Keywords
COVID-19; Non-pharmaceutical interventions; Optimal control;
Comparison of effectiveness
1
2021LATEX template
2 Ranking the Effectiveness of Non-Pharmaceutical Interventions
The epidemic ascribed to the virus called Severe Acute Respiratory Syndrome
Coronavirus 2 (SARS-CoV-2) has greatly impacted society and the economy
around the world. In December 2019, China reported cases of pneumonia of
unknown cause in Wuhan. The World Health Organisation (WHO) declared
the coronavirus disease 2019 (COVID-19) a pandemic in March 11, 2020 [1].
By 3 November 2021, WHO has reported over 246 million cases with more
than 5 million deaths around the world [1].
The virus generally causes respiratory symptoms such as cough, sneezing,
shortness of breath, along with other symptoms including fever, headache [2]
and olfactory or gustatory dysfunctions [3]. Since direct contact and aerosol
transmissions are two important ways of infection [4], symptomatic individuals
are high spreaders. Meanwhile, the virus can also survive on surfaces and
then invade the human body through eyes, nose or mouth via touching [5, 6].
Some carriers are asymptomatic, but they can still infect other susceptible
individuals [7, 8].
Many countries have conducted successful vaccination campaigns. How-
ever, vaccination uptake in most of these countries have platooned at around
70/80% of their total population [9]. Moreover, SARS-CoV-2 has shown a rel-
atively high ability to adapt [10]. Several variants have been reported [11]
with four considered to be of main concern: Alpha (B.1.1.7), Beta (B.1.351),
Gamma (P.1) and Delta (B.1.617.2). In particular, the Delta variant has shown
to be more infectious and more severe, leading to second or third waves in the
UK, India and South Africa [12], in addition to having partial resistance to
vaccines [13, 14]. The fast emergence of viral mutations has also raised wide
considerations on whether current vaccines will be effective on new lineages
appearing in the future [15–17]. Moreover, recent studies also show a decay of
the protection that vaccines offer as time from vaccination increases [18, 19],
which prompted several counties to start a booster campaign. Therefore, in
such a complex situation the implementation of non-pharmaceutical interven-
tions such as mask wearing and social distancing have remained fundamental
measures in containing the disease [20].
This work studies the current situation in British universities which have
re-opened and maintain a combination of non-pharmaceutical measures in
place. The objective of universities is to maximise on-campus activities while
maintaining the spread of the disease under control. Universities are “small-
environments” which have special features for which general purpose models
may be inadequate. For instance, a university is composed of two fundamen-
tally different populations, the students and the staff, which have different
degrees of interaction, vaccination rates and serious symptoms. General pur-
pose models focus mostly on modelling the spread of the disease, but here
we are interested in maximising on-campus activity subject to limited spread.
Our main contribution is two-fold: on one hand we provide a modelling frame-
work to maximise safe on-campus activity. On the other hand, a ranking of
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Ranking the Effectiveness of Non-Pharmaceutical Interventions 3
non-pharmaceutical interventions and their fundamental importance in achiev-
ing the objective naturally emerges from our analysis. Moreover this emergent
behaviour is shown to be relative robust to modelling parameters.
The first block of our framework is a compartmental model. Compartmen-
tal modelling is a popular choice for research on COVID-19. Cooper et al. [21]
used an SIR model with changing total population to estimate the growth of
the epidemic in different nations. To explicitly model details such as incuba-
tion period, hospitalization, and quarantine, Leontitsis et al. [22] proposed an
SEAHIR model. Giordano et al. [23] created a far more complete SIDARTHE
model, reflecting potential effects of non-pharmaceutical interventions imple-
mented by the government. Various stochastic versions with higher complexity
have also been designed to estimate the development of the pandemic under
feasible countermeasures [24–26]. However, most of these models consider the
influence of prevention and control measures by tweaking the model’s param-
eter values. Consequently, the importance of different interventions cannot be
systematically evaluated and compared. In this paper, we propose a new deter-
ministic compartmental model for the spreading of COVID-19 in universities
and investigate the importance of non-pharmaceutical countermeasures using
optimal control techniques.
Consisting of a double SEIQR structure, our model distinguishes the epi-
demic evolution stages of students from those of staff. All individuals can
potentially undergo five statuses: susceptible S (including the vaccinated),
exposed E (asymptomatic), infected I (symptomatic), quarantined Q (hospital-
ized or isolated), and recovered R. Since all members are studying or working
within the same confined space, the coronavirus can also transmit via the
environment. An extra compartment C is used to represent the environmental
virus concentration. The overall structure of the model is depicted in Fig. 1.
This compartmental model automatically assumes that the total population is
homogeneously mixed, which is reasonable because everyone belonging to the
same department is following similar daily routines in the common confined
spaces. The individuals in the compartments also have similar probability of
infections due to the virus surviving in the environment. The model does not
involve the isolation of asymptomatic subjects because it is less likely to occur
in the context of a university population. We still model the vaccinated indi-
viduals as susceptible but with lower infection rates (i.e. vaccine breakthrough
infections). The possibility of re-infection among recovered people is omitted.
Death of vaccinated individuals is also negligible.
To assess the efficacy of the various intervention strategies under study we
first evaluate a baseline scenario in which no countermeasures are implemented.
The parameters for this scenario are taken from the literature. Some of the
values of the parameters are obtained according to the proportion of vaccinated
individuals and vaccine effectiveness reported in the UK [27–29]. A detailed
description of this procedure is reported in the Methods.
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4 Ranking the Effectiveness of Non-Pharmaceutical Interventions
Susceptible
Sy
Exposed
(Asymptomatic)
Ey
Infected
(Symptomatic)
Iy
βyy, βsy, βcy εy
Recovered
Ry
Quarantined
Qy
λy
ηy
ξy
Student Group
ρy
Susceptible
Ss
Exposed
(Asymptomatic)
Es
Infected
(Symptomatic)
Is
βss, βys, βcs εs
Recovered
Rs
Quarantined
Qs
λs
ηs
ξs
Staff Group
ρs
Virus
Environment
Concentration
C
βsyβys
μy
βcy
μs
βcs
Environment
Decaying rate
δ
Fig. 1 Model structure. Flow chart of five epidemic stages among students and staff
in a university department: S, susceptible (including the vaccinated); E, exposed (asymp-
tomatic); I, infected (symptomatic); Q, quarantined (hospitalized or mandatorily isolated);
R, recovered. The subscript “y” stands for students while the subscript “s” denotes staff.
We consider five possible non-pharmaceutical interventions that can be
implemented by the university after reopening: mask wearing, social dis-
tancing, environmental disinfection, quarantine on infected students and
quarantine of infected staff. To study the effectiveness of these measures in the
model, we define five input control variables associated with each of these mea-
sures. We then use optimal control to study four desired scenarios: minimum
number of cases, minimum intervention, minimum non-quarantine interven-
tion and minimum quarantine intervention. In all scenarios, it is assumed that
the University starts to control the epidemic 14 days after the asymptomatic
carriers firstly appear. We also model the desire of keeping the infection under
control as constraints in the optimisation. In particular, we impose constraints
on the number of infected cases and on the number of days required to extin-
guish the epidemic. In the minimum-case scenario, the epidemic is controlled
with no efforts spared, leading to the strongest minimization of COVID-19
cases. For minimum intervention, we study the possibility of minimizing the
total effort of all control measures. In the minimum non-quarantine interven-
tion, we minimise the use of mask wearing, social distancing and environmental
disinfection. In the last scenario, minimum quarantine intervention, we mini-
mize the use of quarantines. By comparing the obtained optimal trajectories
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Ranking the Effectiveness of Non-Pharmaceutical Interventions 5
in different scenarios, we identify an emergent behaviour that shows a ranking
on the importance of the different non-pharmaceutical interventions.
1 Results
1.1 Baseline: no interventions
We first generate a baseline scenario in which no intervention is performed.
We simulate the evolution of the epidemic in one department of the university.
