Study Results
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View full resultsBasic Information
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COMPLETED
NA
54 participants
INTERVENTIONAL
2018-04-11
2019-08-31
Brief Summary
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Detailed Description
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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.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
NONE
Study Groups
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Group I (web-based Indoor Tanning intervention)
Participants receive intervention, weekly text messages about IT reduction, and personalized booster intervention. Participants then receive text messages twice weekly for 4 weeks.
Questionnaire Administration
Questionnaire
Internet-Based Intervention
Intervention
Group II (wait-list)
Participants are placed on wait-list and may receive full intervention after follow-up.
Questionnaire Administration
Questionnaire
Interventions
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Questionnaire Administration
Questionnaire
Internet-Based Intervention
Intervention
Eligibility Criteria
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Inclusion Criteria
* Women
18 Years
25 Years
FEMALE
Yes
Sponsors
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National Cancer Institute (NCI)
NIH
Jerod L Stapleton, PhD
OTHER
Responsible Party
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Jerod L Stapleton, PhD
Associate Professor
Principal Investigators
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Jerod Stapleton, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Kentucky
Locations
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University of Kentucky
Lexington, Kentucky, United States
Countries
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References
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Stapleton JL, Ray AE, Glenn SD, McLouth LE, Parmar V, Manne SL. A randomized controlled trial of a web-based personalized feedback intervention targeting frequent indoor tanning bed users: Engagement, acceptability, and preliminary behavioral outcomes. J Health Psychol. 2022 Mar;27(4):923-935. doi: 10.1177/1359105320982038. Epub 2020 Dec 22.
Provided Documents
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Document Type: Informed Consent Form
Document Type: Study Protocol and Statistical Analysis Plan
Other Identifiers
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NCI-2018-00063
Identifier Type: REGISTRY
Identifier Source: secondary_id
Pro2013003349
Identifier Type: OTHER
Identifier Source: secondary_id
131315
Identifier Type: OTHER
Identifier Source: secondary_id
131315
Identifier Type: -
Identifier Source: org_study_id
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