Behavioral Intervention in Reducing Indoor Tanning

Status Completed

Clinical Trial Summary

This randomized clinical trial tests the efficacy of a behavioral intervention works in reducing indoor tanning. Artificial ultraviolet indoor tanning increases the chance of developing skin cancers. Behavioral interventions use techniques to help participants change the way they react to environmental triggers that may cause a negative reaction.

Clinical Trial Description

PRIMARY OBJECTIVE: To develop and evaluate an online tailored indoor tanning (IT) intervention based on findings from phase 1. OUTLINE: INTERVENTION: Participants are randomized to 1 of 2 groups. GROUP I: Participants receive intervention, weekly text messages about IT reduction, and personalized booster intervention. Participants then receive text messages twice weekly for 4 weeks. GROUP II: Participants are placed on wait-list and may receive full intervention after follow-up. After completion of study, patients are followed up at 3 months. ;

Study Design

Related Conditions & MeSH terms

Healthy Subject

Clinical Trial Details

NCT number	NCT03448224
Study type	Interventional
Source	University of Kentucky
Contact
Status	Completed
Phase	N/A
Start date	April 11, 2018
Completion date	August 31, 2019

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