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BMC Infectious Diseases logoLink to BMC Infectious Diseases
. 2021 Sep 8;21:928. doi: 10.1186/s12879-021-06604-8

Impact of the Covid-19 epidemic and related social distancing regulations on social contact and SARS-CoV-2 transmission potential in rural South Africa: analysis of repeated cross-sectional surveys

Nicky McCreesh 1, Vuyiswa Dlamini 2, Anita Edwards 2, Stephen Olivier 2, Njabulo Dayi 2, Keabetswe Dikgale 2, Siyabonga Nxumalo 2, Jaco Dreyer 2, Kathy Baisley 1,2, Mark J Siedner 3, Richard G White 1, Kobus Herbst 2,4, Alison D Grant 2,5,6,7, Guy Harling 2,8,9,10,
PMCID: PMC8424154  PMID: 34496771

Abstract

Background

South Africa implemented rapid and strict physical distancing regulations to minimize SARS-CoV-2 epidemic spread. Evidence on the impact of such measures on interpersonal contact in rural and lower-income settings is limited.

Methods

We compared population-representative social contact surveys conducted in the same rural KwaZulu-Natal location once in 2019 and twice in mid-2020. Respondents reported characteristics of physical and conversational (‘close interaction’) contacts over 24 hours. We built age-mixing matrices and estimated the proportional change in the SARS-CoV-2 reproduction number (R0). Respondents also reported counts of others present at locations visited and transport used, from which we evaluated change in potential exposure to airborne infection due to shared indoor space (‘shared air’).

Results

Respondents in March–December 2019 (n = 1704) reported a mean of 7.4 close interaction contacts and 196 shared air person-hours beyond their homes. Respondents in June-July 2020 (n = 216), as the epidemic peaked locally, reported 4.1 close interaction contacts and 21 shared air person-hours outside their home, with significant declines in others’ homes and public spaces. Adults aged over 50 had fewer close contacts with others over 50, but little change in contact with 15–29 year olds, reflecting ongoing contact within multigenerational households. We estimate potential R0 fell by 42% (95% plausible range 14–59%) between 2019 and June-July 2020.

Conclusions

Extra-household social contact fell substantially following imposition of Covid-19 distancing regulations in rural South Africa. Ongoing contact within intergenerational households highlighted a potential limitation of social distancing measures in protecting older adults.

Supplementary Information

The online version contains supplementary material available at 10.1186/s12879-021-06604-8.

Keywords: COVID-19, Contact survey, Reproduction number, Social contacts, Indoor

Background

The rapid spread of SARS-CoV-2 in 2020 has harmed populations both directly through Covid-19 morbidity and mortality, and indirectly via both less support for other health conditions [1, 2] and economic impacts arising from government-imposed and self-directed reductions in social interaction [3, 4]. Local physical distancing regulations including mandatory ‘stay at home’ orders, restrictions on public gatherings, and banning of inter-household contact have been common during the pandemic [5]. Such non-pharmaceutical interventions (NPI) were variably implemented and often enforced more stringently in lower-income settings in sub-Saharan Africa [6]. Understanding the impact of both NPIs and personal decisions is vital to determining trade-offs between epidemic control and non-Covid wellbeing.

The impact of NPIs is likely to vary substantially across countries, reflecting differences in both demographic composition and social dynamics. There is particular concern that official movement limitations may have limited impact in settings where informal work is common and economic safety nets are limited [7, 8]. These concerns will be particularly important if the global pandemic follows the example of past infectious diseases and has its greatest impact on marginalized and previously disadvantaged populations [9, 10].

Quantitative data on relevant interpersonal interaction are central to such assessments, both directly for planning locally relevant evidence-based responses and for parameterisation of mathematical models of SARS-CoV-2 transmission and control policies. Movement data from sources linked to smartphones can indicate likely changes in contact patterns, they do not account for the detailed, non-random social interaction that often typifies human behaviour [11], and in settings with low smartphone penetration, reliance on such data can lead to biased results.

Detailed quantitative social contact surveys have been conducted during the Covid-19 pandemic, primarily in higher-income settings. These include online surveys using de novo convenience recruitment in Europe [12, 13], and existing online panels in Europe [14, 15] and the United States [16]. Telephonic surveys have been conducted using random digit dialling in China [17], and existing cohorts in Kenya [18].

Maximizing the benefit of these Covid-19 social contact studies requires careful study design. First, a clear sampling frame rather than a convenience sample allows stronger inference to a source population. Second, having comparable pre-pandemic data allows a clear measure of change to be assessed—there is danger of recall bias if questions are asked retrospectively about pre-pandemic days, and of secular change prior to Covid-19 if using previously collected data from too long ago. Third, longitudinal data within the epidemic’s progress allows judgement of the effects of changing policy and compliance willingness. Fourth, given evidence for aerosolized SARS-CoV-2 transmission [19], adding information on contact-time occurring in indoor congregate settings and transport can broaden our understanding of risk.

South Africa implemented an early, stringent national lockdown in March 2020, which may have initially delayed the national epidemic [20]; however regulations were relaxed from May onwards and case numbers increased rapidly, peaking in July before falling back. In this paper, we compare data from two studies conducted using comparable study instruments in 2019 and 2020, both using samples drawn from the same census sampling frame in rural South Africa. The 2020 data include two rounds of data collection, covering the first wave of Covid-19 in the local area. We use these data to estimate the reduction in potential reproduction number of SARS-CoV-2 between surveys, and to determine where contact beyond the home continued during lockdown periods.

Methods

We used data from two surveys conducted in the southern section of the Africa Health Research Institute (AHRI) demographic surveillance area in 2019 and 2020 [21]. AHRI maintains an active thrice-yearly census of all households ~ 21,000 households in this area of ~ 850 km2 in rural uMkhanyakude district, KwaZulu-Natal province, including one small town [22]. uMkhanyakude ranks among the most deprived districts nationally in terms of health and socioeconomic status.

