Review
Abstract
Background: Vaccination can be viewed as comprising the most important defensive barriers to protect susceptible groups from infection. However, vaccine hesitancy for COVID-19 is widespread worldwide.
Objective: We aimed to systematically review studies eliciting the COVID-19 vaccine preference using discrete choice experiments.
Methods: A literature search was conducted in PubMed, Embase, Web of Science, Scopus, and CINAHL Plus platforms in April 2023. Search terms included discrete choice experiments, COVID-19, and vaccines and related synonyms. Descriptive statistics were used to summarize the study characteristics. Subgroup analyses were performed by factors such as high-income countries and low- and middle-income countries and study period (before, during, and after the pandemic wave). Quality appraisal was performed using the 5-item Purpose, Respondents, Explanation, Findings, and Significance checklist.
Results: The search yield a total of 623 records, and 47 studies with 53 data points were finally included. Attributes were grouped into 4 categories: outcome, process, cost, and others. The vaccine effectiveness (21/53, 40%) and safety (7/53, 13%) were the most frequently reported and important attributes. Subgroup analyses showed that vaccine effectiveness was the most important attribute, although the preference varied by subgroups. Compared to high-income countries (3/29, 10%), a higher proportion of low- and middle-income countries (4/24, 17%) prioritized safety. As the pandemic progressed, the duration of protection (2/24, 8%) during the pandemic wave and COVID-19 mortality risk (5/25, 20%) after the pandemic wave emerged as 2 of the most important attributes.
Conclusions: Our review revealed the critical role of vaccine effectiveness and safety in COVID-19 vaccine preference. However, it should be noticed that preference heterogeneity was observed across subpopulations and may change over time.
Trial Registration: PROSPERO CRD42023422720; https://tinyurl.com/2etf7ny7
doi:10.2196/56546
Keywords
Introduction
Background
Although the World Health Organization has declared the end of COVID-19 as a public health emergency [
], the persistence of this disease as a global threat should not be overlooked or underestimated [ ]. Vaccination has been regarded as one of the most effective strategies against COVID-19 and reduced global COVID-19 mortality, severe disease, symptomatic cases, and COVID-19 infections [ , ]. Furthermore, studies have shown that COVID-19 vaccine also had a preventive effect against post–COVID-19 condition [ - ].Despite significant progress made with vaccination efforts, achieving high vaccination coverage remains a challenge due to disparities in vaccine distribution and vaccine hesitancy [
- ]. Disparities in vaccine distribution have been observed between different countries, with vaccination rates varying markedly between high- and low-income countries [ ]. In addition, COVID-19 vaccine hesitancy has been reported across countries [ ], and booster hesitancy has also become a growing concern for public health officials [ ]. Vaccine hesitancy can change over time and in response to different circumstances. Notably, vaccine hesitancy tends to increase when population-level side-effect studies are released after emergency approvals [ ]. These challenges underline the need for well-designed vaccination programs to ensure equitable access and high uptake.Designing a successful vaccination program, including vaccine selection, rollout, and accessibility, is crucial [
, ]. A thorough understanding of individual needs and preferences will allow us to better tailor vaccination programs, which will facilitate the appeal and uptake of COVID-19 vaccines [ , ]. One approach increasingly used to elicit preferences for vaccines and vaccination programs is the discrete choice experiment (DCE) [ , ]. DCEs are scientific research methods that assess preferences by presenting respondents with a series of hypothetical scenarios. In these scenarios, individuals choose among different alternatives which are characterized by specific attributes. By analyzing these choices, researchers can identify the relative importance of each attribute and estimate utility functions [ , ]. DCEs provide valuable insights into decision-making processes and allow for objective evaluation of attribute-based benefits [ - ]. Published studies have been conducted to identify and review choice-based experiments that assess vaccine preferences [ , ]. However, it is important to note that the nature of various vaccines is different, and the preference for vaccines of COVID-19 was not specifically included in these studies.Objective
The COVID-19 vaccines were developed under emergency conditions where there were no peer-reviewed systematic reviews of DCEs on COVID-19 vaccine preference data to inform global decision-making. The diversity in COVID-19 vaccine preferences may be attributed to disparities in vaccine development and production, vaccination scheduling and management, public trust and uptake, as well as vaccine prioritization strategies across various countries and regions [
]. Moreover, new mutant variants are more likely to infect new individuals, highlighting the need for more effective booster vaccines [ , ]. This study provides empirical evidence on the development, implementation, and follow-up of the COVID-19 vaccine and provides references for vaccine decision-making of other infectious diseases.Methods
We conducted our review following the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) guidelines (
) [ ]. This study was registered in the international prospective register of systematic reviews (PROSPERO CRD42023422720).Search Strategy
A literature search was conducted in PubMed, Embase, Web of Science, Scopus, and CINAHL Plus platforms in April 2023. Search terms included discrete choice experiments, COVID-19, and vaccines and related synonyms. Further details are provided in
.Eligibility Criteria
The inclusion and exclusion criteria are detailed in
.Inclusion criteria
- Study focus: Focused on preferences for COVID-19 vaccine (product, service and distribution, policy intervention, etc)
- Article or study type: First-hand discrete choice experiment (DCE) data analysis research
Exclusion criteria
- Study focus: No preferences for COVID-19 vaccine reported
- Article or study type: Not DCE research; nonoriginal research (including secondary reports, systematic reviews, conference abstracts and presentations, correspondence, editorials, and commentaries); theoretical articles; protocols; book chapters; and duplicates
Data Screening and Extraction
Two reviewers (YH and SF) independently performed a 2-stage screening process to identify eligible studies. In the first stage, titles and abstracts were screened to exclude irrelevant studies using the web-based tool Rayyan (Rayyan Systems, Inc [
]). In the second stage, full-text versions of selected papers were assessed to ensure that the inclusion criteria were met. Both reviewers compared the selected papers at each stage to ensure agreement. Any discrepancy or uncertainty between the reviewers was addressed through discussion until a consensus was reached. If not, a third (senior) reviewer (HJ) was consulted to resolve the disagreement.The extracted data were recorded and managed in Microsoft Excel (Microsoft Corp) software. Full texts were extracted and reviewed independently by 2 authors (YH and YZ), and any disagreements were resolved by a third reviewer (HJ). Data extraction was performed for 3 specific aspects, focusing on their relevance and importance for the analysis of the DCE: (1) study information (author, publication year, study period, country, population, and sample size); (2) information on the DCE methodology (survey administration, attribute and level selection, pilot-tested, experimental study design, choice sets per respondent, options per choice set, inclusion of an opt-out option, and statistical models); and (3) information on the DCE results (number of attributes, included attributes classified into 4 categories [outcome, process, cost, and other], and the most important attribute).