The results are shown in Fig. 2. As case study we consider a department where
the total number of students is 1200 and the number of members of staff is
150 (i.e. similar to the EEE department of Imperial College London). Initially,
we assume 5 students and 2 staff members start as asymptomatic cases. The
effective reproduction number R0 on day 0 is 1 .40, which indicates a poten-
tial outbreak of COVID-19 in this small environment. After two weeks, 1.8%
of students and 3 .1% of staff have caught the disease. Without countermea-
sures, increasingly more individuals will get infected during the coming 120
days. Simultaneously, Rt keeps decreasing and becomes smaller than 1 after
76 days. At day 134, 56% of students and 63% of staff have been infected and
Rt = 0.718. In the end (without considering further infections from outside
the department), the epidemic last around 250 days, rendering 59% of stu-
dents and 66% of staff infected. This prediction result reveals the necessity of
imposing non-pharmaceutical measures at the current UK vaccination levels
(see Methods for the exact percentages).
0 50 100 150 200 250
Time (days)
0
0.2
0.4
0.6
0.8
1
Student Case Proportion
Trajectories of Student Group
Sy(t)
Ey(t)
Iy(t)
Qy(t)
Ry(t)
0 50 100 150 200 250
Time (days)
0
0.2
0.4
0.6
0.8
1
Staff Case Proportion
Trajectories of Staff Group
Ss(t)
Es(t)
Is(t)
Qs(t)
Rs(t)
a
b
Fig. 2 Prediction in the baseline scenario of no interventions. a Evolution of
COVID-19 among students. b Evolution of COVID-19 among staff. Magnitudes are in
proportion to the total number of students or staff.
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6 Ranking the Effectiveness of Non-Pharmaceutical Interventions
1.2 Optimal interventions for four objectives
We now study the effect of non-pharmaceutical interventions. Which inter-
ventions to implement, when and how strongly are all decisions made by the
optimisation method to optimise the objective. We have selected four different
optimisation objectives. In all scenarios, interventions are introduced 14 days
after the initial exposure of 5 students and 2 staff members. In all scenarios, we
impose the constraints that the epidemic must end within 120 days and that
at least 94% of students and staff are not infected. Thus, the overall timeline
is 134 days.
Minimum number of cases: In this scenario the optimisation objective
is formulated to minimise infections, even though this may require that all
non-pharmaceutical interventions are implemented at full strength. The opti-
mal trajectories are depicted in Fig. 3. The epidemic is completely ended at
around the 60 th day when the individuals are only in two states: suscepti-
ble and recovered. More than 97% of students and 96% of staff do not get
infected in this scenario. From the figure we see that this result is achieved by
implementing all interventions unreservedly, from mask wearing to mandatory
quarantine. This reduces Rt to around 0.217. While initially there is a strong
need for all countermeasures, after 30 days the optimal strategy relies mostly
on distancing and masks. All cases have been quarantined by the 45 th day.
After approximately 60 days, the department reaches a steady state and the
infection is stopped. Consequently, at this point the optimal strategy eases the
interventions because the epidemic has been successfully contained.
0 20 40 60 80 100 120
Time (days)
0
0.2
0.4
0.6
0.8
1
Student Case Proportion
Trajectories of Student Group
Sy(t)
Ey(t)
Iy(t)
Qy(t)
Ry(t)
0 20 40 60 80 100 120
Time (days)
0
0.2
0.4
0.6
0.8
1
Staff Case Proportion
Trajectories of Staff Group
Ss(t)
Es(t)
Is(t)
Qs(t)
Rs(t)
0 20 40 60 80 100 120
Time (days)
0
0.2
0.4
0.6
0.8
1
Control Variable Values
m, d and e
m(t)
d(t)
e(t)
0 20 40 60 80 100 120
Time (days)
0
0.2
0.4
0.6
0.8
1
Control Variable Values
qy and qs
qy(t)
qs(t)
a
c
b
d
Fig. 3 Optimal trajectories for the minimum-case scenario. Optimal trajectories
when the department spares no effort to contain the epidemic. a,b, The epidemic evolution
among students and staff, respectively. c, The optimal strategies for mask wearing ( κm),
social distancing (κd), and environmental disinfection ( κe). d, The optimal strategies for
mandatory quarantine on infected students (κqy) and infected staff (κqs).
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Ranking the Effectiveness of Non-Pharmaceutical Interventions 7
Minimum intervention: In this case the objective function is the norm
of all control variables. As a consequence, the aim here is to minimise the use
of all interventions (including quarantine) while still satisfying the constraint
that at least 94% of the population is not infected. The resulting optimal
trajectories are shown in Fig. 4. The epidemic is ended with 4 .3% of students
and 6% of staff having been infected. With respect to before we can see that
there is a decrease in the strength of the interventions. We can also note that
there is an emerging ranking between the interventions. Fig. 4c shows that
the environmental disinfection is far less important than mask wearing. For
what concerns mandatory quarantine shown in Fig. 4d, we notice again that
isolation of infected students plays a more significant role in controlling the
spread of COVID-19 than the isolation of staff. All five control interventions
are strongest at the beginning of the epidemic, and then their magnitude is
attenuated gradually over time.
0 20 40 60 80 100 120
Time (days)
0
0.2
0.4
0.6
0.8
1
Student Case Proportion
Trajectories of Student Group
Sy(t)
Ey(t)
Iy(t)
Qy(t)
Ry(t)
0 20 40 60 80 100 120
Time (days)
0
0.2
0.4
0.6
0.8
1
Staff Case Proportion
Trajectories of Staff Group
Ss(t)
Es(t)
Is(t)
Qs(t)
Rs(t)
0 20 40 60 80 100 120
Time (days)
0
0.2
0.4
0.6
0.8
1
Control Variable Values
m, d and e
m(t)
d(t)
e(t)
0 20 40 60 80 100 120
Time (days)
0
0.2
0.4
0.6
0.8
1
Control Variable Values
qy and qs
qy(t)
qs(t)
a
c
b
d
Fig. 4 Optimal trajectories for the minimum intervention scenario. Optimal tra-
jectories when the department would like to minimise the enforcement of control measures.
a,b, The epidemic evolution among students and staff, respectively. c, The optimal strate-
gies for mask wearing (κ m), social distancing (κd), and environmental disinfection (κe). d,
The optimal strategies for mandatory quarantine on infected students ( κqy) and infected
staff (κqs).
Minimum use of non-quarantine interventions: In this case we want
to minimize the use of masks, social distancing and environmental disinfec-
tion. As a result we expect an increase of the use of quarantines. The resulting
optimal trajectories are shown in Fig. 5. As expected the figures show little
use of non-quarantine interventions, and a strong use of quarantines. We stress
that the primary objective of keeping 94% of the susceptible population infec-
tion free is maintained. Again, Fig. 5d demonstrates the higher importance of
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8 Ranking the Effectiveness of Non-Pharmaceutical Interventions
quarantine among students with respect to staff. This shows the predominant
role played by student quarantine in controlling the epidemic.
0 20 40 60 80 100 120
Time (days)
0
0.2
0.4
0.6
0.8
1
Student Case Proportion
Trajectories of Student Group
Sy(t)
Ey(t)
Iy(t)
Qy(t)
Ry(t)
0 20 40 60 80 100 120
Time (days)
0
0.2
0.4
0.6
0.8
1
Control Variable Values
m, d and e
m(t)
d(t)
e(t)
0 20 40 60 80 100 120
Time (days)
0
0.2
0.4
0.6
0.8
1
Staff Case Proportion
Trajectories of Staff Group
Ss(t)
Es(t)
Is(t)
Qs(t)
Rs(t)
0 20 40 60 80 100 120
Time (days)
0
0.2
0.4
0.6
0.8
1
Control Variable Values
qy and qs
qy(t)
qs(t)
a
c
b
d
Fig. 5 Optimal trajectories for minimum use of non-quarantine interventions.
Optimal trajectories when the departments would like to minimise use of masks, social
distancing and environmental disinfection. a,b, The epidemic evolution among students and
staff, respectively. c, The optimal strategies for mask wearing ( κm), social distancing (κ d),
and environmental disinfection (κe). d, The optimal strategies for mandatory quarantine on
infected students (κqy) and infected staff (κqs).
Minimum quarantine: In this scenario we want to minimise the use of
quarantine, but we allow a strong use of mask wearing, social distancing and
environmental disinfection. The resulting optimal trajectories are shown in
Fig. 6. As a result, the quarantine control variables are zero and the other
three interventions are major tools to resolve the epidemic in this scenario.
Fig. 6c clearly shows the primary role of mask wearing and social distancing in
keeping the infection under control. The figure also shows that environmental
disinfection in comparison play little role when strong mask wearing and social
distancing are in place.
