum 1-2 paragraphs of explanation). Social media is an increasingly important source of information on emerging tobacco products among adolescents. On social media platforms with large youth user bases (e.g., TikTok, Instagram), social media influencers (e.g., public figures, promoters, models, brand ambassadors) can promote novel non-combustible tobacco products on behalf of manufacturers and distributors via social media posts that may attract adolescents to nicotine use. Of concern is the emergence of novel oral nicotine products (ONPs) and e-cigarettes-both of which may leverage social media to market aspects of their products that could attract adolescents to tobacco use. TCORS Project 4 includes two interrelated studies. Study 1 (not a clinical trial) will examine text (Twitter), picture (Instagram), and video (TikTok) posts in social media to determine whether tobacco-related posts that depict products with: a) concept flavors, b) stealth use, and c) other youth-appealing characteristics will generate more engagement (e.g., likes, favorites, shares), compared with tobacco-related posts that do not have these characteristics, respectively. Study 2 (the current clinical trial) will present social media posts adapted from those found in Study 1, with varying combinations of flavor types and mentions of stealth use, to adolescents and determine whether these message characteristics increase adolescents' susceptibility to using these products.
- List the Research Questions.
- Is susceptibility to use the ONP or e-cigarette products higher among youth assigned to view social media posts with concept or characterizing flavors and/or references to stealth use? II. Are the associations between social media post characteristics and susceptibility to use the product mediated by perceived harm and perceived social norms? III. Do the effects of flavors, stealth use, and influencers on susceptibility vary across demographic and tobacco use groups (e.g., age, gender, race/ethnicity, tobacco product use history)?
Inclusion \& Exclusion Criteria
- Describe the inclusion and exclusion criteria for enrollment.
- Provide justification for the population included.
- Please describe (maximum 1-2 paragraphs) how equity, diversity, and inclusion have been considered.
Inclusion and exclusion criteria for enrollment: Adolescents will be eligible to participate if they are students attending the schools where TCORS Project 2 (P2) will be collecting data (but not participating in the P2 cohort) and provide parental consent and youth assent. Exclusion criteria include lack of parent consent or student assent, inability to read English, or any cognitive or physical health condition that would preclude viewing stimuli on a computer screen and answering questions. There are no eligibility criteria based on previous tobacco product use because susceptibility (openness to trying a product in the future) can be assessed among ever-users as well as never-users.
Provide justification for including (or excluding) minors: The study is focused on associations between social media exposure to tobacco content and tobacco product use among adolescents and young adults (AYA), so adolescents (i.e., minors under 18) will be surveyed.
Sample considerations: TCORS P2 recruits from local area high schools and this project will recruit at the same schools. The research questions will look at differences in associations among demographic groups; therefore a diverse sample is needed. Los Angeles area high schools provide sex, racial and ethnic diversity. All eligible students will be invited to participate.
Where will Recruitment occur?
- List all sites or locations where researchers will recruit participants (e.g., on USC campus, place of employment, a specific elementary school, Amazon Turk, Qualtrics panel, specific groups within Facebook, Instagram, etc. Provide exact locations and/or weblinks as applicable). Schools will be recruited in Year 1. Data will not be collected from human subjects until the schools have been recruited and their information has been uploaded here.
- Are the researchers specifically seeking any participants physically present in a country outside of the United States?
X No ☐ Yes If yes, please answer the additional questions regarding International Research.
How will Recruitment happen?
- What format(s) will the researchers use to advertise (find) potential participants (e.g., Listservs, personal emails, public email, flyer, letter, phone call, social media post (e.g., Facebook, Twitter, Instagram)? Email from school personnel to students and parents.
- Who will distribute the recruitment material, and how will it be distributed?