The 2019 data were collected as part of Umoya omuhle (UO), a programme exploring novel approaches to prevention of drug-resistant Mtb transmission in health facilities [23]. UO sampled 3093 census adults (aged 18 and above) residing within the census surveillance area and the catchment area of two primary care centres (one in town, one rural). Sampling was random, stratified by residential area (~ 350 households per area) and with probability proportional to the number of eligible people in each area, based on the most recent census conducted prior to area entry. Data collection was conducted March to December 2019 at respondents’ homes.

The 2020 data were collected as part of a longitudinal Covid-19 surveillance project [24]. The Covid Social Contact (CSC) sub-study used an age/sex stratified sample of one person aged 15 and above from each of 400 census households. Inclusion criteria included participation in Vuk’uzazi, a recent population-wide chronic health screening study [25], allowing intentional oversampling of individuals with locally prevalent health conditions (tuberculosis, hypertension, diabetes, obesity, COPD or asthma). Contact was made telephonically based on previously provided numbers. We analysed two rounds of data collected between 3 June and 16 July (2020 R1), and 16 July and 17 August (2020 R2), as Covid-19 peaked in KwaZulu-Natal (Fig. 1).

Fig. 1.

Fig. 1

South African smoothed Covid-19 case incidence rate, government lockdown and 2020 survey dates in 2020. Levels refer to national non-pharmaceutical interventions (“lockdown”) with strictness declining from level 5 over time (details on interventions at each level in Additional file 1: Material S2). Incidence rates are 7-day running mean values computed from case data collated at [26]

Both studies used structured electronic REDCap interviews (Additional file 1: Material S1). After confirming socio-demographic characteristics, respondents were asked to report on three forms of in-person social interaction. First, they were asked to list all indoor locations visited over a 24 h period. UO asked about a randomly selected day in the past week; CSC asked about the day prior to interview, limiting data largely to Sunday to Thursday. Follow up questions covered the type of location, length of time spent there and the number of people present. Second, respondents were asked who they had directly interacted with over the 24 h period – involving either physical contact or a minimum-three-word conversation (‘close interaction contact’). Respondents were then for each such close interaction contact asked to report their ages and sexes and the duration of time spent together; UO asked these follow-up questions about a random 10 contacts, or all contacts if 10 or fewer were reported while CSC asked about all contacts. Third, respondents were asked about any transport used over the past day, and then how long any trips took and many people shared the transport with them. CSC only asked buildings and transport questions to a random half of sampled individuals per round.

Statistical analyses

We grouped respondents and their close interaction contacts by age into four categories (15–29, 30–49, 50–64 and 65 +) and described respondent characteristics for each survey round. All subsequent analyses weighted the data for sampling and non-response to match the census population and to make methods comparable across surveys (further details in Additional file 1: Material S3). We first calculated the mean number of close interaction contacts per person per day by respondent characteristics (sex, age, household size) and by whether the contact was a household member. We then built social contact age mixing matrices for each round, adjusting our raw results to ensure that the matrices were symmetric using the census population age structure. From these values we calculated the change between 2019 and each 2020 round.

In the absence of a robust estimate of the basic reproduction number (R0) for SARS-CoV-2 in rural South Africa without social distancing (i.e., with 2019 social contact patterns), we estimated the relative reduction in R0 between rounds, assuming the per-contact transmission probability remained constant. (Actual reductions will have been greater to the extent that face coverage increased in 2020 but we cannot precisely estimate either the degree to which this occurred, especially within households, or the degree of protection conferred.) For our estimated reduction we used the next generation matrix of the age-contact matrix, defining R0 as the dominant eigenvalue [27]. To assess uncertainty, we generated mean and 95% plausible intervals using 10,000 independent bootstrapped samples of each survey, and calculated the relative reduction in each pair of samples. The bootstrapped samples were generated by re-sampling respondents with replacement within age categories, and re-sampling contacts with replacement from the set of all contacts of the respondent [28].

Finally, we calculated the change in potential exposure to airborne infection using location and transport data by calculating for each respondent per day: the proportion who visited any location/transport type; mean hours spent in the location if visited; mean people present per visit; mean ‘shared air person-hours’ if visited; and finally mean shared air person-hours across all respondents. For this analysis we merged the two CSC rounds since each respondent provided one datapoint. We tested for significant differences in each measure using logistic or linear bivariate regression including indicator variables for study round.

We conducted several sensitivity analyses: (i) including only data on Sundays to Thursdays, giving each day equal weight, to compare only same-day data across the two surveys; (ii) excluding respondents with any missing close interaction contact age data; iii) excluding close interaction contacts of less than 15 min duration, as the probability of transmission is lower for shorter contact durations [29, 30]; iv) incorporating children into our analysis, using UO and CSC data on adult-reported contact with children, and past South African data about child-child contacts; (v) including only individuals aged ≥ 18, to make the two datasets comparable on age range; (vi) limiting UO data to the period June–August 2019 to ensure seasonal comparability; (vii) weighted the 2019 data to the full census population based on urbanicity (further details in Additional file 1: Material S3).

Ethical approval for UO was granted by the Biomedical Research Ethics Committee (REC) of the University of KwaZulu-Natal (UKZN) (BE662/17) and the London School of Hygiene & Tropical Medicine (14,640); ethical approval for CSC was granted by UKZN BREC (BE290/16) and University College London REC (15231/013). Informed consent for participation was recorded in writing for UO and telephonically for CSC.

Results

Of the 3093 people sampled for UO, 1723 (56%) were successfully contacted, 299 (10%) were dead or reported to have out-migrated, and 1071 (35%) could not be contacted. Of those successfully contacted, 1704 (99%) completed an interview. Of the 400 individuals sampled for CSC, 27 (7%) were dead or had out-migrated, and 102 (26%) could not be contacted. Of those successfully contacted, 216 (80%) completed an interview. At R2 follow-up, 202 of the 216 (94%) completed a second interview and eight previously uncontactable individuals were reached for a first interview. The raw age-sex structures of UO and CSC differed from one-another by design (Table 1).

