- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT01508013
An Appearance-Based Intervention to Reduce Teen Skin Cancer Risk (iSTART)
26. april 2016 opdateret af: Joel Hillhouse, East Tennessee State University
The purpose of this study is to determine whether a skin cancer prevention website is effective at reduce female teenagers' desire to use indoor tanning and ultimately their use of indoor tanning over an 18 month period.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
The project is designed to improve the understanding of, and ability to affect UV risk behavior in teenage populations.
The International Agency for Research in Cancer classifies indoor tanning as "carcinogenic to humans."
There is evidence that female indoor tanning use increases dramatically from freshman to senior years of high school (e.g., 25-40% of older high school girls) making high school a critical time period for anti-tanning interventions to be carried out.
This proposal assesses the effectiveness of a skin cancer prevention website for a nationally representative sample of high school teens in a randomized controlled trial.
Teens exposed to the website will report reduced indoor tanning intentions, frequency and overall percentage of users while increasing sun protective behaviors at long-term (i.e 18 month) follow-up.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
443
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
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Tennessee
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Johnson City, Tennessee, Forenede Stater, 37614
- East Tennessee State University
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Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
12 år til 18 år (Barn, Voksen)
Tager imod sunde frivillige
Ja
Køn, der er berettiget til at studere
Kvinde
Beskrivelse
Inclusion Criteria:
- Teenager between 12 and 18 years old; has either indoor tanned in the past year or has indicated their intentions to indoor tan in the coming year.
Exclusion Criteria:
- None other than not meeting inclusion criteria.
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Forebyggelse
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Dobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
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Eksperimentel: Appearance-Focused Website Intervention
This is a Internet-based appearance-focused prevention intervention based on the Behavioral Alternatives Model.
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The intervention is a teen-friendly website with information concerning the health and appearance effects of indoor tanning.
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Aktiv komparator: Control Website
Control participants viewed an Internet site designed to provide drug and alcohol education for teens.
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The control website contains information about alcohol and drug abuse which is oriented for a teen audience.
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Indoor Tanning Behavior
Tidsramme: 12 months
|
Self-report measure of the number of times the teenager has indoor tanned over 12 month time period.
The self-report measure has been validated in previous studies.
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12 months
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Indoor Tanning Intentions
Tidsramme: 12 months
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A validated measure of the teenagers intentions to use indoor tanning in the next 12 months.
Indoor tanning intentions are measured on a scale that ranges from 1 (definitely do not intend to indoor tan; better) to 7 (definitely do intend to indoor tan; worse).
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12 months
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Indoor Tanning Willingness
Tidsramme: 12 months
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Scale that measures adolescents willingness to indoor tan in the future.
Indoor tanning willingness is measured on a scale that ranges from 1 (definitely not willing; better) to 7 (definitely willing; worse).
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12 months
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Efterforskere
- Ledende efterforsker: Joel J Hillhouse, Ph.D., East Tennessee State University
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart
1. maj 2011
Primær færdiggørelse (Faktiske)
1. maj 2014
Studieafslutning (Faktiske)
1. december 2014
Datoer for studieregistrering
Først indsendt
9. januar 2012
Først indsendt, der opfyldte QC-kriterier
9. januar 2012
Først opslået (Skøn)
11. januar 2012
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
2. juni 2016
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
26. april 2016
Sidst verificeret
1. april 2016
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 1R01CA134891-01A2 (U.S. NIH-bevilling/kontrakt)
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
JA
IPD-planbeskrivelse
The proposed research will include data from high school teenage women who indoor tan.
The final dataset will include self-reported demographic, attitudinal, cognitive and behavioral data from surveys about private personal behaviors.
The final dataset will be stripped of identifiers prior to release for sharing.
We will make the data and associated documentation available to users only under a data-sharing agreement that provides for: (1) a commitment to using the data only for research purposes and to not attempting to identify any individual participant; (2) a commitment to securing the data using appropriate computer technology; and (3) a commitment to destroying or returning the data after analyses are completed.
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
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