A Mobile Text Messaging Intervention for Indoor Tanning Addiction

Sponsor
Georgetown University (Other)
Overall Status
Completed
CT.gov ID
NCT04055272
Collaborator
(none)
265
1
2
26.7
9.9

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Mobile text messaging intervention
N/A

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.

Study Design

Study Type:
Interventional
Actual Enrollment :
265 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
This is a randomized trial with two groups: 1) Indoor tanning education only; 2) Mobile text messaging interventionThis is a randomized trial with two groups: 1) Indoor tanning education only; 2) Mobile text messaging intervention
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
A Mobile Text Messaging Intervention for Indoor Tanning Addiction
Actual Study Start Date :
Jan 7, 2020
Actual Primary Completion Date :
Mar 31, 2022
Actual Study Completion Date :
Mar 31, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Text messaging

Participants in the text messaging intervention arm receive mobile text messages communicating the risks of indoor tanning and motivating cessation on their mobile phones

Behavioral: Mobile 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.

No Intervention: Control

Participants in the control arm receive no intervention

Outcome Measures

Primary Outcome Measures

  1. Motivation to Quit Indoor Tanning [1 month follow up]

    Motivation 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.

  2. Indoor Tanning Cessation [1 month follow up]

    Indoor 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 Outcome Measures

  1. Attempts to Quit Indoor Tanning [1 month follow up and 3 month follow up]

    Attempts 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 Outcome Measures

  1. Risk Appraisals [1 month follow up and 3 month follow up]

    Perceived 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.

  2. Efficacy Beliefs [1 month follow up and 3 month follow up]

    Beliefs 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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 30 Years
Sexes Eligible for Study:
Female
Accepts 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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Georgetown University Washington District of Columbia United States 20007

Sponsors and Collaborators

  • Georgetown University

Investigators

  • Principal Investigator: Darren Mays, PhD, MPH, Georgetown University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Georgetown University
ClinicalTrials.gov Identifier:
NCT04055272
Other Study ID Numbers:
  • STUDY00000474
First Posted:
Aug 13, 2019
Last Update Posted:
Aug 4, 2022
Last Verified:
Jul 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Georgetown University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 4, 2022