Choice-based experiments use different definitions for similar attributes [
]. To address this issue, the attributes were initially grouped into 4 main categories: outcomes, process, cost, and other. The outcomes category encompassed the outcomes or consequences of vaccine administration, such as safety and effectiveness. The process category included activities related to the delivery and administration of vaccines, such as service delivery, dosing, and visits. The cost category focused on the financial aspects of vaccines. Any attributes that did not fit into these 3 categories were classified as other, such as disease risk, incentives or penalties for vaccination, vaccine advice or support, and so on. The classification of outcome, process, cost, and other attributes depended on the aim and design of the studies. It should be noted that vaccine effectiveness and safety were phrased differently in different studies. To facilitate a comparison between studies, efficacy [ , - ], protection rate [ , ], and decreased deaths [ ] were summarized as vaccine effectiveness, whereas side effects [ , , , , , , , , - ], rare but serious risks [ ], and the likelihood of having a flare [ ] were summarized as vaccine safety ( [ , , - ]).High-income countries (HICs) and low- and middle-income countries (LMICs) were classified according to the World Bank [
]. LMICs encompass low-income, lower-middle–income, and upper-middle–income countries. On the basis of previous literatures [ , , ], we hypothesized that individuals’ preferences for vaccines may vary depending on the status of the pandemic. Therefore, we sought to explore how COVID-19 vaccine preferences differed during different study periods. To do this, we used data from the surveillance website [ ] to define the pandemic periods based on daily COVID-19 cases. The first group, before the pandemic wave, referred to the period before the outbreak of the pandemic, when the number of incident cases was low. The second group, during the pandemic wave, represented the peak of the pandemic or was characterized by a rapid increase in the number of incident cases. The third group, after the pandemic wave, was when the number of incident cases decreased and remained low ( [ , , - ]).Quality Appraisal
The 5-item Purpose, Respondents, Explanation, Findings, and Significance (PREFS) checklist, developed by Joy et al [
], is widely accepted and used to assess the reporting quality of preference studies [ , - ]. It evaluates studies based on criteria such as the study’s purpose, respondent sampling, explanation of assessment methods, inclusion of complete response sets in the findings, and use of significance testing.Data Synthesis and Analysis
This review used a combination of text and summary tables to effectively convey information about the characteristics and results of the included studies. Descriptive statistics were used to summarize the study characteristics. The findings were synthesized in a narrative format, providing an overview of the included studies, highlighting the key features of the study designs, and presenting the main findings of the COVID-19 vaccine preference studies. Subgroup analyses were performed by independent factors such as HICs or LMICs and study period (before, during, and after the pandemic wave).
Results
Study Selection
The search yielded a total of 623 records. After title and abstract screening, 513 (82.3%) records were excluded. An additional 63 (10.1%) studies were excluded after full-text assessment. Finally, 47 (7.5%) studies met the eligibility criteria and were included in the review (
).Study and Sample Characteristics
We included 47 studies from 29 countries. Among them, 5 (11%) studies were conducted in multiple countries, with 4 studies conducted in both HICs and LMICs and 1 study conducted in >1 HICs. In addition, 22 (47%) studies were conducted in HICs, while 21 (45%) studies were conducted in LMICs. China stood out with the highest number of preference-based DCEs for COVID-19 vaccines, with 19 (40%) studies. The United States followed closely with 9 (19%) studies, followed by France (n=5, 11%), the United Kingdom (n=4, 9%), Germany (n=4, 9%), and Spain (n=3, 6%). Australia, Canada, India, Italy, Japan, the Netherlands, and South Africa had 2 (4%) studies each. All other countries had only 1 (2%) study (
). The studies were published between the years 2020 and 2023, with sample sizes ranging from 194 to 13,128 participants. The median number of participants per study was 1456 (IQR 872-2109).Most participants were adults, although the specific focus varied. Most studies (36/47, 77%) involved general population samples, whereas some studies (11/47, 23%) included specific groups of participants. These included 5 studies conducted in universities using web-based tools, including 3 studies with university students and 2 studies with both students and staff. In addition, 3 studies involved health care workers (Chinese intensive care unit clinicians, health care workers, and health care and welfare workers); 2 studies involved parents with children aged <18 years, and 1 study involved people with chronic immune-mediated inflammatory diseases (
).Author, year | Study period | Country | Population | Sample size, n |
Asim et al [ | ], 2023February 26 to April 26, 2021 | China | Adults | 208 |
Bansal et al [ | ], 2022May to June, 2021 | India | Adults | 1371 |
Blaga et al [ | ], 2023March to September, 2021 | Hungary | General population | 1011 |
Borriello et al [ | ], 2021March 27 to 31, 2020 | Australia | General population | 2136 |
Bughin et al [ | ], 2023January 25 to 28, 2021 | Germany | General population | 1556 |
Chen et al [ | ], 2023January 24 to March 10, 2021 | China | Middle-aged and older adults aged ≥50 years | 293 |
Chen et al [ | ], 2021January 5 to 12, 2021 | China | Adults | 1066 |
Craig [ | ], 2021November 9 to 11, 2020 | The United States | Adults | 1153 |
Darrudi et al [ | ], 2022March 21 to July 6, 2021 | Iran | Adults | 685 |
Daziano [ | ], 2022October 22 to November 24, 2020 | The United States | Adults | 2723 |
