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SunburnNCT07751406

Randomized Trial of a Sun Safety Intervention for Young Adults

A study testing Healthy Skin and Healthy Lifestyle in people with Sunburn, run by University of Connecticut.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

The goal of this randomized controlled trial is to test the efficacy of a dissonance induction intervention compared to a control group on tanning in 278 young adult tanners. The primary outcome will be tanning at 3-months. Read more about this study

Who is it for?
Ages 18 to 30 yearsHealthy volunteers can take part
Conditions the study is for
Sunburn
What is being tested?
Healthy Skin and Healthy Lifestyle
Could I receive a placebo?
No, everyone receives an active treatment
How many people
278 participants
Where
No sites listed yet
Study dates
1 Feb 2027to 30 Nov 2030
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 18 to 30 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • tanned indoors and/or outdoors at least 5 times in the past year (either intentionally or unintentionally)
  • have intentions of tanning indoors or outdoors in the next 6 months
  • regular social media users (i.e., logged into a social media platform on most days in the past 4 weeks)
  • is and plans to be a full time resident of one of the 12 states with average UV Index ≥5 between April-October (CA, AZ, TX, AL, AR, FL, GA, LA, MS, SC, NM, HI) during the study period.

Who cannot join

  • <100 followers on at least 1 social media account
  • plans to move to a different state during study period

Trial locations and contacts

No sites are listed yet. Contact the study team or a site near you to ask about taking part.

About this study

Official title: Randomized Trial of a Dissonance-Based Sun Safety Intervention for Young Adult Tanners

The goal of this randomized controlled trial is to test the efficacy of a dissonance induction intervention compared to a control group on tanning in 278 young adult tanners. The primary outcome will be tanning at 3-months. Secondary outcomes include tanning at 15-months and sunburn and sun protection use 3- and 15-months post-intervention. The main question it aims to answer is whether the intervention reduces tanning and sunburns and increases use of sunscreen among young adults who tan. Participants will be incentivized to develop sun safety and anti-tanning messaging for a social media campaign and to recruit their social ties to engage with those messages. They will then be asked to complete surveys on tanning and sun protection at baseline, 3-, and 15 months. They will also complete monthly surveys to report sunburns. The dissonance induction intervention is based on a highly effective and internationally disseminated eating disorder prevention program that has reached over 3.5 million people around the world.

Read the detailed description

In this trial, 278 adults will be randomized to one of two campaigns: the Healthy Skin Campaign or the Healthy Lifestyle campaign. Participants must be ages 18-30 years, and have tanned indoors and/or outdoors at least 5 times in the past year (either intentionally or unintentionally), have intentions of tanning indoors or outdoors in the next 6 months, be regular social media users (i.e., logged into a social media platform every day in the past 4 weeks), and be a resident of the 12 states with average UV Index ≥5 between April-October (CA, AZ, TX, AL, AR, FL, GA, LA, MS, SC, NM, HI).

Recruitment will target 12 states with average UV Index is ≥5 during the intervention and follow-up period of April-September. We will use social media advertisements, Research Match, and Qualtrics (internet panel company).

Recruitment advertisements will link to an online survey to evaluate initial eligibility. Those initially eligible will undergo a screening call where they will give verbal consent, learn about the two campaigns, and share their availability to attend an orientation webinar. Following the screening call, eligible candidates will be sent a baseline survey of study measures and upon completion be randomized.

After randomization, participants will attend an orientation webinar where they will learn about their social media campaign, how to create posts, guidelines for appropriate content (e.g., no nudity, explicit language, brand names, images or language that directly or indirectly promoted unhealthy behaviors, or pictures of people without consent), and campaign-related guidance on what to post about (as described below). In the webinar, staff will state that the researchers "are interested in learning how to develop effective health-related social media messages" and "want to examine how engaging young adults find health-related social media posts created by other young adults." Participants will be asked to create social media posts related to the topic of their condition to be posted to the campaign feeds on Facebook and Instagram. In each condition, participants will be instructed to create up to 12 social media posts during the 6-week social media campaign (maximum of 2 in any week). This number of posts would result in a maximum of 5-6 per day in each condition which is consistent with norms reported in social media marketing outlets.

