Abstract
Developing countries have been facing difficulties in reaching out to low-income and underserved communities for COVID-19 vaccination coverage. The rapidity of vaccine development caused a mistrust among certain subgroups of the population, and hence innovative approaches were taken to reach out to such populations. Using a sample of 1760 respondents in five low-income, informal localities of Islamabad and Rawalpindi, Pakistan, we evaluated a set of interventions involving community engagement by addressing demand and access barriers. We used multi-level mixed effects models to estimate average treatment effects across treatment areas. We found that our interventions increased COVID-19 vaccine willingness in two treatment areas that are furthest from city centers by 7.6% and 6.6% respectively, while vaccine uptake increased in one of the treatment areas by 17.1%, compared to the control area. Our results suggest that personalized information campaigns such as community mobilization help to increase COVID-19 vaccine willingness. Increasing uptake however, requires improving access to the vaccination services. Both information and access may be different for various communities and therefore a “one-size-fits-all” approach may need to be better localized. Such underserved and marginalized communities are better served if vaccination efforts are contextualized.
Introduction
The SARS-CoV-2 (COVID-19) outbreak has been one of the largest infectious disease challenges in the past century with 559 million cases and 6.36 million deaths (as of July 15, 2022) [1]. In the initial phase, the only means to curb transmission were measures that limited contact between individuals, such as lockdowns and closures of schools, work, and public places. These, in turn, resulted in tremendous social costs and loss of well-being of individuals and societies [2]. However, the availability of effective vaccines from the first half of 2021 changed how countries and societies approached the contagion and how effective they were in doing so.
The rapidity of the vaccine development process has been unprecedented, as has been the intended scope of its coverage. Until now it took 5–10 years to develop and navigate most vaccines through regulatory approvals, which for most parts were administered to sub-sets of the population such as children, pregnant women, etc. COVID-19 vaccines went from the first identification of the virus to a public rollout of vaccines in under one year and were aimed at nearly all of the world’s adult population.
This swiftness raised issues of mistrust among potential recipients, who questioned both the efficacy and safety of the vaccine [3, 4]. This in turn led to some reluctance and affected the rollout of the vaccine. Several means were attempted to promote vaccination widely, including mandates (e.g., for healthcare workers, other government personnel, or certain patients) [5, 6], tying vaccination to access to public transport or to enter stadiums, or by giving incentives to vaccinate (e.g., discounts on certain purchases). As anticipated, much of the initial vaccinations were in cities, and among well-documented and vaccine-seeking populations. However, the large-scale rollout and the intent to cover the entire population required addressing several complex situations.
For one, globally, about 1 billion people [7, 8] reside in densely populated low-income informal settlements (urban slums), where access and availability to public health facilities are limited [9]. These barriers are further accentuated by a lack of trust by public authorities that are supposed to serve them, which consider them illegal occupants of government lands (sometimes leading to forced evictions and demolitions) and often do not have a full sense of their numbers as these settlements are poorly documented [10–12]. This in turn creates social exclusions and aggravates intra-societal iniquity where the most marginalized individuals are also suspicious of the government and its initiatives to reach them with life-saving services [13–17].
Pakistan started a multi-staged rollout of COVID-19 vaccination in March 2021 that initially prioritized the oldest population, frontline workers, and those with certain risk factors, and then progressively included younger citizens, till vaccinations were opened to everyone aged 18 years or older in July 2021. When the original, voluntary uptake of vaccines slowed down, several strategies were attempted, including reaching out to poor urban communities [18] which form nearly 30% of Pakistan’s total population [19]. The present study explores the effectiveness of interventions aimed at addressing demand and access barriers in such communities.
Theoretical framework for the study
Several socio-demographic factors, communication about COVID-19 and vaccines, perceptions regarding COVID-19 vaccination, and prior experience of COVID-19 infection affect vaccine acceptance. Being male, older in age, highly educated, and employed are associated with higher acceptance; as is the perception of COVID-19 risk towards oneself and a personal or family history of COVID-19 infections [13, 20–29]. In addition, information and communication about COVID-19 vaccination act as signals to influence individual behavior [26, 27].
These factors were included in the context of the Theory of Planned Behavior (TPB) to develop a theoretical framework of vaccine willingness and uptake. The theory suggests that people’s behavioral intentions are motivated by their attitudes, subjective norms, and perceived behavioral control [30]. These behavioral intentions in turn can directly affect an individual’s health behavior [29–31], which we hypothesized in our study as willingness translating to increased vaccine uptake among the targeted population.
Through our community engagement interventions, we aimed to change the behavioral intentions (i.e., COVID-19 vaccine willingness) of residents in the treatment areas. Behavior change communication was carried out in the context of social mobilization to engage the communities [32–34]. Interventions aimed at mobilizing communities for vaccination can help strengthen weak links in the causal chain, as this can enable one to take into account the local characteristics and implement the interventions more effectively [35]. When information is spread through local prominent members (community and religious leaders) of the community, people become more willing to accept it and in turn, implement it.
Engaging communities thus aid to disseminate information in the local language and channels which can have a greater outreach [33]. As found in an earlier study of rural Bangladesh [36], collaboration with non-government organizations (NGOs) to increase immunization rates also results in better service delivery and increases vaccination acceptance as people exhibit more trust in local NGOs. Mobile vaccination camps (MVCs) can help increase access to vaccinations in such underserved communities. The current study explored the roles of community mobilization and vaccination camps in marginalized, low-trust communities to promote awareness and uptake of COVID-19 vaccination and the effects of such interventions in sub-populations of these communities.
Methodology
Study overview, location and sampling
The study used a cross-sectional research design. Residents of five urban poor communities from the Rawalpindi-Islamabad twin cities were included. A baseline survey of 1760 respondents with equal representations of males and females was conducted from June 16 to 26, 2021, followed by an intervention (explained below). An endline survey was conducted from August 24 to September 03, 2021, with the same sampling technique, but not the same respondents. The response rate for the baseline was 98% while it was 96% for the endline.
The study was limited to COVID-19 vaccine-eligible respondents of 18 years of age that were residents of selected communities. The final survey instrument comprised 38 questions divided into multiple sections. Only a few questions were open-ended and the survey was administered in Urdu (local) language for accurate responses. Data collection was carried out in the field on electronic tablets using SurveyCTO.
Five densely populated, low-income, and underserved urban areas were selected in consultation with the Ministry of National Health Services, Regulations and Coordination (MoNHSRC) for their low participation in vaccination efforts, since such areas have historically been more hesitant towards vaccines [37–39]. Based on this experience, from Islamabad, we included I-10 (a middle-class locality), G-7 (Low-income but formal locality), F-7 (France Colony) (informal settlement), and Bhara Kahu (low- to middle-income, completely informal and recent settlement), while Dhok Hassu (low-income, long stand informal locality) was included from Rawalpindi. Each community is located sufficiently away from each other to make any cross-over contamination of the intervention (Information and eased access to local camps through social mobilization) unlikely.