2 Discussion
The figures show an emerging behaviour: non-pharmaceutical interventions
have different importance and this importance arises mathematically from
the evolution of the epidemic. In a typical university department composed
of 1200 students and 150 staff, with a vaccination rate of 68% for students
and 78.8% for staff (see Methods, [27]) we see that the implementation of
non-pharmaceutical interventions is still fundamental to reduce the number of
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Ranking the Effectiveness of Non-Pharmaceutical Interventions 9
0 20 40 60 80 100 120
Time (days)
0
0.2
0.4
0.6
0.8
1
Student Case Proportion
Trajectories of Student Group
Sy(t)
Ey(t)
Iy(t)
Qy(t)
Ry(t)
0 20 40 60 80 100 120
Time (days)
0
0.2
0.4
0.6
0.8
1
Control Variable Values
m, d and e
m(t)
d(t)
e(t)
0 20 40 60 80 100 120
Time (days)
0
0.2
0.4
0.6
0.8
1
Staff Case Proportion
Trajectories of Staff Group
Ss(t)
Es(t)
Is(t)
Qs(t)
Rs(t)
0 20 40 60 80 100 120
Time (days)
0
0.2
0.4
0.6
0.8
1
Control Variable Values
qy and qs
qy(t)
qs(t)
a
c
b
d
Fig. 6 Optimal trajectories for the minimum quarantine scenario. Optimal tra-
jectories when the department would like to minimise the enforcement of mandatory
quarantines. a,b, The epidemic evolution among students and staff, respectively. c, The
optimal strategies for mask wearing (κ m), social distancing (κd), and environmental disin-
fection (κe). d, The optimal strategies for mandatory quarantine on infected students (κ qy)
and infected staff (κqs).
infections to one tenth of the number of infections appearing in a completely
uncontrolled scenario.
The ranking that arises from the study is as follows: wearing masks is the
most effective measure among the considered interventions. Keeping social dis-
tance is ranked close second. This priority of mask wearing is reasonable in a
university, where close contact is often unavoidable. Furthermore, we can also
see that environmental disinfection seems to be far less necessary if both mea-
sures are strongly enforced. As for the enforcement of mandatory quarantines,
the result yields that quarantine of symptomatic students is more significant
than quarantine of staff. This ranking is robust with respect to model param-
eters. This is shown in the sensitivity study presented in Figs. A1 to A8 in
Appendix A.
From a practical perspective, the university should emphasize mask wearing
and social distancing when on-campus teaching is resumed, especially among
students. The study also suggests that the university should invest particular
effort in identifying and quarantining infected students.
The proposed model and optimal control framework can be easily used to
assess other scenarios, e.g. other objectives or other constraints. This tool can
assist universities in predicting and managing the evolution of the epidemic.
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10 Ranking the Effectiveness of Non-Pharmaceutical Interventions
Moreover, our findings demonstrably reflect the importance of different non-
pharmaceutical interventions and help to tackle the trade-off between high-
quality teaching and limiting COVID-19 infections. This is crucial at a time
in which universities are under pressure to increase on-campus activities.
Our study also shows a gap in the epidemiological research of COVID-
19 regarding the evolution of the pandemic in small environments. There are
plenty of small environments, such as schools and companies that have their
very unique population structure ( i.e. populations with different degrees of
interaction, vaccination rates and serious symptoms) and require design tools
to assess the best interventions to be implemented in order to maximise in-
person activities while keeping the infections under control.
We also point out that some factors are not explicitly considered in our
study. Firstly, the model does not consider the infections brought from out-
side the campus. We omitted this aspect because we wanted to focus on the
study of the priority of different mitigation measures. Another limitation is
that the input variables (the interventions) in our optimal control problem are
continuous in magnitude. It may be difficult to give practical significance to
the numerical values representing the interventions. However, we stress that
the optimal trajectories are used here only to compare the relative impor-
tance of different interventions. Further research can be done on discretizing
the magnitude of the input variables into specific levels that correspond to
scientifically-defined interpretable practical meanings.
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Ranking the Effectiveness of Non-Pharmaceutical Interventions 11
3 Methods
3.1 Uncontrolled University Model
The proposed double SEIQR model is described by 11 differential equations,
5 associated to the epidemic evolution of students, 5 associated to the epi-
demic evolution of staff, and 1 representing environmental infection. We
first introduce, describe and analyse the uncontrolled model. In Section 3.3
we modify the model by introducing the control variables that represent
non-pharmaceutical interventions. The double uncontrolled SEIQR model is
described by
dSy(t)
dt =−{βy[Ey(t) +kIy(t) +Es(t) +kIs(t)] +βcyC(t)}Sy(t)
dSs(t)
dt =−{βs [Es(t) +kIs(t) +Ey(t) +kIy(t)] +βcsC(t)}Ss(t)
dEy(t)
dt ={βy[Ey(t) +kIy(t) +Es(t) +kIs(t)] +βcyC(t)}Sy(t)
− (εy +ξy)Ey(t)
dEs(t)
dt ={βs [Es(t) +kIs(t) +Ey(t) +kIy(t)] +βcsC(t)}Ss(t)
− (εs +ξs)Es(t)
dIy(t)
dt =εyEy(t)− (ηy +ρy)Iy(t)
dIs(t)
dt =εsEs(t)− (ηs +ρs)Is(t)
dQy(t)
dt =ηyIy(t)−ϕyQy(t)
dQs(t)
dt =ηsIs(t)−ϕsQs(t)
dRy(t)
dt =ξyEy(t) +ρyIy +ϕyQy(t)
dRs(t)
dt =ξsEs(t) +ρsIs +ϕsQs(t)
dC(t)
dt =µy(Ey(t) +kIi(t)) +µs(Es(t) +kIs(t))−δC(t)
(1)
where all model parameters are denoted by Greek letters with specific biolog-
ical meanings. We now provide a detailed explanation of each parameter. We
stress that this model is uncontrolled, so the values discussed below are for the
baseline scenario, i.e. no intervention is implemented. Also, the parameters are
firstly introduced for unvaccinated population and then modified according to
the UK vaccination proportions.
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12 Ranking the Effectiveness of Non-Pharmaceutical Interventions
• Individual infection rates βy, βs kβy, kβs
The individual infection rates represent the average number of susceptible
individuals who can be infected by a virus carrier via direct contacts in unit
time.βy indicates student-to-student and staff-to-student infection rates.βs
indicates staff-to-staff and student-to-staff infection rates. In other words,
we assume that student-to-student and staff-to-student rates are the same
and staff-to-staff and student-to-staff rates are the same. βs and βy are the
infection rates of the asymptomatic compartments. Considering the age dif-
ference, it is reasonable to expect that βy <β s because staff are more likely
to get infected.kβs andkβy are the infection rates of the symptomatic group.
Since sneezing and coughing play a major role in the direct transmission of
the virus, the symptomatic carriers generally have larger infection rates, i.e.
k > 1. Here it is assumed that k has the same value among students and
staffs. Referring to the scenario 3 of pandemic planning produced by the
CDC [30], k is generally 4. However, in this confined environment case, k
should be smaller because asymptomatic subjects can spread the virus more
easily. We selected a value of k = 1.5. According to the study conducted
by Leontitsis et al. [22], the general infection rate β is 0.1466. This value
is expected to be larger in a confined space because of the higher number
of direct contacts between people. In summary, putting together all these
data and observations, the parameters have been selected as βy = 0.163,
βs = 0.225, kβy = 0.2445 and kβs = 0.3375.
• Environmental infection rates βcy, βcs
These parameters represent how many susceptible people are infected by the
contaminated environment in unit time. They are properties of the virus in
the environment. There is no clear value in the literature and we estimate the
value ofβcy to be 0.171 (based on the expected basic reproduction number).
Moreover, it is reasonable to expect that the ratio βs/βy equals the ratio
p =βcs/βcy. Then βcs =pβcy = 0.236.
• Probability of becoming symptomatic εy, εs
They are the inverse of the average incubation period. According to [31],
this average period is 5 days. Considering that staff are of higher age, we
set εy = 1/5 = 0.2 and εs = 1/10 = 0.1.
• Probability of recovery from an asymptomatic state ξy, ξs
Similarly, the inverses of these quantities denote the average number of days
spent by exposed/asymptomatic subjects to recover ( i.e. they present no
symptom during the whole period). Referring to [30], this portion accounts
for 15%. Since εy = 0.2 and εs = 0.1 (corresponding to 85% of the
population). Then ξy = 0.0353 and ξs = 0.0176.