Table 1.

Descriptive statistics of respondents to the Umoya omuhle (2019) and Covid Social Contacts (2020) studies

2019 2020 R1: June-July 2020 R2: July–August
All Close contact Buildings & transport Close contact Buildings & transport Census population
Age
 15–29 613 36% 36 17% 15 14% 32 15% 17 17% 42%
 30–49 535 31% 50 23% 28 26% 47 22% 23 23% 33%
 50–64 342 20% 64 30% 35 33% 65 31% 28 28% 16%
 65 +  214 13% 66 31% 29 27% 66 31% 33 33% 10%
Sex
 Male 751 44% 101 47% 49 46% 97 46% 48 48% 42%
 Female 953 56% 115 53% 58 54% 113 54% 53 52% 58%
Household size
 1–3 293 17% 61 28% 33 31% 62 30% 27 27% 19%
 4–6 426 25% 60 28% 28 26% 60 29% 29 29% 34%
 7–9 429 25% 54 25% 29 27% 48 23% 22 22% 25%
 10 +  556 33% 41 19% 17 16% 40 19% 23 23% 22%
Residence
 Urban/peri-urban 837 49% 85 39% 37 35% 84 40% 41 41% 32%
 Rural 867 51% 131 61% 70 65% 125 60% 59 58% 59%
 Unknown 0 0 0 1 0.5% 1 1.0% 0.4%
Day reported
 Monday 239 14% 49 23% 22 21% 25 12% 15 15%
 Tuesday 242 14% 52 24% 24 22% 26 12% 12 12%
 Wednesday 239 14% 37 17% 20 19% 73 35% 35 35%
 Thursday 251 15% 40 19% 24 22% 70 33% 33 33%
 Friday 261 15% 0 0 1 0% 1 1%
 Saturday 245 14% 0 0 0 0
 Sunday 227 13% 38 18% 17 16% 15 7% 5 5%
Total 1704 216 107 210 101 36 311

Values are counts and percentages. Census population refers to proportions of residents aged 15 + in the area

The mean number of close interaction contacts varied little by respondent age, sex or household size within rounds, although numbers were lower in the highest age group, and were positively associated with household size (Table 2). Respondents reported a mean of 7.4 close interaction contacts in 2019 (95%CI: 7.1–7.7), 4.1 (95%CI: 3.5–4.6) in 2020 R1 and 4.3 (95%CI: 3.8–4.8) in 2020 R2. Contact reductions were larger for non-household than household member contacts in both absolute and relative terms. Non-household contacts fell from 2.8 (95%CI 2.6–3.1) in 2019 to 0.7 (95%CI 0.4–1.1) in 2020 R1 and 0.5 (95% CI 0.3–0.7) in 2020 R2. Household contacts fell from 4.6 (95% CI 4.5–4.8) in 2019 to 3.4 (95% CI 2.9–3.8) in 2020 R1 and 3.8 (95% CI 3.3–4.3) in 2020 R2.

Table 2.

