- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT03499535
Impact of Smoking Information on Concerns About Radon
17 avril 2019 mis à jour par: Paul Windschitl
Despite a push for tailored messages, health communications are often aimed at, and viewed by, people with varying levels of risk.
This project examined-in the context of radon risk messages-whether information relevant to high-risk individuals can have an unintended influence on lower-risk individuals.
Specifically, the investigators assessed whether information about lung-cancer risk from smoking reduced concerns about lung-cancer risk from radon among nonsmokers.
The investigators hypothesized that non-smokers who read a message that included smoking-relevant information would express less concern about the effects of radon exposure and less interest in testing their home compared to those who read a version in which smoking-relevant information was excluded.
Two studies were conducted.
Although the investigators did not exclude smokers, the focus was on participants self-identifying as nonsmokers (including never smokers and former smokers).
Aperçu de l'étude
Statut
Complété
Les conditions
Description détaillée
Despite a push for tailored messages, health communications are often aimed at, and viewed by, people with varying levels of risk.
This project examined-in the context of radon risk messages-whether information relevant to high-risk individuals can have an unintended influence on lower-risk individuals.
Specifically, the investigators assessed whether information about lung-cancer risk from smoking reduced concerns about lung-cancer risk from radon among nonsmokers.
The investigators hypothesized that non-smokers who read a message that included smoking-relevant information would express less concern about the effects of radon exposure and less interest in testing their home compared to those who read a version in which smoking-relevant information was excluded.
Two studies were conducted.
Although the investigators did not exclude smokers, the focus was on participants self-identifying as nonsmokers (including never smokers and former smokers).
Participants in both studies were recruited through Amazon's Mechanical Turk (MTurk).
Participants viewed radon messages that varied in the information they communicated about smoking's effect on lung cancer.
In Study 1, smoking information was included or excluded from messages assembled from existing radon pamphlets.
In Study 2, versions of a new radon message either excluded smoking information, described smoking as a major cause of lung cancer, or also described smoking's synergistic effect with radon on lung cancer risk.
After viewing a radon health message, participants completed a variety of measures.
Primary measures assessed respondents' anticipated sense of concern and related reactions if they learned that they/their home had been exposed to elevated levels of radon.
Other key measures included questions about participants' interest and intention to test their home for radon.
Type d'étude
Interventionnel
Inscription (Réel)
1390
Phase
- N'est pas applicable
Critères de participation
Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.
Critère d'éligibilité
Âges éligibles pour étudier
18 ans et plus (Adulte, Adulte plus âgé)
Accepte les volontaires sains
Oui
Sexes éligibles pour l'étude
Tout
La description
Inclusion Criteria:
- Live within the US
- Have an Amazon Mechanical Turk account (website where online study was posted)
Exclusion Criteria:
- None
Plan d'étude
Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: La prévention
- Répartition: Randomisé
- Modèle interventionnel: Affectation factorielle
- Masquage: Seul
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Comparateur actif: Study 1: Radon&Smoking Synergistic/EPA
Participants viewed radon and smoking risk information taken from the EPA's pamphlet on the dangers of radon gas exposure.
|
Participants viewed health information detailing the risks of developing lung cancer from exposure to radon gas, smoking, and their synergistic effects.
This intervention represents the type of information most commonly presented in radon risk communications.
Health information modeled after the Environmental Protection Agency's (EPA) pamphlet on radon risk.
|
|
Comparateur actif: Study 1: Radon&Smoking Synergistic/Idaho
Participants viewed radon and smoking risk information taken from Idaho's Department of Health and Human Welfare's pamphlet on the dangers of radon gas exposure.
|
Participants viewed health information detailing the risks of developing lung cancer from exposure to radon gas, smoking, and their synergistic effects.
This intervention represents the type of information most commonly presented in radon risk communications.
Health information modeled after the Idaho Department of Health and Human Welfare's pamphlet on radon risk.
|
|
Expérimental: Study 1: Radon Only / EPA
Participants viewed only radon risk information taken from the EPA's pamphlet on the dangers of radon gas exposure.
|
Health information modeled after the Environmental Protection Agency's (EPA) pamphlet on radon risk.
Participants viewed health information detailing the risks of developing lung cancer from radon exposure.