Population and average household sizes were based on the Census 2017 by the Pakistan Bureau of Statistics and on-site visits (Table 1).
Table 1. Location characteristics of study areas.
| Locality | Actual Population | Actual Households | Average Household Size |
|---|---|---|---|
| Control | |||
| I-10 | 44,580 | 7,984 | 5.6 |
| Treatment | |||
| G-7 (Low-income quarters)/F-7 (France Colony) | 38,722 | 6136 | 6.3 |
| Bhara Kahu | 125,048 | 21,123 | 5.9 |
| Dhok Hassu | 201,212 | 30,032 | 6.7 |
The sample size was calculated using MICS methodology with a 95% confidence interval [40]. We assumed a 50% acceptance rate for vaccination uptake, a design effect of 1.5, a relative margin of error of 0.12, and a 95% response rate. The sample size included 480 respondents from each of the larger communities (population greater than 30,000), while 160 each were from smaller communities.
A two-stage clustered sampling design was applied using GIS mapping, with randomization being done first by selecting a random sample of clusters in each locality of the sampling frame and then randomly selecting households from each cluster. Pins identifying clusters were dropped at random points on the map. Out of those, we randomly selected a total of 110 clusters, 30 each in Dhok Hassu, Bhara Kahu, and I-10, and 10 each in F-7 (France Colony) and G-7 (Low-income quarters) for each round of surveys.
Working in pairs, enumerators reached the pins and started with the nearest household to the left within the cluster. The pair then surveyed fifteen more households in that cluster using the left-hand rule, skipping one household after every successful interview. Each pair surveyed 8 male and 8 female respondents in every cluster, for a total of 16 interviews per cluster. Males and females were surveyed from different households, with no upper age limit restriction.
Ethical review
The ethical review for this study was carried out by Research and Development Solutions (RADS), Islamabad which is registered with the Office for Human Research Protection (OHRP) for Institutional Review Board (IRB) approvals (Reference Number: IRB00010843). The IRB committee reviewed the research methodology, survey consent process, and survey tool, and granted a formal approval on June 8, 2021. All methods were performed in accordance with relevant guidelines and regulations. Informed written consent was taken from respondents prior to surveying given their personal information would be kept confidential and used for research purposes only.
Interventions
Awareness campaign via local mobilizers
The primary intervention focused on building awareness among residents of treatment areas through social mobilization techniques geared towards improving vaccine willingness and uptake. The campaign targeted public places such as shops, markets, mosques, and churches. Within the communities, community leaders (i.e., religious and political leaders) were engaged to spread awareness of COVID-19. Printed information pamphlets (S1 and S2 Figs) were also distributed in the Urdu language via local mobilizers to explain the process of registering and getting vaccinated, while also debunking common myths surrounding vaccines, and identifying COVID-19 vaccination camps (CVCs) nearby.
Mobile vaccination camps (MVCs)
Since there were no CVCs in the vicinity of the selected communities, MVCs were arranged to provide access to COVID-19 vaccination. These camps were organized in treatment areas in collaboration with local community-based organizations (CBOs), NGOs, and community leaders through our team of mobilizers to facilitate the community vaccination process encompassing assembling, counseling, and registering community members for the vaccination. The venue of the vaccination site was chosen by the community as a locally well-known and accessible location, such as a school or other landmarks. Local mobilizers also advertised for these in advance and on the day of the visit, they facilitated them while they were at the camp.
Empirical measurement strategy
We used intent-to-treat (ITT) analysis to measure average treatment effects (ATEs), assuming that households remained in the same treatment groups to which they were originally assigned, whether they received the treatments or not. We estimated ATEs on two primary outcomes: willingness to vaccinate and vaccine uptake. Given both the dependent variables were binary, we estimated non-linear ITT parameters using multi-level mixed effects logistic regressions [41] through the difference-in-differences method. Here, level 2 indicates clusters and level 1 indicates households within those clusters. As suggested by Bruhn and McKenzie [42], we did not report statistical differences between groups at baseline covariates.
The control variables in our analyses were taken based on the theoretical framework explained above as well as their predictive powers to explain the outcome variables [42], which were calculated as having strong correlations with the outcome variables. Controlling for these variables that could be imbalanced at the baseline also controlled for imbalance in the unobservable characteristics [42], and therefore the difference-in-differences analysis was applicable. We conducted all our analyses on the statistical software STATA 17.
The difference-in-differences model in regression form was then specified as follows:
| (1) |
In Eq 1, i referred to each household, j referred to each cluster, z represented each treatment group, t represented pre- and post-time periods and Yij was the relevant outcome. Since we estimated two models, Yvu was vaccine uptake and Ywv was willingness to vaccinate. We also accounted for several control variables () in our models to explain variation in our outcome variables (S1 Table). The fixed part of the model consisted of , μj represented the random part of the model, and εij was the household-level specific error term.
Vaccine uptake (Yvu) was given a value of 1 if the respondent had received at least one dose of COVID-19 vaccination and 0 otherwise, and willingness to vaccinate (Ywv) was assigned a value of 1 if the respondent was willing to get vaccinated if a free of cost government-administered COVID-19 vaccine was provided, and 0 otherwise. Treatijz indicated the localities which we took in treatment and control areas. We defined three treatment areas (T1: G-7/F-7, T2: Bhara Kahu and T3: Dhok Hassu) and one control area (C: I-10). Timeijt was a binary variable indicating a value of 1 for post-intervention and 0 for pre-intervention time periods.
The coefficient (β3) on Treatijz*Timeijt captured the effect of interventions on the treated areas as compared to the control area. Since our model was non-linear in nature, ATEs were calculated by cross derivatives with respect to Timeijt and Treatijz variables [43]:
The R-squared for our models was calculated using a community-distributed STATA program written by Dr Wolfgang Langer [44].
Results
At the baseline, the respondents had a median age of 35 (range: 18–86) years. They were predominantly of Punjabi ethnicity, except for Dhok Hassu, where 42% of respondents were Pashtun (Table 2). The control area (I-10) had more respondents that were Urdu speakers (10%), were better off than any of the treatment areas, and were more educated–the fewest uneducated (9%) and the most university degree holders (47%). Unemployment rates ranged from 61% in I-10 to 48% in Dhok Hassu.