Each year (Years 3-5), the researchers will recruit 1500 students attending the same high schools (across Los Angeles County) in which the USC TCORS is already conducting surveys. P2 will recruit the schools for the survey, using procedures that the school-based research team has developed and refined over the past 30 years. These procedures include obtaining approval from the school district's IRB or similar research review committee and meeting with principals and teachers to introduce the study. P2 will request access to specific classrooms of students for P2's longitudinal survey, and they will also request access to additional classrooms for P4. To avoid contaminating the ongoing observational cohort studies, the researchers will not show tobacco social media posts to students in the cohorts. Instead, the researchers will recruit classrooms of students who are not in the cohorts (e.g., when the cohorts are in 10th grade, the researchers will recruit 9th graders and 11th graders from the same schools). The first half of year in years 3-5, P2 will be collecting data from one grade level, so the researchers will have access to the other 3 grade levels in each high school. After obtaining approval from the district and school, the researchers ask the principal to send an email and paper letter to all parents in the selected classes. The email and letter will state that the school is partnering with USC to administer a 20-minute survey in class. The email will contain a link for parents to provide online consent or opt out. The paper letter will contain a QR code that parents can scan with their phones to provide online consent or opt out. For families that do not respond, the researchers will contact the parents by phone or text, using the contact information provided by the school (under FERPA, schools can provide directory information including parents' names and phone numbers unless they have opted out). After obtaining parental consent, the researchers will invite students to complete an online youth assent form and participate in the survey.
Role of the Investigator/Research Staff
- Will the primary investigator or research staff know any research participants, or have a past or present relationship with participants (e.g., supervisors, principals, any kind of authority or influence over the participants)? X No ☐ Yes: If yes, please explain the relationship.
- Will the primary investigator or research staff have a relationship with the data collection site? X No
- Researchers' relevant experience and background and/or that of research staff as it pertains to supporting and understanding the participants in the study .
Jennifer B. Unger, Ph.D. is Professor of Population and Public Health Sciences (PPHS) at USC. She has led multiple projects and cores in the USC Transdisciplinary Tobacco Use Research Center in the 2000s to investigate cultural influences on adolescent tobacco use, and multiple grants from the California Tobacco-Related Disease Research Program to study tobacco use among Hispanic, African American, and American Indian populations. She served as MPI for USC TCORS projects examining the prevalence, themes, and effects of tobacco content in social media for the 2013-2018 and 2018-2023 cycles and has directed a Population Core from 2018-2023 focused on data collection in local high schools.
Screening of Participants
- Will participants be screened?
X No:
Research Activities
- List all activities (i.e., interviews, focus groups, surveys, interventions etc.) participants will be asked to perform and how long each activity will take. For studies with multiple populations, for each activity, specify which population is doing which activity.
- High school students will be recruited in collaboration with P2 and school site administrators. Information on the study survey will be sent from the school to students and parents. Parents will complete consent forms online. Students will read a description of the study and assent form before they begin the survey, which will be administered online at the school site. No compensation will be given to participants. If the school allows, small gifts (such as USC pens, etc.) may be given to students.
- Participating students will complete an online survey, programmed in REDCap, on their classroom Chromebooks (see measures in Table 1) directly onsite at the schools. In recent school-based surveys, the researchers have found that high schools, even those in low-SES areas, have at least one Chromebook per student. If necessary, the study will provide additional Chromebooks for students to use. After answering questions about their demographic characteristics and tobacco product use, participants will be randomly assigned to view social media posts about e-cigarettes and ONPs with vs. without specific post characteristics.
- All survey data will be captured and stored in USC REDCap, which is password protected and encrypted, and stored on secure servers. No personally identifiable data will be collected.
- Where will researchers meet with participants for each listed activity? At their school site, once sites have agreed to participate.
- How many times will researchers meet with each participant for each activity listed? Once.
- Are researchers using survey instruments, interview/focus group questions, interview guides, etc., to collect data? X Yes:
- Will the research uncover or discover information related to participant suicidality? X No
Secondary/Archival/Existing Data
- Will the researchers be using any existing data sets?
X No:
International Research NA
- Conditions
- Perceptions of Tobacco Products
- Being tested
- Each intervention will be a picture of a social media post. The posts will vary (in a 3X2 factorial design) the type of flavor described and whether concealability is described.