Participants will receive a $10 gift card for each post they create and have a chance to win an additional $50 gift card each week if their post receives the most engagement points in their respective condition within the first 48 hours of posting. The 48-hour time limit allows all posts posted between Monday and Sunday to have the same time frame to garner engagement. Winners each week will be determined on the Tuesday that follows that week (to allow all posts to garner 48 hours of engagement. Social media posts typically get the vast majority of engagement in less than 48 hours.53 The incentive structure is as follows: reactions ("likes") earn 1 point, comments (from unique users because one user can make >1 comments) earn 2 points, and shares/retweets earn 3 points. Shares/reposts earn the most points because this form of engagement has potential to reach a larger audience. This engagement data from the first 48 hours across both Facebook and Instagram will be tallied.

Participants will also earn 2 points for each post they put on one of their personal social media accounts. If they put up a post on more than one of their social media accounts, they will get 2 points for each account they put it on. Participants may use a personal account on any social media platform (e.g., Instagram, TikTok, Snapchat) as long as that account has ≥100 followers at the start of the study. Participants will also get a bonus incentive of $25 if they address all key areas of their assigned topic. On the following Tuesday of each week, research staff will tally the points for each participant and then notify the winner by email. Study staff will email all participants to inform them of the winner's point total each week to nudge them to increase the engagement they are driving to their posts and to post on their own accounts to grow their point totals faster in the next week.

Healthy Skin Campaign. In the orientation webinar, participants assigned to the Healthy Skin campaign will be instructed to create social media posts promoting healthy skin. First, we will discuss the tan ideal and its origins (e.g., media, companies, peer pressure) along with the negative consequences of the tan ideals including ideal internalization, body dissatisfaction, negative mood, premature aging, and skin cancer including the disfiguring ways it is treated and deadly melanoma. We will show a brief video message by a young melanoma survivor and former tanner who will reinforce these points. Second, participants will be encouraged to design posts that reflect the 10 key tenets of dissonance induction interventions, including 1) critique the tan ideal, 2) make arguments against the tan ideal, 3) are messages to younger people and/or their younger self about the costs of attempting to live up to the tan ideal, that promote skin color acceptance (body positivity), 4) speak out about experiences in which they felt pressured to live up to the tan ideal (e.g., being called pale or sick looking), 5) encourage the use of social media to speak out against the tan ideal, 6) share quick catchy verbal comebacks to statements that promote the tan ideal (e.g., "loving the skin I'm in!"), 7) promote sunscreen to protect skin from the harms of UVR, 8) discourage tanning, 9) promote ways to enhance the personal aesthetic via sun safety behaviors (e.g., fashionable protective clothing, hats, and parasols), and 10) promote shade use. They will be shown examples and encouraged to incorporate all 10 topics in their 12 posts. Posts for this campaign will be simultaneously posted to the Skin Smart Campus Initiative Facebook and Instagram pages.

Healthy Lifestyle Campaign. Participants assigned to the Healthy Lifestyle campaign will be asked to create social media posts promoting healthy lifestyle behaviors such as fruit and vegetable consumption, reducing sugary beverages, exercise, sleep, and stress reduction. First, they will be informed of the health benefits of these behaviors and ways to adopt each into a daily routine. Second, they will be asked to create posts that promote engagement in these behaviors, emphasizing the benefits, risks, and any tips and tricks. Posts created by participants in this condition will be posted to the UConn Center for mHealth and Social Media Facebook and Instagram pages.

At the end of 6 weeks and then again at 3- and 15-months, participants will receive a link to complete the survey battery.

Conditions
Sunburn
Being tested
Healthy Skin, Healthy Lifestyle
Keywords
ultraviolet radiation, sun protection, tanning
Medical subject headings
Sunburn

What participants receive

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

  • Healthy SkinBehavioural

    Participants will be instructed to create up to 12 social media posts during the 6-week social media campaign (maximum of 2/week). Participants will receive incentives for the posts they create and be entered into a weekly contest based on the posts that attracted the most engagement on study feeds and their personal feeds. Participants will be instructed to create social media posts that encourage young adults like them to challenge the "tanned skin ideal" portrayed by the media, protect their skin from UVR, avoid tanning, use sun protection, and communicate body positivity. We will explain how tan ideals are perpetuated by the media, how the 'tan ideal' gets internalized and makes people feel worse about their bodies, how the focus on achieving a tan negatively impacts body satisfaction, and how body positivity pertains to all skin types. They will be encouraged to incorporate these ideas in their posts and to role model sun safety.

