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\begin{document}
\begin{center}
  {\noindent \LARGE \bf Simulation protocol:\\[2mm]
    Comparison of confidence intervals summarizing the\\[2mm]
    uncertainty of the combined estimate of a meta-analysis
  }\\
\bigskip
{\noindent \Large Leonhard Held, Felix Hofmann
}\end{center}
\bigskip
\vspace*{.5cm}

For the present protocol is inspired by \citet{burt:etal:06} and \citet{morr:etal:19}.

The simulation is implemented in \texttt{simulate\_all.R}.

\tableofcontents

\newpage 

\section{Aims and objectives}\label{ref:aims}

The aim of this simulation study is the comparison of confidence intervals
(CIs) summarizing the uncertainty of the combined estimate of a meta-analysis.
Specifically, we focus on CIs constructed using p-value functions that
implement the methods from \citet{edgington:72} and \citet{fisher:34}. The
underlying data sets are simulated as described in Section~\ref{sec:simproc}
and Section~\ref{sec:scenario}. The resulting intervals are then compared to CIs
constructed using the other methods listed in Section~\ref{sec:method} using the
measures defined in Section~\ref{sec:meas}.

\section{Simulation of the data sets} \label{sec:simproc}

\subsection{Allowance for failures}
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We expect no failures, \ie, for all simulated data sets all type of CI methods
should lead to a valid CI and all valid CIs should lead to valid CI criteria.
If a failure occurs, we stop the simulation and investigate the reason for the
failure. 

\subsection{Software to perform simulations}
The simulation study is performed using the statistical software R \citep{R}.
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We save the output of \texttt{sessionInfo()} giving information on the used
version of R, packages, and platform with the simulation results.

\subsection{Random number generator}
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We use the package \pkg{doRNG} with its default random number generator to
ensure that random numbers generated inside parallel for loops are independent
and reproducible.


\subsection{Scenarios to be investigated} \label{sec:scenario}
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The $720$ \todo{update number} simulated scenarios consist of all combinations
of the following parameters:
\begin{itemize}
\item Higgin's $I^2$ heterogeneity measure $\in \{0, 0.3, 0.6, 0.9\}$.
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\item We always use an additive heterogeneity model. \todo{Maybe remove this entirely?}
\item Number of studies summarized by the meta-analysis $k \in \{3, 5, 10, 20, 50\}$.
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\item Publication bias is  $\in \{\text{'none'}, \text{'moderate'}, \text{'strong'}\}$
  following the terminology of \citet{henm:copa:10}. 
\item The average study effect $\theta \in \{0.2, 0.5\}$. 
  %, and we set it to $\theta = 0.2$ to
  %obtain a similar scenario as used in \citet{henm:copa:10}.
\item The distribution to draw the true study values $\delta_i$ is either
  'Gaussian' or 't' with 4 degrees of freedom. The latter still has finite mean
    and variance, but leads to more 'outliers'.
\item The sample size $n_i$ of the $i$-th study (number of patients per study)
  is $n_i = 50$ (small study) except for 0, 1, or 2 studies where
  $n_i=500$ (large study). 
\end{itemize}
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Note that \citet{IntHoutIoannidis} use a similar setup.

\subsection{Simulation details}

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% For the \textbf{Additive heterogeneity model without publication bias}, the
% simulation of one meta-analysis dataset is performed as follows:
The simulation of one meta-analysis data set is performed as follows:

\begin{enumerate}
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\item Compute the within-study variance
  \begin{equation} \label{eq:eps2}
    \epsilon^2 = \frac{2}{k} \sum\limits_{i=1}^k \frac{1}{n_i}.
  \end{equation}
\item Compute the between-study variance
  \begin{equation}\label{eq:eq1}
    \tau^2 = \epsilon^2 \frac{I^2}{1-I^2}.
  \end{equation}
\item For a trial $i$ of the meta-analysis with $k$ trials, $i = 1, \dots, k$:
  \begin{enumerate}
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    \item Simulate the true effect size using the Gaussian model:
      $\delta_i \sim \N(\theta, \tau^2)$ or using a Student-$t$ distribution
      with 4 degrees of freedom such that the samples have mean $\theta$ and
      variance $\tau^2$.
    \item Simulate the effect estimates of each trial
      $y_i \sim \N(\delta_i, \frac{2}{n_i})$.
    \item Simulate the standard errors of the trial outcomes:
      $\text{se}_i \sim \sqrt{\frac{\chi^2(2n_i-2)}{(n_i-1)n_i}}$.
  \end{enumerate}
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\end{enumerate}

