Sun Safe Together: Preventing Skin Cancer in Teens

This study, "Sun Safe Together," is testing a digital program to help teenagers and their parents prevent skin cancer. Teens will receive sun safety and general health messages through text messages (MMS) for 12 weeks. Parents will join a private Facebook group for 12 weeks, where they'll see content about teen sun safety and general health. The study wants to see if it's possible to recruit parent-teen pairs and if they find the program helpful and engaging. You can join if you are a teen aged 13-17 and live with a parent, and you've had a sunburn or used an indoor tanning bed in the last year, or don't protect yourself well from the sun. The study is currently unclear about its recruitment status.

Study design
This is a single-arm study, meaning all 104 participants will receive the intervention. It is a pilot trial to test the program's feasibility and acceptability.
What's involved
Teens will receive MMS messages for 12 weeks. Parents will participate in a private Facebook group for 12 weeks. Engagement will be measured for 3 months, and retention for 3 and 6 months.
Compensation
Not stated in the trial record.
Follow-up
Participants will be followed for engagement for 3 months and for retention at 3 and 6 months after the intervention.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07681791

Sun Safe Together: A Digital Skin Cancer Prevention Intervention for Adolescents and Their Parents

Recruiting
NAAges 13+InterventionalPrevention
Rutgers, The State University of New Jersey
~104 participants
Updated 2026-08-05 on ClinicalTrials.gov
What's tested:Teen MMSParent Facebook

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Feasibility of recruitment
Measured over Baseline
+5 more outcomes measured
Skin Cancer Prevention

NCT07681791

Where you'd take part

This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • Rutgers Cancer Institute

    New Brunswick, New Jerseystudy coordinator listed

    Recruiting

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

  • Carolyn Heckman, PhD · PRINCIPAL_INVESTIGATOR · Rutgers, The State University of New Jersey
  • Katie A Devine, PhD · PRINCIPAL_INVESTIGATOR · Rutgers, The State University of New Jersey

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Eligibility criteria

Inclusion

Must be ages 13-17 years
Live with study parent equal to or greater than half time in US
Have experienced sunburn or indoor tanned in the last year or have a suboptimal sun protection score
Have no personal history of melanoma or severe medical condition that prevents participation
Have access to smartphone
Speak and read English
Must be age 18 or older
Live with a teen equal to or greater than half time in US
Have a teen who had experienced sunburn or indoor tanned in the last year or have a suboptimal sun protection score
Have no personal history of melanoma or severe medical condition that prevents participation
Have internet at home, a Facebook account, and be willing to use Facebook daily
Have access to smartphone
Speak and read English
  • Feasibility of recruitmentBaseline

    Feasibility of recruitment will be assessed by the proportion of eligible parent-teen dyads that enroll in the study

  • Acceptability of MMS interventionImmediately after the intervention

    Items were adapted from the Acceptability of Intervention and Feasibility of Intervention Measures to obtain participant feedback about the acceptability, feasibility, ease of use, and impact of the intervention. Individual items are rated on a 5-point likert scale from (1) Completely Disagree to (5) Completely Agree. Higher scores indicated greater acceptability.

  • Engagement with MMS intervention3-months

    Proportion of messages viewed will be calculated to describe engagement.

  • Feasibility of Outcome Data Collection - 7-Day DiariesBaseline, 3-months, 6-months

    Proportion of teens who complete 7-day diaries will be calculated.

  • Feasibility of Outcome Data Collection - UVR DosimeterBaseline, 6 months

    Proportion of teens who return UVR dosimeter with usable data will be calculated.

  • Retention3-months, 6-months

    Proportion of enrolled teens who complete surveys at 3- and 6-months will be calculated.