Skip to main content
PLOS ONE logoLink to PLOS ONE
. 2021 Dec 1;16(12):e0260575. doi: 10.1371/journal.pone.0260575

Will Africans take COVID-19 vaccination?

AbdulAzeez A Anjorin 1, Ismail A Odetokun 2, Ajibola I Abioye 3, Hager Elnadi 4, Mfon Valencia Umoren 5, Bamu F Damaris 6, Joseph Eyedo 1, Haruna I Umar 7, Jean B Nyandwi 8, Mena M Abdalla 9, Sodiq O Tijani 10, Kwame S Awiagah 11, Gbolahan A Idowu 12, Sifeuh N Achille Fabrice 13, Aala M O Maisara 14, Youssef Razouqi 15, Zuhal E Mhgoob 16, Salim Parker 17, Osaretin E Asowata 18, Ismail O Adesanya 19, Maureen A Obara 6, Shameem Jaumdally 20, Gatera F Kitema 21,22, Taofik A Okuneye 23, Kennedy M Mbanzulu 24, Hajj Daitoni 25, Ezekiel F Hallie 26, Rasha Mosbah 27,28, Folorunso O Fasina 29,*
Editor: Prasenjit Mitra30
PMCID: PMC8635331  PMID: 34851998

Abstract

The economic and humanistic impact of COVID-19 pandemic is enormous globally. No definitive treatment exists, hence accelerated development and approval of COVID-19 vaccines, offers a unique opportunity for COVID-19 prevention and control. Vaccine hesitancy may limit the success of vaccine distribution in Africa, therefore we assessed the potentials for coronavirus vaccine hesitancy and its determinants among Africans. An online cross-sectional African-wide survey was administered in Arabic, English, and French languages. Questions on demographics, self-reported health status, vaccine literacy, knowledge and perception on vaccines, past experience, behavior, infection risk, willingness to receive and affordability of the SARS-COV-2 vaccine were asked. Data were subjected to descriptive and inferential statistics. A total of 5,416 individuals completed the survey. Approximately, 94% were residents of 34 African countries while the other Africans live in the Diaspora. Only 63% of all participants surveyed were willing to receive the COVID-19 vaccination as soon as possible and 79% were worried about its side effects. Thirty-nine percent expressed concerns of vaccine-associated infection. The odds of vaccine hesitancy was 0.28 (95% CI: 0.22, 0.30) among those who believed their risk of infection was very high, compared to those who believed otherwise. The odds of vaccine hesitancy was one-fifth (OR = 0.21, 95% CI: 0.16, 0.28) among those who believed their risk of falling sick was very high, compared to those who believed their risk of falling very sick was very low. The OR of vaccine hesitancy was 2.72 (95% CI: 2.24, 3.31) among those who have previously refused a vaccine for themselves or their child compared to counterparts with no self-reported history of vaccine hesitancy. Participants want the vaccines to be mandatory (40%), provided free of charge (78%) and distributed in homes and offices (44%). COVID-19 vaccine hesitancy is substantial among Africans based on perceived risk of coronavirus infection and past experiences.

Introduction

The COVID-19 pandemic has had an undeniable impact on the lives and livelihoods of people globally. The first COVID-19 case in Africa was reported in Egypt on 14 February 2020 [1]. By June 22, 2021, Africa has experienced over 5.1 million cases, with over 137,000 deaths [2]. Initial efforts to combat the pandemic primarily focused on controlling the spread of SARS-CoV-2, through the well-publicized public health measures [3]. However, the accelerated development and approval of COVID-19 vaccines, has added a different dimension to the prevention and control of COVID-19. It is expected to decrease mortality with consequential easing of restrictions on human mobility, a situation that predispose to significant psychosocial, economic and health outcomes [48].

In the context of the global pandemic, high demands for COVID-19 vaccines are warranted despite limited global capacities for production and supplies. The economics of vaccine trade favours the high-income countries against the low and middle-income countries (LMICs). The COVID-19 Vaccines Global Access (COVAX) Facility was formed to facilitate equitable global distribution, with the aim to provide at least two billion doses of vaccines for countries worldwide by the end of 2021 [9]. The African Vaccine Acquisition Task Team is working with the COVAX, to make 720 million doses of COVID-19 vaccines available to achieve 60% coverage across Africa by June 2022 [10]. Vaccine choices in Africa will be dependent on the cost per dose, storage requirements, authorities’ ability to afford and willingness to pay.

On the personal, household and community levels, an important barrier to vaccination is vaccine hesitancy (VH), a phenomenon that remains in the top ten list of the global health threats in 2019 [11]. The SAGE Working Group on Vaccine Hesitancy had earlier stated that ‘Confidence’—trust in the safety and effectiveness of the vaccine, in the delivering health system, and in the motivations of the recommending policymakers; ‘Complacency’—individual risk perception and consequent perceived necessity of vaccination; and ‘Convenience’—issues regarding availability, affordability, and accessibility, are important factors driving vaccine hesitancy [12].

Previous cross-national perception studies from Africa on COVID-19 pandemic have revealed myths, misconceptions, mistrust, beliefs and misinformation about the disease including: the origin and cure (punishment from God for perceived sin; linked to 5G technology; form of biological warfare against Africans; for economic benefits of selected people; Africans are protected naturally; COVID-19 virus does not exist; and can be cured by local herbs [1318]. These sources of misinformation have enormous potential to influence peoples’ perception of risk, with consequential acceptance or refusal of preventative and control measures. Understandably, the novel nature of COVID-19 allows room for speculation and spurious treatments have been promoted by prominent public figures [19]. Currently, variants of potentially more contagious SARS-COV-2 continue to circulate across Africa, and the COVID-19 vaccines are arriving in African countries [20]. Vaccines are now available in approximately half of Africa’s 54 countries, with more than 14 million doses already delivered.

To assess potential coronavirus vaccine hesitancy among Africans and underlying reasons fueling suspicions in African countries, this multinational study was undertaken. The outcome should provide evidence-based insight for public health institutions and authorities involved in management and response to COVID-19 pandemic.

Materials and methods

Study and questionnaire design

An online cross-sectional continent-wide (Africa) survey was designed in English, translated to Arabic and French by native language experts, and distributed using Google Forms (https://forms.gle/b7Q2wXnm7wm54aXk8, Alphabet Inc., California, USA), after pretesting among 30 respondents (Cronbach’s alpha = 0.87). Inclusion criteria was primarily being an African and ≥18 years of age. Demographic variables, socio-economic details, selected epidemiological parameters, knowledge and perceptions related to COVID-19 and associated vaccines were collected between February and March 2021 (S1 Supplement in S1 File). KAP questions had responses on the Likert scale (strongly disagree, disagree, neutral, agree, or strongly agree) and Yes/No scale, as appropriate.

Study participants

Using different social media platforms (Email, Facebook, WhatsApp, LinkedIn, Instagram, Twitter, Telegram, Signal, text messages and voice calls), participants aged 18 years and above were recruited using convenience sampling. Only respondents with internet access were eligible for the study. To improve the response rate, paid adverts were placed on different platforms and individuals who encountered the advertised posts were encouraged to fill the study questionnaire.

A minimum of 386 respondents per country were planned to be recruited. The OpenEpi software was used to determine the number of respondents to be recruited into the study from each country using the sample size formula for cross-sectional (random samples) studies. Assumptions used include 50% of the respondents will accept the COVID-19 vaccine at a precision of 0.05 and 5% level of error at 95% level of confidence. This translated into a computed sample size of 385 per country.

Ethical consideration

Institutional review boards from Nigeria (University of Ilorin) and Egypt (Ahram Canadian University, Faculty of Oral and Dental Medicine) approved the study. All guidelines and ethical codes for human and animal experimentation in research were considered in line with the World Medical Association Declaration of Helsinki (Ethical principles for Medical Research Involving Human Subjects) [21]. The opening question is a participant’s informed consent (acceptance or decline to participate option button), prior to the main survey questions. A click on the decline button automatically ends the session. Study participation was voluntary, allowing participants to withdraw at any time. Confidentiality of all respondents’ data was strictly adhered to by anonymous data collection.

Data analysis

Using descriptive statistics, categorical variables were presented as frequencies and proportions, while continuous variables were presented as means with standard deviations. To assess respondents’ knowledge and perception of vaccines and risk of SARS-COV-2, past experiences/behavior concerning vaccination, the vaccination acceptance, voluntariness, and affordability of the COVID-19 vaccine, a numeric scoring pattern was used to generate specific outcome variables for the sub-scales [18, 22]. These outcome variables were then dichotomized (Satisfactory/Pleasant/Good or Unsatisfactory/Unpleasant/Poor) based on the mean scores/marks obtained by respondents. Single items with Likert scale responses were dichotomized (strongly agree and agree vs don’t know, disagree and strongly disagree).