• Isolation rates ηy, ηs
These parameters denote the proportion of symptomatic individuals who are
isolated due to serious illness or mandatory quarantine. Since we initially
model the unrestricted situation (i.e. no quarantines), infected individuals
are at this point isolated mainly due to hospitalization. According to the
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Ranking the Effectiveness of Non-Pharmaceutical Interventions 13
survey conducted and reported by [32], the values are ηy = 0.06 and ηs =
0.106.
• Recovery rates of infected individuals ρy, ρs
ρ−1
y and ρ−1
s indicate the average time for infected people which are not
isolated to recover. If mandatory quarantine is not implemented, mild cases
will not isolate. These two parameters mainly describe the recovery rate of
this group. According to [33], the average length of recovery is approximately
14 days. In mild cases, we set this length at 10 days for students, and 18
days for staff. Thus, ρy = 1/10 and ρs = 1/18.
• Recovery rates of quarantined individuals ϕy, ϕs
ϕ−1
y and ϕ−1
s indicate the average time for “quarantined” individuals to
recover. In the baseline scenario this refers to hospitalised individuals. It
may take six-nine weeks for severe cases to recover [34]. We set ϕy = 1/40
while ϕs = 1/55.
• Virus shedding rates to the environment µy, µs, kµy, kµs
These parameters measure the spread of the virus from asymptomat-
ic/symptomatic individuals to the environment, with the effects brought by
symptomatic subjects being higher. Similarly to the case of βcy and βcs,
there is no clear value in the literature for these parameters. In this “small
environment” model we expect the values to be µy =µs =µ = 0.25 (based
on the expected basic reproduction number).
• Virus decaying rate in the environment δ
This measures the speed of decay of the virus in the small environment.
Since the airborne virus could stay in aerosol for up to 1 day and survive on
the surface for longer [35–37], this rate δ is set at 0.7.
We denoteNt to be the total population in the department. The total number
of students is represented by Ny and number of staff is labelled by Ns. A
summary of the meaning the parameters is given in Table 1.
These initial values refer to studies on the COVID-19 epidemic before vac-
cination. We now describe how the parameters are adapted to a vaccinated
population. According to the UK data provided by [27], about 68% of young
adults between 18 and 24 years old have been vaccinated by the 1 st Novem-
ber 2021. This quantity become 78.7% among people aged between 25 and 64.
Since vaccines utilized in the UK can reduce COVID-19 infections by around
65% [28, 29], we can see that the 68% vaccinated students will have 65% less
probability of getting infected. The same happens to the 78.7% of staffs. There-
fore, the average reductions in βy andβcy are 0.68× (1− 0.65) + 0.32 = 0.558.
The average reductions inβs andβcs are 0.787×(1−0.65)+0.213 = 0.488. Con-
sequently, due to vaccinations in the current situation, infection rates in this
university model with mixed vaccinated/unvaccinated population becomes:
βy = 0.0910, βcy = 0.0954, βs = 0.1098, and βcs = 0.1152. Since vaccines
can also reduce the probability of symptomatic infections and of severe ill-
ness [38], other parameter values are also tuned accordingly. This adjustment
changed the R0 from 2.50 (totally unvaccinated and no interventions) to 1.40
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14 Ranking the Effectiveness of Non-Pharmaceutical Interventions
T able 1 Model Parameter Definitions.
Parameters Definitions
βy, βs Infection rate for asymptomatic students/staff to susceptible
students/staff (including cross infections)
kβy, kβs Infection rate for symptomatic students/staff to susceptible
students/staff (including cross infections)
βcy, βcs Infection rate from uncleaned environment to susceptible stu-
dents/staff
εy, εs Probability that an asymptomatic student/staff becomes symp-
tomatic
ξy, ξs Probability that an asymptomatic student/staff recovers without
symptoms
ηy, ηs Isolation rate of symptomatic student/staffs
ρy, ρs Recovery rate of infected student/staffs
ϕy, ϕs Recovery rate of quarantined students/staffs
µy, µs Environmental shedding rate by asymptomatic students/staffs
kµy, kµs Environmental shedding rate by symptomatic students/staffs
δ Decaying rate of virus in the environment
(mixed population but still no intervention). Since it is still greater than 1,
the COVID-19 epidemic will still develop in the university model if no other
control or prevention measures are introduced. The values of the parameters
of the model before and after vaccinations are listed in Table 2.
T able 2 Model Parameter Values.
Parameters Before Vaccination After Vaccination
βy 0.163 0.0910
βs 0.225 0.1098
k 1.5 1.5
βcy 0.171 0.0954
βcs 0.236 0.1152
εy 0.2 0.2
εs 0.1 0.1
ξy 0.0353 0.0857
ξs 0.0176 0.0429
ηy 0.06 0.012
ηs 0.106 0.0212
ρy 0.1 0.125
ρs 0.0556 0.0833
ϕy 0.025 0.0714
ϕs 0.0182 0.0714
µy 0.25 0.25
µs 0.25 0.25
δ 0.7 0.7
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3.2 Analysis of the Uncontrolled University Model
3.2.1 Equilibrium Points
Denote x = [Sy, Ss, Ey, Es, Iy, Is, Qy, Qs, Ry, Rs, C]⊤. By equat-
ing all derivatives in (1) to zero, it is easy to determine the equilibria ¯ x =
[ ¯Sy, ¯Ss, 0, 0, 0, 0, 0, 0, ¯Ry, ¯Rs, 0], where
¯Sy + ¯Ss + ¯Ry + ¯Rs = 1, ¯Sy≥ 0, ¯Ss≥ 0, ¯Ry≥ 0, ¯Rs≥ 0 (2)
These equilibria imply that at the end of pandemic, the individuals are either
susceptible to or recovered from the disease.
3.2.2 Basic Reproduction Number
The basic reproduction number is a crucial criterion to measure the average
number of susceptible people that could potentially be infected by a primary
case [39]. This parameter is highly dependent on the fraction of the susceptible
population and it provides information about the potential of the epidemic
outbreak. IfR0 1 increasingly
more people will be infected.
Derivation of the basic reproduction number for the uncontrolled university
model is based on the next generation matrix method described by [40–42].
The university model (1) has five infectious compartments: Ey,Es,Iy,Is and
C. We collect these in the infection state xif = [Ey,Es,Iy,Is,C ]⊤. Let F
denote the rate of increase of secondary cases and V denote the progression
rate. Accordingly,xif obeys the equation
˙xif =F−V (3)
whereF andV given by
F =
Sy (Cβcy +βy (Es +Ey +Isk +Iyk))
Ss (Cβcs +βs (Es +Ey +Isk +Iyk))
0
0
µs (Es +Isk) +µy (Ey +Iyk)
(4)
and
V =
Ey (εy +ξy)
Es (εs +ξs)
Iy (ηy +ρy)−Eyεy
Is (ηs +ρs)−Esεs
Cδ
. (5)
We linearise equation (3) around the equilibrium and we denote the Jacobians
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16 Ranking the Effectiveness of Non-Pharmaceutical Interventions
ofF andV as F and V , respectively. Thus, we obtain
˙xif = (F−V )xif (6)
where
F =
¯Syβy ¯Syβy ¯Syβyk ¯Syβyk ¯Syβcy
¯Ssβyp ¯Ssβyp ¯Ssβykp ¯Ssβykp ¯Ssβcyp
0 0 0 0 0
0 0 0 0 0
µy µs kµy kµs 0
(7)
and
V =
εy +ξy 0 0 0 0
0 εs +ξs 0 0 0
−εy 0 ηy +ρy 0 0
0 −εs 0 ηs +ρs 0
0 0 0 0 δ
. (8)
Denoting σy = ηy +ρy and σs = ηs +ρs, the next generation matrix K is
therefore derived as
K =FV−1
=
¯Syβy (σy +εyk)
σy (εy +ξy)
¯Syβy (σs +εsk)
σs (εs +ξs)
¯Syβyk
σy
¯Syβyk
σs
¯Syβcy
δ
¯Ssβyp (σy +εyk)
σy (εy +ξy)
¯Ssβyp (σs +εsk)
σs (εs +ξs)
¯Ssβykp
σy
¯Ssβykp
σs
¯Ssβcyp
δ
0 0 0 0 0
0 0 0 0 0
µy (σy +εyk)
σy (εy +ξy)
µs (σs +εsk)
σs (εs +ξs)
kµy
σy
kµs
σs
0
.