Mean close contact numbers by respondent characteristics

2019 2020 R1 p-value 2020 R2 p-value
All contacts 7.4 [7.1–7.7] 4.2 [3.5–5.0]  < 0.001 4.3 [3.3–5.8]  < 0.001
Age
 15–29 8.1 [7.6–8.6] 4.7 [3.3–6.8]  < 0.001 4.6 [3.5–5.9]  < 0.001
 30–49 7.0 [6.7–7.4] 3.6 [2.9–4.4]  < 0.001 4.0 [3.2–5.1]  < 0.001
 50–64 7.2 [6.5–8.0] 4.8 [3.7–6.2] 0.001 4.8 [3.7–6.2] 0.001
 65 +  6.1 [5.5–6.7] 3.3 [2.7–4.0]  < 0.001 3.4 [2.7–4.2]  < 0.001
Sex
 Male 7.1 [6.7–7.5] 4.6 [3.3–6.3] 0.001 3.4 [2.6–4.5]  < 0.001
 Female 7.6 [7.3–8.0] 4.0 [3.3–4.7]  < 0.001 4.9 [4.2–5.6]  < 0.001
Household size
 1–3 6.1 [5.4–6.9] 2.6 [2.0–3.3]  < 0.001 2.2 [1.4–3.4]  < 0.001
 4–6 6.9 [6.4–7.4] 4.0 [3.4–4.8]  < 0.001 4.0 [3.3–4.8]  < 0.001
 7–9 7.6 [7.1–8.2] 4.2 [3.4–5.1]  < 0.001 4.7 [3.9–5.7]  < 0.001
 10 +  8.3 [7.9–8.8] 5.8 [3.6–9.2] 0.054 6.0 [4.6–7.7] 0.002
Residence
 Urban/peri-urban 7.1 [6.7–7.5] 4.5 [3.6–5.7]  < 0.001 4.4 [3.3–5.8]  < 0.001
 Rural 7.7 [7.3–8.1] 4.0 [3.1–5.2]  < 0.001 4.4 [3.8–5.0]  < 0.001
All household members 4.6 [4.5–4.8] 3.4 [3.0–3.9]  < 0.001 3.8 [3.3–4.4] 0.01
Age
 15–29 4.8 [4.6–5.1] 3.6 [2.7–4.8] 0.018 4.1 [3.0–5.4] 0.19
 30–49 4.4 [4.2–4.7] 2.9 [2.3–3.6]  < 0.001 3.6 [2.7–4.6] 0.066
 50–64 4.5 [4.2–4.9] 4.2 [3.3–5.5] 0.58 4.0 [3.2–5.1] 0.032
 65 +  4.6 [4.1–5.1] 3.0 [2.5–3.7]  < 0.001 3.1 [2.5–3.9] 0.001
Sex
 Male 3.9 [3.7–4.1] 3.3 [2.7–4.1] 0.090 2.7 [2.0–3.6] 0.002
 Female 5.1 [4.9–5.4] 3.5 [2.9–4.2]  < 0.001 4.5 [3.9–5.2] 0.073
Household size
 1–3 3.2 [2.9–3.5] 1.6 [1.2–2.2]  < 0.001 1.5 [1.0–2.4]  < 0.001
 4–6 3.9 [3.7–4.2] 3.4 [2.9–3.9] 0.025 3.3 [2.7–4.2] 0.11
 7–9 4.8 [4.6–5.1] 3.8 [3.1–4.6] 0.012 4.5 [3.7–5.5] 0.50
 10 +  5.7 [5.4–6.1] 4.5 [3.1–6.6] 0.15 5.3 [4.1–6.8] 0.52
Residence
 Urban/peri-urban 4.3 [4.1–4.6] 3.8 [2.9–4.9] 0.298 3.7 [2.7–5.0] 0.26
 Rural 5.0 [4.8–5.3] 3.3 [2.8–3.9]  < 0.001 4.0 [3.4–4.7] < 0.001
All non-household members 2.8 [2.6–3.1] 0.78 [0.44–1.4]  < 0.001 0.52 [0.52–0.32]  < 0.001
Age
 15–29 3.3 [2.9–3.7] 1.2 [0.42–3.2] < 0.001 0.52 [0.52–0.19]  < 0.001
 30–49 2.7 [2.4–3.0] 0.69 [0.40–1.2]  < 0.001 0.48 [0.48–0.20]  < 0.001
 50–64 2.7 [2.0–3.5] 0.53 [0.24–1.1]  < 0.001 0.76 [0.76–0.39]  < 0.001
 65 +  1.6 [1.2–2.1] 0.28 [0.14–0.54]  < 0.001 0.26 [0.26–0.10]  < 0.001
Sex
 Male 3.3 [2.9–3.7] 1.3 [0.53–3.1] < 0.001 0.79 [0.79–0.41]  < 0.001
 Female 2.5 [2.2–2.9] 0.48 [0.31–0.75]  < 0.001 0.36 [0.36–0.18]  < 0.001
Household size
 1–3 3.0 [2.4–3.8] 1.0 [0.59–1.6]  < 0.001 0.62 [0.62–0.25]  < 0.001
 4–6 3.0 [2.5–3.5] 0.66 [0.38–1.2]  < 0.001 0.68 [0.68–0.32]  < 0.001
 7–9 2.8 [2.4–3.4] 0.37 [0.16–0.85]  < 0.001 0.20 [0.20–0.06]  < 0.001
 10 +  2.6 [2.3–3.0] 1.3 [0.32–5.1] 0.13 0.67 [0.67–0.23]  < 0.001
Residence
Urban/peri-urban 2.8 [2.5–3.1] 0.73 [0.45–1.2]  < 0.001 0.71 [0.71–0.38]  < 0.001
Rural 2.7 [2.4–3.0] 0.70 [0.24–2.1]  < 0.001 0.39 [0.39–0.16]  < 0.001

Values are means with 95% confidence intervals in brackets. p-values are for comparisons within rows vs. 2019 data

In 2019 weighted age-mixing matrices, older individuals had fewer close interaction contacts than younger ones, and contact rates for each age group under 65 were highest within the same age group. By June/July 2020 (2020 R1), contact rates were lower for all age combinations, in most cases statistically significantly. The drop was greatest for contact between those aged 65 + , and smallest for contact between those aged 15–29 and 50–64. The drops in contacts adults reported having with children were lower than for between adults, and in most adult age groups the data were consistent with no change in contact rates between adults and children (Additional file 1: Material S4, panel 4). Contact patterns by age changed little between 2020 R1 and R2. The estimated reduction in R0 between 2019 and 2020 R1 was 45% (95% plausible range 14–59%), and between 2019 and 2020 R2 was 45% (95% plausible range 24–61%) (Fig. 2, a-c).

Fig. 2.

Fig. 2

Age-stratified mean (95% plausible range) number of close contacts from survey respondents. Graphs ac show the mean number of contacts respondents in each age group reported, by contact age group. Graphs df show the mean rate of contact between respondents in each age group and each other person in the target population, by contact age group. Graph g shows the overall estimated relative reduction in R0 from 2019 to 2020. Graphs h and I show the estimated proportional reductions in contact between age groups from 2019 to 2020. *Numbers shown are rates × 105

Sharing of indoor space more generally also fell between 2019 and mid-2020: mean shared air person-time beyond respondents’ own homes (including transport) fell from 196 to 21 person-contact hours (Table 3). Mean time spent at one’s own home rose by almost three hours per day, from an average of 19 to 22 hours, although there was no significant change in person-contact hours. All other location types except public transport saw substantially reduced overall person-contact hours, largely due to fewer people present in the location, rather than changes in the time spent per visit. The proportion of people reporting clinic visits almost doubled, from 2.3% to 4.3%, although the change was not significant (p = 0.20). The proportion of respondents who reported visiting other people’s households and ‘other’ locations fell, from 27 to 6%, and 32% to 24%, respectively.

Table 3.