The chi-square test (and fisher’s exact test for 2×2 tables) was used to test for significance between the outcome variables and the demographic (independent) variables. Bivariate logistic regression models examined potential predictors of vaccine acceptance. Variables considered included demographic characteristics such as age (categories), gender, educational attainment, region, community type (rural, urban, semi-urban), income (categories) and marital status, and questionnaire items concerning risk perception and previous practices.

No adjustments were made for missing data, and all analysis used complete case analysis. P-values were two-sided, and all analyses were carried out at the 95% confidence interval. Analyses were performed using the Statistical Package for the Social Sciences (SPSS) software, v.22, and the Open-Source Epidemiologic Statistics for Public Health (OpenEpi), v.3.03a.

Results

Demographic information of respondents

A total of 5,416 individuals completed the survey but only 5,212 (96%) agreed that their data can be used for analysis. Approximately 94% were residents of 34 African countries while the others were African resident in other countries outside Africa and were considered as Diaspora (Fig 1).

Fig 1. Percentage distribution of COVID-19 vaccine acceptability and hesitancy in Africa.

Fig 1

A total of 5211 count data was used for this analysis. Specific number of data count per country are available in the S1 Table.

Seven countries met the recruitment criteria of 386 respondents (Cameroon, Ghana, Nigeria, Egypt, South Africa, Democratic Republic of Con/go and Sudan). Participants were predominantly urban dwellers (67%), with educational attainment above secondary school (85%) and aged 18–44 years (83%). Males were 54% of the population while females were 46%. Monthly income was <$500 for 63% of the surveyed population. About 60% of the participants were employed, 38% were unemployed and approximately 50.6% were trained in health-related fields.

Past experiences/behavior

About 25% of participants (n = 1,355) identified reasons they had missed on vaccinations in the past (Table 1). The reasons proffered included the unavailability of vaccines (35.1%), inability to afford the cost associated with a vaccine (22.7%), not having the required time to obtain vaccines (19.8%) and distance to the health centres (14.2%). About 23% said they knew someone who had a “serious side effect” from a vaccination in the past.

Table 1. Respondent’s attitudes and past experiences related to COVID-19 vaccination.

Attitude Percent
Vaccine acceptability (n = 5,212)
 If there was a vaccine available to prevent corona virus (SARS CoV 2), I would prefer to get it as soon as possible. 63%
 If there was a vaccine available to prevent corona virus (SARS CoV 2), I would wait and see how other people react to it before I get it. 5%*
 I will ONLY get the corona virus (SARS CoV 2) vaccine if it is mandatory 33%
 I will get the corona virus (SARS CoV 2) vaccine even if it is NOT mandatory 58%#
 I would be willing to participate in a clinical trial for a corona virus (SARS CoV 2) vaccine. 28%
 I do not think a corona virus (SARS CoV 2) vaccine is necessary. 26%
 I believe that there are other (better) ways to protect against corona virus (SARS CoV 2) than the usage of a vaccine. 43%
 I am worried that people are using the corona virus (SARS CoV 2) vaccine as an excuse to ‘experiment’ on Africans. 30%
 I am worried that the corona virus (SARS CoV 2) vaccine will not actually work to prevent COVID-19. 31%
Safety (n = 5,212)
 I am worried about the possible side effects of the corona virus (SARS CoV 2) vaccine. 79%
 I am worried that I can get infected with corona virus (SARS CoV 2) by getting the vaccine 39%
Risk perception (n = 5,212)
 I know a family member or friend who has been sick with corona virus (SARS CoV 2) 65%
 I believe my risk of becoming infected with corona virus (SARS CoV 2) is medium, high or very high 65%
 I believe my risk of falling sick if I get infected with corona virus (SARS CoV 2) is medium, high or very high 60%
Past experiences (n = 5,212)
 I know someone who has gotten a vaccine-preventable disease because they did not get the vaccine 36%
 I know someone who has had a serious side effect from a vaccination 23%
 In the past I have been advised not to give my child a recommended vaccine 12%
 In the past, I have refused a vaccine that was recommended for me or my child 9%
 In the past, I have done my best to get all the recommended vaccines for me or my child 59%
 In the past, I have not been able to get a vaccine that I planned to get 21%

*These additional 5% who indicated some hesitation will be added to 63% who wanted to be vaccinated as soon as possible to make 68% of total who wanted to be vaccinated.

#Only 58% of the 63% who wanted to be vaccinated as soon as possible will only do so if it is not mandatory.

Perceived SARS-CoV-2 risk and acceptance of COVID-19 vaccine

Most survey participants (65%) believed that their risk of getting infected with the SARS-CoV-2 was medium to high (Table 1). Slightly fewer (60%) thought that their risk of falling sick was medium to high if they became infected. About 65% of participants knew a family member or friend who had been sick with the infection.

Only 63% of participants surveyed were willing to receive the COVID-19 vaccination as soon as possible (Fig 1). A total of 79% were worried about the side effects of the vaccine, and 39% actually expressed concerns that they might get infected by receiving the vaccine (Table 1). In all, 68% of the total populations were willing to receive the vaccine (63% without hesitation and 5% with some hesitation after observing potential reactions in earlier vaccinated subjects) (Table 1). While 49% did not have a preference for the route of administration, others were more likely to take the vaccine if it was in the form of injections (29%), oral (19%) or nasal spray (3%).

In the univariable logistic regression models, age, gender, employment status, income level, region of residence, and, rural versus urban settlement were significantly related to vaccine hesitancy (Table 2). The odds ratio (OR) of vaccine hesitancy was lower with advancing age– 0.69 (95% CI: 0.59–0.79) in 25–34-year-old respondents, 0.76 (95% CI: 0.64–0.89) in 35–44-year-old respondents, 0.59 (95% CI: 0.48–0.73) in 45–54-year-old respondents, 0.55 (95% CI: 0.42–0.71) in 55–64-year-old respondents, and 0.42 (95% CI: 0.26–0.69) in >65-year-old respondents, compared to 18–24-year-old respondents. The OR of vaccine hesitancy was 0.87 (95% CI: 0.78–0.97) in females compared to males, and it was 0.61 (95% CI: 0.57–0.71) in employed individuals compared to unemployed counterparts. In addition, the odds of vaccine hesitancy was 0.61 (95% CI: 0.49–0.74) among residents of urban settings compared to rural counterparts, and it was 2.85 (95% CI: 2.35–3.47) in Central Africa and 0.54 (95% CI: 0.43–0.68) in Southern Africa compared to North Africa. Details of other variables evaluated are available in Table 2.

Table 2. Sociodemographic predictors of COVID-19 vaccine hesitancy.

Variables Categories Frequency (%) Vaccine accepting (n) Vaccine hesitant (n) Vaccine hesitancy
OR 95% CI P–value
Age 18–24 1185 (22.8) 588 597 1 - <0.001
25–34 1978 (38.0) 1162 816 0.69 0.59, 0.79
35–44 1166 (22.4) 660 506 0.76 0.64, 0.89
45–54 497 (9.6) 311 186 0.59 0.48, 0.73
55–64 291 (5.9) 187 104 0.55 0.42, 0.71
>65 83 (1.6) 58 25 0.42 0.26, 0.69
Gender Male 2790 (53.7) 1548 1242 1 - 0.008
Female 2410 (46.3) 1418 992 0.87 0.78, 0.97
Education None 24 (0.5) 12 12 1 - <0.001
Primary School 40 (0.8) 11 29 2.64 0.91, 7.60
Secondary School 731 (14.1) 344 387 1.13 0.49, 2.54
OND/Technical degree 361 (6.9) 147 214 1.56 0.64, 3.33
University Degree (Undergraduate) 1827 (35.1) 1078 749 0.69 0.31, 1.56
Graduate Degree 2217 (42.6) 1374 843 0.61 0.27, 1.37
Region Northern Africa 944 (18.2) 555 389 1 - <0.001
Eastern Africa 999 (19.2) 664 335 0.72 0.59, 0.87
Central Africa 810 (15.6) 270 540 2.85 2.35, 3.47
Southern Africa 573 (11.0) 415 158 0.54 0.43, 0.68
Western Africa 1555 (29.8) 859 693 1.15 0.98, 1.36
Africans living in the Diaspora 322 (6.2) 203 119 0.84 0.64, 1.09
Community Rural 441 (8.5) 209 232 1 - <0.001
Semi-Urban 1258 (24.2) 669 589 0.79 0.64, 0.99
Urban 3501 (67.3) 2088 1413 0.61 0.49, 0.74
Employed No 1953 (37.6) 978 975 1 - <0.001
Yes 3247 (62.4) 1988 1259 0.61 0.57, 0.71
Monthly income up to $99 1572 (30.2) 783 789 1 - <0.001
$100-$499 1684 (32.4) 941 743 0.78 0.68, 0.89
$500-$999 847 (16.3) 479 368 0.76 0.64, 0.90
$1000-$4999 743 (14.3) 513 230 0.44 0.37, 0.54
$5000-$9999 196 (3.8) 144 52 0.36 0.26, 0.49
$10000-$14,999 63 (1.2) 43 20 0.46 0.27, 0.79
$15,000 and above 95 (1.8) 63 32 0.40 0.33, 0.78
Religion None 117 (2.3) 55 62 1 - <0.001
Christianity 2523 (48.5) 1346 1177 0.78 0.54, 1.13
Islam 2433 (46.8) 1506 927 0.55 0.38, 0.79
Traditional 49 (0.9) 20 29 1.29 0.65, 2.53
Others 78 (1.5) 39 39 0.89 0.50, 1.57
Marital status Single 2661 (51.2) 1445 1216 1 - <0.001
Married 2332 (44.8) 1425 907 0.76 0.68, 0.85
Widow(er) 77 (1.5) 48 29 0.72 0.45, 1.15
Cohabiting 130 (2.5) 48 82 2.03 1.41, 2.92