- Keywords
- tobacco, e-cigarette, social media
- Medical subject headings
- Vaping
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Each intervention will be a picture of a social media post. The posts will vary (in a 3X2 factorial design) the type of flavor described and whether concealability is described.Behavioural
The researchers are making stimuli that will appear to be social media posts about tobacco products. They will vary on two dimensions in a 3X2 design:
Type of flavor portrayed (flavored, unflavored, or concept flavor name) Whether the post portrays the tobacco product as concealable
| Study group | Role | What they receive |
|---|---|---|
| Unflavored tobacco product, no depiction of concealment of product | Placebo comparator | A picture of a social media post Receives: Behavioral: Each intervention will be a picture of a social media post. The posts will vary (in a 3X2 factorial design) the type of flavor described and whether concealability is described. |
| Flavored tobacco product, no depiction of concealment of product | Experimental | A picture of a social media post Receives: Behavioral: Each intervention will be a picture of a social media post. The posts will vary (in a 3X2 factorial design) the type of flavor described and whether concealability is described. |
| Concept flavor tobacco product, no depiction of concealment of product | Experimental | A picture of a social media post Receives: Behavioral: Each intervention will be a picture of a social media post. The posts will vary (in a 3X2 factorial design) the type of flavor described and whether concealability is described. |
| Unflavored tobacco product, depiction of concealment of product | Experimental | A picture of a social media post Receives: Behavioral: Each intervention will be a picture of a social media post. The posts will vary (in a 3X2 factorial design) the type of flavor described and whether concealability is described. |
| Flavored tobacco product, depiction of concealment of product | Experimental | A picture of a social media post Receives: Behavioral: Each intervention will be a picture of a social media post. The posts will vary (in a 3X2 factorial design) the type of flavor described and whether concealability is described. |
| Concept flavor tobacco product, depiction of concealment of product | Experimental | A picture of a social media post Receives: Behavioral: Each intervention will be a picture of a social media post. The posts will vary (in a 3X2 factorial design) the type of flavor described and whether concealability is described. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Tobacco product use: Lifetime and past-month use of tobacco products Perceived harm of product Social norms about product use Susceptibility to tobacco use
All of these are standard psychosocial measures from the Population Assessment of Tobacco and Health (PATH) survey.
Measured: Immediately after viewing the stimuli
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted23 Jul 2026
- Study start1 Jul 2025
- Primary completion1 Nov 2027 (estimated)
- Study completion1 May 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Perceptions of Tobacco ProductsStudies of the same condition, open and under way.
- More trials run by University of Southern CaliforniaThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Basic science
- Allocation
- Randomised
- Intervention model
- Factorial
- Model description
- Adolescents will view social media posts about tobacco products with varying characteristics. After viewing the posts, they will report their perceptions of tobacco products.
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 4,500 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University of Southern California
- Sponsor type
- University, hospital or other
- Collaborators
- National Cancer Institute (NCI)
- Responsible party
- Principal investigator, Jennifer Unger, University of Southern California
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07721883
- Sponsor's protocol ID
- UP-23-00724
- Other IDs
- U54CA180905
- Acronym
- USC TCORS P4
- Status last verified
- Jul 2026
- First submitted
- 16 Jul 2026
- Last updated
- 23 Jul 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: There is no need to share IPD with other researchers.
Study at a glance
From the registry record, last updated by the sponsor on 23 Jul 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- USC Tobacco Center of Regulatory Science - Project 4: Social Media Influences on Engagement and Susceptibility to Non-combustible Tobacco Product Use Among Youth and Young Adults (AYA)
- ClinicalTrials.gov ID
- NCT07721883
- Acronym / sponsor ID
- USC TCORS P4 / UP-23-00724
- Conditions
- Perceptions of Tobacco Products
- Keywords
- tobacco, e-cigarette, social media
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 4,500 participants (estimated)
- Lead sponsor
- University of Southern CaliforniaUniversity, hospital or other
- Collaborators
- National Cancer Institute (NCI)
- Study start
- 1 Jul 2025 (actual)
- Primary completion
- 1 Nov 2027 (estimated)
- Study completion
- 1 May 2028 (estimated)
- First posted
- 23 Jul 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The purpose of this study is to present social media posts with varying combinations of flavor types and mentions of stealth use, to adolescents and determine whether these message characteristics increase adolescents' perceptions of these products and susceptibility to using these products.