(9)
The obtained matrix K is nonnegative and has rank 2. In particular, it has
three zero eigenvalues and two positive eigenvalues. According to [40], R0 is
the spectral radius ofK, i.e. its largest eigenvalue. By computing det(λI−K),
the characteristic polynomial is
pk(λ) =λ3
[
λ2−
( ¯Syβy (σy +εyk)
σy (εy +ξy) +
¯Ssβyp (σs +εsk)
σs (εs +ξs)
)
λ
− 1
δ
( ¯Syβcyµy(σy +εyk)
σy (εy +ξy) +
¯Ssβcypµs(σs +εsk)
σs (εs +ξs)
)]
.
(10)
We recall that we have assumed thatµy =µs =µ, which means that students
and staff have equal rates of spreading the virus into the environment. The
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two non-zero eigenvalues can be derived by finding the roots of the polynomial
˜pk(λ) =λ2−βy
( ¯Sy (+εyk)
σy (εy +ξy) +
¯Ssp (σs +εsk)
σs (εs +ξs)
)
λ
− µβcy
δ
( ¯Sy (σy +εyk)
σy (εy +ξy) +
¯Ssp (σs +εsk)
σs (εs +ξs)
)
.
(11)
Denote
a =βy
( ¯Sy (σy +εyk)
σy (εy +ξy) +
¯Ssp (σs +εsk)
σs (εs +ξs)
)
, c = µβcy
δβyy
. (12)
Then
˜pk(λ) =λ2−aλ−ac (13)
Since the constants a and c are both positive, the quadratic equation has two
real roots and R0 will be the larger one. Therefore, we can express R0 as
R0 = a(1 +
√
1 + 4c/a)
2 . (14)
In the next section we show how R0 is related to the stability of the
equilibrium point.
3.2.3 Stability Analysis
Proposition 1 If R0 < 1, the equilibrium points ¯x of the uncontrolled university
model (1) is asymptotically stable.
Proof Model (1) can be reformulated into a feedback interconnection. Compartments
Ey, Es, Iy, Is, Qy, Qs, C form a positive linear subsystem with output feedback
topology. Defining xl = [Ey,Es,Iy,Is,Qy,Qs,C ]⊤, ys = [Sy,Ss]⊤, yR = [Ry,Rs]⊤,
the subsystem can be formulated as
˙xl(t) =Axl(t) +Bu(t)
=
−ry 0 0 0 0 0 0
0 −rs 0 0 0 0 0
εy 0 −σy 0 0 0 0
0 εs 0 −σs 0 0 0
0 0 ηy 0 −ϕy 0 0
0 0 0 ηs 0 −ϕs 0
µy µs kµy kµs 0 0 −δ
xl(t) +
1 0
0 1
0 0
0 0
0 0
0 0
0 0
u(t)
(15)
ys(t) =Csxl(t) =
[βy βy βyk βyk 0 0 βcy
βs βs βsk βsk 0 0 βcs
]
xl(t) (16)
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yR(t) =CRxl(t) =
[ξy 0 ρy 0 ϕy 0 0
0 ξs 0 ρs 0 ϕs 0
]
xl(t) (17)
where ry = εy +ηy, rs = εs +ηs. Since output yR does not contribute to the
variations of the state variable xl, we can represent the overall system dynamics by
the output feedback loop as
u(t) =Ks(t)ys(t) =
[Sy(t) 0
0 Ss(t)
]
ys(t). (18)
Derivatives of the remaining compartments can be calculated as[ ˙Sy(t)
˙Ss(t)
]
= −
[Sy(t) 0
0 Ss(t)
]
ys(t) (19)
[ ˙Ry(t)
˙Rs(t)
]
=yR(t). (20)
Note that the system has a time-varying feedback Ks(t). Around the equilibrium ¯x,
the system behaviour is determined by using the constant feedback term ¯Ks as
¯Ks =
[ ¯Sy 0
0 ¯Ss
]
ys(t). (21)
Therefore, the dynamics of the original model is equivalent to that of this closed-loop
system. To study its stability, we firstly derive the closed-loop system matrix Acl as
Acl =A +BKsCs
=
¯Syβy −ry ¯Syβy ¯Syβyk ¯Syβyk 0 0 ¯Syβcy
¯Ssβyp ¯Ssβyp −rs ¯Ssβykp ¯Ssβykp 0 0 ¯Ssβcyp
εy 0 −σy 0 0 0 0
0 εs 0 −σs 0 0 0
0 0 ηy 0 −ϕy 0 0
0 0 0 ηs 0 −ϕs 0
µy µs kµy kµs 0 0 −δ
.
(22)
To determine its closed-loop poles, we compute its characteristic equation, i.e.
det(λI −Acl). Since all parameters are positive,Acl must have two negative eigenval-
ues at −ϕy and −ϕs. The remaining five eigenvalues are the roots of the polynomial
p5(λ):
p5(λ) =
λ +ry − ¯Syβy − ¯Syβy − ¯Syβyk − ¯Syβyk − ¯Syβcy
−¯p (λ +ry) λ +rs 0 0 0
−εy 0 λ +σy 0 0
0 −εs 0 λ +σs 0
−µy −µs −kµy −kµs δ +λ
=
λ +ry − ¯Syβy −λ −ry 0 0 − ¯Syβcy
−¯p (λ +ry) λ +rs + ¯p (λ +ry) −k (λ +rs) 0 0
−εy εy λ +σy −λ −σy 0
0 −εs εsk λ +σs 0
−µ 0 0 0 δ +λ
(23)
where we have defined ¯p =
¯Ssp
¯Sy
and used thatµy =µs =µ according to the previous
analysis. The polynomial is finally derived as
p5(λ) =λ5 +α4λ4 +α3λ3 + +α2λ2 +α1λ +α0, (24)
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where
α4 =δ +rs +ry +σs +σy − ¯Syβy − ¯Ssβyp
α3 =δrs +δry +δσs +δσy +rsry +rsσs +rsσy +ryσs +ryσy +σsσy
− ¯Syβyδ − ¯Syβcyµ − ¯Syβyrs − ¯Syβyσs − ¯Syβyσy − ¯Syβyεyk
− ¯Ssβyδp − ¯Ssβcyµp − ¯Ssβypry − ¯Ssβypσs − ¯Ssβypσy
− ¯Ssβyεskp
α2 =δrsry +δrsσs +δrsσy +δryσs +δryσy +δσsσy +rsryσs +rsryσy
+rsσsσy +ryσsσy − ¯Syβyδrs − ¯Syβyδσs − ¯Syβyδσy − ¯Syβcyµrs
− ¯Syβcyµσs − ¯Syβcyµσy − ¯Syβyrsσs − ¯Syβyrsσy − ¯Syβyσsσy
− ¯Syβyδεyk − ¯Syβcyεykµ − ¯Syβyεykrs − ¯Syβyεykσs
− ¯Ssβyδpr y − ¯Ssβyδpσ s − ¯Ssβyδpσ y − ¯Ssβcyµpr y − ¯Ssβcyµpσ s
− ¯Ssβcyµpσ y − ¯Ssβypryσs − ¯Ssβypryσy − ¯Ssβypσsσy
− ¯Ssβyδεskp − ¯Ssβcyεskµp − ¯Ssβyεskpr y − ¯Ssβyεskpσ y
α1 =δrsryσs +δrsryσy +δrsσsσy +δryσsσy +rsryσsσy − ¯Syβyδrsσs
− ¯Syβyδrsσy − ¯Syβyδσsσy − ¯Syβcyµrsσs − ¯Syβcyµrsσy
− ¯Syβcyµσsσy − ¯Syβyrsσsσy − ¯Syβyδεykrs − ¯Syβyδεykσs
− ¯Syβcyεykµr s − ¯Syβcyεykµσ s − ¯Syβyεykrsσs − ¯Ssβyδpr yσs
− ¯Ssβyδpr yσy − ¯Ssβyδpσ sσy − ¯Ssβcyµpr yσs − ¯Ssβcyµpr yσy
− ¯Ssβcyµpσ sσy − ¯Ssβypryσsσy − ¯Ssβyδεskpr y − ¯Ssβyδεskpσ y
− ¯Ssβcyεskµpr y − ¯Ssβcyεskµpσ y − ¯Ssβyεskpr yσy
α0 =δrsryσsσy − ¯Syβyδrsσsσy − ¯Syβcyµrsσsσy − ¯Syβyδεykrsσs
− ¯Syβcyεykµr sσs − ¯Ssβyδpr yσsσy − ¯Ssβcyµpr yσsσy
− ¯Ssβyδεskpr yσy − ¯Ssβcyεskµpr yσy
(25)
The conditions to obtain a stable equilibrium point can be determined using the
Routh-Hurwitz stability criterion. The Routh table is given in Table 3.