A total of 5,200 responses were available for the assessment in Table 2.

Participants’ risk perceptions were also significantly related to vaccine hesitancy (Table 3). Those who know someone sick with COVID-19 are twice as likely to take vaccine acceptance more seriously (p < 0.0001). Compared to those with very high perceived infection risk, the ORs of vaccine acceptance among others with very low to high risks of infection range between 0.26–0.70 (p < 0.0001) (Table 3), an indication that those with very low risk perception of infection are the highest vaccine hesitant group. Similar vaccine hesitancy were 5-folds for those who believe that their risk of getting severely sick if infected is very low (OR = 0.20, 95% CI = 0.15, 0.26, p < 0.0001) (Table 3).

Table 3. Risk perception, past experiences and COVID-19 vaccine hesitancy.

Variable Classification Vaccine acceptance (%) Vaccine hesitancy (%) OR CI95% P-value
Risk perception
I know a family member or friend who has been sick with coronavirus Yes 2300 (44.1) 1089 (20.9) 1 - NA
No 977 (18.7) 845 (16.2) 0.55 0.49; 0.62 <0.0001
I believe my risk of becoming infected with coronavirus is: Very low 423 (8.1) 483 (9.3) 0.26 0.20; 0.32 <0.0001
Low 524 (10.1) 405 (7.8) 0.38 0.30; 0.48 <0.0001
Medium 1151 (22.1) 608 (11.7) 0.55 0.44; 0.69 <0.0001
High 735 (14.1) 308 (5.9) 0.7 0.55; 0.88 0.003
Very high 444 (8.5) 130 (2.5) 1 - NA
I believe my risk of falling very sick IF I get infected with coronavirus is: Very low 368 (7.1) 464 (8.9) 0.2 0.15; 0.26 <0.0001
Low 726 (13.9) 531 (10.2) 0.34 0.26; 0.45 <0.0001
Medium 1210 (23.2) 648 (12.4) 0.46 0.35; 0.61 <0.0001
High 671 (12.9) 216 (4.1) 0.77 0.57; 1.04 0.08
Very high 302 (5.8) 75 (1.4) 1 - NA
Past Experiences
I know someone who has gotten a vaccine-preventable disease because they did not get the vaccine. Yes 1339 (25.7) 537 (10.3) 1 - NA
No 1938 (37.2) 1397 (26.8) 0.56 0.49; 0.63 <0.0001
I know someone who has had a serious side effect from a vaccination. Yes 596 (11.4) 599 (11.5) 1 - NA
No 2681 (51.4) 1335 (25.6) 2.02 1.77; 2.30 <0.0001
In the past, I was advised not to give my child a recommended vaccine. Yes 347 (6.7) 279 (5.4) 1 - NA
No 2930 (56.2) 1655 (31.8) 1.42 1.20; 1.69 <0.0001
In the past, I have refused a vaccine that was recommended for my child or me. Yes 213 (4.1) 266 (5.1) 1 - NA
No 3064 (58.8) 1668 (32.0) 2.29 1.88; 2.78 <0.0001
In the past, I have done my best to get all the recommended vaccines for me or my child. Yes 2089 (40.1) 959 (18.4) 1 - NA
No 1188 (22.8) 975 (18.7) 0.56 0.50; 0.63 <0.0001
In the past, I have not been able to get a vaccine that I planned to get. Yes 708 (13.6) 363 (7.0) 1 - NA
No 2569 (49.3) 959 (18.4) 1.37 1.19; 1.59 <0.0001

A total of 5,211 data was used for this analysis. OR = Odds ratio; CI95% = 95% Confidence interval.

Participants’ previous vaccine-related behavior and experiences were also related to vaccine hesitancy. Participants who had refused a vaccine for themselves or their child in the past had a 2.29-folds greater odds of vaccine hesitancy compared to counterparts with no previous history of vaccine hesitancy (Table 3, S1 Table in S1 File). Participants were more likely to be vaccine-hesitant if they believed they knew someone who had a serious side effect from other vaccinations (OR = 2.02; 95% CI: 1.77, 2.30), who has been advised in time past not to take vaccines (OR = 1.42; 95% CI: 1.20, 1.69), or those who have not been able to get the necessary vaccines (OR = 1.37; 95% CI: 1.19, 1.59). Contrastingly, those who know persons who became ill because of avoidance of vaccine (OR = 0.56; 95% CI: 0.49, 0.63), and those who have did their best to get all the necessary vaccines (OR = 0.56; 95% CI: 0.50, 0.63) are less likely to be vaccine-hesitant.

Only 28% were willing to participate in a vaccine trial. A similar proportion (26%) did not think that vaccination was necessary and 43% believed that there are suitable alternatives to COVID-19 vaccination.

Self-reported health status and health literacy

Approximately 10% of all respondents believed that they had health conditions that should prevent them from being vaccinated, and 92% report being comfortable making decisions about their health based on the sources of information available to them.

Most participants said they get their health information from healthcare workers (51%), scientists (44%), news media (43%) and schools (41%). Only 29% said they got health information from the government. Notably, some participants also got their health information from celebrities (12%) and religious leaders (5%) S2 & S3 Tables in S1 File.

The overall self-rated knowledge, perception and awareness of vaccines were high with 78% claiming to understand how vaccines work, 90% were aware of routine childhood vaccination and 89% knew that some vaccines are recommended for adults. Awareness that there are vaccines recommended for children (90%) and adults (88%) was very high. In addition, 78% of participants said they understood how vaccines work. Eighty-two percent (82%) of participants believed that vaccines can prevent serious infectious diseases, and 76% think it is important for everyone to get recommended vaccinations S4 Table in S1 File. Approximately 86% of all respondents with children were able to take decisions on whether their children receive vaccination.

Preferences for COVID-19 vaccination program

About 40% agreed or strongly agreed that COVID-19 vaccines should be made mandatory when available and 78% suggested that it should be provided free of charge. If they had to pay for the vaccine, 67% thought that one to three US dollars was a reasonable price range. 49% of all respondents advocated for more knowledge about the risks and benefits of any COVID-19 vaccine and 44% will want the healthcare workers to conduct home or office-based vaccinations S4 Table in S1 File. A total of 92% of respondents have health centres or hospitals within 15–60 minutes of their homes, and 79% will be willing to travel up to an hour to obtain COVID-19 Vaccine S5 Table in S1 File.

Discussion

We conducted a cross-sectional online survey among African residents in 29 African countries and Africans in the diaspora. It should be clear that this study has a degree of bias to urban populace, comparatively more educated, and with internet access. In addition, a significant percentage of respondents (50.6%) have some forms of healthcare training, which may skew perception. These results should therefore be taken with caution as it may not represent the whole of African population. We evaluated perceived SARS-CoV-2 risk and vaccine hesitancy among respondents and identified sociodemographic factors related to vaccine hesitancy. We also examined previous practices regarding vaccination as a significant predictor of future practices.

Our study occurred in the context of COVID-19 vaccine rollouts across the continent [23], and was necessitated by the intense debates on the pandemic and the place of vaccination in the continent [2426]. By 8th March 2021, globally, more than 312 million COVID-19 vaccine doses had been administered, out of which 5 million doses of the vaccine (1.65% of global total) were administered in Africa. Morocco alone accounts for 90% of all the doses used in Africa [27].