Table 2. Descriptive baseline characteristics in percentages across groups.
| Variables | Categories | Control Group | Treatment Groups | ||||||
|---|---|---|---|---|---|---|---|---|---|
| I-10 | G-7/F-7 | Bhara Kahu | Dhok Hassu | ||||||
| Baseline | Endline | Baseline | Endline | Baseline | Endline | Baseline | Endline | ||
| Age Group | 18–29 | 32.2 | 28.3 | 31.7 | 36.0 | 29.2 | 26.6 | 30.8 | 29.2 |
| 30–39 | 24.5 | 24.0 | 27.3 | 21.9 | 31.9 | 33.2 | 31.0 | 28.0 | |
| 40–49 | 19.0 | 18.7 | 19.1 | 19.3 | 22.9 | 22.7 | 22.8 | 20.9 | |
| 50–59 | 11.2 | 14.8 | 13.2 | 12.8 | 9.7 | 12.6 | 9.4 | 12.9 | |
| 60+ | 12.6 | 14.3 | 8.8 | 10.0 | 6.3 | 5.0 | 6.1 | 9.1 | |
| Education level | None | 8.8 | 6.3 | 19.5 | 24.6 | 15.8 | 15.9 | 34.5 | 34.6 |
| Up to 12 years | 44.0 | 42.3 | 57.9 | 60.1 | 63.0 | 64.5 | 58.5 | 58.1 | |
| University degree | 47.3 | 51.4 | 22.6 | 15.3 | 21.2 | 19.6 | 7.1 | 7.2 | |
| Ethnicity | Punjabi | 58.0 | 59.1 | 84.0 | 90.7 | 50.6 | 63.9 | 45.1 | 48.7 |
| Pashtun | 16.74 | 15.2 | 5.6 | 4.7 | 16.2 | 13.6 | 42.4 | 39.0 | |
| Urdu Speaking | 10.3 | 16.1 | 2.2 | 0.6 | 3.4 | 5.0 | 0.4 | 0.62 | |
| Hindko | 3.6 | 2.7 | 1.3 | 0 | 4.4 | 3.1 | 6.9 | 7.2 | |
| Others | 11.5 | 7.0 | 6.9 | 4.1 | 25.4 | 14.4 | 5.2 | 4.5 | |
| Employment | Self Employed | 15.7 | 11.9 | 6.9 | 10.3 | 19.3 | 21.3 | 29.4 | 25.0 |
| Employed | 23.1 | 22.8 | 39.8 | 38.6 | 26.9 | 22.1 | 22.4 | 21.4 | |
| Unemployed | 61.2 | 65.3 | 53.3 | 51.1 | 53.8 | 56.6 | 48.2 | 53.6 | |
| Self-infection of COVID-19 | Yes | 13.5 | 13.7 | 7.3 | 4.4 | 4.3 | 3.5 | 1.5 | 2.7 |
| Family infection of COVID-19 | Yes | 16.9 | 19.7 | 11.6 | 6.0 | 7.0 | 6.4 | 2.3 | 3.3 |
| Sought treatment for last illness | Yes | 79.3 | 72.2 | 79.6 | 70.0 | 80.6 | 74.8 | 83.3 | 81.4 |
| Family vaccination | Yes | 57.4 | 85.5 | 66.9 | 89.3 | 36.4 | 69.0 | 18.9 | 57.0 |
| Distance from CVC | Up to 2 kms | 5.0 | 23.3 | 45.3 | 20.6 | 43.9 | 49.6 | 8.2 | 55.5 |
| More than 2 kms | 49.4 | 40.3 | 42.8 | 67.6 | 29.4 | 28.1 | 37.1 | 22.3 | |
| Don’t Know | 45.6 | 36.4 | 12.0 | 11.8 | 26.7 | 22.3 | 54.6 | 22.3 | |
| Risk perception of COVID-19 | Worried | 65.8 | 68.5 | 63.6 | 61.7 | 59.0 | 77.9 | 71.4 | 74.1 |
| Uncertain | 17.2 | 10.9 | 4.8 | 6.2 | 14.8 | 9.3 | 10.7 | 9.1 | |
| Unworried | 17.0 | 20.6 | 31.7 | 32.1 | 26.2 | 12.8 | 17.9 | 16.8 | |
| Sources of information: | |||||||||
| Television | Yes | 26.6 | 35.0 | 33.2 | 24.6 | 25.4 | 14.2 | 23.4 | 28.3 |
| Government Call/SMS | Yes | 26.8 | 17.8 | 16.3 | 19.9 | 37.6 | 41.0 | 27.6 | 32.4 |
| Family/Friends | Yes | 46.2 | 24.2 | 49.2 | 53.0 | 46.0 | 65.2 | 44.1 | 63.1 |
| Medical professionals | Yes | 8.6 | 8.4 | 9.1 | 18.1 | 6.1 | 11.6 | 4.2 | 15.9 |
| Religious leaders | Yes | 0 | 0 | 0.3 | 7.5 | 1.5 | 2.7 | 0.4 | 6.2 |
| Any NGO/CBO working in area | Yes | 88.7 | 66.6 | 56.1 | 48.3 | 74.4 | 71.6 | 74.1 | 73.4 |
Few respondents (1% to 17%) reported any prior COVID-19 infection for themselves or among their families from any location. The highest rates were reported from the control area (I-10). However, 59–71% of all respondents reported being worried about COVID-19. The history of at least one member of the family having received the COVID-19 vaccine was the highest in G7/F7 (67%), followed by I-10 (57%), and the lowest in Dhok Hassu (19%). Distance from a CVC was the least for residents of G7/F7 and Bhara Kahu and the most for I-10 residents. Respondents from all areas reported similar proportions of sources of COVID-19 vaccination information and similar rates of treatment-seeking during a prior illness. 89% of respondents from I-10 were aware of NGOs and CBOs working in the area, compared with 56% in G-7/F-7 and 74% in Bhara Kahu and Dhok Hassu (Table 2).
Willingness to vaccinate and COVID-19 vaccine uptake
Willingness to receive vaccines increased substantially from baseline (67%) to endline (80%), more for men than women (Table 3). The control area (I-10) had the highest willingness for both men and women across both time periods, with an exception that G7/F7 had the highest willingness for men at the endline (94%).
Table 3. Willingness to vaccinate and vaccine uptake segregated by gender and location.
| Willingness to vaccinate | Vaccine uptake | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Willing | Uncertain | Unwilling | Unvaccinated | Only registered | At least partially vaccinated | ||||||||
| Baseline | Endline | Baseline | Endline | Baseline | Endline | Baseline | Endline | Baseline | Endline | Baseline | Endline | ||
| TOTAL | 67% | 80% | 12% | 9% | 21% | 10% | 65% | 39% | 13% | 14% | 22% | 47% | |
| Male | C: I-10 | 82% | 88% | 9% | 2% | 9% | 10% | 59% | 20% | 12% | 31% | 29% | 49% |
| T1: G-7/F-7 | 81% | 94% | 2% | 4% | 17% | 2% | 43% | 16% | 16% | 6% | 40% | 78% | |
| T2: Bhara Kahu | 64% | 77% | 25% | 18% | 12% | 5% | 64% | 35% | 12% | 14% | 24% | 51% | |
| T3: Dhok Hassu | 64% | 85% | 13% | 10% | 23% | 5% | 76% | 38% | 14% | 22% | 10% | 40% | |
| Total | 72% | 85% | 13% | 9% | 15% | 6% | 62% | 28% | 13% | 19% | 24% | 52% | |
| Female | C: I-10 | 73% | 83% | 9% | 9% | 18% | 9% | 49% | 32% | 18% | 11% | 33% | 57% |
| T1: G-7/F-7 | 71% | 72% | 8% | 8% | 21% | 20% | 58% | 43% | 13% | 6% | 29% | 51% | |
| T2: Bhara Kahu | 51% | 80% | 13% | 4% | 36% | 16% | 79% | 60% | 8% | 7% | 12% | 32% | |
| T3: Dhok Hassu | 55% | 67% | 17% | 18% | 28% | 15% | 83% | 59% | 11% | 12% | 7% | 28% | |
| Total | 62% | 76% | 12% | 10% | 26% | 14% | 68% | 49% | 12% | 9% | 20% | 41% | |
Correspondingly, refusal to receive vaccine dropped sharply in the endline. For men, the highest dip in refusals occurred in Dhok Hassu (18%), while Bhara Kahu had the highest decrease for women (20%). Registrations and vaccinations mirror willingness. Vaccine uptake increased from 22% to 47%, with men receiving more vaccination than women (Table 3).
