Evidence map›Paper›PMID 33334616›Full record

ArticleVaccine2021

Broad cross-national public support for accelerated COVID-19 vaccine trial designs.

David Broockman, Joshua Kalla, Alexander Guerrero, Mark Budolfson, Nir Eyal, Nicholas P Jewell, Monica Magalhaes, Jasjeet S Sekhon

Abstract read
In one paragraph

Article in Vaccine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. The next viral pandemic-where do we stand?Folia microbiologica · 2025
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Evolving ethics of COVID-19 challenge trials.The Lancet. Infectious diseases · 2021
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

David BroockmanDepartment of Political Science, University of California, Berkeley, United States.
Joshua KallaDepartment of Political Science and Department of Statistics & Data Science, Yale University, United States. Electronic address: josh.kalla@yale.edu.
Alexander GuerreroDepartment of Philosophy, Rutgers University, United States.
Mark BudolfsonDepartment of Environmental and Occupational Health and Justice, Rutgers University, United States.
Nir EyalDepartment of Health Behavior, Society and Policy and Center for Population-Level Bioethics, Rutgers University, United States.
Nicholas P JewellLondon School of Hygiene & Tropical Medicine and Division of Biostatistics, School of Public Health, University of California, Berkeley, United States.
Monica MagalhaesCenter for Population-Level Bioethics, Rutgers University, United States.
Jasjeet S SekhonDepartment of Statistics & Data Science and Department of Political Science, Yale University, United States.

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
HIV cure studies: risk, risk perception, and ethicsR01AI114617 · NIAID · RUTGERS BIOMEDICAL/HEALTH SCIENCES-RBHS · PI EYAL, NIR · 2015 to 2018
$3.2M
NCATS NIH HHS UL1 TR001863NIAID NIH HHS R01 AI114617
6 · The paper itself

Abstract

A vaccine for COVID-19 is urgently needed. Several vaccine trial designs may significantly accelerate vaccine testing and approval, but also increase risks to human subjects. Concerns about whether the public would see such designs as ethical represent an important roadblock to their implementation; accordingly, both the World Health Organization and numerous scholars have called for consulting the public regarding them. We answered these calls by conducting a cross-national survey (n = 5920) in Australia, Canada, Hong Kong, New Zealand, South Africa, Singapore, the United Kingdom, and the United States. The survey explained key differences between traditional vaccine trials and two accelerated designs: a challenge trial or a trial integrating a Phase II safety and immunogenicity trial into a larger Phase III efficacy trial. Respondents' answers to comprehension questions indicate that they largely understood the key differences and ethical trade-offs between the designs from our descriptions. We asked respondents whether they would prefer scientists to conduct traditional trials or one of these two accelerated designs. We found broad majorities prefer for scientists to conduct challenge trials (75%) and integrated trials (63%) over standard trials. Even as respondents acknowledged the risks, they perceived both accelerated trials as similarly ethical to standard trial designs. This high support is consistent across every geography and demographic subgroup we examined, including vulnerable populations. These findings may help assuage some of the concerns surrounding accelerated designs.

Indexed as

Decision MakingResearch DesignAsiaAustraliaChoice BehaviorClinical Trials as TopicCOVID-19COVID-19 VaccinesFemaleHumansImmunity, InnateImmunization ScheduleImmunogenicity, VaccineMaleNorth AmericaPandemicsCOVID-19 VaccinesChallenge trialsCOVID-19Public opinionVaccine ethics

Identifiers

PMID33334616
PMCPMC7831807

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.