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NCT Number: NCT07681791

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

The goal of this pilot clinical trial is to learn if a digital intervention to improve sun safety, Sun Safe Together (SST), is feasible and acceptable to teenagers and their parents.

Recruiting

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Key information

Age range

13 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Rutgers Cancer Institute

New Brunswick, New Jersey, 08901, United States

Location status: Recruiting

Location contact

Anna Mitarotondo, MS

CONTACT

[email protected]

732-514-2891

Carolyn J. Heckman, PhD

CONTACT

[email protected]

Carolyn J. Heckman, PhD

PRINCIPAL_INVESTIGATOR

Katie A. Devine, PhD, MPH

PRINCIPAL_INVESTIGATOR

About this study

Melanoma is a leading cause of invasive cancer in teens and young adults aged 15-39. Most skin cancers are preventable with skin protection such as minimizing UVR exposure and wearing protective clothing and sunscreen. However, teens have low levels of sun protection. Thus, interventions targeting skin cancer risk reduction among teens are needed. The proposed Sun Safe Together (SST) intervention is a 12-week program consisting of sun safety and general health messages sent via multimedia messaging service (MMS) to teens and via a private Facebook group for parents.

This pilot trial is a single arm test of SST to determine:

  • feasibility of enrolling parent-teen dyads
  • engagement with/acceptability of the intervention via message views and acceptability ratings
  • outcome data collection feasibility (i.e., daily diary, UVR exposure measured by UVR dosimeter)
  • retention rates for teens and parents at 3 and 6 months

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Parents and teens are participating as dyads, meaning both the parent and the teen need to be deemed eligible based on the criteria below to be able to participate.

Teens

  • 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

Parents/Guardians

  • 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

Treatment and study plan

Teen MMS

Behavioral

Teens will receive MMS messages regarding sun safety behaviors and other general health issues for 12 weeks.

Parent Facebook

Behavioral

Parents of teenagers join a private Facebook group where membership, activities, and content are only viewable by invited members. Content related to teen sun safety and general health will be posted for 12 weeks. Research staff will moderate the group.

Primary outcomes

  1. Feasibility of recruitment

    Time frame: Baseline

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

  2. Acceptability of MMS intervention

    Time frame: Immediately 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.

  3. Engagement with MMS intervention

    Time frame: 3-months

    Proportion of messages viewed will be calculated to describe engagement.

  4. Feasibility of Outcome Data Collection - 7-Day Diaries

    Time frame: Baseline, 3-months, 6-months

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

  5. Feasibility of Outcome Data Collection - UVR Dosimeter

    Time frame: Baseline, 6 months

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

  6. Retention

    Time frame: 3-months, 6-months

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

Sponsors and collaborators

Lead sponsor

Rutgers, The State University of New Jersey

Other

Collaborators

  • National Cancer Institute (NCI)

Registry information

Official study title

A Digital Skin Cancer Prevention Intervention for Adolescents and Their Parents

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Jul 2, 2026
Registry last updated
Jul 2, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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