Detailed description
University of Southern California Social Behavioral and/or Secondary Research Protocol Template
General Information Study Title: TCORS3 Project 4: Social media influences on engagement and susceptibility to non-combustible tobacco product use among youth and young adults (AYA)
PI Name: Jennifer Unger, Ph.D.
Study Information
- What is the general purpose of the study? What do the investigators hope to learn? (Maximum 1-2 paragraphs of explanation). Social media is an increasingly important source of information on emerging tobacco products among adolescents. On social media platforms with large youth user bases (e.g., TikTok, Instagram), social media influencers (e.g., public figures, promoters, models, brand ambassadors) can promote novel non-combustible tobacco products on behalf of manufacturers and distributors via social media posts that may attract adolescents to nicotine use. Of concern is the emergence of novel oral nicotine products (ONPs) and e-cigarettes-both of which may leverage social media to market aspects of their products that could attract adolescents to tobacco use. TCORS Project 4 includes two interrelated studies. Study 1 (not a clinical trial) will examine text (Twitter), picture (Instagram), and video (TikTok) posts in social media to determine whether tobacco-related posts that depict products with: a) concept flavors, b) stealth use, and c) other youth-appealing characteristics will generate more engagement (e.g., likes, favorites, shares), compared with tobacco-related posts that do not have these characteristics, respectively. Study 2 (the current clinical trial) will present social media posts adapted from those found in Study 1, with varying combinations of flavor types and mentions of stealth use, to adolescents and determine whether these message characteristics increase adolescents' susceptibility to using these products.
- List the Research Questions.
- Is susceptibility to use the ONP or e-cigarette products higher among youth assigned to view social media posts with concept or characterizing flavors and/or references to stealth use? II. Are the associations between social media post characteristics and susceptibility to use the product mediated by perceived harm and perceived social norms? III. Do the effects of flavors, stealth use, and influencers on susceptibility vary across demographic and tobacco use groups (e.g., age, gender, race/ethnicity, tobacco product use history)?
Inclusion \& Exclusion Criteria
- Describe the inclusion and exclusion criteria for enrollment.
- Provide justification for the population included.
- Please describe (maximum 1-2 paragraphs) how equity, diversity, and inclusion have been considered.
Inclusion and exclusion criteria for enrollment: Adolescents will be eligible to participate if they are students attending the schools where TCORS Project 2 (P2) will be collecting data (but not participating in the P2 cohort) and provide parental consent and youth assent. Exclusion criteria include lack of parent consent or student assent, inability to read English, or any cognitive or physical health condition that would preclude viewing stimuli on a computer screen and answering questions. There are no eligibility criteria based on previous tobacco product use because susceptibility (openness to trying a product in the future) can be assessed among ever-users as well as never-users.
Provide justification for including (or excluding) minors: The study is focused on associations between social media exposure to tobacco content and tobacco product use among adolescents and young adults (AYA), so adolescents (i.e., minors under 18) will be surveyed.
Sample considerations: TCORS P2 recruits from local area high schools and this project will recruit at the same schools. The research questions will look at differences in associations among demographic groups; therefore a diverse sample is needed. Los Angeles area high schools provide sex, racial and ethnic diversity. All eligible students will be invited to participate.
Where will Recruitment occur?
- List all sites or locations where researchers will recruit participants (e.g., on USC campus, place of employment, a specific elementary school, Amazon Turk, Qualtrics panel, specific groups within Facebook, Instagram, etc. Provide exact locations and/or weblinks as applicable). Schools will be recruited in Year 1. Data will not be collected from human subjects until the schools have been recruited and their information has been uploaded here.
- Are the researchers specifically seeking any participants physically present in a country outside of the United States?
X No ☐ Yes If yes, please answer the additional questions regarding International Research.
How will Recruitment happen?