Díaz Luévano et al [ | ], 2021December 18, 2020, to February 1, 2021 | France | Health care and welfare workers | 4346 |
Dong et al [ | ], 2020June to July, 2020 | China | Adults | 1236 |
Dong et al [ | ], 2022January 29 to February 13, 2021 | India, the United Kingdom, Germany, Italy, and Spain | Adults | 812 |
Donin et al [ | ], 2022March 22 to May 3, 2021 | Czech Republic | University students | 445 |
Eshun-Wilson et al [ | ], 2021March 15 to March 22, 2021 | United States | General population | 2985 |
Fu et al [ | ], 2020March 17 to 18, 2020 | China | Health care workers | 541 |
Fung et al [ | ], 2022July 20 to September 21, 2021 | China | University students and staff members | 3423 |
George et al [ | ], 2022November 18 to December 24, 2021 | South Africa | University students and staff members | 1836 |
Hazlewood et al [ | ], 2023May to August, 2021 | Canada | People with chronic immune-mediated inflammatory diseases | 551 |
Hess et al [ | ], 2022Summer 2020 to the start of March 2021 | Africa: Namibia, South Africa; Asia: China Japan, and South Korea; Europe: Denmark, France, Germany, Spain, and the Kingdom; North America: the United States; Oceania: Australia and New Zealand; and South America: Brazil, Chile, Colombia, and Ecuador | General population | 13,128 |
Huang et al [ | ], 2021March 24 to April 10, 2021 | China | Chinese ICUa clinicians | 11,951 |
Igarashi et al [ | ], 2022November 19 to 27, 2020 | Japan | General population | 2155 |
Krueger and Daziano [ | ], 2022March 4 to 10, 2021 | The United States | General population | 1421 |
Leng et al [ | ], 2021NRb | China | Adults | 1883 |
Li et al [ | ], 2021January 25 to February 25, 2021 | China | University students | 194 |
Li et al [ | ], 2023January 28 to February 27, 2021 | China and the United States | Middle-aged and older adult population (aged ≥41 years) | 3444 |
Liu et al [ | ], 2021January 29 to February 13, 2021 | China and the United States | General population | 2480 |
Luyten et al [ | ], 2022October 6 to 16, 2020 | Belgium | Adults | 1944 |
McPhedran et al [ | ], 2022March 25 to April 2, 2021 | The United Kingdom | Adults | 2012 |
McPhedran et al [ | ], 2021August 27 to September 3, 2020 | The United Kingdom | General population | 1501 |
Morillon and Poder [ | ], 2022October 19 to November 17, 2020 | Canada | Adults | 1599 |
Mouter et al [ | ], 2022November 4 to 10, 2020 | The Netherlands | General population | 895 |
Mouter et al [ | ], 2022December 1 to 4, 2020 | The Netherlands | Adults | 747 |
Panchalingam and Shi [ | ], 2022October to November, 2021 | United States | Parents with children aged <18 years | 1456 |
Prosser et al [ | ], 2023May 21 to June 9, 2021 | The United States | Adults | 1040 |
Schwarzinger et al [ | ], 2021June 22 to July 3, 2020 | France | Working-age population (aged 18-64 years) | 1942 |
Steinert et al [ | ], 2022Germany in April 2021; France, Italy, Poland, Spain, and Sweden in June 2021 | France, Germany, Italy, Poland, Spain, and Sweden | Adults | 6030 |
Teh et al [ | ], 2022March 2021 | Malaysia | Adults | 2028 |
Tran et al [ | ], 2023April to August, 2022 | Vietnam | Adults | 871 |
Velardo et al [ | ], 2021November 30 to December 16, 2020 | France | Working-age population (aged 18-64 years) | 5519 |
Wang et al [ | ], 2022August 2020 | China | Adults | 873 |
Wang et al [ | ], 2021February 26 to 28, 2021 | China | Working-age population (aged 18-64 years) | 1773 |
Wang et al [ | ], 2022Mid-September to the end of October, 2021 | China | Parents with children <18 years old | 298 |
Wang et al [ | ], 2022May 2021 | China | University students | 1138 |
Wang et al [ | ], 2022May to June, 2021 | China | Adults | 849 |
Xiao et al [ | ], 2022January 28 to 31, 2021 | China | Adults | 1576 |
Zhang et al [ | ], 2022July 15 to August 10, 2021 | China | Adults | 1200 |
aICU: intensive care unit.
bNR: not reported.
The Implementation of DCEs
Among these 47 studies, researchers commonly used a multifaceted approach to identify and select attributes and levels. Among the studies reviewed, 23 (49%) studies reported a literature review with qualitative assessments such as expert interviews and public surveys. A total of 25 (53%) studies reported a pilot DCE survey. In terms of survey administration, most studies (40/47, 85%) reported that the DCE was conducted through web-based surveys (
).Author, year | Survey administration | Attributes and levels selection | Pilot-tested DCE | Experimental study design | Choice sets per respondent | Options per choice set | Statistical models |
Asim et al [ | ], 2023Web based | Focus group | Yes | D-optimal algorithm design | 8 | 2+opt out | Latent class logit model and nested logistic model |
Bansal et al [ | ], 2022Web based | Literature review | NRa | D-efficient design | 6 | 2 | Conditional logit model and nonparametric logit mixed logit model |
Blaga et al [ | ], 2023NR | Focus group and expert interviews | Yes | D-efficient design | 8 | 3+opt out | Latent variable models, random parameters logit model, and hybrid random parameters logit model |
Borriello et al [ | ], 2021Web based | Literature review and judgment of respondent understanding and plausibility | NR | Bayesian d-efficient design | 8 | 3+opt out | Latent class model |
Bughin et al [ | ], 2023Web based | On the basis of the purpose of the research and necessary calibration of the conjoint | NR | NR | 10 | 3 | Hierarchical multinomial logit model |
Chen et al [ | ], 2023NR | Literature review, expert interviews, and current COVID-19 vaccine development progress | Yes | Orthogonal design | 12 | 2 | Multinomial logistic regression model |
Chen et al [ | ], 2021Web based | Literature review | NR | D-efficient design | 16 | 2 | Conditional logit model and panel mixed logit model |
Craig [ | ], 2021Web based | Literature review, expert interviews, and the CDCb interim playbook version 2.0 | Yes | NR | 8 | 3+opt out | Conditional logit model, latent class model, and opt-out inflated logit model |
Darrudi et al [ | ], 2022Web based | Literature review and expert interviews | Yes | D-efficient design | Group 1:9 and group 2:10 | Group 1: 2 and group 2: 2 | Conditional logit model |
