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Clinical Trials/NCT03448224
NCT03448224
Completed
N/A

The Development and Evaluation of a Behavioral Intervention to Reduce Indoor Tanning

Jerod L Stapleton, PhD1 site in 1 country54 target enrollmentApril 11, 2018
ConditionsHealthy Subject

Overview

Phase
N/A
Intervention
Not specified
Conditions
Healthy Subject
Sponsor
Jerod L Stapleton, PhD
Enrollment
54
Locations
1
Primary Endpoint
Number of Prior 2-Month Indoor Tanning Sessions Reported by Participants on a Follow-up Survey
Status
Completed
Last Updated
5 years ago

Overview

Brief 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.

Detailed 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.

Registry
clinicaltrials.gov
Start Date
April 11, 2018
End Date
August 31, 2019
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Jerod L Stapleton, PhD
Responsible Party
Sponsor Investigator
Principal Investigator

Jerod L Stapleton, PhD

Associate Professor

University of Kentucky

Eligibility Criteria

Inclusion Criteria

  • Use of IT at least 25 times in the past year

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Number of Prior 2-Month Indoor Tanning Sessions Reported by Participants on a Follow-up Survey

Time Frame: Up to 3 months

On the follow-up assessment administered 3 months after the baseline assessment, participants will estimate the number of times they used a tanning bed or booth with tanning lamps in the past 2 months with an open-ended response.

Secondary Outcomes

  • Perceived Difficulty (Self-efficacy) in Quitting Tanning(At 3 months post-intervention)
  • Intentions to Use Indoor Tanning(Up to 3 months)
  • Sunburns(Up to 3 months)
  • Number of Participants Expressing Positive Interest in Changing Tanning(3 months)

Study Sites (1)

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