We found substantial vaccine hesitancy among Africans living in Africa as well as in the diaspora. Only 63% of participants would receive COVID-19 vaccination as soon as possible, and an additional 5% would receive vaccines after considering their safety among earlier vaccinated individuals. Previous surveys worldwide have reported diverse estimates, ranging from 23–97% [28, 29]. Previous surveys have reported COVID-19 vaccine acceptance rates of 15% in Cameroun [30], 28% for the Democratic Republic of the Congo [31], 54% for Egypt [32], 65% for Nigeria [28] and 82% for South Africa [28]. All the surveys in African settings, including ours, were conducted by convenience sampling, had relatively small sample sizes per country, and potentially not genuinely representative of the respective countries. Nonetheless, our estimates are comparable to the other online-only surveys [28], that found higher vaccine acceptance rates (61–82%), while surveys with some in-person data collection [30, 31], reported lower acceptance rates (15–28%). Vaccine hesitancy could severely limit the opportunity to attain herd immunity against the SARS-CoV-2 and prevent hospitalization, catastrophic health expenditures and deaths [12]. Our study may, however, be highly valuable in predicting individuals and groups likely to be vaccine-hesitant, and thereby guide comprehensive vaccination programs across the continent. Noteworthy is the high percentage (10%) of respondents who believed that they have other health conditions, which should prevent them from being vaccinated. While we did not probe into these ‘other health conditions’ to avoid straying outside the context of this study, this information should prompt the health authorities in Africa to consider further study to know such specifics and assess whether hospital records of debilitating and chronic conditions tally with these assertions.

We found that respondents’ risk perception was related to their attitude to COVID-19 vaccines. The odds of vaccine hesitancy was substantially low if participant’s perceived risk of infection or sickness was very high. Most respondents in our study (≥60%) knew at least one person infected with the coronavirus, and believed that they had a medium to very high risk of being infected and developing severe illness. Nonetheless, vaccine hesitancy was high in our population– 26% believed the vaccines were unnecessary, and 43% believed alternatives to COVID-19 vaccination exist. Vaccine hesitancy was more common among young people than older adults and in rural areas compared to urban ones. The burden of COVID-19 was considerably less among young people, partly due to their lower risk of comorbidities [1, 33, 34]. Urban residents experienced a more significant disease burden and suffered a greater economic impact as a result of the pandemic [34, 35]. The overall self-rated knowledge, perception, and awareness of vaccines were high in our study. Most respondents claimed to understand how vaccines work, the routes of vaccination, and which vaccines are recommended for adults. Our findings that perceived risk is a crucial driver of hesitancy is consistent with the SAGE Working Group’s Confidence, Complacency and Convenience Model of Vaccine Hesitancy [12], and suggests that individuals with the low perceived risk of COVID-19 were complacent to vaccination. Strategies that clarify the balance of relevant risks and benefits may improve vaccine uptake.

Concerns about vaccine safety were common in our study. The majority of respondents were worried about the vaccines’ side effects, and many were even concerned that they might get infected with the coronavirus by obtaining the vaccine. Concerns about vaccine safety could strongly worsen any vaccines’ hesitancy, and planning for COVID-19 vaccination programs should proactively anticipate this challenge [36]. Prior studies have shown that perception of COVID-19 vaccine safety is related to the willingness to receive vaccines [37]. The COVID-19 pandemic, however, poses unique vaccination challenges. First, some of the vaccines are based on novel mRNA technology that most people were unfamiliar with. Second, misinformation campaigns, often led by populist leaders, have been frequent during the pandemic, creating division and undermining trust in public institutions and scientists [38, 39]. Third, nine European countries temporarily suspended the administration of the Oxford-AstraZeneca COVID-19 vaccines following reports of thromboembolism and death [40]. Though analysis of safety data from >10 million vaccination records found no increased risk of the events, the global media coverage was extensive, and its impact on perceived vaccine safety and hesitancy is unclear.

We investigated whether and how past experience regarding vaccines may be related to vaccine hesitancy in the present study. A fair proportion of the population (23%) said they know someone who had experienced side-effects of vaccination in the past, though we did not ask which. About 9% of participants had even refused vaccinations to their children. An analysis of 250,000 medical records among Israel residents found that whether and when an individual received seasonal influenza vaccines in previous seasons represents a default that strongly predicts whether and when they would receive the same vaccines in the subsequent year [41]. Individuals with previous vaccine hesitancy have almost 3-fold increased odds of COVID-19 vaccine hesitancy unavailability of vaccines (35%), inability to afford the cost associated with a vaccine (22%), not having the required time to obtain vaccines (20%) and distance to the health centres (14%) were some reasons why respondents did not get vaccines in times past. Understanding these “defaults” could guide the design of future vaccination programs.

Considerable variability in COVID-19 vaccine acceptance rates has been reported in different countries and regions of the world [29]. We observed that Central Africa has a significantly low vaccine acceptance rate (< 35%) compared to Southern Africa (≈ 75%) (Table 2), and this has implications for continental control of the current COVID-19 pandemic. Nonetheless, the factors driving vaccine hesitancy in each African country are likely to differ to some extent. For instance, Central Africa countries may serve as passageways to connect Africa, have health infrastructural deficit, and have experienced repeated conflicts. Geographical variation highlights the critical social aspects of vaccine hesitancy, and solutions focused on the individual alone may not suffice [42]. Strategies that consider these unique characteristics in each country within the context of the regional plan to reduce vaccine hesitancy and improve health promotion may be warranted.

We asked respondents about their desired features for a COVID-19 vaccination program. Only 40% wanted mandatory vaccination. Mandatory vaccination could potentially accelerate vaccine uptake and the attainment of herd immunity. It could, however, undermine patients’ trust in healthcare workers, threaten individual agency, and pose ethical risks if it burdens the most vulnerable in the population unduly [43]. Many respondents advocated for information campaigns as part of vaccination programs. Respondents receive COVID-19 information from healthcare workers (51%), scientists (44%), news media (43%), and schools (41%); multi-channel information campaigns may therefore be beneficial for optimal coverage. Behavioral insights relating to social norms could guide these campaigns’ design [44]. Finally, respondents identified the value of convenience to improve the accessibility of vaccinations. Although many of them were willing to travel up to an hour to receive vaccines, they recommended vaccination at beneficiaries’ homes or offices. Addressing these “last-mile issues” could drastically reduce vaccine hesitancy [44].

Our study has some limitations. By recruiting participants and collecting data online, we inadvertently selected a more urban, young-to-middle age, and highly educated population. Standardization to obtain acceptance rates that are more reflective of national population estimates was not done due to each country’s complex demographic structures. However, leveraging the internet for the survey minimized contact and associated COVID-19 infection risk while generating valuable insights from the survey. The sample size for each country was small, limiting our ability to obtain reasonable country-level inferences to guide policy. Its dependence on self-report also limited our study. For instance, the stated desire to receive the vaccine may not translate to actual practice, though our use of online data collection limits the possibility of social desirability bias.

Supporting information

S1 File

(DOCX)

Data Availability

The basic minimum data required to replicate all study findings reported in the article, as well as related metadata and methods are included in the supplementary materials (Supplement 1, S1-4 Table and Supplementary Figure S1) including the 1) Questionnaire, 2) Location surveyed, 3) Biodata of surveyed participants, and 4) methods and data analysis sections of the study.

Funding Statement

The authors received no specific funding for this work.