No information about the risks for developing lung cancer associated with smoking or its synergistic effect with radon exposure are included.
|
|
Expérimental: Study 1: Radon Only / Idaho
Participants viewed only radon risk information taken from Idaho's Department of Health and Human Welfare's pamphlet on the dangers of radon gas exposure.
|
Health information modeled after the Idaho Department of Health and Human Welfare's pamphlet on radon risk.
Participants viewed health information detailing the risks of developing lung cancer from radon exposure.
No information about the risks for developing lung cancer associated with smoking or its synergistic effect with radon exposure are included.
|
|
Expérimental: Study 2: Radon Only
Participants viewed a radon-only message that focused only on the effect of radon on lung-cancer risk.
|
Participants viewed health information detailing the risks of developing lung cancer from radon exposure.
No information about the risks for developing lung cancer associated with smoking or its synergistic effect with radon exposure are included.
|
|
Autre: Study 2: Radon and Smoking Isolated
Participants viewed a radon-and-smoking-isolated message that covered the individual effects of radon and of smoking on lung cancer, but without mentioning their synergistic effect.
|
Participants viewed health information detailing the risks of developing lung cancer from radon exposure and smoking.
No information describing the synergistic effects of smoking and radon exposure on lung cancer risk are included.
|
|
Comparateur actif: Study 2: Radon & Smoking Synergistic
Participants viewed a radon-and-smoking-synergistic message that covered the individual effects of radon and of smoking but that also included information about their synergistic effect.
|
Participants viewed health information detailing the risks of developing lung cancer from exposure to radon gas, smoking, and their synergistic effects.
This intervention represents the type of information most commonly presented in radon risk communications.
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Conditional Concern Composite
Délai: Immediately post-intervention (approx. 1 minute)
|
Composite formed from 4 conditional questions assessing concern, perceived impact on risk and comparative risk, and threat--if exposed to radon
|
Immediately post-intervention (approx. 1 minute)
|
|
Interest in Testing Composite
Délai: Immediately post-intervention (approx. 2 minutes)
|
Composite formed from 2 questions assessing importance and intention to test home for radon
|
Immediately post-intervention (approx. 2 minutes)
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Worry Elicited by Health Message
Délai: Immediately post-intervention (approx. 2 minutes)
|
Single question assessing worry elicited by the health communication material
|
Immediately post-intervention (approx. 2 minutes)
|
|
Likelihood Judgments about Lung Cancer
Délai: Immediately post-intervention (approx. 4 minutes)
|
Three items assessing perceived likelihood of developing lung cancer
|
Immediately post-intervention (approx. 4 minutes)
|
|
Elect to Leave Email for Raffle
Délai: Immediately post-intervention (approx. 4 minutes)
|
Participants given option to leave email address in case they won one of the 20 radon kits being raffled (Study 2).
|
Immediately post-intervention (approx. 4 minutes)
|
|
Elect to Read More
Délai: Immediately post-intervention (approx. 4 minutes)
|
Participants given option to be presented with more information at the end of the session about testing for radon (Study 2).
|
Immediately post-intervention (approx. 4 minutes)
|
|
Concern about Loved Ones If Exposed to Radon
Délai: Immediately post-intervention (approx. 4 minutes)
|
Rated how concerned they would be about loved ones if they learned their home had high radon (Study 2)
|
Immediately post-intervention (approx. 4 minutes)
|
Collaborateurs et enquêteurs
C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.
Parrainer
Dates d'enregistrement des études
Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.
Dates principales de l'étude
Début de l'étude (Réel)
7 août 2015
Achèvement primaire (Réel)
22 avril 2016
Achèvement de l'étude (Réel)
22 avril 2016
Dates d'inscription aux études
Première soumission
30 mars 2018
Première soumission répondant aux critères de contrôle qualité
13 avril 2018
Première publication (Réel)
17 avril 2018
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
19 avril 2019
Dernière mise à jour soumise répondant aux critères de contrôle qualité
17 avril 2019
Dernière vérification
1 avril 2019
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- 201507727
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
OUI
Description du régime IPD
De-identified data and guide will be made available to other investigators upon request.
Délai de partage IPD
Requested data will be made available upon publication of the project.
Critères d'accès au partage IPD
Please contact corresponding author Dr. Paul Windschitl at paul-windschitl@uiowa.edu
Type d'informations de prise en charge du partage d'IPD
- ANALYTIC_CODE
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Non
Étudie un produit d'appareil réglementé par la FDA américaine
Non
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .
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