Location and transport patterns of respondents in 2019 and 2020

Location Proportion visited (%) p-value Hours if visited p-value People per visit p-value Contact-hours if visited p-value Contact-hours p-value
Own home 2019 98.6 [97.9, 99.1] 19.0 [18.7, 19.2] 5.34 [5.18, 5.50] 107 [103, 111] 106 [102, 110]
2020 96.2 [88.7, 98.8] 0.11 21.9 [20.9, 22.9]  < 0.001 5.63 [4.96, 6.39] 0.43 121 [104, 140] 0.14 116 [99.6, 136] 0.26
Other house 2019 26.9 [24.8, 29.1] 6.2 [5.72, 6.77] 10.7 [6.90, 16.6] 71.3 [48.4, 105] 19.1 [12.9, 28.4]
2020 6.26 [2.89, 13.9]  < 0.001 12.8 [6.15, 26.7] 0.11 2.67 [2.02, 3.53]  < 0.001 33.1 [16.8, 65.2] 0.027 2.07 [0.63, 6.81]  < 0.001
Clinic 2019 2.27 [1.65, 3.12] 5.08 [3.76, 6.85] 135 [67.6, 269] 561 [258, 1219] 12.8 [5.72, 28.4]
2020 4.27 [1.76, 10.0] 0.19 4.88 [3.27, 7.27] 0.86 26.5 [15.1, 46.6] 0.025 150 [78.5, 285] 0.069 6.4 [2.69, 15.1] 0.28
Other locations 2019 32.3 [30.1, 34.6] 6.09 [5.78, 6.42] 92.4 [76.8, 111] 492 [392, 618] 159 [125, 202]
2020 24.5 [17, 33.9] 0.11 5.38 [3.77, 7.68] 0.46 16.0 [7.53, 34.0]  < 0.001 39.0 [24.6, 61.8]  < 0.001 9.2 [5.21, 16.1]  < 0.001
Private transport 2019 10.5 [9.10, 12.0] 1.75 [1.37, 2.24] 7.34 [6.19, 8.71] 8.27 [6.21, 11.0] 0.87 [0.63, 1.19]
2020 9.26 [5.4, 15.4] 0.66 2.57 [0.69, 9.52] 0.61 2.69 [2.05, 3.54]  < 0.001 3.52 [1.42, 8.75] 0.014 0.33 [0.12, 0.90] 0.013
Public transport 2019 13.5 [11.9, 15.2] 1.52 [1.29, 1.79] 31.2 [27.1, 36.1] 28.3 [23.4, 34.3] 3.81 [3.04, 4.78]
2020 14.1 [8.78, 21.8] 0.85 1.99 [0.90, 4.40] 0.54 12.4 [6.35, 24.1]  < 0.001 21.8 [9.27, 51.3] 0.49 3.07 [1.25, 7.54] 0.61

Values are means, aside from the “proportion visited” columns. Values in brackets are the 95% confidence intervals. All p-values are for coefficients for a year indicator variable in a bivariate regression of each column outcome. Detailed information on other locations reported are provided in Additional file 1: Material S5

Our sensitivity analyses did not substantively change our conclusions (Additional file 1: Material S4). Estimated reductions in R0 between 2019 and 2020 R1 and 2020 R2 ranged from 40 to 50% and 38 to 48% respectively in the sensitivity analyses, compared to 42 and 45% respectively in the primary analysis. Excluding Fridays/Saturdays, contacts under 15 min, respondents with any missing contact age data or those aged 15–17 had no qualitative effect on age-mixing patterns. Adding children to the analysis highlighted the large number of contacts adults had with children pre-Covid, but did not affect the estimated reduction in R0 between 2019 and 2020. However, it was notable that adults’ close personal contact with children fell by less than almost any other age combination, looking similar to the pattern between 15 and 29 and 50–64 year olds.

Discussion

We compared rates of close interaction contact and time spent with others indoors or on transport from surveys conducted in the same rural South African setting, both pre-Covid-19 in 2019 and during the first wave of cases in mid-2020. We found substantial declines in close contact numbers and in time spent at most indoor locations other than respondents’ own homes by 2020, suggesting that the combination of government NPIs and the ongoing epidemic substantially affected behaviour. Under the assumptions that close interaction contacts are the most important for infection transmission, and qualitatively the same in both years, we estimate a 42–45% reduction in the likely basic reproduction number between the two surveys. Given the substantial level of use of face coverings outside the home required and observed in South Africa [31], this reduction is likely to be an underestimate.

While it is difficult to disentangle the effects of NPIs and the state of the local epidemic, the fact that much of the decline between 2019 and 2020 was present by the first interview round – the majority of which occurred prior to the local mass arrival of Covid-19 – suggests that respondents in this area were complying with government mobility NPIs. By June and July these had been relaxed somewhat from the initial strict stay-at-home requirements, but entertainment and alcohol availability remained highly limited. The continuation of limited close interaction contact, even as NPIs were relaxed into August and beyond, highlights that the changes made in response to NPIs were maintained subsequently; it is hard to tell whether this was due to increased concern due to widespread local transmission or slow adjustment to changing policies.

Declines in close interaction contact were not homogenous. The age group with the greatest decreases in contact were those aged over 65, particularly for contact with others aged 50 and older, with declines of around three-quarters compared to pre-Covid. In contrast, the lowest declines were seen between those aged 15–29 and older adults—particularly those aged 30–49 years, i.e. one generation older. This pattern reflects the notably larger decline in non-household member contacts compared to household members in combination with the common presence of multiple adult generations within each household. This finding is similar that seen in other contact studies of rural Africans [32], and highlights the likely difficulty of protecting those most vulnerable to Covid-19 in settings such as this. A fuller understanding of the implications of these ongoing within-household intergenerational contacts will require focused qualitative work to determine whether young adults living in multigenerational households are able to maintain some social distance within houses, and how to potentially target messages to this population.

To consider the implications of behaviour change for an infection with aerosol transmission potential, we also measured time spent in indoor locations, and numbers of people present. Unsurprisingly, we found that time spent at home rose, while shared person-time spent in other homes dropped by 89% and at ‘other locations’ (largely school, work and shops) by 94%. This reduced potential for exposure in both public and private suggests that people are following rules both when they can and cannot be seen; these data are also consistent with other evidence from this area of reduced mobility in July and August compared even to earlier in 2020 [31]. Our respondents reported similar time spent attending health clinics in the two years, but reported that fewer others were present when they attended in 2020, perhaps reflecting improved social distancing policies within clinics. Overall, our indoor location data suggested nuanced decision-making by respondents during Covid-19, reducing less vital trips but maintaining necessary ones.