- What format(s) will the researchers use to advertise (find) potential participants (e.g., Listservs, personal emails, public email, flyer, letter, phone call, social media post (e.g., Facebook, Twitter, Instagram)? Email from school personnel to students and parents.
- Who will distribute the recruitment material, and how will it be distributed?
Each year (Years 3-5), the researchers will recruit 1500 students attending the same high schools (across Los Angeles County) in which the USC TCORS is already conducting surveys. P2 will recruit the schools for the survey, using procedures that the school-based research team has developed and refined over the past 30 years. These procedures include obtaining approval from the school district's IRB or similar research review committee and meeting with principals and teachers to introduce the study. P2 will request access to specific classrooms of students for P2's longitudinal survey, and they will also request access to additional classrooms for P4. To avoid contaminating the ongoing observational cohort studies, the researchers will not show tobacco social media posts to students in the cohorts. Instead, the researchers will recruit classrooms of students who are not in the cohorts (e.g., when the cohorts are in 10th grade, the researchers will recruit 9th graders and 11th graders from the same schools). The first half of year in years 3-5, P2 will be collecting data from one grade level, so the researchers will have access to the other 3 grade levels in each high school. After obtaining approval from the district and school, the researchers ask the principal to send an email and paper letter to all parents in the selected classes. The email and letter will state that the school is partnering with USC to administer a 20-minute survey in class. The email will contain a link for parents to provide online consent or opt out. The paper letter will contain a QR code that parents can scan with their phones to provide online consent or opt out. For families that do not respond, the researchers will contact the parents by phone or text, using the contact information provided by the school (under FERPA, schools can provide directory information including parents' names and phone numbers unless they have opted out). After obtaining parental consent, the researchers will invite students to complete an online youth assent form and participate in the survey.
Role of the Investigator/Research Staff
- Will the primary investigator or research staff know any research participants, or have a past or present relationship with participants (e.g., supervisors, principals, any kind of authority or influence over the participants)? X No ☐ Yes: If yes, please explain the relationship.
- Will the primary investigator or research staff have a relationship with the data collection site? X No
- Researchers' relevant experience and background and/or that of research staff as it pertains to supporting and understanding the participants in the study .
Jennifer B. Unger, Ph.D. is Professor of Population and Public Health Sciences (PPHS) at USC. She has led multiple projects and cores in the USC Transdisciplinary Tobacco Use Research Center in the 2000s to investigate cultural influences on adolescent tobacco use, and multiple grants from the California Tobacco-Related Disease Research Program to study tobacco use among Hispanic, African American, and American Indian populations. She served as MPI for USC TCORS projects examining the prevalence, themes, and effects of tobacco content in social media for the 2013-2018 and 2018-2023 cycles and has directed a Population Core from 2018-2023 focused on data collection in local high schools.
Screening of Participants
- Will participants be screened?
X No:
Research Activities
- List all activities (i.e., interviews, focus groups, surveys, interventions etc.) participants will be asked to perform and how long each activity will take. For studies with multiple populations, for each activity, specify which population is doing which activity.
- High school students will be recruited in collaboration with P2 and school site administrators. Information on the study survey will be sent from the school to students and parents. Parents will complete consent forms online. Students will read a description of the study and assent form before they begin the survey, which will be administered online at the school site. No compensation will be given to participants. If the school allows, small gifts (such as USC pens, etc.) may be given to students.
- Participating students will complete an online survey, programmed in REDCap, on their classroom Chromebooks (see measures in Table 1) directly onsite at the schools. In recent school-based surveys, the researchers have found that high schools, even those in low-SES areas, have at least one Chromebook per student. If necessary, the study will provide additional Chromebooks for students to use. After answering questions about their demographic characteristics and tobacco product use, participants will be randomly assigned to view social media posts about e-cigarettes and ONPs with vs. without specific post characteristics.
- All survey data will be captured and stored in USC REDCap, which is password protected and encrypted, and stored on secure servers. No personally identifiable data will be collected.
- Where will researchers meet with participants for each listed activity? At their school site, once sites have agreed to participate.
