- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT03499535
Impact of Smoking Information on Concerns About Radon
17 aprile 2019 aggiornato da: 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).
Panoramica dello studio
Stato
Completato
Condizioni
Descrizione dettagliata
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.
Tipo di studio
Interventistico
Iscrizione (Effettivo)
1390
Fase
- Non applicabile
Criteri di partecipazione
I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.
Criteri di ammissibilità
Età idonea allo studio
18 anni e precedenti (Adulto, Adulto più anziano)
Accetta volontari sani
Sì
Sessi ammissibili allo studio
Tutto
Descrizione
Inclusion Criteria:
- Live within the US
- Have an Amazon Mechanical Turk account (website where online study was posted)
Exclusion Criteria:
- None
Piano di studio
Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Prevenzione
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione fattoriale
- Mascheramento: Separare
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Comparatore attivo: 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.
|
|
Comparatore attivo: 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.
|
|
Sperimentale: 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.
|
|
Sperimentale: 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.
|
|
Sperimentale: 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.
|
|
Altro: 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.
|
|
Comparatore attivo: 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.
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Conditional Concern Composite
Lasso di tempo: 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
Lasso di tempo: 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)
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Worry Elicited by Health Message
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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)
|
Collaboratori e investigatori
Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.
Sponsor
Studiare le date dei record
Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.
Studia le date principali
Inizio studio (Effettivo)
7 agosto 2015
Completamento primario (Effettivo)
22 aprile 2016
Completamento dello studio (Effettivo)
22 aprile 2016
Date di iscrizione allo studio
Primo inviato
30 marzo 2018
Primo inviato che soddisfa i criteri di controllo qualità
13 aprile 2018
Primo Inserito (Effettivo)
17 aprile 2018
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
19 aprile 2019
Ultimo aggiornamento inviato che soddisfa i criteri QC
17 aprile 2019
Ultimo verificato
1 aprile 2019
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- 201507727
Piano per i dati dei singoli partecipanti (IPD)
Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?
SÌ
Descrizione del piano IPD
De-identified data and guide will be made available to other investigators upon request.
Periodo di condivisione IPD
Requested data will be made available upon publication of the project.
Criteri di accesso alla condivisione IPD
Please contact corresponding author Dr. Paul Windschitl at paul-windschitl@uiowa.edu
Tipo di informazioni di supporto alla condivisione IPD
- CODICE_ANALITICO
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
No
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
No
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
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