T able 3 Routh Table.
λ5 1 α3 α1
λ4 α4 α2 α0
λ3 b31 = − 1
a4
(α2 −α4α3) b32 = − 1
a4
(α0 −α1α4) 0
λ2 b21 = − 1
b31
(α4b32 −α2b31) α0 0
λ1 b11 = − 1
b21
(α0b31 −b32b21) 0 0
λ0 α0 0 0
From the Routh-Hurwitz stability criterion follows that the equilibrium point is
asymptotically stable if and only if α4 > 0, b31 > 0, b21 > 0, b11 > 0 and α0 > 0.
We evaluate these coefficients numerically for different values of R0. The results are
shown in Table 4 for R0 1. Since α0 > 0 in Table 4 and
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α0 < 0 in Table 5, the Routh-Hurwitz stability criterion confirms that the R0 found
in (14) is consistent with the expected epidemic dynamics.
T able 4 Values of the first column of the Routh table when R0 < 1.
R0 0.9957 0.9966 0.9974 0.9983 0.9992
α4 1.3087 1.3086 1.3085 1.3084 1.3083
b31 0.4609 0.4608 0.4607 0.4606 0.4605
b21 0.0648 0.0648 0.0647 0.0647 0.0646
b11 0.0036 0.0036 0.0036 0.0036 0.0036
α0 2.2031e-06 1.7561e-06 1.3091e-06 8.6205e-07 4.1504e-07
T able 5 Values of the first column of the Routh table when R0 > 1.
R0 1.0001 1.0009 1.0018 1.0027 1.0036
α4 1.3082 1.3081 1.3079 1.3078 1.3077
b31 0.4604 0.4603 0.4602 0.4601 0.4600
b21 0.0646 0.0646 0.0646 0.0645 0.0645
b11 0.0036 0.0036 0.0036 0.0036 0.0036
α0 -3.1972e-08 -4.7898e-07 -9.2600e-07 -1.3730e-06 -1.8200e-06
□
3.3 Control of the University Model
3.3.1 Formulation of the Controlled University Model
In this study we consider five non-pharmaceutical interventions that the
university can implement.
1. Compulsory mask wearing: how strongly this measure is implemented is
represented by the normalised variable 0≤κm≤ 1.
2. Keep safe social distance: how strongly this measure is implemented is
represented by the normalised variable 0≤κd≤ 1.
3. Environment disinfection: how strongly this measure is implemented is
represented by the normalised variable 0≤κe≤ 1.
4/5. Mandatory quarantines: how strongly these measures are implemented is
represented by the normalised variables 0 ≤ κqy ≤ 1 (for students) and
0≤κqs≤ 1 (for staff).
A group of five variables is initially defined to represent the reduction
factors in the infection rates, shedding rates, environmental decaying rate, and
isolation rates. Denoting these factors as u = [up, um, ue, uqy, uqs]⊤, the
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university model at this stage is expressed as
dSy(t)
dt =−{(1−up)βy[Ey(t) +kIy(t) +Es(t) +kIs(t)]
− (1−um)βcyC(t)}Sy(t)
dSs(t)
dt =−{(1−up)pβy [Es(t) +kIs(t) +Ey(t) +kIy(t)]
− (1−um)pβcyC(t)}Ss(t)
dEy(t)
dt ={(1−up)βy[Ey(t) +kIy(t) +Es(t) +kIs(t)]
+ (1−um)βcyC(t)}Sy(t)− (εy +ξy)Ey(t)
dEs(t)
dt ={(1−up)pβy [Es(t) +kIs(t) +Ey(t) +kIy(t)]
+ (1−um)pβcyC(t)}Ss(t)− (εs +ξs)Es(t)
dIy(t)
dt =εyEy(t)−uqyηyIy(t)
dIs(t)
dt =εsEs(t)−uqsηsIs(t)
dQy(t)
dt =uqyηyIy(t)−ϕyQy(t)
dQs(t)
dt =uqsηsIs(t)−ϕsQs(t)
dRy(t)
dt =ξyEy(t) +ϕyQy(t)
dRs(t)
dt =ξsEs(t) +ϕsQs(t)
dC(t)
dt = (1−um)µ (Ey(t) +kIi(t) +Es(t) +kIs(t))−ueδC (t)
(26)
Note that up, um, ue, uqyηy, and uqsηs should vary within [0, 1].
Since a reduction factor can be influenced by multiple interventions, we
need to identify the relationship between the reduction factors ( u’s) and
intervention variables (κ’s).
1. Reduction of interpersonal infection rates βy and βs
The person-to-person infection rates are directly influenced by two measures:
wearing masks and keeping social distance. Wearing masks could reduce
the probability of infections during contacts while social distancing could
reduce the number of direct contacts between individuals. Study conducted
by Karaivanov et al, [43] argued that the mandatory mask-wearing policy
in confined spaces could reduce the number of infected cases by up to 40%
weekly. Furthermore, Jarvis et al. [44] conducted a survey which showed
that the physical distancing could reduce the number of direct contacts by
74%. However, since this survey might have selection and recall bias, the
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actual result should be lower than 74% to obtain a conservative estimate.
In this case, we set the maximum reduction at 65%. Hence, 1 −up = (1−
0.4κm)(1− 0.65κm).
2. Reduction of shedding rates and environment-to-person infection rates: µy,
µs, βcy, βcs
Shedding rates as well as infections due to unclean environment can be
reduced by the use of masks. According to laboratory-based investigations
by [45, 46], masks could block approximately 50% to 70% droplets and
aerosol, greatly reducing the transmission of virus. In this case, we set the
maximum reduction of shedding rate to be 60% for a conservative estimate.
Therefore, 1−um = 1− 0.6κm.
3. Enhancement of virus environmental decaying rate δ
The environmental decaying rate could be magnified by disinfection of the
confined space. Recall that the uncontrolled decaying rate was δ = 0.7.
It is hard to determine how much this rate is increased. A conservative
estimate is that the rate is increased at the maximum by 30%, yielding a
maximum new rateueδ = 0.91. The linear relationship can be finally defined
as ue = 1 + 0.3κe.
While the analysis above is derived from considerations extracted from the
literature, these still assumed an ideal enforcement of the interventions. Since
the university cannot guarantee full compliance, we limit κm, κd, and κe to
70% of their values.
4. Quarantine enhancement
Recall that in model (1) the quarantined populations were simply equiva-
lent to the populations who developed serious symptoms and their rate were
ηy and ηs. To consider the effects of mandatory quarantines we replace ηy
andηs byuqyηy anduqsηs, respectively. (uqyηy)−1 and (uqsηs)−1 now indi-
cate the average time that unisolated symptomatic students/staff stay in
campus before being detected by the university. We set these values to 2,
meaning that the university takes two days in average to detect and iso-
late infected individuals after their symptoms develop. Thus, the maximum
values of (uqsηs)−1 and (uqsηs)−1 are both 0 .5. These values correspond
to the situation where the enforcement of mandatory quarantines reaches
the strongest degree, which means that κqy andκqs are 1. On the contrary,
when mandatory quarantines are not implemented, i.e. κqy = κqs = 0, we
want that the resulting quarantine rates uqyηy anduqsηs are stillηy andηs,
respectively. These relations are formulated as uqyηy = (0.5−ηy)κqy +ηy
and uqsηs = (0.5−ηs)κqs +ηs.
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In summary, the following relations hold
1−up = (1− 0.4· 0.7κm)(1− 0.65· 0.7κd)
1−um = 1− 0.6· 0.7κm
ue = 1 + 0.3· 0.7κe
uqyηy = (0.5−ηy)κqy +ηy
uqsηs = (0.5−ηs)κqs +ηs.