Daziano [ | ], 2022Web based | Literature review and focus group | Yes | Bayesian efficient design | 7 | 2+opt out | Latent class logit model, conditional logit model, and random effects logit model |
Díaz Luévano et al [ | ], 2021Web based | Literature review | Yes | Efficient design | 8 | 1+opt out | Random intercept logit models |
Dong et al [ | ], 2020Web based | Literature review, expert interviews, and public interviews | Yes | D-optimal algorithm design | 10+validity | 2 | Mixed logit regression model |
Dong et al [ | ], 2022Web based | NR | Yes | NR | NR | NR | Conditional logit model |
Donin et al [ | ], 2022Web based | Literature review | Yes | D-efficient design | NR | 2+opt out | Hierarchical Bayes |
Eshun-Wilson et al [ | ], 2021Web based | Expert interviews, expert discussion, and literature review | Yes | Fractional factorial design | 10 | 2+opt out | Mixed logit model and latent class model |
Fu et al [ | ], 2020Web based | Literature review, focus group, and expert interviews | Yes | Fractional factorial design | 8+ validity | 2 | Binary logistic regression model |
Fung et al [ | ], 2022Web based | Literature review and expert interviews | NR | Orthogonal design | 8 | 2+opt out | Mixed logit model |
George et al [ | ], 2022Web based | Literature review and a series of meetings and discussions with the study team and key stakeholders at UKZNc | NR | Fractional factorial design | 8 | 2 | Mixed effects logit model |
Hazlewood et al [ | ], 2023Web based | Guideline panel discussion | Yes | Fractional factorial design | 10 | 2+opt out | Main-effects multinomial logit model |
Hess et al [ | ], 2022Web based | NR | NR | D-efficient design | 6 | 4+opt out | Ordered logit model, latent class model, and nested logit |
Huang et al [ | ], 2021Web based | Expert interviews | Yes | Fractional factorial design | 4 | 2 | Multivariable conditional logistic regression model |
Igarashi et al [ | ], 2022Web based | Literature review | NR | Orthogonal design | 12 | 2+opt out | Panel logit model |
Krueger and Daziano [ | ], 2022NR | Literature review and focus group | NR | Bayesian efficient design | 7 | 2+opt out | Normal error components mixed logit model |
Leng et al [ | ], 2021Face to face | Literature review | Yes | D-efficient partial profile design | 8 | 2 | Conditional logit model |
Li et al [ | ], 2021Web based | NR | NR | Orthogonal design | 6 | 2 | Conditional logit model |
Li et al [ | ], 2023Web based | Literature review and expert interviews | NR | Fractional factorial design | 13 | 2+opt out | Conditional logit model |
Liu et al [ | ], 2021Web based | Literature review and expert interviews | Yes | NR | NR | 2 | Conditional logit model |
Luyten et al [ | ], 2022Web based | Literature review | Yes | Bayesian d-optimal design | 10+ validity | 2 | Panel mixed logit model |
McPhedran et al [ | ], 2022Web based | Literature review | NR | D-optimal fractional factorial design | 6 | 2+opt out | Mixed logit model |
McPhedran et al [ | ], 2021Web based | Literature review | NR | Rotation design | 6 | 2+opt out | Clustered conditional logit model and hybrid logit model |
Morillon and Poder [ | ], 2022Web based | Literature review, expert interviews, and public interviews | NR | Orthogonal design | 11+ validity | 2+opt out | Mixed logit model, latent class logit model, and multinomial logistic regression |
Mouter et al [ | ], 2022Web based | Literature review, expert consultations, and feedback | Yes | Bayesian d-efficient design | 8 | 2 | Panel mixed logit model |
Mouter et al [ | ], 2022Web based | Literature review, expert discussion, and pretest | Yes | Bayesian d-optimal design | 9 | 2 | Panel mixed logit model |
Panchalingam and Shi [ | ], 2022Web based | Literature review | NR | D-efficient design | 10+ validity | 2+opt out | Logistic regressions model and random parameter logit regressions model |
Prosser et al [ | ], 2023Web based | Literature review and public interviews | NR | Fractional factorial design | 6 | 2+opt out | Bayesian logit regression and latent class analyses |
Schwarzinger et al [ | ], 2021Web based | Literature review and expert interviews | NR | D-efficient design | 8 | 2+opt out | Conditional logit model |
Steinert et al [ | ], 2022Web based | NR | NR | D-efficient design | 8 | 2 | Conditional logit model, and fixed-effects model |
Teh et al [ | ], 2022Web based | Literature review, expert interviews, and focus group | Yes | Bayesian d-optimal design | 10+ validity | 2+opt out | Mixed logit model,and nested logit model |
Tran et al [ | ], 2023Web based | Literature review and expert interviews | Nr | NR | 7 | 2 | Hierarchical Bayes |
Velardo et al [ | ], 2021Web based | NR | NR | D-efficient design | 8 | 2+opt out | Conditional logit model |
Wang et al [ | ], 2022Web based | Expert interviews and public interviews | Yes | D-efficient design | 6 | 2+opt out | Multinominal mixed effects logit model |
Wang et al [ | ], 2021Web based | Individual interviews | Yes | D-optimal algorithm design | 8 | 2+opt out | Multiple logistic regression model, nested logistic model, and separate logistic model |
Wang et al [ | ], 2022Web based | Literature review, qualitative interview and background information, and levels of the attributes | Yes | D-efficient design | 8 | 2+opt out | Multiple logistic model and mixed logit model |
Wang et al [ | ], 2022Face to face | Literature review | NR | D-efficient partial profile design | 8+ validity | 2 | Conditional logit model |
Wang et al [ | ], 2022Face to face | Literature review and expert interviews | Yes | D-efficient partial profile design | 8 | 2 | Conditional logit model, mixed logit model, and latent class model |
Xiao et al [ | ], 2022Web based | Literature review, research team discussions, official report, expert discussion, and pretest | Yes | Full factorial design | 4 | 2+opt out | Random parameter logit model and constrained latent class model |
Zhang et al [ | ], 2022NR | Literature review, expert interviews, and several vaccines on the market | NR | Fractional factorial design | 11 | 2+opt out | Conditional logit model |
aNR: not reported.
bCDC: Center for disease control and prevention.
cUKZN: the University of KwaZulu-Natal.