Intent-to-treat (ITT) and average treatment effects (ATEs)
Average marginal treatment effects from multi-level mixed effects logistic regressions show that, compared to the control area (I-10), willingness to receive vaccination increased by 7.6% in Bhara Kahu (Coef: 0.0764, CI: 0.0121, 0.1406) and 6.6% in Dhok Hassu (Coef: 0.0661, CI: 0.00498, 0.1272) respectively. However, the change in G7/F7 was not significant.
Whereas, this willingness did not translate into an increase in vaccination rates in either of the areas. Vaccine uptake increased by 17.1% (Coef: 0.1709, CI: 0.0417, 0.3) in G-7/F-7 only (Table 4). Our adjusted models with all controls showing odds ratios are provided in S2 Table.
Table 4. Pairwise comparisons of average marginal treatment effects.
| (1) | (2) | |||
|---|---|---|---|---|
| Comparison | Willingness to vaccinate | Vaccine Uptake | ||
| Unadjusted | Adjusted | Unadjusted | Adjusted | |
| Difference-in-differences | ||||
| T1: G-7/F-7 vs C: I-10 | 0.0312 | 0.0611 | 0.077 | 0.1709** |
| (-0.0578, 0.1203) | (-0.0197, 0.1419) | (-0.0354, 0.1894) | (0.0417, 0.3) | |
| T2: Bhara Kahu vs C: I-10 | 0.1189*** | 0.0764** | 0.0078 | 0.0418 |
| (0.0424, 0.1954) | (0.0121, 0.1406) | (-0.0994, 0.115) | (-0.0817, 0.1652) | |
| T3: Dhok Hassu vs C: I-10 | 0.1314*** | 0.0661** | 0.0385 | 0.0398 |
| (0.0566, 0.2063) | (0.00498, 0.1272) | (-0.066, 0.143) | (-0.0767, 0.1563) | |
| Observations | 3107 | 2,904 | 3448 | 3216 |
| Number of clusters | 220 | 220 | 220 | 220 |
| Intra-class correlation | 0.044 | 0.046 | 0.042 | 0.048 |
| McKelvey & Zavoina R2 (FE and RE) | 0.083 | 0.395 | 0.198 | 0.533 |
Robust standard errors were used, CI in parentheses
*** p<0.01
** p<0.05
* p<0.1
The Intra class correlation (ICC) is the correlation among observations within the same cluster. In our models, ICC indicates that only around 4.2–4.8% of the total variance in willingness to vaccinate and uptake is explained by between-cluster differences (i.e., due to clustering). The Mckelvey & Zavoina Pseudo R-squares of adjusted models show that 40% and 53% of the variations in willingness and uptake respectively are captured by the independent variables. Both models show good fits to predict the relevant outcomes.
Determinants of willingness and vaccine uptake
Willingness to vaccinate was twice as likely in the control area at baseline but this effect disappeared at the endline. On the other hand, the likelihood of vaccine uptake increased in G-7/F-7 compared to the control locality (AOR: 1.975, CI: 1.079, 3.617) but not anywhere else. Women were half as likely to express willingness to vaccinate but were not any different from men in terms of vaccine uptake. Increasing age, higher education, and employment were important determinants of willingness and uptake of vaccination at the baseline. While these factors remained important at the endline as well, their significance decreased as seen by their lowered odds at the endline. Pashtuns became less likely and Urdu speakers more likely to receive the vaccine at the endline.
Previous infection with COVID-19 for self was not a key determinant for willingness but a significant one for uptake of vaccination (AOR: 2.286, CI: 1.142, 4.576). Similarly, infection or vaccination of a family member and a high-risk perception were motivators for both willingness and uptake of vaccination. The effect of all these factors increased at the endline. Having sought treatment for a recent illness was positively correlated with uptake (AOR: 1.471, CI: 1.078, 2.009).
Having received an SMS or call from the government was a major motivator that led to increased willingness (AOR: 2.414, CI: 1.420, 4.103) and uptake (AOR: 1.310, CI: 1.004, 1.708) in the endline. Advice from friends, family, medical professionals, and religious leaders did not sway opinions about the willingness or uptake of vaccination. Living near a CVC was correlated with higher willingness compared to those who resided so far away that they did not know about the distance to a nearby CVC, and closer distances were associated with higher uptake (AOR: 4.14, CI: 2.370, 7.233 for less than 2 kms and AOR: 3.969, CI: 2.452, 6.423 for 2+ kms). The odds of vaccine uptake also increased if an NGO/CBO was working in the area in the pre-intervention period (AOR: 1.657, CI: 1.093, 2.514) (Table 5).
Table 5. Odds ratios of factors influencing willingness to vaccinate and vaccine uptake.