Even prior to Covid-19, the numbers of close interaction contacts reported in this area was substantially lower than that seen elsewhere in Africa [18, 3235]. Low numbers of contacts may reflect the very large proportion of our respondents’ days spent at home – a mean of 19 h in 2019 and almost 22 h in 2020. This lack of mobility reflects very high local unemployment – under 25% of resident working-aged adults reported employment during the late-2019 demographic census. As a result, while household contact numbers are comparable to other African studies, contacts beyond the household appear to be substantially lower. In the context of a South African first wave of the Covid-19 epidemic that saw much smaller outbreaks in rural than urban areas, this lower baseline suggests a low rural R0 even before individuals increased their social distance.

Strengths and limitations

There are limitations to this study. As with any observational study of human behaviour, care must be taken in generalising to other populations. While the pre-Covid-19 contact patterns we show here are consistent with those elsewhere in rural Africa [32], as are the changes seen with the arrival of Covid-19 [18], it is important to consider whether close contact patterns in rural lower-income settings may have different implications for disease prevention than patterns seen elsewhere.

In contrast to social contact surveys that used prospective diaries to capture information, we relied on recent recall – this may have led to some misreporting, but the delay was in all cases less than one week, limiting this concern. Our data were also self-reported rather than, for example, based on proximity detectors or mobility tracking. Self-report can lead to misreporting, although this effect is unlikely to have affected measures of change since we used the same approach for both years. Nevertheless, given the uncertainty of self-reports, absolute values of contact numbers should be treated with caution. It is also possible that respondents underreported more in 2020 insofar as they had visited places in contravention of the law and at the risk of fines or court appearances [36], if they believed that interviewers would report this or were ashamed of their behaviour. Self-report also has the benefit of providing richer data on the nature of each interaction. Conversely, we kept our questionnaires brief to minimize respondent fatigue, and as a result we do not have certain details about each contact, including whether a facemask was used during each interaction (although any such use of masks should have increased the drop in infectious potential from 2019 to 2020). We also do not have detailed information on how respondents changed their work, educational or other patterns of daily life; more in-depth interviews potentially using qualitative data collection methods would thus provide important additional insight into the effect of the epidemic and lockdowns on infection risk.

There are substantial strengths to this work. We were able to compare two studies with respondents drawn from the same well-defined sampling frame asking very similar questions about behaviour both shortly before and after the arrival of Covid-19 in the study area. The availability of longitudinal response data during the Covid-19 outbreak allowed us to observe behaviour changed as government NPIs and epidemic situations changed; although while patterns of behaviour over time can suggest effects, we cannot prove causality, something important if using our findings to design preventative interventions.

Conclusion

In comparable surveys about social contacts conducted in the same rural South African location in 2019 and mid-2020, we find substantial declines in close physical and conversational contacts, and also in beyond-household sharing of indoor space. These findings suggest that the strict government NPIs implemented to mitigate the Covid-19 epidemic, in combination with the arrival of the epidemic itself in the local area, led to highly protective behaviours. It will be important to triangulate these findings with other information on the wider impact of such behaviour.

Supplementary Information

12879_2021_6604_MOESM1_ESM.docx (6.6MB, docx)

Additional file 1: Material S1. Study instruments. Material S2. Lockdown levels and regulations. Material S3. Extended methods for statistical analysis. Material S4. Sensitivity analyses. Material S5. Detailed description of ‘other locations’ from non-close contact questions

Acknowledgements

We acknowledge the generosity of all participants. We gratefully acknowledge the efforts of all the study research assistants: in 2019 Nkosingiphile Buthelezi, Zilethile Khumalo, Sifundesihle Malembe, Zodwa Mkwanazi, Sanele Mthiyane; in 2020 Gugu Buthelezi, Ngenzeni Buthelezi, Duduzile Mkhwanazi, Siyabonga Mnyango, Nondumiso Mpanza, Mxolisi Nhlenyama. We thank Indira Govender for helpful suggestions on an earlier draft.

Abbreviations

AHRI

Africa Health Research Institute

COPD

Chronic Obstructive Pulmonary Disease

CSC

Covid Social Contact

NPI

Non-pharmaceutical interventions

R0

Reproduction number

REC

Research Ethics Committee

UKZN

University of KwaZulu-Natal

UO

Umoya omuhle

Authors' contributions

Conceptualization: NM, RGW, ADG, GH. Design: NM, MJS, KH, ADG, GH. Data acquisition: VD, AE, SO, ND, KD, SN, JD. Data analysis: NM, SO, KB. Data interpretation: NM, GH. Writing – original draft: NM, GH. All authors contributed to critical revision of the work, final revisions to the text and agree to be accountable for the work. All authors read and approved the final manuscript.

Funding

Data collection in the Umoya omuhle programme is funded in part by the UK Economic and Social Research Council (ES/P008011/1), one of seven research councils underpinning the Antimicrobial Resistance Cross Council Initiative. It is also supported by the UK Medical Research Council (MRC) and the UK Department for International Development (DFID) under the MRC/DFID Concordat agreement that is also part of the EDCTP2 programme supported by the European Union (MR/P002404/1). The Covid Social Contacts study was funded by internal seed funding from the Africa Health Research Institute (AHRI), which is core funded by the Wellcome Trust (201433/Z/16/Z). GH is supported by a fellowship from the Royal Society and the Wellcome Trust (210479/Z/18/Z). NM, RGW and ADG are supported by the UK ESRC (ES/P008011/1); NM and RGW are supported by the Wellcome Trust (218261/Z/19/Z). RGW is additionally funded NIH (R01-AI147321), EDTCP (RIA208D-2505B), UK MRC (CCF17-7779 via SET Bloomsbury), BMGF (OPP1084276, OPP1135288 & INV-001754), and the WHO (2020/985800–0). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Availability of data and materials

The datasets supporting the conclusions of this article are available through the AHRI data repository (https://data.ahri.org) in pseudonymized form  at 10.23664/ahri.uoandcsc.dataset.2021. Data can be requested directly from this repository and the corresponding author (Guy Harling) can be contacted to assist in this process.