Attributes in DCE Studies
Of the 286 attributes identified in the 47 studies, 126 (44.1%) were categorized as outcome attributes, followed by 82 (28.7%) as process attributes, and 22 (7.7%) as cost attributes. The remaining 55 (19.2%) attributes were categorized as other attributes (
and ).Author, year | Attributes, n | Outcome | Process | Cost | Other | Most important attribute |
Asim et al [ | ], 20237 | Efficacya and safetya | Venue for vaccinationa and vaccine branda | —b | Exemption of quarantine for vaccinated travelersa, uptake of recommendations from professionals, and vaccine by people around | Brand |
Bansal et al [ | ], 20227 | Effectiveness of vaccinea, side effectsa, and duration of protection offered by the vaccinea | Developera, and place where vaccination is administereda | Out-of-pocket costa | The proportion of friends and family members who have taken the vaccinea | Vaccinated friends or family |
Blaga et al [ | ], 20234 | Effectiveness of the vaccinea, type of possible side effectsa, and duration of protection provided by the vaccinea | Country of origina | — | — | Duration of protection |
Borriello et al [ | ], 20217 | Effectivenessa, mild side effectsa, and major side effectsa | Mode of administrationa, locationa, and time period when the vaccine was availablea | Costa | — | Safety |
Bughin et al [ | ], 20235 | Effectivenessa | Time of COVID-19 vaccinationa | Work sitea, restriction levela, choices to get vaccinateda, and advantages or penaltiesa | Time of COVID-19 vaccination | |
Chen et al [ | ], 20235 | Risk of adverse effectsa, protective durationa, and effectivenessa | Injection dosesa and injection perioda | — | — | Safety |
Chen et al [ | ], 20215 | Protection rate a, adverse effect a, and protection durationa | Convenience of vaccinationa | Cost of the vaccinea | — | Safety |
Craig [ | ], 20215 | Duration of immunity a, risk of severe side effects a, and vaccine effectivenessa | Vaccination settinga | — | Proof of vaccinationa | Effectiveness |
Darrudi et al [ | ], 20226 | Group 1: effectiveness a, risk of severe complications a, and duration of protectiona | Group 1: location of vaccine productiona; group 2: age | Group 1: pricea; group 2: cost to the communitya | Group 1: underlying diseasea, employment in the health sector a, potential capacity to spread the virus (virus spread)a, and the necessary job for societya | Group 1: effectiveness; group 2: potential capacity to spread the virus |
Daziano [ | ], 20229 | Effectiveness a, days for antibodies to developa, duration of protectiona, number of people out of 10 with mild side effects a, and the number of people out of 1,000,000 with severe side effectsa | Country where vaccine was developeda and introduced (months)a | Out-of-pocket costa | Who recommends this specific vaccinea | Recommenders |
Díaz Luévano et al [ | ], 20215 | Efficacya, indirect protectiona, safetya, and protection durationa | — | — | Recommendation or incentive sourcea | Effectiveness |
Dong et al [ | ], 20206 | Effectivenessa, duration of protectiona, and adverse eventa | The total number of injectionsa and origin of the producta | Price (Chinese Yuan)a | — | Effectiveness |
Dong et al [ | ], 20226 | Adverse effectsa, efficacy a, duration of the vaccine a, and time taken for the vaccine to worka | Vaccine types | The cost of vaccinationa | — | Effectiveness |
Donin et al [ | ], 20226 | Protection durationa, efficacya, and risk of mild side effectsa | Route of vaccinationa and travel time to vaccination sitea | — | Recommender of the vaccinea | Protection duration |
Eshun-Wilson et al [ | ], 20217 | — | Vaccine frequency, waiting time at vaccination site, vaccination location, number of doses required per vaccination episode, and vaccination appointment scheduling | — | Vaccination enforcement and who has already received the vaccine in your community? | Vaccine frequency |
Fu et al [ | ], 20207 | Vaccine safetya and vaccine efficacya | — | Out-of-pocket costsa | Infection probabilitya, case fatality ratioa, possible trends of the epidemica, and acceptance of social contactsa | Possible trends of the epidemic |
Fung et al [ | ], 20227 | Risk of a mild or moderate adverse event after vaccinationa, risk of a severe adverse event after vaccinationa, efficacy against COVID-19 infectiona, efficacy against severe manifestation of COVID-19 infectiona, and duration of protection after vaccinationa | — | Out-of-pocket costsa | Incentives for completing vaccinationa | Quarantine-free travel |
George et al [ | ], 20227 | Effectivenessa | Vaccination locationa, waiting time at the vaccination sitea, number of dosesa, boosters requireda, and vaccine origina | — | Incentives for vaccinationa | Effectiveness |
Hazlewood et al [ | ], 20234 | Effectivenessa, rare but serious risksa, and likelihood of having a flarea | Dosinga | — | — | Effectiveness |
Hess et al [ | ], 20229 | Estimated protection duration, risk of mild side effects, and risk of severe side effects | — | Fee | Exemption from international travel restrictions, risk of infection, and risk of serious illness, and population coverage | Effectiveness |
Huang et al [ | ], 20214 | Effectivenessa, risk of adverse reactionsa, and duration of immunitya | — | — | Whether coworkers have been vaccinateda | Effectiveness |
Igarashi et al [ | ], 20225 | Safetya, efficacya, and immunity durationa | — | Pricea | Disease prevalence | Effectiveness |
Krueger, and Daziano [ | ], 20229 | Effectivenessa, protection perioda, risk of severe side effectsa, risk of mild side effectsa, and incubation perioda | Origin of the vaccinea, number of required dosesa, and whether the vaccine has a booster against variants | Out-of-pocket costa | — | Effectiveness |
Leng et al [ | ], 20217 | Vaccine effectivenessa, side effectsa, and duration of vaccine protectiona | Accessibilitya, number of dosesa, and vaccination sitesa | — | Proportion of acquaintances vaccinateda | Effectiveness |
Luyten et al [ | ], 20225 | — | Agea, essential professiona, and medical risk groupa | Cost to societya | Virus spreadera | Medical risk group |
Li et al [ | ], 20216 | Nonsevere adverse reactionsa, efficacya, and protection duration | Required number of dosesa, and origin of the vaccinea | Out-of-pocket pricea | — | Safety |
Li et al [ | ], 20236 | Adverse effecta, efficacya, duration of vaccine effecta, and time for the vaccine to start workinga | Vaccine varietiesa | Cost of vaccinationa | — | China: cost; The United States: effectiveness |
Liu et al [ | ], 20216 | Adverse effecta, efficacya, duration of vaccine effecta, and time for the vaccine to start working | Vaccine varietiesa | Cost of vaccinationa | — | China: cost; the United States: effectiveness |
McPhedran et al [ | ], 20224 | — | Delivery modea, appointment timinga, and proximitya | — | Sendera | SMS text message invitation sender |
McPhedran et al [ | ], 20215 | Level of protection offereda | Location in which the vaccine is administereda and the number of doses needed for full protectiona | — | Recommender of the vaccinea and coverage in the mediaa | Effectiveness |
Morillon and Poder [ | ], 20227 | Effectivenessa, safetya, and durationa | Waiting timea, priority populationa, and origina | — | Recommendationa | Effectiveness |
Mouter et al [ | ]4 | The percentage of vaccinated individuals protected against COVID-19a, the number of cases of mild side effectsa, and the number of cases of severe side effectsa | The month when the vaccine would become available to the respondenta | — | — | Safety |