| Willingness to Vaccinate | Vaccine Uptake | |||
|---|---|---|---|---|
| (1) | (2) | (3) | (4) | |
| VARIABLES | Baseline | Endline | Baseline | Endline |
| Group (Control: I-10) | ||||
| T1: G-7/F-7 | 0.501** | 0.766 | 0.883 | 1.975** |
| (0.275, 0.911) | (0.365, 1.608) | (0.513, 1.520) | (1.079, 3.617) | |
| T2: Bhara Kahu | 0.567** | 0.670 | 0.669 | 0.741 |
| (0.354, 0.908) | (0.328, 1.368) | (0.405, 1.104) | (0.422, 1.301) | |
| T3: Dhok Hassu | 0.718 | 1.091 | 0.483*** | 0.639 |
| (0.435, 1.187) | (0.492, 2.418) | (0.294, 0.792) | (0.373, 1.095) | |
| Female | 0.546*** | 0.477*** | 1.049 | 0.766 |
| (0.349, 0.853) | (0.278, 0.818) | (0.656, 1.676) | (0.520, 1.129) | |
| Age Group (18–29) | ||||
| 30–39 | 1.332 | 2.072*** | 2.215*** | 1.631*** |
| (0.924, 1.920) | (1.347, 3.187) | (1.407, 3.489) | (1.136, 2.342) | |
| 40–49 | 1.699*** | 2.413*** | 6.775*** | 3.154*** |
| (1.153, 2.502) | (1.424, 4.087) | (4.255, 10.79) | (2.135, 4.659) | |
| 50–59 | 1.761** | 2.502** | 12.32*** | 4.595*** |
| (1.010, 3.070) | (1.225, 5.111) | (7.350, 20.65) | (3.022, 6.988) | |
| 60–69 | 2.913*** | 2.391** | 31.23*** | 4.890*** |
| (1.498, 5.661) | (1.061, 5.386) | (17.22, 56.64) | (3.002, 7.966) | |
| Education level (None) | ||||
| Up to 12 years | 1.237 | 0.920 | 1.122 | 0.728* |
| (0.863, 1.771) | (0.580, 1.459) | (0.695, 1.810) | (0.530, 1.001) | |
| University degree | 1.941** | 0.614 | 1.735* | 0.918 |
| (1.167, 3.227) | (0.324, 1.163) | (0.955, 3.153) | (0.576, 1.460) | |
| Ethnicity (Others) | ||||
| Punjabi | 0.935 | 0.996 | 1.042 | 1.054 |
| (0.583, 1.501) | (0.483, 2.055) | (0.665, 1.635) | (0.654, 1.698) | |
| Pashtun | 1.154 | 0.618 | 1.003 | 0.605* |
| (0.667, 1.995) | (0.274, 1.393) | (0.615, 1.636) | (0.337, 1.087) | |
| Urdu Speaking | 0.820 | 1.153 | 1.630 | 2.033** |
| (0.352, 1.908) | (0.361, 3.680) | (0.808, 3.288) | (1.026, 4.027) | |
| Hindko | 0.832 | 1.100 | 0.595 | 1.202 |
| (0.357, 1.938) | (0.283, 4.269) | (0.207, 1.716) | (0.530, 2.727) | |
| Employment status (Unemployed) | ||||
| Self-employed | 1.339 | 2.296** | 1.009 | 1.272 |
| (0.827, 2.166) | (1.167, 4.520) | (0.598, 1.702) | (0.834, 1.941) | |
| Employed | 2.279*** | 2.396*** | 3.390*** | 2.332*** |
| (1.412, 3.681) | (1.322, 4.339) | (2.190, 5.248) | (1.545, 3.522) | |
| Self-infection of COVID-19 | 1.079 | 0.699 | 1.095 | 2.286** |
| (0.507, 2.299) | (0.265, 1.847) | (0.606, 1.980) | (1.142, 4.576) | |
| Family infection of COVID-19 | 3.005*** | 3.607*** | 1.877** | 1.443 |
| (1.416, 6.376) | (1.591, 8.176) | (1.075, 3.278) | (0.840, 2.477) | |
| Family vaccination (No) | ||||
| Yes | 2.816*** | 4.679*** | 8.181*** | 5.766*** |
| (1.951, 4.064) | (2.905, 7.537) | (5.175, 12.93) | (4.070, 8.169) | |
| Not applicable | 0.296*** | 1.308 | 1.347 | 1.121 |
| (0.168, 0.521) | (0.619, 2.767) | (0.377, 4.821) | (0.501, 2.510) | |
| Risk perception of COVID-19 (Unworried) | ||||
| Worried | 2.494*** | 5.627*** | 1.295 | 1.427** |
| (1.765, 3.523) | (3.609, 8.772) | (0.833, 2.014) | (1.020, 1.995) | |
| Uncertain | 0.938 | 4.021*** | 1.279 | 2.308*** |
| (0.572, 1.540) | (1.687, 9.583) | (0.716, 2.284) | (1.247, 4.274) | |
| Source of information on COVID-19 vaccine | ||||
| Television | 1.107 | 1.279 | 0.823 | 1.012 |
| (0.774, 1.585) | (0.849, 1.927) | (0.566, 1.194) | (0.752, 1.361) | |
| Government Call/SMS | 1.159 | 2.414*** | 0.931 | 1.310** |
| (0.807, 1.664) | (1.420, 4.103) | (0.637, 1.361) | (1.004, 1.708) | |
| Family/friends | 1.211 | 0.889 | 0.657** | 0.774* |
| (0.894, 1.641) | (0.559, 1.413) | (0.472, 0.916) | (0.589, 1.016) | |
| Medical professionals | 2.057* | 1.046 | 1.360 | 1.187 |
| (0.931, 4.549) | (0.544, 2.012) | (0.827, 2.236) | (0.849, 1.659) | |
| Religious leaders | 0.0437*** | 2.177 | 0.131 | 1.752* |
| (0.007, 0.265) | (0.672, 7.053) | (0.0112, 1.531) | (0.959, 3.203) | |
| Distance from CVC (Do not know) | ||||
| Less than 2 kms | 1.591** | 1.474 | 4.140*** | 2.273*** |
| (1.029, 2.460) | (0.913, 2.379) | (2.370, 7.233) | (1.528, 3.381) | |
| 2+ kms | 2.163*** | 2.320*** | 3.969*** | 1.765*** |
| (1.511, 3.096) | (1.334, 4.035) | (2.452, 6.423) | (1.171, 2.661) | |
| Any NGO/CBO working in area | 1.384* | 1.165 | 1.657** | 1.334* |
| (0.988, 1.938) | (0.791, 1.717) | (1.093, 2.514) | (1.000, 1.780) | |
| Sought treatment for last illness | 1.758*** | 1.470 | 0.772 | 1.471** |
| (1.236, 2.499) | (0.882, 2.451) | (0.500, 1.192) | (1.078, 2.009) | |
| Constant | 0.365** | 0.293* | 0.00392*** | 0.0306*** |
| (0.144, 0.924) | (0.0852, 1.005) | (0.001, 0.0141) | (0.012, 0.078) | |
| Observations | 1,417 | 1,487 | 1,613 | 1,603 |
| Number of clusters | 110 | 110 | 110 | 110 |
| Intra-class correlation | 0.038 | 0.084 | 0 | 0.087 |
| McKelvey & Zavoina R2 (FE and RE) | 0.401 | 0.434 | 0.584 | 0.423 |
Robust standard errors, CI eform in parentheses
*** p<0.01
** p<0.05
* p<0.1
Discussion
We found that interventions that raised awareness through community mobilization and removed access barriers helped improve vaccine willingness by 7% and uptake by 17% in some low-income and underserved communities. However, there is a two-stage process. In the first, awareness increased and hesitancy decreased, following our awareness interventions. In the second stage, some of those that became convinced took up the vaccines. Uptake was dependent on access to vaccinations, which our interventions addressed only in part.
