SunSmart Intervention in Schools
3. januar 2022 opdateret af: University of Colorado, Denver
A prevention study to improve sun exposure behaviors in children after an educational classroom-based intervention.
Studieoversigt
Detaljeret beskrivelse
This study aims to demonstrate that learning about sun exposure using a more classroom-based intervention will motivate classroom students to reduce exposure at a critical life period and will create lifetime learned sun exposure behaviors.
Students' sun exposure behaviors will be assessed prior to the educational intervention.
The educational intervention consists of three educational sessions and one lab lesson.
At the conclusion of the intervention, students' sun exposure behaviors will be assessed again via a post-intervention questionnaire.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
76
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
Colorado
-
Aurora, Colorado, Forenede Stater, 80045
- University of Colorado
-
-
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
9 år til 15 år (Barn)
Tager imod sunde frivillige
Ja
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- Any children between grades 4 and 8 enrolled in one of the participating schools.
Exclusion Criteria:
- No exclusions, but children or their parents may opt out of participating.
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: N/A
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: Testing
This is a preventative study model.
All students who choose to participate will receive a pre and post test regarding their sun exposure behaviors and knowledge on sun exposure risk.
|
Students participating in this study will receive a pre test, instruction regarding sun safety, and a post test.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Sun Exposure Knowledge
Tidsramme: From the administration of the questionnaire to the end of the followup questionnaire, up to 3 years
|
Determining children's knowledge of sun exposure risk through a self-completed questionnaire
|
From the administration of the questionnaire to the end of the followup questionnaire, up to 3 years
|
|
Sun Exposure Attitudes
Tidsramme: From the administration of the questionnaire to the end of the followup questionnaire, up to 3 years
|
Determining children's attitude toward sun exposure through a self-completed questionnaire
|
From the administration of the questionnaire to the end of the followup questionnaire, up to 3 years
|
|
Sun Exposure Behavior
Tidsramme: From the administration of the questionnaire to the end of the followup questionnaire, up to 3 years
|
Determining children's behavior toward sun exposure through a self-completed questionnaire
|
From the administration of the questionnaire to the end of the followup questionnaire, up to 3 years
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Mediators of Program Effects: Attitudes
Tidsramme: During the followup questionnaire, which is given 3 to 4 weeks post intervention, up to three years
|
Assessing children's attitude toward sun exposure through a self-completed questionnaire
|
During the followup questionnaire, which is given 3 to 4 weeks post intervention, up to three years
|
|
Mediators of Program Effects: Norms
Tidsramme: During the followup questionnaire, which is given 3 to 4 weeks post intervention, up to three years
|
Determining children's understanding of social norms regarding tanning and sun protection through a self-completed questionnaire
|
During the followup questionnaire, which is given 3 to 4 weeks post intervention, up to three years
|
|
Mediators of Program Effects: Personal Agency
Tidsramme: During the followup questionnaire, which is given 3 to 4 weeks post intervention, up to three years
|
Determining children's understanding of behavioral control regarding sun protection through a self-completed questionnaire
|
During the followup questionnaire, which is given 3 to 4 weeks post intervention, up to three years
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Efterforskere
- Ledende efterforsker: Evelinn Borrayo, PhD, University of Colorado, Denver
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 (Faktiske)
26. september 2017
Primær færdiggørelse (Faktiske)
30. august 2021
Studieafslutning (Faktiske)
30. august 2021
Datoer for studieregistrering
Først indsendt
15. november 2018
Først indsendt, der opfyldte QC-kriterier
15. november 2018
Først opslået (Faktiske)
19. november 2018
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
4. januar 2022
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
3. januar 2022
Sidst verificeret
1. januar 2022
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 17-0667.cc
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Ingen
Studerer et amerikansk FDA-reguleret enhedsprodukt
Ingen
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 .