Mouter et al [ | ], 20226 | Decrease in deaths, decrease in health damage, and decrease in households with income loss | Vaccination at home and vaccination when and where convenient | One-time tax increase | Vaccination ambassadors, pay €250 (US $280.75) if does not get vaccinateda, receive €100 (US $113) if gets vaccinateda, vaccination passport daily activities during outbreaka, vaccination passport large eventsa, counseling if does not get vaccinateda, and mandatory testing at own cost if does not get vaccinateda | Mandatory testing at own cost if does not get vaccinated |
Panchalingam and Shi [ | ], 20225 | Risk of severe side effectsa, and effectivenessa, and duration of vaccine-induced protectiona | — | — | Risk of unvaccinated children requiring hospitalization for COVID-19a and local coveragea | Safety |
Prosser et al [ | ], 20236 | Effectivenessa, mild common side effectsa, and rare adverse eventsa | Number of dosesa, total time required to get vaccinateda, and regulatory approvala | — | — | Effectiveness |
Schwarzinger et al [ | ], 20214 | Safetya and efficacya | Place to be vaccinateda and country of vaccine manufacturera | — | — | Region of vaccine manufacturer |
Steinert et al [ | ], 20224 | — | Agea | — | Employment statusa, country of residence and health care system capacitya, and mortality riska | Mortality risk |
Teh et al [ | ], 20225 | Effectivenessa and risk of developing severe side effectsa | Vaccination schedule during office hoursa, distance from home to vaccination centera, and halal contenta | — | — | Halal content |
Tran et al [ | ]c, 20236 | Immunity duration, effectiveness, and side effects | — | Cost of the vaccine | Limitations if not vaccinated and COVID-19 mortality rate | Mortality rate |
Velardo et al [ | ], 20215 | Efficacya, risk of serious side effects per 100,000a, and duration of vaccine immunitya | Place of vaccine administration and location of vaccine manufacturera | — | — | Effectiveness |
Wang et al [ | ], 20226 | Probability of fever, side effectsa and effectivenessa | Location of vaccinationa, number of dosesa, and origin of vaccinea | Price (CNY)a | — | Effectiveness |
Wang et al [ | ], 20217 | Probability of COVID-19 infectiona and probability of serious adverse eventa | Branda and venue for vaccinationa | — | Recommendations from professionals, quarantine for vaccinated travelersa, and vaccine uptake of people arounda | Effectiveness |
Wang et al [ | ] 20227 | Efficacya and probability of serious adverse eventa | Venue for vaccination and branda | — | Recommendations from professionals, vaccination coverage among all children aged <18 yearsa, and vaccine uptake among acquaintances’ minor children | Effectiveness |
Wang et al [ | ], 20226 | Self-assessed vaccine-related side effectsa, duration of vaccine protectiona, and effectivenessa | Vaccination sitesa | — | Risk perceptiona and acquaintances vaccinateda | Safety |
Wang et al [ | ], 20226 | Effectivenessa, side effectsa, and duration of protectiona | Vaccination sitesa | — | Perceived probability of infection of individuals or acquaintancesa and percentage of acquaintances vaccinateda | Effectiveness |
Xiao et al [ | ], 20224 | Effectivenessa, adverse reactionsa, and protection perioda | — | Pricea | — | Effectiveness |
Zhang et al [ | ], 20226 | Efficacya, durationa, adverse effecta, and time period when the vaccine starts workinga | Varietiesa | Costa | — | Cost |
aAttribute is significant (P<.05).
bNot available.
cThe corresponding coefficients and P values are not provided.
The Most Important Attribute Reported in DCE Studies
In total, 2 of the 5 multicountry studies did not report preferences for each country and were therefore excluded from the synthesis of the most important attribute. A total of 53 data points on COVID-19 vaccine preferences were collected from the study population of the corresponding country. In the outcome category, among the 30 attributes examined, effectiveness emerged as the most prominent, accounting for 40% (21/53) of the studies [
, , , - , , - , , , - , - ]. Safety was addressed in 13% (7/53) of the studies [ , , , , , , ], while protection duration was mentioned in 4% (2/53) [ , ]. In the process category, 13 attributes were identified. Brand (1/53, 2%) [ ], region of vaccine manufacturer (1/53, 2%) [ ], and halal content (1/53, 2%) [ ] were associated with vaccine production. In addition, waiting time for COVID-19 vaccination (1/53, 2%) [ ] and vaccine frequency (1/53, 2%) [ ] were considered. Furthermore, 3 (6%) studies on vaccine distribution prioritized vaccination for the medical risk group (1/53, 2%) [ ], those who had a higher COVID-19 mortality risk (6/53, 11%) [ ], and those who had the potential capacity to spread the virus (1/53, 2%) [ ]. In the cost category, personal vaccination cost accounted for 6% (3/53) [ , , ]. Among the other attributes (7/53, 13%), disease risk threat was of particular importance, including possible trends of the epidemic (1/53, 2%) [ ] and COVID-19 mortality rate (1/53, 2%) [ ]. In addition, incentives and penalties for vaccination were identified, including quarantine-free travel (1/53, 2%) [ ] and mandatory testing at own expense if not vaccinated (1/53, 2%) [ ]. Vaccine advice or support included vaccination invitation sender (1/53, 2%) [ ] and recommenders (1/53, 2%) [ ]. The proportion of friends and family members who had received the vaccine (1/53, 2%) [ ] was also among the other attributes influencing decision-making ( ).Although effectiveness remained the most important attribute, it is worth noting that variations in preferences were also observed among different subgroups. A higher proportion of studies conducted in LMICs (4/24, 17%) than in HICs (3/29, 10%) prioritized on safety (
). In addition, COVID-19 mortality risk was the second most important attribute (6/29, 21%) after effectiveness in HICs. Cost was considered to be another most important attribute (3/24, 13%) in LMICs. Interestingly, many other attributes also became more important as the pandemic progressed. Protection duration (2/24, 8%) emerged as one of the most important attributes during the pandemic wave. COVID-19 mortality risk (5/25, 20%) and cost (3/25, 12%) were considered as the most important attributes after the pandemic wave ( ).Study Quality
The overall reporting quality was deemed acceptable but there is room for improvement. The PREFS scores of the 47 studies ranged from 2 to 4, with a mean of 3.23 (SD 0.52). No study scored 5. Most studies scored 3 (32/47, 68%) or 4 (13/47, 28%), while 2 studies (2/47, 4%) scored 2 (
[ , , - ]).Discussion
Principal Findings
This systematic review synthesizes existing data on preference for COVID-19 vaccine using DCE, with the aim of informing improvements in vaccine coverage and vaccine policy development. We identified 47 studies conducted in 29 countries, including 21 HICs and 8 LMICs. HICs had an adequate supply of vaccine since the early emergency availability of COVID-19 vaccine, and HICs had 1.5 times more doses of COVID-19 vaccinations than LMICs by September 2023 [
]. In total, 19 (40%) studies were conducted in China and 9 (19%) in the United States, demonstrating their significant contribution to the research and their leadership in vaccine research and development. Vaccine effectiveness and safety were the most important attributes in DCEs, although preferences differed among subgroups.Recent years have seen new trends in the design, implementation, and validation of the DCE. For example, most studies (40/47, 85%) reported that the DCE was administered through web-based surveys, which have become a quick and cost-effective way to collect DCE data [
