- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT05244356
Health Communication to Influence COVID-19 Vaccination Intent and Message Propagation (CONVINCE)
Effective Public Health Communication to Influence COVID-19 Vaccination Intent and Message Propagation: A Randomized Controlled Experiment
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
Studientyp
Einschreibung (Tatsächlich)
Phase
- Unzutreffend
Kontakte und Standorte
Studienorte
-
-
Selangor
-
Shah Alam, Selangor, Malaysia, 40170
- Institute for Clinical Research, National Institutes of Health, Malaysia
-
-
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Beschreibung
Inclusion Criteria:
- Willing and able to give informed consent for participation in the trial
- Malaysian nationality.
- Can understand either the English or Malay language.
- Aged 18 years or above
Exclusion Criteria:
- Received at least one COVID-19 vaccination dose
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Sonstiges
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Single
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Experimental: Descriptive Norm (70%)
Intervention in the form of a message likened to a social media post. Composed of 3 parts:
|
Participants exposed to a health message and requested to read it completely.
Subsequently requested to answer post intervention questions that form basis for outcome measures.
|
|
Experimental: Descriptive Norm
Intervention in the form of a message likened to a social media post. Composed of 3 parts:
|
Participants exposed to a health message and requested to read it completely.
Subsequently requested to answer post intervention questions that form basis for outcome measures.
|
|
Experimental: Healthcare worker (HCW) recommendation
Intervention in the form of a message likened to a social media post. Composed of 3 parts:
|
Participants exposed to a health message and requested to read it completely.
Subsequently requested to answer post intervention questions that form basis for outcome measures.
|
|
Experimental: Negative attribute framing
Intervention in the form of a message likened to a social media post. Composed of 3 parts:
|
Participants exposed to a health message and requested to read it completely.
Subsequently requested to answer post intervention questions that form basis for outcome measures.
|
|
Experimental: Positive attribute framing
Intervention in the form of a message likened to a social media post. Composed of 3 parts:
|
Participants exposed to a health message and requested to read it completely.
Subsequently requested to answer post intervention questions that form basis for outcome measures.
|
|
Experimental: Risky choice framing (Safety)
Intervention in the form of a message likened to a social media post. Composed of 3 parts:
|
Participants exposed to a health message and requested to read it completely.
Subsequently requested to answer post intervention questions that form basis for outcome measures.
|
|
Experimental: Risky choice framing (Side effects)
Intervention in the form of a message likened to a social media post. Composed of 3 parts:
|
Participants exposed to a health message and requested to read it completely.
Subsequently requested to answer post intervention questions that form basis for outcome measures.
|
|
Experimental: Control message
Control message containing only rally slogan: "It's safe and effective!"
|
Participants exposed to a health message and requested to read it completely.
Subsequently requested to answer post intervention questions that form basis for outcome measures.
|
|
Experimental: Combination message: Descriptive Norm (70%) + Descriptive Norm
Participants received 2 messages which were exposed one at a time.
Sequence of message appearing randomly rotated.
|
Participants exposed to a health message and requested to read it completely.
Subsequently requested to answer post intervention questions that form basis for outcome measures.
|
|
Experimental: Combination message: Descriptive Norm (70%) + HCW recommendation
Participants received 2 messages which were exposed one at a time.
Sequence of message appearing randomly rotated.
|
Participants exposed to a health message and requested to read it completely.
Subsequently requested to answer post intervention questions that form basis for outcome measures.
|
|
Experimental: Combination message: Descriptive Norm (70%) + Negative attribute framing
Participants received 2 messages which were exposed one at a time.
Sequence of message appearing randomly rotated.
|
Participants exposed to a health message and requested to read it completely.
Subsequently requested to answer post intervention questions that form basis for outcome measures.
|
|
Experimental: Combination message: Descriptive Norm (70%) + Positive attribute framing
Participants received 2 messages which were exposed one at a time.
Sequence of message appearing randomly rotated.
|
Participants exposed to a health message and requested to read it completely.
Subsequently requested to answer post intervention questions that form basis for outcome measures.
|
|
Experimental: Combination message: Descriptive Norm (70%) + Risky choice framing (Safety)
Participants received 2 messages which were exposed one at a time.