\paragraph{Note: The marginal variance}\mbox{}\\
The marginal variance of this simulation procedure is
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$\tau^2 + 2/n_i$, so follows the additive heterogeneity model as intended.
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% For the \textbf{Multiplicative model without publication bias}, the simulation
% of one meta-analysis dataset is performed as follows:
% \begin{enumerate}
% \item Compute the within-study variance
%   $\epsilon^2 = \frac{2}{k} \sum\limits_{i=1}^k \frac{1}{n_i}$.
%   \item Compute the multiplicative heterogeneity factor
%     $\phi = \frac{1}{1-I^2}$. Compute the corresponding
%     \begin{equation}\label{eq:eq2}
%       \tau^2 = \epsilon^2 \, (\phi-1) .
%     \end{equation}
% \item For a trial $i$ of the meta-analysis with $k$ trials, $i = 1, \dots, k$:
%   \begin{enumerate}
%     \item Simulate the true effect size using the Gaussian model:
%       $\delta_i \sim \N(\theta, \tau^2)$ or using a Student-$t$ distribution
%       such that the samples have mean $\theta$ and variance $\tau^2$.
%     \item Simulate the effect estimates of each trial
%       $y_i \sim \N(\delta_i, \frac{2}{n_i})$.
%     \item Simulate the standard errors of the trial outcomes:
%       $\text{se}_i \sim \sqrt{\frac{\chi^2(2n_i-2)}{(n_i-1)n_i}}$.
%   \end{enumerate}
% \end{enumerate}
%
%
% \paragraph{Note: The marginal variance}\mbox{}\\
% The marginal variance of this simulation procedure is
% $\frac{2}{n} \, (\phi-1) + \frac{2}{n} = \frac{2\phi}{n} = \phi \, \epsilon^2$,
% so follows the multiplicative model as intended.

\paragraph{Note: Publication bias}\mbox{}\\
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To simulate studies under \textbf{publication bias}, we follow the suggestion
of \citet{henm:copa:10} and accept each simulated study with probability
\begin{equation} \label{eq:pbias}
\exp(-4\, \Phi(-y_i / \text{se}_i)^\gamma ),
\end{equation}
where $\gamma = 3$ and $\gamma = 1.5$ correspond to \emph{moderate} and
\emph{strong} publication bias, respectively.
This is, accepted studies are kept and for a rejected study we replace $y_i$
and $\text{se}_i$ by newly simulated values, which are then again accepted
with the given probability above. This procedure is repeated until the required
number of studies is simulated. 

To obtain a similar scenario as in \citet{henm:copa:10} we set
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$$
\theta / \sqrt{2/n_i}  \overset{!}{=} 1 \Rightarrow \theta = \sqrt{2/n_i}
\vadjust{\todo{Where does this come from? Does this still apply when $\theta =
0.5$?}}
$$
However, we assume that only small studies with $n_i = 50$ are subject to
publication bias. Thus, larger studies with $n_i = 500$ are always accepted.
As described in Section~\ref{sec:scenario}, we set $\theta \in \{0.2, 0.5\}$. See the R function \texttt{simREbias()}.

% The mean study effect $\theta$ and the sample size $n_i$ have an influence
% on the acceptance probability 

% \paragraph{Note: Unbalanced sample sizes}\mbox{}\\
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% To study the effect of unbalanced sample sizes $n_1, \ldots, n_k$ we consider
% the following setup:
% \begin{enumerate}
% \item Increase the sample size of \textbf{one} of the $k$ by a factor 10. 
% \item Increase the sample size of \textbf{two} of the $k$ by a factor 10. 
% \end{enumerate}
%% See the argument \texttt{large} of \texttt{simREbias()}.

\subsection{Simulation procedure}
For each scenario in Section~\ref{sec:scenario} we
\begin{enumerate}
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\item simulate 10'000 meta-analysis data sets
\item compute the CIs listed in Section~\ref{sec:method} for each meta-analysis
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\item summarize the performance of the CIs by the criteria listed in
  Section~\ref{sec:meas}
\end{enumerate}

\section{Analysis of the confidence intervals}

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This section contains an overview over the construction methods for CIs
that we consider in this simulation. Moreover, we explain what measures we
use in order to compare the different CIs with each other.