]. Almost half of the studies (25/47, 53%) did not report a pilot test. However, piloting in multiple stages throughout the development of a DCE is conducive to identifying appropriate and understandable attributes, considering whether participants can effectively evaluate the full profiles, and producing an efficient design [ , , ].Overall, vaccine effectiveness and safety have emerged as the most commonly investigated attributes in the outcome category. Despite heterogeneity in preferences across subpopulations, effectiveness remains the primary driver for COVID-19 vaccination across the studies [
, , , - , , , , , , - , - ], similar to the previous findings [ ]. A study conducted in India and Europe found that respondents’ preference for the COVID-19 vaccine increased with effectiveness and peaked at 95% effectiveness [ ]. Another study conducted among university staff and students in South Africa found that vaccine effectiveness not only was a concern but also significantly influenced vaccine choice behavior [ ]. Interestingly, a nationwide stated choice survey in the United States found a strong interaction between effectiveness and other attributes [ ]. These findings support the ongoing efforts to maximize vaccine effectiveness while emphasizing the importance of communicating information on vaccine effectiveness to the target population for promotion [ ].Safety has also been identified as a crucial factor influencing the acceptance of COVID-19 vaccine [
, , , , , , ]. One study indicated that the likelihood of the general public choosing vaccines with low or moderate side effects increased by 75% and 63%, respectively, compared with vaccines with high side effects. While the likelihood changed within a 30% range when most attributes other than effectiveness and safety were changed [ ]. In addition, respondents in Australia expressed a willingness to wait an additional 0.04 and 1.2 months to reduce the incidence of mild and severe adverse events by 1/10,000, respectively [ ].Similar to the results of previous systematic reviews of DCEs for various vaccines [
, ], the most common predictors of COVID-19 vaccine acceptance are effectiveness and safety, particularly during the rapid development and rollout of COVID-19 vaccines, which essentially boils down to trust in the vaccine [ ]. Respondents expressed the importance of having a safe and effective COVID-19 vaccine available as soon as possible, but the majority preferred to wait a few months to observe the experience of others rather than be the first in line [ ]. Therefore, collaborating to enhance vaccine effectiveness while reducing the risk of severe side effects could be a highly effective strategy to address vaccine hesitancy and augment vaccine desirability. Dissemination of this important vaccine-related information by governments and health care institutions, along with effective communication by health care professionals, can help build public trust and ultimately increase vaccination rates [ ]. However, these inherent vaccine attributes are typically beyond the control of a vaccination program, and given the ongoing mutations of SARS-CoV-2, it is challenging to predict the effectiveness of the vaccines currently in development [ ]. Global collaboration between scientists and pharmaceutical companies is therefore essential to improve vaccine effectiveness and minimize side effects [ ].Vaccine production, including its origin, brand, vaccine frequency, and content, are key considerations in the process category. Vaccine brand also has a significant impact on vaccine choice [
], independent of effectiveness and safety, due to factors such as reputation, country of origin, technological advances, and reported side effects associated with the brands [ ]. For vaccine origin, some studies found that participants preferred domestic vaccines to imported vaccines, which may depend on the availability or the approval of vaccines in different countries [ , , ] or the incidence of side effects among different types of COVID-19 vaccines [ ]. However, some studies found that imported vaccines were more likely to be accepted than domestically produced vaccines, which may be attributed to less trust in domestically produced vaccines [ , ]. A study on vaccine preferences among the Malaysian population found that the composition and production process of the COVID-19 vaccine, which complied with Islamic dietary requirements (ie, halal content) was an important factor for many Malaysians when deciding whether to be vaccinated. This underscores the substantial influence of religion on vaccine choice [ ].Vaccine frequency was emphasized to play an important role in the choice of COVID-19 vaccine among the US public, while the 90% efficacy with low side effect rate of the COVID-19 vaccine was set. The prospect of vaccinating once to get lifelong immunity was very attractive, reflecting the fact that people were effort minimizers [
]. This is similar to the nature of the 2 studies referenced in the outcome attribute, where the protection duration is prioritized. Given the threat of COVID-19, people expect the protection duration to be as long as possible [ , ].When vaccine supply is limited, people tend to prioritize vaccination for those who are more susceptible to the disease, have higher mortality rates from infectious diseases, or have greater potential to spread the virus. A study in Iran found that individuals tend to prioritize vaccination for those in the community with higher potential for virus transmission [
]. In addition, results from a study in 6 European countries revealed unanimous agreement among respondents that candidates with higher mortality and infection risks should be prioritized for vaccination [ ]. While another study conducted among Belgians also found that respondents would prioritize populations at higher medical risk [ ].Cost was another important factor influencing COVID-19 vaccine preferences, mostly related to out-of-pocket costs [
, , ]. In 2 studies comparing public preferences for COVID-19 vaccines in China and the United States, vaccine efficacy emerged as the most important driver for the American public, whereas the cost of vaccination had the greatest impact on the Chinese public. This difference was likely due to the relatively stable pandemic situation in China at the time and the lower perceived risk of COVID-19. As a result, the Chinese population was more price sensitive and reluctant to pay for vaccination [ , , ].For the other category, several different attributes were highlighted, depending on the specific population or situation. When people perceive the threat of a disease, their desire to be vaccinated becomes more urgent. In a study among health care workers in China, participants’ expectations about the future development of COVID-19 had a greater impact on their decision to be vaccinated than their perceived risk of infection or actual case rates, which may have been influenced by their previous experience with seasonal influenza vaccination [
]. The mortality rate of COVID-19 was considered the most influential factor in the uptake of COVID-19 booster shots in Vietnam. This study was conducted during a pandemic wave in Vietnam, which may have led to an increased perception of public health risks and a greater inclination toward COVID-19 vaccination [ ]. To achieve herd immunity, government authorities can implement policies of incentives and penalties for vaccination to encourage population-wide uptake. A study conducted in the Netherlands revealed that respondents particularly disliked policies that penalized those who were not vaccinated, such as mandatory testing at their own expense if they were not vaccinated [ ]. Instead, they favored policies that rewarded vaccination, such as giving vaccinated individuals additional privileges through a vaccination passport. This finding is consistent with a study in Hong Kong, which found that quarantine-free travel was considered the most important motivator among university students and staff, given their frequent engagement in international travel [ ].The source of vaccine information also influences vaccine decision-making [
