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NCT04693689
Novelty, Conformity and Trust in COVID-19 Vaccines
NA trial testing RNA vaccine in Trust in 35,180 participants. Completed in 30 March 2021.
30 March 2021
Quick facts
| Lead sponsor | National University of Singapore |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | health services research |
| Enrollment | 35,180 |
| Start date | 1 February 2021 |
| Primary completion | 30 March 2021 |
| Estimated completion | 30 March 2021 |
| Sites | 1 location across United States |
Drugs / interventions tested
- RNA vaccine
- 20% adoption rate
- 40% adoption rate
- 60% adoption rate
- 80% adoption rate
- Conventional vaccine
- 0% adoption rate
Conditions studied
- Trust — all drugs for Trust →
Sponsor
National University of Singapore
Who can join
18 and older, any sex, with Trust. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Despite their established benefits as public measures, vaccines continue to be treated with suspicion by many people, in the US and other parts of the world (Larson et al. 2014; Olive et al. 2018; Lazarus et al. 2020). Since the success of vaccines depends on their high uptake level (Anderson and May, 1985; Fine et al. 2011; Fontanet and Cauchemez, 2020), identifying factors that influence low trust and decision-making in relation to vaccines is essential in order to combat diseases such as the novel Coronavirus (COVID-19). The investigators study factors that could potentially influence public's trust in COVID-19 vaccines through a large-scale online field experiment. The investigators conduct an online survey of 32,400 subjects in nine countries (USA, Brazil, Mexico, China, India, Indonesia, Russia, Germany, and UK). The investigators study how willingness to receive the COVID-19 vaccine is affected by (1) the "novelty" of the vaccine technology (conventional vs. RNA vaccines), and (2) the adoption rate of the new vaccine in the country. That is - the impact of controversial science and the force of conformity on the rates of adoption. The latter will also allow us to calculate the "tipping point" adoption rate for each country that will allow the country to achieve herd immunity from COVID-19. The investigators have four hypotheses, below. H1 (Conformity): People are more willing to receive a vaccine as the cumulative adoption rate in their community increases. H2 (Novelty): People are less willing to get a COVID-19 vaccine that uses the new RNA technology, compared to a conventional vaccine H3 (Interaction between H1 and H2): As the cumulative adoption rate in a community increases, the difference between people's willingness to adopt conventional rather than RNA vaccines decreases. H4 (Tipping Point): Each country will have a different "tipping point". This is the cumulative adoption rate after which unvaccinated people are significantly more willing to get the vaccine. Countries that have a higher "honesty index" will have the tipping point appear at a lower cumulative adoption rate. Please note that this study is not a clinical trial. This study is a randomized controlled trial in the form of an online survey.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Assessing the impact of novelty and conformity on hesitancy towards COVID-19 vaccines using mRNA technology.
Leong C, Jin L, Kim D, Kim J, et al · · 2022 · cited 32× · PMID 35664455 · DOI 10.1038/s43856-022-00123-6
Verify or expand the search:
- PubMed search for NCT04693689
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT04693689 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by National University of Singapore
- Last refreshed: 22 February 2022
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04693689.
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