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Screen Time ExposureNCT07199660

Reactions to Social Media Warning Labels Among Teens and Young Adults

A study testing Human-developed negative body image warning, Voluntary warning and Human-developed depression and anxiety warning in people with Screen Time Exposure, run by Stanford University at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The primary objective of this study is to evaluate whether social media warnings are perceived as more effective than control labels among teens and young adults, and to identify the most promising topics for social media warnings for these age groups. Read more about this study

Who is it for?
Ages 13 to 29 yearsHealthy volunteers can take part
Conditions the study is for
Screen Time Exposure
What is being tested?
Human-developed negative body image warning, Voluntary warning and Human-developed depression and anxiety warning
Could I receive a placebo?
No, everyone receives an active treatment
How many people
1,012 participants
Where
1 siteUnited States
Study dates
2 Dec 2025to 16 Dec 2025
Phase
Interventional
Are there results?
None posted in the registry

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 13 to 29 years
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult

Who may be able to join

  • Age between 13-29 years
  • Reside in the United States
  • Able to complete a survey in English
  • Access to the internet

Who cannot join

  • Younger than 13 or older than 29 years
  • Reside outside of the United States
  • Unable to complete a survey in English
  • Lacks access to the internet

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Stanford School of Medicine

    Palo Alto, California, 94304

Other trials in United States

About this study

Official title: An Evaluation of Social Media Warning Labels for Teens and Young Adults: A Randomized Controlled Trial

The primary objective of this study is to evaluate whether social media warnings are perceived as more effective than control labels among teens and young adults, and to identify the most promising topics for social media warnings for these age groups. A secondary objective is to compare perceived message effectiveness of warnings refined using artificial intelligence (AI) vs. those not refined using AI.

Read the detailed description

Participants will complete a within-subjects online randomized experiment in which they will view and rate messages on the risk of social media use. Participants will view messages about 9 topics: 8 warning topics and 1 control topic. The 8 warning topics include 7 potential mandatory warnings (depression and anxiety, body image, addiction, sleep, mental health harms to children, not been proven safe, and California's proposed warning) and 1 voluntary warning (similar to a message used on TikTok to encourage users to take breaks). For each topic, participants will view 1-2 messages and respond to survey items about that message. All messages will be shown in random order.

Being tested
Human-developed negative body image warning, Voluntary warning, Human-developed depression and anxiety warning, Human-developed addiction warning, Human-developed sleep warning
Keywords
teenagers, young adults, warning labels, social media

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Human-developed negative body image warningBehavioural

    Participants will view a message about the risk of social media use contributing to negative body. The message was developed by humans without using artificial intelligence.

  • Voluntary warningBehavioural

    Participants will view a message suggesting user take a break from scrolling on social media. The message was developed by humans without using artificial intelligence.

  • Human-developed depression and anxiety warningBehavioural

    Participants will view a message about the risk of social media use contributing to depression and anxiety. The message was developed by humans without using artificial intelligence.

  • Human-developed addiction warningBehavioural

    Participants will view a message warning that social media can be addictive. The message was developed by humans without using artificial intelligence.

  • Human-developed sleep warningBehavioural

    Participants will view a message that social media use can contribute to poor sleep quality. The message was developed by humans without using artificial intelligence.

  • Human-developed mental health harms to young people warningBehavioural

    Participants will view a message about the risk of social media use contributing to mental health harms for some young people. The message was developed by humans without using artificial intelligence.

  • Human-developed warning that social media has not been proven safeBehavioural

    Participants will view a message warning that the use of social media has not been proven safe for young people. The message was developed by humans without using artificial intelligence.

  • Control messageBehavioural

    Participants will view a message about encouraging seatbelt use while traveling in a vehicle.

  • California's proposed social media warningBehavioural

    Participants will view a message warning about the harms of social media use that mirrors the language the state of California has proposed for mandatory social media warnings.

  • Artificial-intelligence-developed depression and anxiety warningBehavioural

    Participants will view a message about the risk of social media use contributing to depression and anxiety. The message was developed using artificial intelligence.