References

  • 1.Anjorin A, Abioye A, Asowata O, Soipe A, Kazeem M, Adesanya I, et al. Comorbidities and the COVID-19 pandemic dynamics in Africa. Tropical Medicine & International Health. 2021;26(1):2–13. doi: 10.1111/tmi.13504 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.World Health Organization—Africa Region (WHO-AFRO). Coronavirus Dashboard 2021 [24th June 2021]. https://www.afro.who.int/health-topics/coronavirus-covid-19.
  • 3.Anjorin AA. The coronavirus disease 2019 (COVID-19) pandemic: A review and an update on cases in Africa. Asian Pacific Journal of Tropical Medicine. 2020;13(5):199. [Google Scholar]
  • 4.Africa-CDC. Outbreak Brief 15: COVID-19 Pandemic-28 April 2020: Africa CDC; 2020 [29th April, 2020]. https://africacdc.org/download/outbreak-brief-15-covid-19-pandemic-28-april-2020/
  • 5.World Health Organization (WHO). COVID-19 vaccines 2021 [16th March 2021]. https://www.who.int/emergencies/diseases/novel-coronavirus-2019/covid-19-vaccines.
  • 6.Iwasaki A, Omer SB. Why and how vaccines work. Cell. 2020;183(2):290–5. doi: 10.1016/j.cell.2020.09.040 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Chung JY, Thone MN, Kwon YJ. COVID-19 vaccines: The status and perspectives in delivery points of view. Advanced drug delivery reviews. 2020. doi: 10.1016/j.addr.2020.12.011 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Tregoning JS, Brown ES, Cheeseman HM, Flight KE, Higham SL, Lemm NM, et al. Vaccines for COVID-19. Clinical & Experimental Immunology. 2020;202(2):162–92. doi: 10.1111/cei.13517 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.World Health Organization (WHO). COVAX: WOrking for global equitable access to COVID-19 vaccines Geneva, Switzerland2020 [21 March, 2021]. https://www.who.int/initiatives/act-accelerator/covax.
  • 10.AMSP opens COVID-19 vaccines pre-orders for 55 African Union Member States [Internet]. Addis Ababa, Ethiopia; 2021; 19 January, 2021. https://africacdc.org/news-item/amsp-opens-covid-19-vaccines-pre-orders-for-55-african-union-member-states/#:~:text=African%20Vaccine%20Acquisition%20Task%20Team%20(AVATT)%20established%20by%20the%20African,on%2020th%20of%20August%2C%202020.
  • 11.World Health Organization (WHO). Ten threats to global health in 2019 2019 [21 March, 2021]. https://www.who.int/news-room/spotlight/ten-threats-to-global-health-in-2019.
  • 12.World Health Organization (WHO). REPORT OF THE SAGE WORKING GROUP ON VACCINE HESITANCY. 2014.
  • 13.International Federation of Red Cross and Red Crescent (IFRC). COVID-19: Rapport sur les retours d’information de la communauté. #7. Dakar: 2020 13 May, 2020. Report No.: Contract No.: 7.
  • 14.Ovenseri-Ogbomo G, Ishaya T, Osuagwu UL, Abu EK, Nwaeze O, Oloruntoba R, et al. Factors associated with the myth about 5G network during COVID-19 pandemic in sub-Saharan Africa. Journal of Global Health Reports. 2020. [Google Scholar]
  • 15.Singh JA. The case for why africa should host COVID-19 candidate vaccine trials. The Journal of infectious diseases. 2020;222(3):351–5. doi: 10.1093/infdis/jiaa303 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Thomas E, Zhang A. ID2020, Bill Gates and the Mark of the Beast: How Covid-19 catalyses existing online conspiracy movements. Australian Strategic Policy Institute, 2020. [Google Scholar]
  • 17.Aiyewumi O, Okeke MI. The myth that Nigerians are immune to SARS-CoV-2 and that COVID-19 is a hoax are putting lives at risk. Journal of global health. 2020;10(2). doi: 10.7189/jogh.10.020375 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Elnadi H, Odetokun IA, Bolarinwa O, Ahmed Z, Okechukwu O, Al-Mustapha AI. Correction: Knowledge, attitude, and perceptions towards the 2019 Coronavirus Pandemic: A bi-national survey in Africa. Plos one. 2021;16(2):e0247351. doi: 10.1371/journal.pone.0247351 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.British Broadcasting Corporation (BBC). Coronavirus: What misinformation has spread in Africa? 2020 [updated 2020 April 24February 17, 2021]. https://www.bbc.com/news/world-africa-51710617.
  • 20.COVID-19 cases in Africa to top 4 million, vaccine rollout underway [Internet]. Brazzaville, Congo; 2021; 11 March 2021. https://www.afro.who.int/news/covid-19-cases-africa-top-4-million-vaccine-rollout-underway
  • 21.World Medical Association (WMA). World Medical Association Declaration of Helsinki: ethical principles for medical research involving human subjects. Jama. 2013;310(20):2191–4. doi: 10.1001/jama.2013.281053 [DOI] [PubMed] [Google Scholar]
  • 22.Odetokun IA, Akpabio U, Alhaji NB, Biobaku KT, Oloso NO, Ghali-Mohammed I, et al. knowledge of antimicrobial resistance among veterinary students and their personal antibiotic use practices: A National cross-sectional survey. Antibiotics. 2019;8(4):243. doi: 10.3390/antibiotics8040243 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.World Health Organization—Africa Region (WHO-AFRO). COVID-19 cases in Africa to top 4 million, vaccine rollout underway 2021 [updated 11 March, 202119 March, 2021]. https://www.afro.who.int/news/covid-19-cases-africa-top-4-million-vaccine-rollout-underway.
  • 24.Islam MS, Sarkar T, Khan SH, Kamal A-HM, Hasan SM, Kabir A, et al. COVID-19–related infodemic and its impact on public health: A global social media analysis. The American Journal of Tropical Medicine and Hygiene. 2020;103(4):1621. doi: 10.4269/ajtmh.20-0812 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Schmidt T, Cloete A, Davids A, Makola L, Zondi N, Jantjies M. Myths, misconceptions, othering and stigmatizing responses to Covid-19 in South Africa: A rapid qualitative assessment. PloS one. 2020;15(12):e0244420. doi: 10.1371/journal.pone.0244420 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Makoni M. Tanzania refuses COVID-19 vaccines. The Lancet. 2021;397(10274):566. doi: 10.1016/S0140-6736(21)00362-7 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.University of Oxford. Our World in Data 2021 [18 March, 2021]. https://ourworldindata.org/covid-vaccinations.
  • 28.Lazarus JV, Ratzan SC, Palayew A, Gostin LO, Larson HJ, Rabin K, et al. A global survey of potential acceptance of a COVID-19 vaccine. Nature medicine. 2021;27(2):225–8. doi: 10.1038/s41591-020-1124-9 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Sallam M. COVID-19 vaccine hesitancy worldwide: A concise systematic review of vaccine acceptance rates. Vaccines. 2021;9(2):160. doi: 10.3390/vaccines9020160 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Dinga JN, Sinda LK, Titanji VP. Assessment of vaccine hesitancy to a COVID-19 vaccine in Cameroonian adults and its global implication. Vaccines. 2021;9(2):175. doi: 10.3390/vaccines9020175 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Nzaji MK, Ngombe LK, Mwamba GN, Ndala DBB, Miema JM, Lungoyo CL, et al. Acceptability of Vaccination Against COVID-19 Among Healthcare Workers in the Democratic Republic of the Congo. Pragmatic and observational research. 2020;11:103. doi: 10.2147/POR.S271096 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Saied SM, Saied EM, Kabbash IA, Abdo SAEF. Vaccine Hesitancy: Beliefs and Barriers Associated with COVID-19 Vaccination among Egyptian Medical Students. Journal of medical virology. 2021. doi: 10.1002/jmv.26910 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Osibogun A, Abayomi A, Kanma-Okafor O, Idris J, Bowale A, Wright O, et al. Morbidity and mortality outcomes of COVID-19 patients with and without hypertension in Lagos, Nigeria: A retrospective cohort study. 2020. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Diop BZ, Ngom M, Biyong CP, Biyong JNP. The relatively young and rural population may limit the spread and severity of COVID-19 in Africa: a modelling study. BMJ global health. 2020;5(5):e002699. doi: 10.1136/bmjgh-2020-002699 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Chirisa I, Mutambisi T, Chivenge M, Mabaso E, Matamanda AR, Ncube R. The urban penalty of COVID-19 lockdowns across the globe: manifestations and lessons for Anglophone sub-Saharan Africa. GeoJournal. 2020:1–14. doi: 10.1007/s10708-020-10281-6 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.DeRoo SS, Pudalov NJ, Fu LY. Planning for a COVID-19 vaccination program. Jama. 2020;323(24):2458–9. doi: 10.1001/jama.2020.8711 [DOI] [PubMed] [Google Scholar]
  • 37.Karlsson LC, Soveri A, Lewandowsky S, Karlsson L, Karlsson H, Nolvi S, et al. Fearing the disease or the vaccine: The case of COVID-19. Personality and Individual Differences. 2021;172:110590. doi: 10.1016/j.paid.2020.110590 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Lasco G. Medical populism and the COVID-19 pandemic. Global Public Health. 2020;15(10):1417–29. doi: 10.1080/17441692.2020.1807581 [DOI] [PubMed] [Google Scholar]
  • 39.Woods ET, Schertzer R, Greenfeld L, Hughes C, Miller-Idriss C. COVID-19, nationalism, and the politics of crisis: A scholarly exchange. Nations and Nationalism. 2020. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Wise J. Covid-19: European countries suspend use of Oxford-AstraZeneca vaccine after reports of blood clots. British Medical Journal Publishing Group; 2021. doi: 10.1136/bmj.n699 [DOI] [PubMed] [Google Scholar]
  • 41.Shaham A, Chodick G, Shalev V, Yamin D. Personal and social patterns predict influenza vaccination decision. BMC public health. 2020;20(1):222. doi: 10.1186/s12889-020-8327-3 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42.Wiysonge CS, Ndwandwe D, Ryan J, Jaca A, Batouré O, Anya B-PM, et al. Vaccine hesitancy in the era of COVID-19: could lessons from the past help in divining the future? Human vaccines & immunotherapeutics. 2021:1–3. doi: 10.1080/21645515.2021.1893062 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.Gur-Arie R, Jamrozik E, Kingori P. No Jab, No Job? Ethical Issues in Mandatory COVID-19 Vaccination of Healthcare Personnel. BMJ global health. 2021;6(2):e004877. doi: 10.1136/bmjgh-2020-004877 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Chevallier C, Hacquin A-S, Mercier H. COVID-19 vaccine hesitancy: Shortening the last mile. Trends in cognitive sciences. 2021. doi: 10.1016/j.tics.2021.02.002 [DOI] [PMC free article] [PubMed] [Google Scholar]