(27)
Substituting these relationships into equation (26), we obtain the final
controlled university model
dSy(t)
dt =−{(1− 0.28κm)(1− 0.455κd)βy[Ey(t) +kIy(t) +Es(t) +kIs(t)]
− (1− 0.42κm)βcyC(t)}Sy(t)
dSs(t)
dt =−{(1− 0.28κm)(1− 0.455κd)pβy [Es(t) +kIs(t) +Ey(t) +kIy(t)]
− (1− 0.42κm)pβcyC(t)}Ss(t)
dEy(t)
dt ={(1− 0.28κm)(1− 0.455κd)βy[Ey(t) +kIy(t) +Es(t) +kIs(t)]
+ (1− 0.42κm)βcyC(t)}Sy(t)− (εy +ξy)Ey(t)
dEs(t)
dt ={(1− 0.28κm)(1− 0.455κd)pβy [Es(t) +kIs(t) +Ey(t) +kIy(t)]
+ (1− 0.42κm)pβcyC(t)}Ss(t)− (εs +ξs)Es(t)
dIy(t)
dt =εyEy(t)− [(0.5−ηy)κqy +ηy +ρy]Iy(t)
dIs(t)
dt =εsEs(t)− [(0.5−ηs)κqs +ηs +ρs]Is(t)
dQy(t)
dt = [(0.5−ηy)κqy +ηy]Iy(t)−ϕyQy(t)
dQs(t)
dt = [(0.5−ηs)κqs +ηs]Is(t)−ϕsQs(t)
dRy(t)
dt =ξyEy(t) +ρyIy(t) +ϕyQy(t)
dRs(t)
dt =ξsEs(t) +ρsIs(t) +ϕsQs(t)
dC(t)
dt = (1− 0.42κm)µ (Ey(t) +kIi(t) +Es(t) +kIs(t))
− (1 + 0.21κe)δC (t).
(28)
In this model, the variables κ = [κm, κd, κe, κqy, κqs]⊤ are the control
variables that need to be optimised.
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24 Ranking the Effectiveness of Non-Pharmaceutical Interventions
3.3.2 Formulation of the Optimal Control Problem
Now we formulate the optimal control problem that, once solved, provides the
optimal trajectories that give the best combination of interventions to contain
the epidemic within the university. The optimal control problem is defined as
J∗ = min
x(·),κ(·)
J =∥x(tf)−xtar∥2
H +
∫ tf
t0
∥x(τ)−xtar∥2
Q +∥κk(τ)∥2
R dτ
s.t. ˙ x(t) =f(x(t),κ(t),t),
xmin≤x(t)≤xmax,
xf,min≤x(tf)≤xf,max,
κmin≤κ(t)≤κmax,
x(0) =x14,
(29)
wherextar represents the target state vector,∥·∥H/Q/R indicates the Euclidean
matrix norm weighted byH/Q/R and the square matricesH,Q andR contain
the weights for the final states, running states and running control variables,
respectively. The values of xtar and the weights are changed depending on
the scenario that we need to solve (see next section). The problem has also
constraints on both states and control variables. In fact, we need that the
states lie between 0 and 1. Thus, even without further requirement the state
constraints are at least xmin =xf,min = [0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0]⊤ and
xmax =xf,max = [1, 1, 1, 1, 1, 1, 1, 1, 1, 1, 1]⊤. Similarly, the lower bounds
of the control variables should be κmin = [0, 0, 0, 0, 0]⊤ while their upper
constrains are κmax = [1, 1, 1, 1, 1]⊤. The initial condition sets the starting
point of the system. We assume that the university starts to react two weeks
after the first exposed subjects appear among students or staff. Thus, we first
run the simulation of the original un-controlled model for 14 days and get the
resulting state values on day 14, namely x14. Then this state is used as the
initial condition for the optimisation problem, namely x(0) = x14. We finally
require that the epidemic is eliminated within 120 days, sot0 = 0 andtf = 120.
3.3.3 Implementation of Four Different Scenarios
Balancing the trade-off between controlling the spread of COVID-19 and
resuming the normal campus activity is the main question considered in this
study. According to different trade-off’s between these two objectives, four
scenarios are studied: minimum number of cases, minimum intervention, min-
imum non-quarantine interventions, and minimum quarantine interventions.
Each scenario corresponds to different weight matrices and different path
constraints.
For the first scenario (minimum number of cases), the university does not
impose any limitations on the strength of the interventions to lead to the
fastest mitigation of the epidemic. Mathematically, the controller is designed
to maximise the number of susceptible people during the whole period, i.e.,
2021 LATEX template
Ranking the Effectiveness of Non-Pharmaceutical Interventions 25
the proportions of the susceptible students/staff are maintained as close to one
as possible. In contrast, the values of the other compartments need to be as
close as possible to zero in this scenario. Therefore, we set the target state as
xtar = [1, 1, 0, 0, 0, 0, 0, 0, 0, 0, 0]⊤. (30)
Meanwhile, the weight matrices are set as
H =diag([100; 100; 0; 0; 0; 0; 0; 0; 0; 0; 0])
Q =diag([100; 100; 0; 0; 0; 0; 0; 0; 0; 0; 0])
R =diag([10−2; 10 −2; 10 −2; 10 −2; 10 −2]).
(31)
where in the matrix R we use 10−2 instead of 0 to improve numerical stability
of the solver. The constraints on both states and control variables remain the
same as the basic requirements discussed before, namely
xmin =[0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0]⊤
xmax =[1, 1, 1, 1, 1, 1, 1, 1, 1, 1, 1]⊤
xf,min =[0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0]⊤
xf,max =[1, 1, 1, 1, 1, 1, 1, 1, 1, 1, 1]⊤
κmin = [0, 0, 0, 0, 0]⊤
κmax = [1, 1, 1, 1, 1]⊤.
(32)
For the other three scenarios, we require that the number of susceptible
students and staff cannot go below 94% of the total population (i.e. the number
of infected individuals is equal or below 6%). We can easily achieve this by
setting more restrictive state constraints. Consequently, we do not need to
use the weights H andQ (also because it is difficult to intuitively understand
the meaning of the weights on the states in these scenarios). Hence, we select
H = 0 and Q = 0 and xtar is not used. Additionally, to ensure that the
epidemic is completely concluded after 134 days, the number of exposed and
infected individuals should become zero at the final state. Recall that Ny,Ns,
and Nt indicate the total number of student, staff, and the total population,
respectively. Then the constraints on states should be
xmin = [0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0]⊤
xmax = [1, 1, 1, 1, 1, 1, 1, 1, 1, 1, 1]⊤
xf,min = [0.94Ny
Nt
, 0.94Ns
Nt
, 0, 0, 0, 0, 0, 0, 0, 0, 0]⊤
xf,max = [1, 1, 10−4, 10−4, 10−4, 10−4, 1, 1, 1, 1, 1]⊤,
(33)
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26 Ranking the Effectiveness of Non-Pharmaceutical Interventions
while the input constraints remain unchanged
κmin = [0, 0, 0, 0, 0]⊤
κmax = [1, 1, 1, 1, 1]⊤.
(34)
The only difference in the formulation of the other three scenarios is the value
of the weight matrixR. In the minimum intervention scenario, the solver aims
to minimize the total norm of the control signal while satisfying the 94%
constraint. Thus, all control variables are heavily weighted and the matrix R
is selected as
R =diag([100; 100; 100; 100; 100]) . (35)
In the scenario of minimisation of non-quarantine interventions, the strength
of first three interventions (wearing masks κm, keeping social distance κd and
disinfecting the environmentκe) are minimised, while the quarantines are not.
In this situation, the matrix R becomes
R =diag([100; 100; 100; 10 −2; 10 −2]). (36)
In the minimum quarantine scenario, the norm of quarantine rates for the
infected students (κqy) and staff (κqs) are minimised. Since mandatory quaran-
tine has the largest impact on campus activities, this scenario aims to find how
the spread can be minimised while avoiding quarantine enforcement. Hence,
the matrix R is
R =diag([10−2; 10 −2; 10 −2; 100; 100]). (37)
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Ranking the Effectiveness of Non-Pharmaceutical Interventions 27
Code availability
The code is available at https://github.com/ZiruiNiu/University Epidemic
Model with Control.git.
Data availability
All model’s parameters taken from the literature are opportunely referenced
in the main text. No further data is used.