Declarations

Ethical approval and consent to participate

Ethical approval for UO was granted by the Biomedical Research Ethics Committee (REC) of the University of KwaZulu-Natal (UKZN) (BE662/17) and the London School of Hygiene & Tropical Medicine (14640); ethical approval for CSC was granted by UKZN BREC (BE290/16) and University College London REC (15231/013). Informed consent for participation was recorded in writing for UO and telephonically for CSC.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Footnotes

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

  • 1.Hogan AB, Jewell BL, Sherrard-Smith E, Vesga JF, Watson OJ, Whittaker C, Hamlet A, Smith JA, Winskill P, Verity R. Potential impact of the COVID-19 pandemic on HIV, tuberculosis, and malaria in low-income and middle-income countries: a modelling study. Lancet Glob Health. 2020;8(9):e1132–e1141. doi: 10.1016/S2214-109X(20)30288-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Richards M, Anderson M, Carter P, Ebert BL, Mossialos E. The impact of the COVID-19 pandemic on cancer care. Nature Cancer. 2020;1:565–567. doi: 10.1038/s43018-020-0074-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.McKibbin WJ, Fernando R. The global macroeconomic impacts of COVID-19: seven scenarios. SSRN J. 2020 doi: 10.2139/ssrn.3547729. [DOI] [Google Scholar]
  • 4.Ataguba JE. COVID-19 pandemic, a war to be won: understanding its economic implications for Africa. Appl Health Econ Health Policy. 2020;18:325–328. doi: 10.1007/s40258-020-00580-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Hale T, Petherick A, Phillips T, Kira B. Oxford COVID-19 government response tracker. Oxford: Blavatnik School of Government; 2020. [DOI] [PubMed] [Google Scholar]
  • 6.Dyer O. Covid-19: Africa records over 10 000 cases as lockdowns take hold. Br Med J. 2020;369:m1439. doi: 10.1136/bmj.m1439. [DOI] [PubMed] [Google Scholar]
  • 7.Alon TM, Kim M, Lagakos D, VanVuren M: How Should Policy Responses to the COVID-19 Pandemic Differ in the Developing World? Working paper 27273. Cambridge: National Bureau of Economic Research.; 2020.
  • 8.Ozili PK. COVID-19 in Africa: socioeconomic impact, policy response and opportunities. Germany: University Library of Munich; 2020. [Google Scholar]
  • 9.Shadmi E, Chen Y, Dourado I, Faran-Perach I, Furler J, Hangoma P, Hanvoravongchai P, Obando C, Petrosyan V, Rao KD. Health equity and COVID-19: global perspectives. Int J Equity Health. 2020;19(1):1–16. doi: 10.1186/s12939-020-01218-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Blundell R, Costa Dias M, Joyce R, Xu X. COVID-19 and inequalities. Fisc Stud. 2020;41(2):291–319. doi: 10.1111/1475-5890.12232. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Bansal S, Grenfell BT, Meyers LA. When individual behaviour matters: homogeneous and network models in epidemiology. J R Soc Interface. 2007;4(16):879–891. doi: 10.1098/rsif.2007.1100. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Bosetti P, Huynh B-T, Abdou AY, Sanchez M, Eisenhauer C, Courtejoie N, Accardo J, Salje H, Guillemot D, Moslonka-Lefebvre M. Lockdown impact on age-specific contact patterns and behaviours in France. MedRxiv. 2020 doi: 10.1101/2020.1110.1107.20205104. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Del Fava E, Cimentada J, Perrotta D, Grow A, Rampazzo F, Gil-Clavel S, Zagheni E. The differential impact of physical distancing strategies on social contacts relevant for the spread of COVID-19. MedRxiv. 2020;10:21885. doi: 10.1136/bmjopen-2021-050651. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Jarvis CI, Van Zandvoort K, Gimma A, Prem K, Klepac P, Rubin GJ, Edmunds WJ. Quantifying the impact of physical distance measures on the transmission of COVID-19 in the UK. BMC Med. 2020;18:124. doi: 10.1186/s12916-020-01597-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Backer JA, Mollema L, Vos ER, Klinkenberg D, Van Der Klis FR, De Melker HE, Van Den Hof S, Wallinga J. Impact of physical distancing measures against COVID-19 on contacts and mixing patterns: repeated cross-sectional surveys, the Netherlands, 2016–17, April 2020 and June 2020. Eurosurveillance. 2021;26(8):2000994. doi: 10.2807/1560-7917.ES.2021.26.8.2000994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Feehan D, Mahmud A. Quantifying interpersonal contact in the United States during the spread of COVID-19: first results from the Berkeley Interpersonal Contact Study. MedRxiv. 2020;395:931. [Google Scholar]
  • 17.Zhang J, Litvinova M, Liang Y, Wang Y, Wang W, Zhao S, Wu Q, Merler S, Viboud C, Vespignani A. Changes in contact patterns shape the dynamics of the COVID-19 outbreak in China. Science. 2020;368(6498):1481–1486. doi: 10.1126/science.abb8001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Quaife M, van Zandvoort K, Gimma A, Shah K, McCreesh N, Prem K, Barasa E, Mwanga D, Kangwana B, Pinchoff J, et al. The impact of COVID-19 control measures on social contacts and transmission in Kenyan informal settlements. BMC Med. 2020;18:316. doi: 10.1186/s12916-020-01779-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Morawska L, Milton DK. It is time to address airborne transmission of COVID-19. Clin Infect Dis. 2020;71(9):2311–2313. doi: 10.1093/cid/ciaa939. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Abdool Karim SS. The South African Response to the Pandemic. N Engl J Med. 2020;382(24):e95. doi: 10.1056/NEJMc2014960. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.McCreesh N, Dlamini V, Edwards A, Olivier S, Dayi N, Dikgale K, Nxumalo S, Dreyer J, Baisley K, Siedner MJ, White RG, Herbst K, Grant A, Harling G. Social contact information from PIPSA residents in uMkhanyakude before and during the Covid-19 pandemic – data from the Umoya Omuhle and Covid Social Contacts studies (Version 1) [Data set]. Africa Health Research Institute (AHRI). 2021. Available from: 10.23664/AHRI.UOANDCSC.DATASET.2021. Accessed 31 August 2021.