Decision Letter 0

Prasenjit Mitra

16 Jun 2021

PONE-D-21-13734

Will Africans take COVID-19 Vaccination?

PLOS ONE

Dear Dr. Fasina,

Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process.

==============================

ACADEMIC EDITOR: Please check the reviewers comments.

==============================

Please submit your revised manuscript by Jul 31 2021 11:59PM. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at plosone@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pone/ and select the 'Submissions Needing Revision' folder to locate your manuscript file.

Please include the following items when submitting your revised manuscript:

  • A rebuttal letter that responds to each point raised by the academic editor and reviewer(s). You should upload this letter as a separate file labeled 'Response to Reviewers'.

  • A marked-up copy of your manuscript that highlights changes made to the original version. You should upload this as a separate file labeled 'Revised Manuscript with Track Changes'.

  • An unmarked version of your revised paper without tracked changes. You should upload this as a separate file labeled 'Manuscript'.

If you would like to make changes to your financial disclosure, please include your updated statement in your cover letter. Guidelines for resubmitting your figure files are available below the reviewer comments at the end of this letter.

If applicable, we recommend that you deposit your laboratory protocols in protocols.io to enhance the reproducibility of your results. Protocols.io assigns your protocol its own identifier (DOI) so that it can be cited independently in the future. For instructions see: http://journals.plos.org/plosone/s/submission-guidelines#loc-laboratory-protocols. Additionally, PLOS ONE offers an option for publishing peer-reviewed Lab Protocol articles, which describe protocols hosted on protocols.io. Read more information on sharing protocols at https://plos.org/protocols?utm_medium=editorial-email&utm_source=authorletters&utm_campaign=protocols.

We look forward to receiving your revised manuscript.

Kind regards,

Prasenjit Mitra, MD, MRSB, MIScT, FLS, FACSc, FAACC

Academic Editor

PLOS ONE

Journal Requirements:

When submitting your revision, we need you to address these additional requirements.

1. Please ensure that your manuscript meets PLOS ONE's style requirements, including those for file naming. The PLOS ONE style templates can be found at

https://journals.plos.org/plosone/s/file?id=wjVg/PLOSOne_formatting_sample_main_body.pdf and

https://journals.plos.org/plosone/s/file?id=ba62/PLOSOne_formatting_sample_title_authors_affiliations.pdf

2.  Please include additional information regarding the survey or questionnaire used in the study and ensure that you have provided sufficient details that others could replicate the analyses. For instance, if you developed a questionnaire as part of this study and it is not under a copyright more restrictive than CC-BY, please include a copy, in both the original language and English, as Supporting Information. Moreover, please include more details on how the questionnaire was pre-tested, and whether it was validated. "

3. Please consider modifying your title to ensure that it is specific, descriptive, concise, and comprehensible to readers outside the field (for example by specifying the type of study and its location).

4. We note that you have indicated that data from this study are available upon request. PLOS only allows data to be available upon request if there are legal or ethical restrictions on sharing data publicly. For information on unacceptable data access restrictions, please see http://journals.plos.org/plosone/s/data-availability#loc-unacceptable-data-access-restrictions.

In your revised cover letter, please address the following prompts:

a) If there are ethical or legal restrictions on sharing a de-identified data set, please explain them in detail (e.g., data contain potentially identifying or sensitive patient information) and who has imposed them (e.g., an ethics committee). Please also provide contact information for a data access committee, ethics committee, or other institutional body to which data requests may be sent.

b) If there are no restrictions, please upload the minimal anonymized data set necessary to replicate your study findings as either Supporting Information files or to a stable, public repository and provide us with the relevant URLs, DOIs, or accession numbers. Please see http://www.bmj.com/content/340/bmj.c181.long for guidelines on how to de-identify and prepare clinical data for publication. For a list of acceptable repositories, please see http://journals.plos.org/plosone/s/data-availability#loc-recommended-repositories.

We will update your Data Availability statement on your behalf to reflect the information you provide.

5. Please include captions for your Supporting Information files at the end of your manuscript, and update any in-text citations to match accordingly. Please see our Supporting Information guidelines for more information: http://journals.plos.org/plosone/s/supporting-information.

[Note: HTML markup is below. Please do not edit.]

Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: Yes

**********

2. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: Yes

**********

3. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

**********

4. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: Yes

**********

5. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: MAJOR COMMENTS:

• Line 98 (abstract, and elsewhere): “Only 62% of all participants surveyed were willing to receive the COVID-19 vaccination.” This is not clear from the data presented in the results section. The results indicate that 62% would “prefer to get it as soon as possible” if it were available. This has a different meaning.

• Were all questions answered by all participants. If not, then raw numbers need to be shown in Table 1 for each question.

• Table 1 results (vaccine acceptability): was there Boolean logic in the questionnaire or were all questions asked of all participants? It doesn’t seem to make sense that 62% of participants indicated they would prefer to be vaccinated as soon as possible vs. 67% would prefer to wait and see how others react before getting it vs. only 58% would get the vaccine even if it was not mandatory to do so.

• All the logistic regression results described in lines 280-289 are different to the results shown in Table 2. The authors need to review their analyses to establish which results are the correct ones and present their findings consistently.

MINOR COMMENTS:

• What is the justification for including “Africans who live in the Diaspora” and how was this group defined? (e.g. born in Africa vs African ancestry; which parts of the world do they live in?)

• Line 141: total deaths reported appears too low, please check references. South Africa alone had >50 000 deaths by the end of March 2021.

• Line 166-168: this section of misconceptions should be rewritten more clearly; I suggest use of semicolons to separate the different misconceptions.

• Figure 1: consider changing this to a stacked bar chart, with countries arranged from low to high hesitancy.

• Table 2 and S1 Table show duplicated data.

• A result is missing in Table 1 (‘other(better) ways to protect’ – it is blank).

• The discussion section needs more emphasis on the fact that the participants are not representative of all Africans: this is a select group of Africans who are largely from urban areas, who have high levels of education and who have internet access. Furthermore, nearly half were “employed in the healthcare field” yet this was not highlighted in the discussion section, nor were stratified ORs shown for the group who were employed in healthcare fields vs employed in different settings.

• Line 267: 67% reported whereas 65% is reported in the Table. Which is correct?

• Line 271: “Only 62% of participants surveyed were willing to receive the COVID-19 vaccination” – again, this is not the same meaning as 62% would “prefer to get it as soon as possible” if it were available. Please be clear on the meaning and be consistent with how questions were worded in the questionnaire. The same applies for line 362.

• Line 317-318: these findings were previously described (line 272).

• Line 326: “Approximately 10% of all respondents knew they had health conditions that should prevent them from being vaccinated, and most (92%) said they were comfortable taking their health decisions based on this.” This high percentage (10%) is concerning and I think should be a discussion point. The word “believed” would be more accurate than “knew.” What sort of conditions would these likely be? HIV? The second half of the sentence doesn’t make sense (92%...) – would it be better to report that 92% report being comfortable making decisions about their health based on the sources of information available to them? That would be more in keeping with the question in the questionnaire.

• Line 347: the result is not shown in Table 1 as specified.

• Line 348-349: the results are not shown in S5 Table as indicated.

• Line 408: “said they had experienced side effects” should be “said they know someone who had experienced side-effects.”

• Line 421: these results were not presented in the results section. Please include them in the results, especially if they are a discussion point.