- How many times will researchers meet with each participant for each activity listed? Once.
- Are researchers using survey instruments, interview/focus group questions, interview guides, etc., to collect data? X Yes:
- Will the research uncover or discover information related to participant suicidality? X No
Secondary/Archival/Existing Data
- Will the researchers be using any existing data sets?
X No:
International Research NA
Study design
- Primary purpose
- Basic science
- Allocation
- Randomised
- Intervention model
- Factorial
- Masking
- Single blind (participant)
- Number of arms
- 6
- Model description
- Adolescents will view social media posts about tobacco products with varying characteristics. After viewing the posts, they will report their perceptions of tobacco products.
| Arm | Type | Receives |
|---|---|---|
| Unflavored tobacco product, no depiction of concealment of product | Placebo comparator | Behavioral: Each intervention will be a picture of a social media post. The posts will vary (in a 3X2 factorial design) the type of flavor described and whether concealability is described.A picture of a social media post |
| Flavored tobacco product, no depiction of concealment of product | Experimental | Behavioral: Each intervention will be a picture of a social media post. The posts will vary (in a 3X2 factorial design) the type of flavor described and whether concealability is described.A picture of a social media post |
| Concept flavor tobacco product, no depiction of concealment of product | Experimental | Behavioral: Each intervention will be a picture of a social media post. The posts will vary (in a 3X2 factorial design) the type of flavor described and whether concealability is described.A picture of a social media post |
| Unflavored tobacco product, depiction of concealment of product | Experimental | Behavioral: Each intervention will be a picture of a social media post. The posts will vary (in a 3X2 factorial design) the type of flavor described and whether concealability is described.A picture of a social media post |
| Flavored tobacco product, depiction of concealment of product | Experimental | Behavioral: Each intervention will be a picture of a social media post. The posts will vary (in a 3X2 factorial design) the type of flavor described and whether concealability is described.A picture of a social media post |
| Concept flavor tobacco product, depiction of concealment of product | Experimental | Behavioral: Each intervention will be a picture of a social media post. The posts will vary (in a 3X2 factorial design) the type of flavor described and whether concealability is described.A picture of a social media post |
Who may qualify
- Ages
- 14 to 17 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child
Key inclusion criteria (2 listed)
- High school student
- Provides parental consent and youth assent
Key exclusion criteria (2 listed)
- No parental consent or youth assent
- Can't read or speak English
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Each intervention will be a picture of a social media post. The posts will vary (in a 3X2 factorial design) the type of flavor described and whether concealability is described.The researchers are making stimuli that will appear to be social media posts about tobacco products. They will vary on two dimensions in a 3X2 design: Type of flavor portrayed (flavored, unflavored, or concept flavor name) Whether the post portrays the tobacco product as concealable | Behavioural | Concept flavor tobacco product, depiction of concealment of product, Concept flavor tobacco product, no depiction of concealment of product, Flavored tobacco product, depiction of concealment of product, Flavored tobacco product, no depiction of concealment of product, Unflavored tobacco product, depiction of concealment of product, Unflavored tobacco product, no depiction of concealment of product |
Primary outcome
Tobacco product use: Lifetime and past-month use of tobacco products Perceived harm of product Social norms about product use Susceptibility to tobacco use
Time frame: Immediately after viewing the stimuli
All of these are standard psychosocial measures from the Population Assessment of Tobacco and Health (PATH) survey.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 23 Jul 2026.
- We will de-identify the data and upload it to an NIH-approved repository after the end of the study.Link provided by the sponsor.
- Individual participant dataSharing planned: No. There is no need to share IPD with other researchers.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Each intervention will be a picture of a social media post. The posts will vary (in a 3X2 factorial design) the type of flavor described and whether concealability is described. in people with Perceptions of Tobacco Products, run by University of Southern California at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 23 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Jennifer B Unger, PhD (323-442-8234, unger@usc.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Tobacco product use: Lifetime and past-month use of tobacco products Perceived harm of product Social norms about product use Susceptibility to tobacco use (time frame: Immediately after viewing the stimuli). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 23 Jul 2026.