Our intervention results suggest that raising awareness of COVID-19 vaccination through more personalized means at community levels using printed material in local languages, engaging with community leaders, and building partnerships with local CBOs and NGOs can improve vaccine willingness by changing the behavioral intentions of residents, which is in line with previous literature on the topic [13, 32, 35]. By contrast, merely informing the public through television, the internet or newspaper, etc., i.e., non-personalized means, may be less effective, as was seen in the control area. However, benefits from this approach may saturate beyond a certain point. For example, our interventions were successful in improving vaccine willingness in Bhara Kahu and Dhok Hassu by 7.6 and 6.6 percentage points compared to I-10, but to a lesser extent in G7/F7 where there had already been high willingness at baseline.
While willingness improved, it did not always translate into increased uptake. A major barrier to achieving COVID-19 vaccination coverage in some settlements is the difficulty that residents have in accessing CVCs, which were often several kilometers away. While our set of interventions included some mobile vaccination centers (MVC), these were insufficient to fulfill the extent of demand for vaccination. Thus, vaccine uptake increased the most in G-7/F-7 by 17.1 percentage points compared to the control area, possibly because these areas are located in the center of Islamabad with easier access to multiple CVCs nearby–as compared to Bhara Kahu, a peri-urban slum outside Islamabad, and Dhok Hassu, an urban slum of Rawalpindi.
Table 5 tracks changes in willingness and uptake before and after the intervention. Odds of willingness to receive vaccination which was lower in all urban slums at baseline when compared to the control area became indistinguishable at the endline. Similarly, the odds of willingness for university-educated respondents, which were initially twice as much as those with lesser education, became insignificant. On the other hand, the odds of willingness rose for those that had experienced infection for self or family, if someone was already worried about infections, or if a family member had received vaccination. It appears that the interventions may have helped mitigate the disadvantage of residence in an urban slum or from lower education and accentuated the willingness of those who had encountered infection or vaccines.
Similarly, the odds of uptake of vaccination rose by two-fold in G-7/F-7, which is located in the city center, and for the 18–39 years age groups compared to all older groups. On the other hand, there appeared to be little effect from education or employment and a slight loss of advantage for those with a previous vaccination in the family. In short, in the endline period, there appears to be a homogenization effect in terms of who would take up vaccination, or a loss of disadvantage of the less educated, younger individuals, and residents of marginalized communities.
Our interventions also helped to increase vaccine willingness for people whose family members had a prior experience with COVID-19 but did not affect their uptake, which was more associated with a previous infection for self. Although our results are consistent with a prior study that uses a sample of Pakistan’s adult population to the extent that an incidence of COVID-19 among family members influences perception about COVID-19 vaccination [45], the effect is not strong enough to translate this willingness into action.
Vaccine uptake was higher among those with a previous infection with COVID-19, those with risk-aversion (who were worried about getting infected), and those who sought treatment for their illness. Previous research has shown a positive association between health concerns and vaccine willingness [46–48], therefore our interventions may have nudged them to seek vaccination [49]. This implies that raising awareness, dispelling rumors, and communicating the benefits of COVID-19 vaccines can change the behavior of people who are more concerned about their health.
A prior study on routine immunizations in urban slums of Pakistan found that the source of information also plays an important role in shaping trust and risk perceptions of vaccines [39]. Given the social norms and inaccurate information especially in low-income settlements, people might not get vaccinated due to social hesitancy regarding COVID-19 vaccination. We also found that government calls and SMS about COVID-19 vaccination in the endline were associated with both increased willingness and uptake. Given the high tele-density of cellphone users in Pakistan—85.3% penetration as of October 2021 [50], cellphone campaigns communicating COVID-19 and the benefits of vaccination may be cost-effective.
Limitations
One limitation is that a group (set) of interventions–community outreach through local leaders, local vaccination campaigns, and information–was implemented for all treatment groups. Therefore, we cannot isolate the effect of each intervention to analyze its relative effectiveness. Secondly, although MVCs were deployed in each treatment area and each reached around 150–250 vaccinations a day compared to 30–50 when they merely showed up without our intervention, such MVC visits were too few. Only 5% of the respondents out of the total vaccinated reported that they had been vaccinated through MVCs, suggesting that CVCs were the predominant source of vaccinations and subject to the distance effect mentioned above. This may have limited the impact on vaccination uptake in distant communities (Bara Kahu and Dhok Hassu). Data for previous self and family infection of COVID-19 are self-reported and not verified through laboratory means which may have skewed our results to some extent. The results of vaccine willingness may have suffered from the social desirability bias as some respondents may have provided socially acceptable responses in view of the enumerators, which may not be aligned with their actual intentions. Finally, the baseline and endline were separated by 2 months, during which the national vaccination campaign had ramped up. Some of the homogenization of uptake may be explained by this rather than an intervention effect, although the difference-in-differences analysis shows a significant change.
Conclusion
We show that personalized information campaigns such as community mobilization and direct messaging are superior to general messaging in helping overcome COVID-19 vaccine hesitancy. However, increasing uptake of the vaccine requires an additional step of improving access to vaccination services. Both information and access may be different for various communities and therefore a “one-size-fits-all” approach may need to be better localized. These findings may apply to other vaccinations and possibly to other health initiatives where the public may require motivation to uptake services such as diabetes or hypertension screening or testing. A key lesson is that low-income or marginalized communities would be better served if the services are brought to them locally.
Supporting information
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Data Availability
All relevant data are within the paper and its Supporting Information files.