• Line 424: it does not seem likely that Central Africa is more of a tourist destination than other African regions. Please revise this statement.

**********

6. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

If you choose “no”, your identity will remain anonymous but your review may still be made public.

Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: No

[NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files.]

While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Registration is free. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email PLOS at figures@plos.org. Please note that Supporting Information files do not need this step.

PLoS One. 2021 Dec 1;16(12):e0260575. doi: 10.1371/journal.pone.0260575.r002

Author response to Decision Letter 0


1 Jul 2021

Reviewer #1: MAJOR COMMENTS:

Query 1: Line 98 (abstract, and elsewhere): “Only 62% of all participants surveyed were willing to receive the COVID-19 vaccination.” This is not clear from the data presented in the results section. The results indicate that 62% would “prefer to get it as soon as possible” if it were available. This has a different meaning.

Response: These are now corrected with the addition of ‘as soon as possible’ to the abstract, and in the body of the manuscript in line 271-272 and in line 362.

Query 2: Were all questions answered by all participants. If not, then raw numbers need to be shown in Table 1 for each question.

Response: A total of 5,212 answered the question completely and these were included in the analysis. This is now indicated in Table 1. Where there are needs for breakdown of the numbers, we provided it in Tables 2 and 3.

Query 3: Table 1 results (vaccine acceptability): was there Boolean logic in the questionnaire or were all questions asked of all participants? It doesn’t seem to make sense that 62% of participants indicated they would prefer to be vaccinated as soon as possible vs. 67% would prefer to wait and see how others react before getting it vs. only 58% would get the vaccine even if it was not mandatory to do so.

Responses: First, Boolean Logic was not used for all responses. It was only applied where true or false responses were taken. Where a response could invoke another response, it was ignored; For instance, “Will you take COVID-19 vaccine?; Will you take COVID-19 Vaccine immediately?; The responders in the first question who answered “Yes” will still be included in the responders to the second question “Yes or No” even though it was expected that the percentage may be less.

This section was revised to read, ‘In all, 67% of the total populations were willing to receive the vaccine (62% without hesitation and 5% with some hesitation after observing potential reactions in earlier vaccinated subjects)’.

The 67% was also adjusted in the table to read 5% but with some footnotes for clarity as follows, ‘* These additional 5% who indicated some hesitation will be added to 62% who wanted to be vaccinated as soon as possible to make 67% of total who wanted to be vaccinated. #Only 58% of the 62% who wanted to be vaccinated as soon as possible will only do so if it is not mandatory.’.

Query 4: All the logistic regression results described in lines 280-289 are different to the results shown in Table 2. The authors need to review their analyses to establish which results are the correct ones and present their findings consistently.

Response: We thank the reviewer for this keenness and eagle eyes in picking these errors. We rechecked and confirmed that the one presented in the table was correct. We have now adjusted the text appropriately. Thank you. It now reads, ‘The odds ratio (OR) of vaccine hesitancy was lower with advancing age – 0.69 (95% CI: 0.59 – 0.79) in 25 – 34-year-old respondents, 0.76 (95% CI: 0.64 – 0.89) in 35 – 44-year-old respondents, 0.59 (95% CI: 0.48 – 0.73) in 45 – 54-year-old respondents, 0.55 (95% CI: 0.42 – 0.71) in 55 – 64-year-old respondents, and 0.42 (95% CI: 0.26 – 0.69) in >65-year-old respondents, compared to 18 – 24-year-old respondents. The OR of vaccine hesitancy was 0.87 (95% CI: 0.78 – 0.97) in females compared to males, and it was 0.61 (95% CI: 0.57 – 0.71) in employed individuals compared to unemployed counterparts. In addition, the odds of vaccine hesitancy was 0.61 (95% CI: 0.49 – 0.74) among residents of urban settings compared to rural counterparts, and it was 2.85 (95% CI: 2.35 – 3.47) in Central Africa and 0.54 (95% CI: 0.43 – 0.68) in Southern Africa compared to North Africa. Details of other variables evaluated are available in Table 2’.

MINOR COMMENTS:

• What is the justification for including “Africans who live in the Diaspora” and how was this group defined? (e.g. born in Africa vs African ancestry; which parts of the world do they live in?)

Response: The questionnaire was non-discriminatory. It was shared with Africans, and individual who considered himself as still tied to Africa (those who went abroad for study or works, but not Africans born abroad) were included in the study. A figure displaying where they were sampled from is now included as supplementary material.

• Line 141: total deaths reported appears too low, please check references. South Africa alone had >50 000 deaths by the end of March 2021.

Response: Yes, your observation is correct. It should be emphasized that data on death is a moving target. As at the time of submission, the figure that we supplied is correct. It is now adjusted to reflect the new total. It reads, ‘By June 22, 2021, Africa has experienced over 5.1 million cases, with over 137,000 deaths’.

• Line 166-168: this section of misconceptions should be rewritten more clearly; I suggest use of semicolons to separate the different misconceptions.

Response: This is now rewritten to read, ‘Previous cross-national perception studies from Africa on COVID-19 pandemic have revealed myths, misconceptions, mistrust, beliefs and misinformation about the disease including: the origin and cure (punishment from God for perceived sin; linked to 5G technology; form of biological warfare against Africans; for economic benefits of selected people; Africans are protected naturally; COVID-19 virus does not exist; and can be cured by local herbs’.

• Figure 1: consider changing this to a stacked bar chart, with countries arranged from low to high hesitancy.

Response: This is now revised.

• Table 2 and S1 Table show duplicated data.

Response: Table S1 is now deleted.

• A result is missing in Table 1 (‘other (better) ways to protect’ – it is blank).

Response: 43% is now added.

• The discussion section needs more emphasis on the fact that the participants are not representative of all Africans: this is a select group of Africans who are largely from urban areas, who have high levels of education and who have internet access. Furthermore, nearly half were “employed in the healthcare field” yet this was not highlighted in the discussion section, nor were stratified ORs shown for the group who were employed in healthcare fields vs employed in different settings.

Response: The following statement is now added to the discussion: ‘It should be clear that this study has a degree of bias to urban populace, comparatively more educated, and with internet access. In addition, a significant percentage of respondents (50.6%) have some forms of healthcare training, which may skew perception. These results should therefore be taken with caution as it may not represent the whole of African population’.

• Line 267: 67% reported whereas 65% is reported in the Table. Which is correct?

Response: 65% is correct and is now revised.

• Line 271: “Only 62% of participants surveyed were willing to receive the COVID-19 vaccination” – again, this is not the same meaning as 62% would “prefer to get it as soon as possible” if it were available. Please be clear on the meaning and be consistent with how questions were worded in the questionnaire. The same applies for line 362.

Responses: These are now corrected alongside the queries in the abstract.

• Line 317-318: these findings were previously described (line 272).

Responses: The repetition is now deleted

• Line 326: “Approximately 10% of all respondents knew they had health conditions that should prevent them from being vaccinated, and most (92%) said they were comfortable taking their health decisions based on this.” This high percentage (10%) is concerning and I think should be a discussion point. The word “believed” would be more accurate than “knew.” What sort of conditions would these likely be? HIV? The second half of the sentence doesn’t make sense (92%...) – would it be better to report that 92% report being comfortable making decisions about their health based on the sources of information available to them? That would be more in keeping with the question in the questionnaire.

Response: ‘Knew’ was changed to ‘believed that’. The high percentage (10%) is now mentioned in the discussion, however, we did not probe these other health conditions in this study because such question was considered invasive by the authorities that provided clearance. A statement which reads, ‘Noteworthy is the high percentage (10%) of respondents who believed that they have other health conditions, which should prevent them from being vaccinated. While we did not probe into these ‘other health conditions’ to avoid straying outside the context of this study, this information should prompt the health authorities in Africa to consider further study to know such specifics and assess whether hospital records of debilitating and chronic conditions tally with these assertions’ is now added.

• The second half of the sentence doesn’t make sense (92%...) – would it be better to report that 92% report being comfortable making decisions about their health based on the sources of information available to them? That would be more in keeping with the question in the questionnaire.

Response: This was revised as suggested. The whole statement now reads, ‘Approximately 10% of all respondents believed that they had health conditions that should prevent them from being vaccinated, and 92% report being comfortable making decisions about their health based on the sources of information available to them’.

• Line 347: the result is not shown in Table 1 as specified.

Response: It is revised and now reflected in S3 Table.

• Line 348-349: the results are not shown in S5 Table as indicated.

Response: These values are now reflected in S3 Table.

• Line 408: “said they had experienced side effects” should be “said they know someone who had experienced side-effects.”

Responses: This is corrected.