Sequence of message appearing randomly rotated.
|
Participants exposed to a health message and requested to read it completely.
Subsequently requested to answer post intervention questions that form basis for outcome measures.
|
|
Experimental: Combination message: Descriptive Norm (70%) + Risky choice framing (Side effects)
Participants received 2 messages which were exposed one at a time.
Sequence of message appearing randomly rotated.
|
Participants exposed to a health message and requested to read it completely.
Subsequently requested to answer post intervention questions that form basis for outcome measures.
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Change in intent to accept the COVID-19 vaccine amongst the Malaysian adult population.
Zeitfenster: Immediately before and after message exposure during questionnaire administration.
|
Outcome measure was assessed using a questionnaire answered through a 4 point ordinal scale.
Scale ranges from '"Definitely no", "Not sure, but probably no", "Not sure, but probably yes"to Definitely yes".
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Immediately before and after message exposure during questionnaire administration.
|
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Change in intent to recommend the COVID-19 vaccine to healthy adults.
Zeitfenster: Immediately before and after message exposure during questionnaire administration.
|
Outcome measure was assessed using a questionnaire answered through a 5 point ordinal scale.
Scale ranges from "Strongly disagree", "Disagree", "Not sure", "Agree", and "Strongly agree".
|
Immediately before and after message exposure during questionnaire administration.
|
|
Change in intent to recommend the COVID-19 vaccine to elderly.
Zeitfenster: Immediately before and after message exposure during questionnaire administration.
|
Outcome measure was assessed using a questionnaire answered through a 5 point ordinal scale.
Scale ranges from "Strongly disagree", "Disagree", "Not sure", "Agree", and "Strongly agree".
|
Immediately before and after message exposure during questionnaire administration.
|
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Change in intent to recommend the COVID-19 vaccine to people with existing health conditions.
Zeitfenster: Immediately before and after message exposure during questionnaire administration.
|
Outcome measure was assessed using a questionnaire answered through a 5 point ordinal scale.
Scale ranges from "Strongly disagree", "Disagree", "Not sure", "Agree", and "Strongly agree".
|
Immediately before and after message exposure during questionnaire administration.
|
|
Intent to share message on social media platform.
Zeitfenster: Immediately after message exposure during questionnaire administration.
|
Outcome measure was assessed using a questionnaire answered through a 5 point ordinal scale.Scale ranges from "Strongly disagree", "Disagree", "Not sure", "Agree", and "Strongly agree".
|
Immediately after message exposure during questionnaire administration.
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Moderators of vaccination intent.
Zeitfenster: Immediately after message exposure during questionnaire administration.
|
Outcome measure assessed using a series of questions answered through a 5 point ordinal scale.
Scale ranges from "Strongly disagree", "Disagree", "Not sure", "Agree", and "Strongly agree".
|
Immediately after message exposure during questionnaire administration.
|
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Reliability of various information sources about COVID-19.
Zeitfenster: Immediately after message exposure during questionnaire administration.
|
Outcome measure assessed using a questionnaire that list out various types of information sources and having participants to rate the reliability for each source using a 5 point ordinal scale.
Scale ranges from "Strongly not reliable", "Not reliable, "Not sure", "Reliable", and "Strongly reliable".
|
Immediately after message exposure during questionnaire administration.
|
Mitarbeiter und Ermittler
Mitarbeiter
Ermittler
- Hauptermittler: Yee Liang Hing, MSc., Clinical Research Centre, Malaysia
Publikationen und hilfreiche Links
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Tatsächlich)
Primärer Abschluss (Tatsächlich)
Studienabschluss (Tatsächlich)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
- Pathologische Prozesse
- Coronaviridae-Infektionen
- Nidovirales-Infektionen
- RNA-Virusinfektionen
- Viruserkrankungen
- Krankheitsattribute
- COVID-19
- Coronavirus-Infektionen
- Lungenkrankheit
- Infektionen
- Übertragbare Krankheiten
- Lungenentzündung
- Pneumonie, viral
- Infektionen der Atemwege
- Atemstörungen
- Erkrankungen der Atemwege
Andere Studien-ID-Nummern
- NMRR-21-26-58107
Plan für individuelle Teilnehmerdaten (IPD)
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Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
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