Funding Statement
This work was supported, in whole or in part, by the Bill & Melinda Gates Foundation [grant number: INV-025171]. Under the grant conditions of the Foundation, a Creative Commons Attribution 4.0 Generic License has already been assigned to the Author Accepted Manuscript version that might arise from this submission. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
References
- 1.John Hopkins University. Coronavirus Resource Center. 2022 [cited 15 Jul 2022]. Available: https://coronavirus.jhu.edu/
- 2.Schneiders ML, Naemiratch B, Cheah PK, Cuman G, Poomchaichote T, Ruangkajorn S, et al. The impact of COVID-19 non-pharmaceutical interventions on the lived experiences of people living in Thailand, Malaysia, Italy and the United Kingdom: A cross-country qualitative study. PLoS One. 2022;17: e0262421. doi: 10.1371/journal.pone.0262421 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Rosiello DF, Anwar S, Yufika A, Adam RY, Ismaeil MI, Ismail AY, et al. Acceptance of COVID-19 vaccination at different hypothetical efficacy and safety levels in ten countries in Asia, Africa, and South America. Narra J. 2021;1. doi: 10.52225/NARRA.V1I3.55 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Rayhan MA, Mudatsir M, Nurjannah N, Ichsan I, Amir-Behghadami M, Khader YS, et al. Acceptance and willingness to purchase a hypothetical COVID-19 vaccine in a region under Shariah law: A cross-sectional study in Aceh, Indonesia. Narra J. 2022;2. doi: 10.52225/NARRA.V2I2.85 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Opel DJ, Diekema DS, Ross LF. Should We Mandate a COVID-19 Vaccine for Children? JAMA Pediatr. 2021;175: 125–126. doi: 10.1001/jamapediatrics.2020.3019 [DOI] [PubMed] [Google Scholar]
- 6.Ross LF, Opel DJ. The case against COVID-19 vaccine mandates in pediatric solid organ transplantation. Pediatr Transplant. 20220212th ed. 2022; e14243. doi: 10.1111/petr.14243 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Buckley RM. Targeting the World’s Slums as Fat Tails in the Distribution of COVID-19 Cases. Journal of Urban Health. Journal of Urban Health; 2020. pp. 358–364. doi: 10.1007/s11524-020-00450-w [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Mehrolhassani MH, Yazdi-Feyzabadi V, Rafiee N, Ghasemi S. Health protection challenges of slums residents during the COVID-19 pandemic, according to the social determinants of health framework: A case study of Kerman city in Iran. J Educ Health Promot. 2022;11: 197. doi: 10.4103/jehp.jehp_958_21 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Armand A, Augsburg B, Bancalari A, Augsburg B. Coping with COVID-19 in Slums Evidence from India. 2020. [cited 17 Dec 2021]. Available: https://www.theigc.org/wp-content/uploads/2021/01/Armand-et al. -2020-Final-report.pdf [Google Scholar]
- 10.Winayanti L, Lang HC. Provision of urban services in an informal settlement: a case study of Kampung Penas Tanggul, Jakarta. Habitat Int. 2004;28: 41–65. doi: 10.1016/S0197-3975(02)00072-3 [DOI] [Google Scholar]
- 11.Minnery J, Argo T, Winarso H, Hau D, Veneracion CC, Forbes D, et al. Slum upgrading and urban governance: Case studies in three South East Asian cities. Habitat Int. 2013;39: 162–169. doi: 10.1016/J.HABITATINT.2012.12.002 [DOI] [Google Scholar]
- 12.Sheridan D, Njogu M, Maki A, Agyemang F. Voicing the urban poor: experience from an energy justice program for and by slum dwellers Electronic reference. F Actions Sci Reports. 2020; 46–51. Available: http://journals.openedition.org/factsreports/6287 [Google Scholar]
- 13.Razai MS, Chaudhry UAR, Doerholt K, Bauld L, Majeed A. Covid-19 vaccination hesitancy. BMJ. 2021;373: 1136–1139. doi: 10.1136/bmj.n1138 [DOI] [PubMed] [Google Scholar]
- 14.Clouston S, Kidman R, Palermo T. Social inequalities in vaccination uptake among children aged 0–59 months living in Madagascar: An analysis of Demographic and Health Survey data from 2008 to 2009. Vaccine. 2014;32: 3533–3539. doi: 10.1016/j.vaccine.2014.04.030 [DOI] [PubMed] [Google Scholar]
- 15.Opel DJ, Lo B, Peek ME. Addressing mistrust about COVID-19 vaccines among patients of color. Ann Intern Med. 20210209th ed. 2021;174: 698–700. doi: 10.7326/M21-0055 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Opel DJ, Salmon DA, Marcuse EK. Building Trust to Achieve Confidence in COVID-19 Vaccines. JAMA Netw open. 20201001st ed. 2020;3: e2025672. doi: 10.1001/jamanetworkopen.2020.25672 [DOI] [PubMed] [Google Scholar]
- 17.Simione L, Vagni M, Gnagnarella C, Bersani G, Pajardi D. Mistrust and Beliefs in Conspiracy Theories Differently Mediate the Effects of Psychological Factors on Propensity for COVID-19 Vaccine. Front Psychol. 20210707th ed. 2021;12: 683684. doi: 10.3389/fpsyg.2021.683684 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Omer SB, Benjamin RM, Brewer NT, Buttenheim AM, Callaghan T, Caplan A, et al. Promoting COVID-19 vaccine acceptance: recommendations from the Lancet Commission on Vaccine Refusal, Acceptance, and Demand in the USA. Lancet. 20211115th ed. 2021;398: 2186–2192. doi: 10.1016/S0140-6736(21)02507-1 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Ellis P, Roberts M. Leveraging Urbanization in South Asia: Managing Spatial Transformation for Prosperity and Livability. World Bank. Washington, DC: Washington, DC: World Bank; 2016. doi: 10.1596/978-1-4648-0662-9 [DOI] [Google Scholar]
- 20.Solís Arce JS, Warren SS, Meriggi NF, Scacco A, McMurry N, Voors M, et al. COVID-19 vaccine acceptance and hesitancy in low- and middle-income countries. Nat Med. 20210716th ed. 2021;27: 1385–1394. doi: 10.1038/s41591-021-01454-y [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Abedin M, Islam MA, Rahman FN, Reza HM, Hossain MZ, Hossain MA, et al. Willingness to vaccinate against COVID-19 among Bangladeshi adults: Understanding the strategies to optimize vaccination coverage. PLoS One. 2021;16: e0250495. doi: 10.1371/journal.pone.0250495 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Guidry JPD, Laestadius LI, Vraga EK, Miller CA, Perrin PB, Burton CW, et al. Willingness to get the COVID-19 vaccine with and without emergency use authorization. Am J Infect Control. 20201120th ed. 2021;49: 137–142. doi: 10.1016/j.ajic.2020.11.018 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Lin Y, Hu Z, Zhao Q, Alias H, Danaee M, Wong LP. Understanding COVID-19 vaccine demand and hesitancy: A nationwide online survey in China. PLoS Negl Trop Dis. 20201217th ed. 2020;14: e0008961. doi: 10.1371/journal.pntd.0008961 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Walker AN, Zhang T, Peng XQ, Ge JJ, Gu H, You H. Vaccine acceptance and its influencing factors: An online cross-sectional study among international college students studying in china. Vaccines. 20210602nd ed. 2021;9: 585. doi: 10.3390/vaccines9060585 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Joshi A, Kaur M, Kaur R, Grover A, Nash D, El-Mohandes A. Predictors of COVID-19 Vaccine Acceptance, Intention, and Hesitancy: A Scoping Review. Front Public Heal. 20210813th ed. 2021;9: 1152. doi: 10.3389/fpubh.2021.698111 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26.Loomba S, de Figueiredo A, Piatek SJ, de Graaf K, Larson HJ. Measuring the impact of COVID-19 vaccine misinformation on vaccination intent in the UK and USA. Nat Hum Behav. 20210205th ed. 2021;5: 337–348. doi: 10.1038/s41562-021-01056-1 [DOI] [PubMed] [Google Scholar]