• Line 421: these results were not presented in the results section. Please include them in the results, especially if they are a discussion point.

Response: This information are available in Table 2 and are now added to the discussion.

• Line 424: it does not seem likely that Central Africa is more of a tourist destination than other African regions. Please revise this statement.

Response: The statement is revised to read, ‘Central Africa countries may serve as passageways to connect Africa, have health infrastructural deficit, and have experienced repeated conflicts’.

Attachment

Submitted filename: Reviewer_PONE.docx

Decision Letter 1

Prasenjit Mitra

28 Jul 2021

PONE-D-21-13734R1

Will Africans take COVID-19 Vaccination?

PLOS ONE

Dear Dr. Fasina,

Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process.

==============================

ACADEMIC EDITOR: Please go through the comments of the reviewer and revise your manuscript accordingly. 

==============================

Please submit your revised manuscript by Sep 11 2021 11:59PM. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at plosone@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pone/ and select the 'Submissions Needing Revision' folder to locate your manuscript file.

Please include the following items when submitting your revised manuscript:

  • A rebuttal letter that responds to each point raised by the academic editor and reviewer(s). You should upload this letter as a separate file labeled 'Response to Reviewers'.

  • A marked-up copy of your manuscript that highlights changes made to the original version. You should upload this as a separate file labeled 'Revised Manuscript with Track Changes'.

  • An unmarked version of your revised paper without tracked changes. You should upload this as a separate file labeled 'Manuscript'.

If you would like to make changes to your financial disclosure, please include your updated statement in your cover letter. Guidelines for resubmitting your figure files are available below the reviewer comments at the end of this letter.

If applicable, we recommend that you deposit your laboratory protocols in protocols.io to enhance the reproducibility of your results. Protocols.io assigns your protocol its own identifier (DOI) so that it can be cited independently in the future. For instructions see: http://journals.plos.org/plosone/s/submission-guidelines#loc-laboratory-protocols. Additionally, PLOS ONE offers an option for publishing peer-reviewed Lab Protocol articles, which describe protocols hosted on protocols.io. Read more information on sharing protocols at https://plos.org/protocols?utm_medium=editorial-email&utm_source=authorletters&utm_campaign=protocols.

We look forward to receiving your revised manuscript.

Kind regards,

Prasenjit Mitra, MD, MRSB, MIScT, FLS, FACSc, FAACC

Academic Editor

PLOS ONE

[Note: HTML markup is below. Please do not edit.]

Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. If the authors have adequately addressed your comments raised in a previous round of review and you feel that this manuscript is now acceptable for publication, you may indicate that here to bypass the “Comments to the Author” section, enter your conflict of interest statement in the “Confidential to Editor” section, and submit your "Accept" recommendation.

Reviewer #1: All comments have been addressed

**********

2. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: Yes

**********

3. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: I Don't Know

**********

4. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

**********

5. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: Yes

**********

6. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: Thank you for addressing the concerns and suggestions.

A few additional points:

• Inaccuracies remain in the tables, has the analysis been carefully rechecked? For example, in Table 2, vaccine accepting number plus vaccine hesitant number in most rows does not add up correctly to the Total Frequency (eg. 588 + 597 in first row = 1185, not 1187 as listed). Furthermore, the proportions (%) are not shown and if calculated, they often do not match the results in the text. Eg. For vaccine accepting, male + female = 1548 + 1418 = 2966/5212 = 57%. Whereas the study’s main finding is that 62% (or 67%, depending on definition used) were vaccine accepting. Why do the figures not correlate? In Table 3, what are the denominators? It is unclear how the reported percentages were derived.

• I recommend omitting “(distribution of location of the diasporas is available in the supplementary figure)” from the abstract.

• Reference 2 needs citation date to be amended in the reference list

• “(50.6%) have some forms of healthcare training” was added yet elsewhere it states “46% were trained in health-related fields”. This needs to be corrected after checking the data for the “employed in the healthcare field” question and stating results accordingly.

**********

7. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

If you choose “no”, your identity will remain anonymous but your review may still be made public.

Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: No

[NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files.]

While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Registration is free. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email PLOS at figures@plos.org. Please note that Supporting Information files do not need this step.

PLoS One. 2021 Dec 1;16(12):e0260575. doi: 10.1371/journal.pone.0260575.r004

Author response to Decision Letter 1


4 Aug 2021

6. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: Thank you for addressing the concerns and suggestions.

A few additional points:

Query 1: • Inaccuracies remain in the tables, has the analysis been carefully rechecked? For example, in Table 2, vaccine accepting number plus vaccine hesitant number in most rows does not add up correctly to the Total Frequency (eg. 588 + 597 in first row = 1185, not 1187 as listed). Furthermore, the proportions (%) are not shown and if calculated, they often do not match the results in the text. Eg. For vaccine accepting, male + female = 1548 + 1418 = 2966/5212 = 57%. Whereas the study’s main finding is that 62% (or 67%, depending on definition used) were vaccine accepting. Why do the figures not correlate? In Table 3, what are the denominators? It is unclear how the reported percentages were derived.

Response: The Tables were now checked and corrected for errors. The original errors were regretted. There was a mix up in the course of harmonizing the data and the wrong tables were uploaded. The current table is correct and the statistics were checked again. The figure 1 is now also readjusted as per the rechecked data and improved. The table 3 is also completely reviewed and updated in the document.

Query 2: • I recommend omitting “(distribution of location of the diasporas is available in the supplementary figure)” from the abstract.

Response: This is now deleted from the abstract.

Query 3: • Reference 2 needs citation date to be amended in the reference list

Response: Reference 2 is now updated to June 24 after the date cited.

Query 4: • “(50.6%) have some forms of healthcare training” was added yet elsewhere it states “46% were trained in health-related fields”. This needs to be corrected after checking the data for the “employed in the healthcare field” question and stating results accordingly.

Response: 50.6% is correct. The erroneous 46% is now corrected to 50.6%.

________________________________________

Attachment

Submitted filename: Review round 2_PONE.docx

Decision Letter 2

Prasenjit Mitra

15 Nov 2021

Will Africans take COVID-19 Vaccination?

PONE-D-21-13734R2

Dear Dr. Fasina,

We’re pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it meets all outstanding technical requirements.

Within one week, you’ll receive an e-mail detailing the required amendments. When these have been addressed, you’ll receive a formal acceptance letter and your manuscript will be scheduled for publication.

An invoice for payment will follow shortly after the formal acceptance. To ensure an efficient process, please log into Editorial Manager at http://www.editorialmanager.com/pone/, click the 'Update My Information' link at the top of the page, and double check that your user information is up-to-date. If you have any billing related questions, please contact our Author Billing department directly at authorbilling@plos.org.

If your institution or institutions have a press office, please notify them about your upcoming paper to help maximize its impact. If they’ll be preparing press materials, please inform our press team as soon as possible -- no later than 48 hours after receiving the formal acceptance. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information, please contact onepress@plos.org.

Kind regards,

Prasenjit Mitra, MD, CBiol, MRSB, MIScT, FLS, FACSc, FAACC

Academic Editor

PLOS ONE

Additional Editor Comments (optional):

Reviewers' comments:

Acceptance letter

Prasenjit Mitra

18 Nov 2021

PONE-D-21-13734R2

Will Africans take COVID-19 Vaccination?

Dear Dr. Fasina:

I'm pleased to inform you that your manuscript has been deemed suitable for publication in PLOS ONE. Congratulations! Your manuscript is now with our production department.

If your institution or institutions have a press office, please let them know about your upcoming paper now to help maximize its impact. If they'll be preparing press materials, please inform our press team within the next 48 hours. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information please contact onepress@plos.org.

If we can help with anything else, please email us at plosone@plos.org.

Thank you for submitting your work to PLOS ONE and supporting open access.

Kind regards,

PLOS ONE Editorial Office Staff

on behalf of

Dr. Prasenjit Mitra

Academic Editor

PLOS ONE

Associated Data

    This section collects any data citations, data availability statements, or supplementary materials included in this article.

    Supplementary Materials

    S1 File

    (DOCX)

    Attachment

    Submitted filename: Reviewer_PONE.docx

    Attachment

    Submitted filename: Review round 2_PONE.docx

    Data Availability Statement

    The basic minimum data required to replicate all study findings reported in the article, as well as related metadata and methods are included in the supplementary materials (Supplement 1, S1-4 Table and Supplementary Figure S1) including the 1) Questionnaire, 2) Location surveyed, 3) Biodata of surveyed participants, and 4) methods and data analysis sections of the study.


    Articles from PLoS ONE are provided here courtesy of PLOS

    RESOURCES