Skip to main content
Clinical Trials/NCT02192918
NCT02192918
Completed
N/A

Pilot Investigation of Behavioral Alternatives to Indoor Tanning

University of Massachusetts, Worcester1 site in 1 country74 target enrollmentApril 2012
ConditionsSkin Cancer

Overview

Phase
N/A
Intervention
Not specified
Conditions
Skin Cancer
Sponsor
University of Massachusetts, Worcester
Enrollment
74
Locations
1
Primary Endpoint
Effort of alternatives
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

The goal of this research is to develop and test the feasibility of an intervention that stimulates uptake of healthy alternatives to tanning by providing free access to them for a limited time. Free access gives participants a low-risk opportunity to try something new that is consistent with their motivations. Free access also allows them to experience the reinforcing properties of the alternatives which could prime continued use after the free trial period. The objective of the present study is to determine the feasibility and short-term efficacy of providing free alternatives to indoor tanners in an effort to "nudge" them to switch from indoor tanning to healthy alternatives.

Detailed Description

Melanoma is the second most common cancer diagnosed in young women and is responsible for nearly 8,000 US deaths per year. Exposure to ultraviolet radiation (UVR) increases risk for melanoma. The International Agency for Research on Cancer assigned indoor tanning (IT; use of tanning beds or booths), as a class 1 carcinogen joining arsenic, asbestos, and mustard gas. Unfortunately, interventions educating tanners about the risks have not been very effective. Many tanners are more motivated by the immediate consequences of tanning than the delayed consequence of possibly getting cancer. Research shows the primary motivation for indoor tanning is to improve physical appearance, but a secondary motivation is stress reduction. Behavioral economics theory suggests that the rate of a behavior depends on 1) the reinforcing value of that behavior relative to alternatives, 2) the cost of engaging in the behavior relative to alternatives, and 3) the availability of the behavior relative to alternatives. The purpose of the present study is to determine whether exposure to healthy alternatives changes the behavior of indoor tanners. The investigators will randomize tanners to conditions differing in physical appearance and stress reduction alternatives to determine whether they can get their motivational needs met in healthier ways.

Registry
clinicaltrials.gov
Start Date
April 2012
End Date
April 2015
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
University of Massachusetts, Worcester
Responsible Party
Principal Investigator
Principal Investigator

Sherry Pagoto

Associate Professor

University of Massachusetts, Worcester

Eligibility Criteria

Inclusion Criteria

  • Ages 16-65
  • Report minimum of 10 indoor tanning visits in the last year with intentions to continue

Exclusion Criteria

  • Ages \<16 or \>65
  • Pregnant, breastfeeding, or planning to become pregnant during the study period
  • Reporting less than 10 indoor tanning visits per year
  • No intention to continue indoor tanning
  • Using sunless tanning more than once in the last year and ever in the last 3 months
  • Physically limited to do yoga or dance classes
  • DHA allergy
  • Inability to consent
  • Prisoners

Outcomes

Primary Outcomes

Effort of alternatives

Time Frame: 6-month follow-up

Perceived effort of alternatives will be discussed in a focus group setting.

Retention

Time Frame: 12 month follow-up

% sessions complete and total withdrawn from study

Satisfaction

Time Frame: up to 12 months

A measure of satisfaction will be assessed for each alternative visit on a scale of 1-10 immediately after each activity is completed. Visits occur between baseline and 12 months of participation. Timing of visits depend on which condition is assigned.

Recruitment rate

Time Frame: baseline

Total randomized and total screened out.

Secondary Outcomes

  • abstinence(12-month follow-up)

Study Sites (1)

Loading locations...

Similar Trials