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A Mobile Text Messaging Intervention for Indoor Tanning Addiction

A Mobile Text Messaging Intervention for Indoor Tanning Addiction

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04055272
Enrollment
265
Registered
2019-08-13
Start date
2020-01-07
Completion date
2022-03-31
Last updated
2022-08-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Indoor Tanning

Keywords

indoor tanning, skin cancer, mobile health, text messaging

Brief summary

The purpose of this study is to test the effects of messages communicating the risks (i.e., health harms, addictiveness) of indoor tanning delivered via mobile text messaging among young adult women ages 18 to 30 years who meet screening criteria for indoor tanning addiction.

Detailed description

This is a two arm randomized controlled trial to test the effects of messages communicating the risks of indoor tanning delivered via mobile text messaging as a strategy for promoting cessation among young adult women who meet screening criteria for indoor tanning addiction. Eligible participants are young adult women ages 18 to 30 years who meet screening criteria for indoor tanning addiction and have access to the internet and a personal mobile phone to complete study procedures. Participants will complete baseline measures and then be randomized to the study arms. The text messaging intervention exposure in the intervention arm will last for four weeks. The control arm will be given basic indoor tanning education information and will not receive any intervention. Follow up assessments capturing study outcomes will be administered at 1 month (i.e., immediately post-intervention) and three months post-intervention.

Interventions

BEHAVIORALMobile text messaging intervention

Participants in the intervention arm will receive text messages to their mobile phones designed to communicate the risks of indoor tanning and motivate cessation. The intervention exposure lasts for 4 weeks with messages sent 2 days each week. It is an interactive intervention that engages participants by asking them to respond to prompts, and sending indoor tanning message content in return on message days.

Sponsors

Georgetown University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

This is a randomized trial with two groups: 1) Indoor tanning education only; 2) Mobile text messaging intervention

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 30 Years
Healthy volunteers
No

Inclusion criteria

* Female * Age between 18 and 30 years * Meet self-report criteria for tanning addiction * Has access to the internet to complete study procedures * Has personal mobile phone to complete study procedures

Exclusion criteria

* Male * Age less than 18 or greater than 30 * Does not meet self-report criteria for tanning addiction * Does not have access to the internet to complete study procedures * Does not have a personal mobile phone to complete study procedures

Design outcomes

Primary

MeasureTime frameDescription
Motivation to Quit Indoor Tanning1 month follow upMotivation to quit is measured by participant report by a single question with a 1 to 7 response scale. Higher scores indicate greater motivation to quit and are considered better outcomes. This question is administered at 1 month follow up and at 3 month follow up.
Indoor Tanning Cessation1 month follow upIndoor tanning cessation is measured by participant report by a single question asking if participants have stopped indoor tanning completely. Responses indicating cessation are considered better outcomes. This item is administered at 1-month follow-up and at 3 month follow up.

Secondary

MeasureTime frameDescription
Attempts to Quit Indoor Tanning1 month follow up and 3 month follow upAttempts to quit indoor tanning are measured by participant report by a single question asking if participants have attempted to quit indoor tanning since the last assessment. Responses indicating any attempt(s) to quit are considered a better outcome. This item is administered at 1 month follow up and at 3 month follow up.

Other

MeasureTime frameDescription
Risk Appraisals1 month follow up and 3 month follow upPerceived risk of harm are measured by asking participants how likely harms are to occur (1 = no chance, 7 = certain to happen). Worry about harms are measured by asking participants how worried they are about harms of indoor tanning (1 = not at all, 7 = very much). Greater risk appraisals are considered a better outcome. The items are administered at 1 month follow up and at 3 month follow up.
Efficacy Beliefs1 month follow up and 3 month follow upBeliefs about the health benefits of quitting indoor tanning, efficacy beliefs, are measured using 6 questions asking about health benefits occurring from quitting indoor tanning (1 = No Chance, 7 = Certain to Happen). Greater efficacy beliefs are considered a better outcome. These items are administered at 1 month follow up and at 3 month follow up.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026