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RecruitingNCT07721883USC TCORS P4Updated Jul 23, 2026

Social Media Influences on Engagement and Susceptibility to Non-combustible Tobacco Product Use Among Youth and Young Adults (AYA)

An interventional study of 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 Perceptions of Tobacco Products, sponsored by University of Southern California. Recruiting at 1 site in United States. Open to participants aged 14 Years to 17 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-07-23.

Sponsored by University of Southern California · Not applicable, Interventional, and Basic science

From the registry’s dates

  • Registered 1 year after the study started (first participant enrolled Jul 2025, registered Jul 2026).
  • Started Jul 2025; still recruiting 1 year 4 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
4,500
Allocation
Randomized
Ages
14 Years to 17 Years
Sex
All
01

Study 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 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

  1. 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.

  2. List the Research Questions.

I. 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

  1. Describe the inclusion and exclusion criteria for enrollment.
  2. Provide justification for the population included.
  3. 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?

  1. 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.

  2. 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?

  1. 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.

  2. 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

  1. 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.
  2. Will the primary investigator or research staff have a relationship with the data collection site? X No

4. 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

1. Will participants be screened?

X No:

Research Activities

  1. 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.

    1. 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.
    2. 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.
    3. 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.
  2. Where will researchers meet with participants for each listed activity? At their school site, once sites have agreed to participate.
  3. How many times will researchers meet with each participant for each activity listed?

    Once.

  4. Are researchers using survey instruments, interview/focus group questions, interview guides, etc., to collect data?

    X Yes:

  5. Will the research uncover or discover information related to participant suicidality? X No

Secondary/Archival/Existing Data

1. Will the researchers be using any existing data sets?

X No:

International Research NA

02

Conditions studied

  • Perceptions of Tobacco Products

Browse trials for

Keywords

  • tobacco, e-cigarette, social media
03

In context

Vaping

402 studies on the registry are indexed under Vaping; 95 are open to participants now.

This study's planned enrollment of 4,500 is above the median of 79 across 322 interventional studies indexed under Vaping.

Browse Vaping studies →

Lead sponsor

University of Southern California is the lead sponsor of 791 studies on the registry; 136 are open to participants now.

Of its 70 completed or terminated interventional studies of FDA-regulated products, 32 (46%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
14 Years to 17 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • High school student
  • Provides parental consent and youth assent

Exclusion criteria

Exclusion Criteria:

  • No parental consent or youth assent
  • Can't read or speak English
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Factorial assignment
Masking
Single (Participant)
Enrollment
4,500 participants (estimated)

Study arms

  • Placebo comparator
    Unflavored tobacco product, no depiction of concealment of product

    A picture of a social media post

    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.

  • Experimental
    Flavored tobacco product, no depiction of concealment of product

    A picture of a social media post

    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.

  • Experimental
    Concept flavor tobacco product, no depiction of concealment of product

    A picture of a social media post

    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.

  • Experimental
    Unflavored tobacco product, depiction of concealment of product

    A picture of a social media post

    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.

  • Experimental
    Flavored tobacco product, depiction of concealment of product

    A picture of a social media post

    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.

  • Experimental
    Concept flavor tobacco product, depiction of concealment of product

    A picture of a social media post

    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.

Interventions

  • BehavioralEach 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

06

What researchers measure

Primary outcomes

  1. 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.

    Time frame: Immediately after viewing the stimuli

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: No — There is no need to share IPD with other researchers.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Jul 2025 (actual). Primary completion is estimated for Nov 2027, 28 months after the start.

Of 184 non-industry interventional studies with no phase under Vaping, half reached primary completion within 20 months of starting (the median), counting those still running; a quarter within 9 and three quarters within 35. This study's planned 28 months is above that.

Counting every sponsor, half of 208 studies reached it within 18 months; a quarter within 6 and three quarters within 31.

How these figures are worked out, and which studies are left out of them.

Registered
Jul 16, 2026
First posted
Jul 23, 2026
StartActual
Jul 1, 2025
Primary completionEst.
Nov 1, 2027
CompletionEst.
May 1, 2028
Last update
Jul 23, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jul 23, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07721883
Responsible party
Jennifer Unger (Professor, University of Southern California) — Principal investigator
First posted
Jul 23, 2026
Start date
Jul 1, 2025
Primary completion
Nov 1, 2027 (estimated)
Completion
May 1, 2028 (estimated)
Last update
Jul 23, 2026

Study contacts

Jennifer B Unger, PhD
Contact
unger@usc.edu
323-442-8234

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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