- 27.Cerda AA, García LY. Hesitation and Refusal Factors in Individuals’ Decision-Making Processes Regarding a Coronavirus Disease 2019 Vaccination. Front Public Heal. 20210421st ed. 2021;9: 229. doi: 10.3389/fpubh.2021.626852 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Zewude B, Habtegiorgis T. Willingness to Take COVID-19 Vaccine Among People Most at Risk of Exposure in Southern Ethiopia. Pragmatic Obs Res. 2021;Volume 12: 37–47. doi: 10.2147/POR.S313991 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29.Hossain MB, Alam MZ, Islam MS, Sultan S, Faysal MM, Rima S, et al. Health Belief Model, Theory of Planned Behavior, or Psychological Antecedents: What Predicts COVID-19 Vaccine Hesitancy Better Among the Bangladeshi Adults? Front Public Heal. 20210816th ed. 2021;9: 1172. doi: 10.3389/fpubh.2021.711066 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.Ajzen I. The theory of planned behavior. Organ Behav Hum Decis Process. 1991;50: 179–211. doi: 10.1016/0749-5978(91)90020-T [DOI] [Google Scholar]
- 31.Ullah I, Lin CY, Malik NI, Wu TY, Araban M, Griffiths MD, et al. Factors affecting Pakistani young adults’ intentions to uptake COVID-19 vaccination: An extension of the theory of planned behavior. Brain Behav. 20210920th ed. 2021;11: e2370. doi: 10.1002/brb3.2370 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Dutta T, Agley J, Meyerson BE, Barnes PA, Sherwood-Laughlin C, Nicholson-Crotty J. Perceived enablers and barriers of community engagement for vaccination in India: Using socioecological analysis. PLoS One. 2021;16. doi: 10.1371/journal.pone.0253318 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33.World Health Organisation. Conducting community engagement for COVID-19 vaccines: interim guidance. Geneva; 2021. Available: https://www.who.int/publications/i/item/WHO-2019-nCoV-vaccination-community-engagement-2021.1
- 34.Olufadewa II, Adesina MA, Ekpo MD, Akinloye SJ, Iyanda TO, Nwachukwu P, et al. Lessons from the coronavirus disease 2019 (COVID-19) pandemic response in China, Italy, and the U.S.: a guide for Africa and low- and middle-income countries. Glob Heal J. 2021;5: 56–61. doi: 10.1016/j.glohj.2021.02.003 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Sabarwal S, Bhatia R, Dhody B, Perumal S, Howard W, Puri J. Engaging communities for increasing immunisation coverage What do we know? July 2015 Scoping Paper 3. 2015. [cited 10 Dec 2021]. Available: https://www.3ieimpact.org/sites/default/files/2019-01/3ie_immunisation_scoping_report_3.pdf [Google Scholar]
- 36.Amin R, Li Y. NGO-Promoted women’s credit program, immunization coverage, and child mortality in rural Bangladesh. Women Heal. 1997;25: 71–87. doi: 10.1300/J013v25n01_05 [DOI] [PubMed] [Google Scholar]
- 37.Ahmed KA, Grundy J, Hashmat L, Ahmed I, Farrukh S, Bersonda D, et al. An analysis of the gender and social determinants of health in urban poor areas of the most populated cities of Pakistan. Int J Equity Health. 2022;21: 52. doi: 10.1186/s12939-022-01657-w [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38.Crocker-Buque T, Mindra G, Duncan R, Mounier-Jack S. Immunization, urbanization and slums—A systematic review of factors and interventions. BMC Public Health. 2017;17. doi: 10.1186/S12889-017-4473-7 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 39.Yazdani AT, Muhammad A, Nisar MI, Khan U, Shafiq Y. Unveiling and addressing implementation barriers to routine immunization in the peri-urban slums of Karachi, Pakistan: a mixed-methods study. Heal Res Policy Syst. 2021;19: 1–9. doi: 10.1186/s12961-021-00691-4 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 40.UNICEF. MULTIPLE INDICATOR CLUSTER SURVEY MANUAL 2005. New York, USA.: Division of Communication, UNICEF; 2005. Available: https://mics.unicef.org/files?job=W1siZiIsIjIwMTUvMDQvMDIvMDYvMzcvMDYvMTE5L011bHRpcGxlX0luZGljYXRvcl9DbHVzdGVyX1N1cnZleV9NYW51YWxfMjAwNS5wZGYiXV0&sha=dd2e54d1ddd61cdb [Google Scholar]
- 41.Banerjee AV, Duflo E, Glennerster R, Kothari D. Improving immunisation coverage in rural India: Clustered randomised controlled evaluation of immunisation campaigns with and without incentives. BMJ. 2010;340: 1291. doi: 10.1136/bmj.c2220 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.Bruhn M, McKenzie D. In pursuit of balance: Randomization in practice in development field experiments. Am Econ J Appl Econ. 2009;1: 200–232. doi: 10.1257/app.1.4.200 [DOI] [Google Scholar]
- 43.Puhani PA. The treatment effect, the cross difference, and the interaction term in nonlinear “difference-in-differences” models. Econ Lett. 2012;115: 85–87. doi: 10.1016/j.econlet.2011.11.025 [DOI] [Google Scholar]
- 44.Langer W. Stata Page. 2019 [cited 6 Dec 2021]. Available: https://langer.soziologie.uni-halle.de/stata/index.html
- 45.Hawlader MDH, Rahman ML, Nazir A, Ara T, Haque MMA, Saha S, et al. COVID-19 vaccine acceptance in South Asia: a multi-country study. Int J Infect Dis. 2022;114: 1–10. doi: 10.1016/j.ijid.2021.09.056 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 46.Qamar MA, Irfan O, Dhillon RA, Bhatti A, Sajid MI, Awan S, et al. Acceptance of COVID-19 Vaccine in Pakistan: A Nationwide Cross-Sectional Study. Cureus. 2021;13: e16603. doi: 10.7759/cureus.16603 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 47.Ahmed TF, Ahmed A, Ahmed S, Ahmed HU. Understanding COVID-19 vaccine acceptance in Pakistan: an echo of previous immunizations or prospect of change? Expert Rev Vaccines. 2021;20: 1185–1193. doi: 10.1080/14760584.2021.1964963 [DOI] [PubMed] [Google Scholar]
- 48.Zakar R, Momina A ul, Shahzad S, Hayee M, Shahzad R, Zakar MZ. COVID-19 Vaccination Hesitancy or Acceptance and Its Associated Factors: Findings from Post-Vaccination Cross-Sectional Survey from Punjab Pakistan. Int J Environ Res Public Health. 2022;19. doi: 10.3390/ijerph19031305 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 49.Ledderer L, Kjær M, Madsen EK, Busch J, Fage-Butler A. Nudging in Public Health Lifestyle Interventions: A Systematic Literature Review and Metasynthesis. Heal Educ Behav Off Publ Soc Public Heal Educ. 2020;47: 749–764. doi: 10.1177/1090198120931788 [DOI] [PubMed] [Google Scholar]
- 50.Pakistan Telecom Authorities. Telecom Indicators in Pakistan| PTA. In: Pta [Internet]. 2021 [cited 17 Dec 2021]. Available: https://www.pta.gov.pk/en/telecom-indicators
