Skip to main content
OpenTrials
Completed

NCT Number: NCT02147080

A Tailored Internet Intervention to Reduce Skin Cancer Risk Behaviors Among Young Adults

Skin cancer is the most common cancer in the US, with over a million new cases diagnosed yearly. Young adults are increasingly at risk of melanoma. Contributing to the increasing skin cancer risk is the fact that US adolescents have the lowest skin protection rates of all age groups and also demonstrate increased exposure to natural and artificial UV radiation. Innovative interventions are needed to have an impact on skin cancer risk among young people. Unlike previous interventions, our skin cancer risk reduction intervention will be tailored (or personalized) to each individual participant and delivered via the Internet. The intervention will emphasize appearance concerns, which are known to be the primary motivation for UV exposure and lack of skin protection among young adults. This will be accomplished in part through the use of personalized facial images showing UV damage as well as computerized age progression demonstrations.

Primary Aim 1. To examine the efficacy of a tailored intervention delivered via the Internet designed to increase skin protection and decrease sun exposure behavior among young adults at moderate to high risk of developing skin cancer. Participants will be randomized to the tailored intervention, the Skin Cancer Foundation website, or an assessment only condition.

Aim 2. To evaluate whether sociodemographic variables (sex, race/ethnicity, skin type, family history of skin cancer), appearance consciousness, and past exposure and protective behaviors moderate intervention effects.

Aim 3. To evaluate whether Integrative Model constructs (UV-related knowledge, risk perception, beliefs, norms, self-efficacy, and intentions) mediate intervention effects.

The goals of future research would be to enhance the tailored intervention, for example, by adding additional contacts or Internet technologies or features, disseminate the intervention, assess the longevity of effects, and/or adapt the tailored intervention for use with other cancer risk behaviors or at risk groups.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–25 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Fox Chase Cancer Center

Philadelphia, Pennsylvania, 19111, United States

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Age 18-25 years old
  • Moderate to high risk of skin cancer (cut-off of >=27 on the Brief Skin Cancer Risk Assessment Tool)

Exclusion criteria

  • History of skin cancer

Treatment and study plan

UV4me

Behavioral

Tailored website includes: personalized responses to quizzes, information on skin type and burn risk, UV damage photo of similar individual, avatar activity, age progression images, personal risk calculator, SPF (sun protection factor) calculator

Other names: Tailored Intervention for Skin Cancer Risk Reduction

Skin Cancer Foundation website

Behavioral

Current best practice website for skin cancer and prevention. Includes information, images, news, and opportunities for advocacy.

Primary outcomes

  1. Sun protection

    Time frame: Follow-up 1 (3 weeks after baseline)

    Continuous measure examining frequency of sun protection behaviors (e.g., sunscreen use, clothing, shade, sunglasses), using items adapted from Glanz and colleagues (2008)

  2. Sun protection

    Time frame: Follow-up 2 (12 weeks after baseline)

    Continuous measure examining frequency of sun protection behaviors (e.g., sunscreen use, clothing, shade, sunglasses), using items adapted from Glanz and colleagues (2008)

  3. Outdoor UV Exposure

    Time frame: Follow-up 1 (3 weeks after baseline)

    How many hours participants spend in the sun during peak daylight hours during the week

  4. Outdoor UV exposure

    Time frame: Follow-up 2 (12 weeks after baseline)

    How many hours participants spend in the sun during peak daylight hours during the week

Secondary outcomes

  1. Indoor Tanning

    Time frame: Follow-up 1 (3 weeks after baseline)

    Number of indoor tanning sessions in past month

  2. Indoor Tanning

    Time frame: Follow-up 2 (12 weeks after baseline)

    Number of indoor tanning sessions in past month

Other outcomes

  1. Spray-on tan

    Time frame: Follow-up 1 (3 weeks after baseline)

    Number of spray-on tanning sessions in past month

  2. Spray-on tan

    Time frame: Follow-up 2 (12 weeks after baseline)

    Number of spray-on tanning sessions in past month

  3. Sunless tanning creams

    Time frame: Follow-up 1 (3 weeks after baseline)

    Number of times sunless tanning cream has been used in the past month

  4. Sunless tanning creams

    Time frame: Follow-up 2 (12 weeks after baseline)

    Number of times sunless tanning cream has been used in the past month

Sponsors and collaborators

Lead sponsor

Fox Chase Cancer Center

Other

Collaborators

  • National Cancer Institute (NCI)

Registry information

Acronym: UV4me

Important dates

Study start
2011
Primary completion
2014
Study completion
2014
First posted
May 26, 2014
Registry last updated
Jul 3, 2018

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.

Published trials that share one or more normalized conditions with this study.