  • 22.Tanser F, Hosegood V, Bärnighausen T, Herbst K, Nyirenda M, Muhwava W, Newell C, Viljoen J, Mutevedzi T, Newell M-L. Cohort profile: Africa Centre Demographic Information System (ACDIS) and population-based HIV survey. Int J Epidemiol. 2008;37(5):956–962. doi: 10.1093/ije/dym211. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Kielmann K, Karat AS, Zwama G, Colvin C, Swartz A, Voce AS, Yates TA, MacGregor H, McCreesh N, Kallon I. Tuberculosis infection prevention and control: why we need a whole systems approach. Infect Dis Poverty. 2020;9(1):1–4. doi: 10.1186/s40249-020-00667-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Siedner MJ, Harling G, Derache A, Smit T, Khoza T, Gunda R, Mngomezulu T, Gareta D, Majozi N, Ehlers E, et al. Protocol: Leveraging a demographic and health surveillance system for Covid-19 Surveillance in rural KwaZulu-Natal. Wellcome Open Res. 2020;5(109):109. doi: 10.12688/wellcomeopenres.15949.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Myambo Magodoro I, Oliver S, Gareta D, Modise TH, Koole O, Herbst K, Pillay D, Wong E, Siedner MJ. Engagement in HIV care as an avenue to primary care in rural South Africa: results from the vukuzazi population health platform. Open Forum Infect Dis. 2019;2019:S13–14. doi: 10.1093/ofid/ofz359.029. [DOI] [Google Scholar]
  • 26.Statistics South Africa . P0302—mid-year population estimates, 2019. Pretoria: Statistics South Africa; 2019. [Google Scholar]
  • 27.Diekmann O, Heesterbeek JAP, Metz JA. On the definition and the computation of the basic reproduction ratio R 0 in models for infectious diseases in heterogeneous populations. J Math Biol. 1990;28(4):365–382. doi: 10.1007/BF00178324. [DOI] [PubMed] [Google Scholar]
  • 28.Funk S. Socialmixr: social mixing matrices for infectious disease modelling [Internet]. The Comprehensive R Archive Network; 2018. Available from: https://CRAN.Rproject.org/package=socialmixr.
  • 29.World Health Organization . Roadmap to improve and ensure good indoor ventilation in the context of COVID-19. Geneva: World Health Organization; 2021. [Google Scholar]
  • 30.Greenhalgh T, Jimenez JL, Prather KA, Tufekci Z, Fisman D, Schooley R. Ten scientific reasons in support of airborne transmission of SARS-CoV-2. Lancet. 2021;397(10285):1603–1605. doi: 10.1016/S0140-6736(21)00869-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Harling G, Gómez-Olivé FX, Tlouyamma J, Mutevedzi T, Kabudula CW, Mahlako R, Singh U, Ohene-Kwofie D, Buckland R, Ndagurwa P, et al. Protective behaviours and secondary harms from non-pharmaceutical interventions during the COVID-19 epidemic in South Africa: a multisite prospective longitudinal study. JMIR Public Health Surveill . 2021;7(5):e26073. doi: 10.2196/26073. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Melegaro A, Del Fava E, Poletti P, Merler S, Nyamukapa C, Williams J, Gregson S, Manfredi P. Social contact structures and time use patterns in the Manicaland Province of Zimbabwe. PLoS ONE. 2017;12(1):e0170459. doi: 10.1371/journal.pone.0170459. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Johnstone-Robertson SP, Mark D, Morrow C, Middelkoop K, Chiswell M, Aquino LD, Bekker L-G, Wood R. Social mixing patterns within a South African township community: implications for respiratory disease transmission and control. Am J Epidemiol. 2011;174(11):1246–1255. doi: 10.1093/aje/kwr251. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Dodd PJ, Looker C, Plumb ID, Bond V, Schaap A, Shanaube K, Muyoyeta M, Vynnycky E, Godfrey-Faussett P, Corbett EL. Age-and sex-specific social contact patterns and incidence of Mycobacterium tuberculosis infection. Am J Epidemiol. 2016;183(2):156–166. doi: 10.1093/aje/kwv160. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Kiti MC, Kinyanjui TM, Koech DC, Munywoki PK, Medley GF, Nokes DJ. Quantifying age-related rates of social contact using diaries in a rural coastal population of Kenya. PLoS ONE. 2014;9(8):e104786. doi: 10.1371/journal.pone.0104786. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.Administrative Region 6, Kwazulu-Natal: Judicial Circular 11 of 2020—Determination of Admission of Guilt Fines in Respect of Offences Committed in Terms of Regulations Promulgated Under the Disaster Management Act, 2002 https://www.judiciary.org.za/images/Determinations/Kwazulu-Natal_Province/Determination_of_Admission_of_Guilt_Fines_in_Respect_of_Offences_Committed_in_Terms_of_Regulations_Promulgated_Under_the_Disaster_Management_Act_2002_Published_in_Government_Gazzette_43258_Dated_29_April_2020.pdf]. Accessed 31 August 2021.

Associated Data

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

Supplementary Materials

12879_2021_6604_MOESM1_ESM.docx (6.6MB, docx)

Additional file 1: Material S1. Study instruments. Material S2. Lockdown levels and regulations. Material S3. Extended methods for statistical analysis. Material S4. Sensitivity analyses. Material S5. Detailed description of ‘other locations’ from non-close contact questions

Data Availability Statement

The datasets supporting the conclusions of this article are available through the AHRI data repository (https://data.ahri.org) in pseudonymized form  at 10.23664/ahri.uoandcsc.dataset.2021. Data can be requested directly from this repository and the corresponding author (Guy Harling) can be contacted to assist in this process.


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