]. Variation in the sender of vaccination appointment invitation via SMS text messaging and recommenders may potentially influence the public’s willingness to vaccinate against a disease [ , , ]. Furthermore, the acceptance of vaccines was observed to change as the firsthand information about vaccine side effects and effectiveness was provided by friends and family in India [ ].In HICs, COVID-19 mortality risk was the second most important attribute after effectiveness, as respondents in all 6 high-income European countries from a study of public preferences for COVID-19 vaccine distribution prioritized candidates with higher mortality risks [
]. However, individuals from LMICs appeared to be more concerned about vaccine safety than those from HICs. This may be related to greater confidence in vaccine safety in HICs due to the earlier initiation and higher rates of COVID-19 vaccination [ ]. In contrast, in some LMICs, vaccine safety was reported as the main reason influencing the willingness to vaccinate due to the rapid development of the COVID-19 vaccines [ , , , , , , , ].Interestingly, the preference for COVID-19 vaccines may also have changed as the pandemic progressed [
]. Similarly, effectiveness remained the most important attribute in all periods, possibly due to the continuing severity of the pandemic and the fear of the possible emergence of new coronavirus strains [ ]. Before the pandemic wave, the information on vaccine effectiveness was limited [ ], but people still considered vaccine effectiveness to be the most important driver of vaccination. However, during the pandemic, the public’s perception of the health risk increased. As vaccines were introduced and used, people seemed to become more concerned about the duration of vaccine protection and preferred a longer vaccine protection [ , ]. After the pandemic wave, as the pandemic situation gradually stabilized, cost, combined with their perception of the risk of susceptibility, became more important in their preferences. However, despite this shift, most of the public still believed that people who are at higher risk of infection or death should be vaccinated first [ ].Limitations
Our study had several limitations. First, not all studies used the same attributes and levels, which limited our ability to perform a quantitative synthesis and directly compare the estimates of model parameters. Instead, we qualitatively synthesized and summarized the range of attributes that may be useful in the formative stage of attribute selection in future DCE surveys investigating the preference for COVID-19 vaccine. Second, although DCEs have been shown to be a valid method for eliciting preferences, the experiment may not represent real market choices but rather hypothetical scenarios with plausible and realistic attributes. However, it offers opportunities to evaluate vaccines that are not yet available in the market or to specific population [
]. Third, the commonly used classification of outcome, cost, and process was used in order to better explain the public’s preference for vaccine attributes. However, several attributes could not be properly classified, and a fourth category (ie, other attributes) had to be added [ ]. Meanwhile, the variety of attributes included may make it difficult to appropriately name and interpret this category as a whole. Fifth, the PREFS checklist is limited to 5 questions and fails to elicit several criteria that should be reported in DCE studies. Also, it does not provide sufficient tools to assess the biases in a DCE, such as selection bias and nonresponse bias [ , ]. Finally, although there was no specific theoretical framework to structure our qualitative analysis from the 4 identified categories, our classification was based on previous studies [ , , , , ] and our own findings. This synthesis led us to categorize attributes into 4 main classes, providing a clear structure for analyzing and presenting participants’ vaccine preferences and making it easier to compare their preferences across different studies.Conclusions
In conclusion, this systematic review synthesized the global evidence on preferences for COVID-19 vaccines using the DCE methodology. Vaccine effectiveness and safety were found to be the main drivers for COVID-19 vaccination, highlighting the importance of global collaboration to improve vaccine effectiveness and minimize side effects, as well as the importance of communicating this vaccine-related information to the public to maximize the uptake of COVID-19 vaccines. The subgroup analyses emphasized the importance of differences in vaccine preference of specific populations and time periods in optimizing the acceptance of COVID-19 vaccines. These findings may serve as valuable insights for government agencies involved in the social mobilization process for COVID-19 vaccination. However, the response to the pandemic is a continuous learning process [
]. It is crucial for policy makers to consider preference evidence when designing policies to promote vaccination.Acknowledgments
The authors have not received a specific grant for this research from any funding agency in the public, commercial, or not-for-profit sectors.
Data Availability
All data relevant to the study are included in the article or uploaded as supplemental information. Data sets of this study are available upon reasonable request to the corresponding author.
Authors' Contributions
YH, SF, and YZ are joint first authors. HJ conceived the study and its methodology. YH, SF, and YZ designed, refined, and implemented the search strategy; screened articles for inclusion; and extracted and curated the data. All authors contributed to the interpretation of the results. YH, SF, and YZ wrote the initial draft of the manuscript. HJ and HW critically reviewed the manuscript. HJ supervised the study design and provided overall guidance. All authors approved the final draft of the manuscript. HJ had full access to all the data used in this study, and all authors had final responsibility for the decision to submit for publication.
Conflicts of Interest
None declared.
PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) 2020 checklist.
DOCX File , 31 KBSearch strategies.
DOCX File , 12 KBAttributes included in each category.
DOCX File , 61 KBThe detailed distribution of the study period across countries.
DOCX File , 3172 KBPreference for COVID-19 vaccines among high-income countries and low- and middle-income countries (n=53).
DOCX File , 12 KBPreference for COVID-19 vaccines in the different study periods (n=53).
DOCX File , 14 KBAssessment of 47 included studies quality using the Purpose, Respondents, Explanation, Findings, and Significance checklist.
DOCX File , 22 KBReferences
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Abbreviations
DCE: discrete choice experiment |
HIC: high-income country |
LMIC: low- and middle-income country |
PREFS: Purpose, Respondents, Explanation, Findings, and Significance |
PRISMA: Preferred Reporting Items for Systematic Reviews and Meta-Analyses |
Edited by A Mavragani; submitted 19.01.24; peer-reviewed by T Ricks, I Saha; comments to author 11.04.24; revised version received 01.05.24; accepted 26.05.24; published 29.07.24.
Copyright©Yiting Huang, Shuaixin Feng, Yuyan Zhao, Haode Wang, Hongbo Jiang. Originally published in JMIR Public Health and Surveillance (https://publichealth.jmir.org), 29.07.2024.
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