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28 Ranking the Effectiveness of Non-Pharmaceutical Interventions
Appendix A Sensitivity Figures
0 20 40 60 80 100 120
Time (days)
0
0.01
0.02
0.03
0.04
Curves of Ey(t)
y Testing Result - Exposed Students
0 20 40 60 80 100 120
Time (days)
0
0.005
0.01
Curves of Es(t)
y Testing Result - Exposed Staff
0 20 40 60 80 100 120
Time (days)
0
0.02
0.04
0.06
Curves of Iy(t)
y Testing Result - Infected Students
0 20 40 60 80 100 120
Time (days)
0
0.005
0.01
Curves of Is(t)
y Testing Result - Infected Staff
y = 0.07
y = 0.075
y = 0.08
y = 0.085
y = 0.09
y = 0.095
y = 0.1
y = 0.105
y = 0.11
y = 0.115
a
c
b
d
Fig. A1 Numerical testing of student-to-student infection rate βy. Trajectories of
cases among students and staffs whenβy varying from 0.07 to 0.115. With differentβy, panels
a and b show the proportion trajectories of exposed students and staffs respectively while
panels c and d depict the proportion trajectories of infected students and staffs respectively.
0 50 100 150
Time (days)
0
0.01
0.02
0.03
Curves of Ey(t)
s Testing Result - Exposed Students
0 50 100 150
Time (days)
0
2
4
6
8
Curves of Es(t)
10-3 s Testing Result - Exposed Staff
0 50 100 150
Time (days)
0
0.01
0.02
0.03
0.04
Curves of Iy(t)
s Testing Result - Infected Students
0 50 100 150
Time (days)
0
2
4
6
8
Curves of Is(t)
10-3 s Testing Result - Infected Staff
s = 0.08
s = 0.085
s = 0.09
s = 0.095
s = 0.1
s = 0.105
s = 0.11
s = 0.115
s = 0.12
s = 0.125
a
c
b
d
Fig. A2 Numerical testing of student-to-student infection rate βs. Trajectories of
cases among students and staffs whenβs varying from 0.08 to 0.125. With differentβs, panels
a and b show the proportion trajectories of exposed students and staffs respectively while
panels c and d depict the proportion trajectories of infected students and staffs respectively.
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Ranking the Effectiveness of Non-Pharmaceutical Interventions 29
0 50 100 150
Time (days)
0
0.01
0.02
0.03
0.04
Curves of Ey(t)
cy Testing Result - Exposed Students
0 50 100 150
Time (days)
0
0.005
0.01
Curves of Es(t)
cy Testing Result - Exposed Staff
0 50 100 150
Time (days)
0
0.01
0.02
0.03
0.04
Curves of Iy(t)
cy Testing Result - Infected Students
0 50 100 150
Time (days)
0
2
4
6
8
Curves of Is(t)
10-3 cy Testing Result - Infected Staff
cy = 0.075
cy = 0.08
cy = 0.085
cy = 0.09
cy = 0.095
cy = 0.1
cy = 0.105
cy = 0.11
cy = 0.115
cy = 0.12
a
c
b
d
Fig. A3 Numerical testing of student-to-student infection rate βcy. Trajectories
of cases among students and staffs when βcy varying from 0.075 to 0.12. With different
βcy, panels a and b show the proportion trajectories of exposed students and staffs respec-
tively while panels c and d depict the proportion trajectories of infected students and staffs
respectively.
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30 Ranking the Effectiveness of Non-Pharmaceutical Interventions
0 50 100 150
Time (days)
0
0.01
0.02
0.03
Curves of Ey(t)
cs Testing Result - Exposed Students
0 50 100 150
Time (days)
0
2
4
6
8
Curves of Es(t)
10-3 cs Testing Result - Exposed Staff
0 50 100 150
Time (days)
0
0.01
0.02
0.03
0.04
Curves of Iy(t)
cs Testing Result - Infected Students
0 50 100 150
Time (days)
0
2
4
6
8
Curves of Is(t)
10-3 cs Testing Result - Infected Staff
cs = 0.095
cs = 0.1
cs = 0.105
cs = 0.11
cs = 0.115
cs = 0.12
cs = 0.125
cs = 0.13
cs = 0.135
cs = 0.14
a
c
b
d
Fig. A4 Numerical testing of student-to-student infection rate βcs. Trajectories
of cases among students and staffs when βcs varying from 0.095 to 0.14. With different
βcs, panels a and b show the proportion trajectories of exposed students and staffs respec-
tively while panels c and d depict the proportion trajectories of infected students and staffs
respectively.
0 50 100 150
Time (days)
0
0.01
0.02
0.03
Curves of Ey(t)
y Testing Result - Exposed Students
0 50 100 150
Time (days)
0
2
4
6
8
Curves of Es(t)
10-3 y Testing Result - Exposed Staff
0 50 100 150
Time (days)
0
0.01
0.02
0.03
0.04
Curves of Iy(t)
y Testing Result - Infected Students
0 50 100 150
Time (days)
0
2
4
6
8
Curves of Is(t)
10-3 y Testing Result - Infected Staff
y = 0.007
y = 0.008
y = 0.009
y = 0.01
y = 0.011
y = 0.012
y = 0.013
y = 0.014
y = 0.015
y = 0.016
a
c
b
d
Fig. A5 Numerical testing of student-to-student infection rate ηy. Trajectories of
cases among students and staffs whenηy varying from 0.007 to 0.016. With differentηy, pan-
els a and b show the proportion trajectories of exposed students and staffs respectively while
panels c and d depict the proportion trajectories of infected students and staffs respectively.
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0 50 100 150
Time (days)
0
0.01
0.02
0.03
Curves of Ey(t)
s Testing Result - Exposed Students
0 50 100 150
Time (days)
0
2
4
6
8
Curves of Es(t)
10-3 s Testing Result - Exposed Staff
0 50 100 150
Time (days)
0
0.01
0.02
0.03
0.04
Curves of Iy(t)
s Testing Result - Infected Students
0 50 100 150
Time (days)
0
2
4
6
8
Curves of Is(t)
10-3 s Testing Result - Infected Staff
s = 0.016
s = 0.017
s = 0.018
s = 0.019
s = 0.02
s = 0.021
s = 0.022
s = 0.023
s = 0.024
s = 0.025
a
c
b
d
Fig. A6 Numerical testing of student-to-student infection rate ηs. Trajectories of
cases among students and staffs whenηs varying from 0.016 to 0.025. With differentηs, pan-
els a and b show the proportion trajectories of exposed students and staffs respectively while
panels c and d depict the proportion trajectories of infected students and staffs respectively.
0 50 100 150
Time (days)
0
0.01
0.02
0.03
0.04
Curves of Ey(t)
Testing Result - Exposed Students
0 50 100 150
Time (days)
0
0.005
0.01
Curves of Es(t)
Testing Result - Exposed Staff
0 50 100 150
Time (days)
0
0.02
0.04
0.06
Curves of Iy(t)
Testing Result - Infected Students
0 50 100 150
Time (days)
0
0.005
0.01
Curves of Is(t)
Testing Result - Infected Staff
= 0.5
= 0.55
= 0.6
= 0.65
= 0.7
= 0.75
= 0.8
= 0.85
= 0.9
= 0.95
a
c
b
d
Fig. A7 Numerical testing of student-to-student infection rate δ. Trajectories of
cases among students and staffs when δ varying from 0.5 to 0.95. With different δ, panels
a and b show the proportion trajectories of exposed students and staffs respectively while
panels c and d depict the proportion trajectories of infected students and staffs respectively.
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32 Ranking the Effectiveness of Non-Pharmaceutical Interventions
0 50 100 150
Time (days)
0
0.02
0.04
0.06
Curves of Ey(t)
Testing Result - Exposed Students
0 50 100 150
Time (days)
0
0.005
0.01
0.015
Curves of Es(t)
Testing Result - Exposed Staff
0 50 100 150
Time (days)
0
0.02
0.04
0.06
0.08
Curves of Iy(t)
Testing Result - Infected Students
0 50 100 150
Time (days)
0
0.005
0.01
0.015
Curves of Is(t)
Testing Result - Infected Staff
= 0.05
= 0.1
= 0.15
= 0.2
= 0.25
= 0.3
= 0.35
= 0.4
= 0.45
= 0.5
a
c
b
d
Fig. A8 Numerical testing of student-to-student infection rate µ. Trajectories of
cases among students and staffs when µ varying from 0.05 to 0.5. With different µ, panels
a and b show the proportion trajectories of exposed students and staffs respectively while
panels c and d depict the proportion trajectories of infected students and staffs respectively.
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