  • Artificial-intelligence-developed negative body image warningBehavioural

    Participants will view a message about the risk of social media use contributing to negative body. The message was developed using artificial intelligence

  • Artificial-intelligence-developed addiction warningBehavioural

    Participants will view a message warning that social media can be addictive. The message was developed using artificial intelligence.

  • Artificial-intelligence-developed sleep warningBehavioural

    Participants will view a message that social media use can contribute to poor sleep quality. The message was developed using artificial intelligence.

  • Artificial-intelligence-developed mental health harms to young people warningBehavioural

    Participants will view a message about the risk of social media use contributing to mental health harms for some young people. The message was developed using artificial intelligence.

  • Artificial-intelligence-developed warning that social media has not been proven safeBehavioural

    Participants will view a message warning that the use of social media has not been proven safe for young people. The message was developed using artificial intelligence.

Study groups in NCT07199660
Study groupRoleWhat they receive
Warning labelsExperimentalParticipants view 15 messages in random order: 6 warning messages about social media developed by a team of human experts (1 each about 6 different topics), 6 warning messages about social media developed by artificial intelligence (1 each about the same 6 topics as the human-developed messages), an additional 1 warning message that mirrors the language proposed by the state of California, 1 voluntary warning message developed by human experts, and 1 control message.
Receives: Behavioral: Human-developed negative body image warning; Behavioral: Voluntary warning; Behavioral: Human-developed depression and anxiety warning; Behavioral: Human-developed addiction warning; Behavioral: Human-developed sleep warning; Behavioral: Human-developed mental health harms to young people warning; Behavioral: Human-developed warning that social media has not been proven safe; Behavioral: Control message; Behavioral: California's proposed social media warning; Behavioral: Artificial-intelligence-developed depression and anxiety warning; Behavioral: Artificial-intelligence-developed negative body image warning; Behavioral: Artificial-intelligence-developed addiction warning; Behavioral: Artificial-intelligence-developed sleep warning; Behavioral: Artificial-intelligence-developed mental health harms to young people warning; Behavioral: Artificial-intelligence-developed warning that social media has not been proven safe

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Perceived message effectiveness for discouraging social media use

    The study will assess perceived message effectiveness for discouraging social media use with 1 item: "How much does this message discourage you from wanting to use social media?" Response options will range from "Not at all" (coded as 1) to "A great deal" (coded as 5). Higher scores indicate higher perceived message effectiveness.

    Measured: The survey will measure perceived message effectiveness immediately after participants are exposed to the message.

Secondary outcomes (1)
  1. Awareness of the harms of social media use

    The study will assess awareness of the harms of social media use with 1 item: "How much does this message increase your awareness of the harms of using social media?" Response options will range from "Not at all" (coded as 1) to "A great deal" (coded as 5). Higher scores indicate greater awareness.

    Measured: The survey will measure awareness of the harms of social media use immediately after participants are exposed to the message.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted30 Sep 2025
  2. Study start2 Dec 2025
  3. Primary completion16 Dec 2025
  4. Study completion16 Dec 2025

Resources

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
Prevention
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
1,012 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07199660
Sponsor's protocol ID
81445
Status last verified
Mar 2026
First submitted
22 Sep 2025
Last updated
16 Mar 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: Investigators will post de-identified individual participant data in a publicly available repository.

Publications

  • Grummon AH, Ulm C, Zeitlin AB, Hall MG, Falbe J, Kline NA, Robinson TN. Designing Social Media Health Warnings for Teenagers and Young Adults: A Randomized Clinical Trial. JAMA Health Forum. 2026 Sep 4;7(9):e263014. doi: 10.1001/jamahealthforum.2026.3014.

    PubMed 42696289

Questions about this trial

What is this clinical trial studying?

A study testing Human-developed negative body image warning, Voluntary warning and Human-developed depression and anxiety warning in people with Screen Time Exposure, run by Stanford University 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 4 inclusion and 4 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: finished, as of the sponsor's last update on 16 Mar 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. 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?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Perceived message effectiveness for discouraging social media use (time frame: The survey will measure perceived message effectiveness immediately after participants are exposed to the message.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07199660, which also lists 1 linked publication.

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 16 Mar 2026.

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