  • Healthy LifestyleBehavioural

    Participants will be instructed to create up to 12 social media posts during the 6-week social media campaign (maximum of 2/week). Participants will receive incentives for the posts they create and be entered into a weekly contest based on the posts that attracted the most engagement on study feeds and their personal feeds. Participants will be instructed to create social media posts that encourage young adults like them to consume a healthy diet (e.g., 5 servings of fruit and vegetables, eliminate sugary beverages), get moderate intensity exercise for 150 minutes per week, get 7-8 hours of sleep per night, and engage in stress management. They will receive guidance on healthy lifestyle targets and how these lifestyle behaviors prevent disease.They will be encouraged to incorporate these ideas in their posts and to role model these healthy lifestyle behaviors.

Study groups in NCT07751406
Study groupRoleWhat they receive
Healthy SkinExperimentalParticipants will be incentivized to create, attract engagement to, and post social media content that argues for sun safety and against tanning in a 6-week social media campaign.
Receives: Behavioral: Healthy Skin
Healthy LifestyleActive comparatorParticipants will be incentivized to create, attract engagement to, and post social media content that promotes exercise, healthy diet, sleep, and stress management in a 6-week social media campaign.
Receives: Behavioral: Healthy Lifestyle

What is being measured

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

  1. tanning

    total number of self-reported outdoor and indoor tanning episodes

    Measured: 3 months post-intervention

Secondary outcomes (8)
  1. tanning

    total number of self-reported outdoor and indoor tanning episodes

    Measured: post-intervention (6 weeks)

  2. tanning

    total number of self-reported outdoor and indoor tanning episodes

    Measured: 15 months post-intervention

  3. sunburn

    total number of sunburns

    Measured: 3 months post-intervention

  4. sunburn

    total number of sunburns

    Measured: post-intervention (6 weeks)

  5. sunburn

    total number of sunburns

    Measured: 15 months post-intervention

  6. unprotected sun exposure

    minutes per day weighted by percentage of the body that was unprotected from the sun (per the Daily Minutes of Unprotected Sun Exposure (MUSE) Inventory)

    Measured: 3 months post-intervention

  7. unprotected sun exposure

    minutes per day weighted by percentage of the body that was unprotected from the sun (per the Daily Minutes of Unprotected Sun Exposure (MUSE) Inventory)

    Measured: post-intervention (6 weeks)

  8. unprotected sun exposure

    minutes per day weighted by percentage of the body that was unprotected from the sun (per the Daily Minutes of Unprotected Sun Exposure (MUSE) Inventory)

    Measured: 15 months post-intervention

Timeline

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

  1. First posted7 Aug 2026
  2. Study start1 Feb 2027 (estimated)
  3. Primary completion30 Nov 2030 (estimated)
  4. Study completion30 Nov 2030 (estimated)

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
Randomised
Intervention model
Parallel groups
Model description
This is a two-arm randomized controlled trial
Masking
Double blind
Who is masked
Investigator, Outcomes assessor
Enrolment
278 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07751406
Sponsor's protocol ID
26-100
Other IDs
R01CA309495
Status last verified
Sep 2026
First submitted
3 Aug 2026
Last updated
11 Sep 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: Even though the final dataset will be de-identified prior to release for sharing, participant social media posts will not be made available to protect their privacy. We will make the data and associated documentation available to users only under a data-sharing agreement that provides for: (1) a commitment to using the data only for research purposes and not to identify any individual participant; (2) a commitment to securing the data using appropriate computer technology; and (3) a commitment to destroying or returning the data after analyses are completed. Datasets will be stored with encryption and will be shared only after verification of IRB approval is obtained.

Questions about this trial

What is this clinical trial studying?

A study testing Healthy Skin and Healthy Lifestyle in people with Sunburn, run by University of Connecticut.

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 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: opening soon, as of the sponsor's last update on 11 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

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?

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 Denise Fernandes (860-515-8186, denise.fernandes@uconn.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

tanning (time frame: 3 months post-intervention). 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 11 Sep 2026.

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