\subsection{Construction methods for confidence intervals} \label{sec:method}

For this project, we will calculate 95\% CIs according to the following methods.

\begin{enumerate}
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\item Hartung Knapp Sidik Jonkman (HK) \citep{IntHoutIoannidis}.
\item Random effects model (with REML estimate of the heterogeneity variance).
\item Henmi and Copas (HC) \citep{henm:copa:10}.
\item Harmonic mean analysis with alternative \texttt{none} \citep{Held2020b}
  and without variance adjustment. % Check
% \item Harmonic mean analysis with alternative {\texttt two.sided}
%  \cite{Held2020b} % This was also thrown out
\item Harmonic mean analysis with alternative \texttt{none}, additive variance
  adjustment with $\hat \tau^2$. An extension of the idea in \citet{Held2020b}. 
\item Harmonic mean analysis with alternative \texttt{none}, multiplicative
  variance adjustment \citep{mawd:etal:17}.
\item $k$-trials rule with alternative \texttt{none} and without
  variance adjustment.
\item $k$-trials rule with alternative \texttt{none}, additive variance
  adjustment with $\hat \tau^2$. 
\item $k$-trials rule with alternative \texttt{none}, multiplicative variance
  adjustment.
\end{enumerate}

\subsection{Definition of the $k$-trials rule} \label{sec:ktrial}

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Similar to the harmonic mean method, the $k$-trials rule takes a mean value
under the null hypothesis $\mu_{0}$ as well as effect estimates
$\hat{\theta_{i}}, i = 1, \dots, k$ and the corresponding standard errors
$\text{se}(\hat{\theta_i})$ from $k$ different studies as input and calculates
the resulting $p$-value according to Equation~\ref{f:ktrial}.

\begin{equation}\label{f:ktrial}
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p(\mu_0) = \text{max} \left( 
  \Phi \left( \frac{\hat{\theta_i} - \mu_0}{\text{se}(\hat{\theta_{i}})} \right)
  \right)^k
\end{equation}

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As the effect estimates $\hat{\theta_i}$ and the corresponding standard
errors $\text{se}(\hat{\theta_i})$ are usually given in the context of
meta-analyses, the above $p$-value function only depends on $\mu_{0}$.
Therefore, CI limits are computed by searching for those values of $\mu_0$ for
which $p(\mu_0) = 0.05$. This may result in confidence sets containing more
than one confidence interval. 
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In case of variance adjustments, the term $\text{se}(\hat{\theta_i})$  in
Equation~\ref{f:ktrial} is replaced with
$\text{se}_{\text{adj}}(\hat{\theta_i})$, which is defined in
Subsection~\ref{sec:varadj}.

\subsection{Definition of the variance adjustments} \label{sec:varadj}

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As stated in Subsection~\ref{sec:method}, the harmonic mean and $k$-trials
methods can be extended such that heterogeneity between the individual studies
is taken into account. In scenarios where the additive variance adjustment is
used, we estimate the between study variance $\tau^2$ using the REML method
implemented in the \texttt{metagen} \texttt{R}-package ``meta'' and adjust
the study-specific standard errors such that
$\text{se}_{\text{adj}}(\hat{\theta_i}) = \sqrt{\text{se}(\hat{\theta_i})^2 + \tau^2}$.
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In case of the multiplicative variance adjustment, we estimate the
multiplicative parameter $\phi$ as described in \citet{mawd:etal:17} and adjust
the study-specific standard errors such that
$\text{se}_{\text{adj}}(\hat{\theta_i}) = \text{se}(\hat{\theta_i}) \cdot \sqrt{\phi}$.

\subsection{Measures considered} \label{sec:meas}

We assess the CIs using the following criteria
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\begin{enumerate}
  \item CI coverage of combined effect, \ie, the proportion of intervals
    containing the true effect % coverage_true
  \item CI coverage of study effects, \ie, the proportion of intervals
    containing the true study-specific effects % coverage_effects
  \item CI coverage of all study effects, \ie, whether or not the CI covers
    all of the study effects %coverage_all
  \item CI coverage of at least one of the study effects, \ie, whether or not
    the CI covers at least one of the study effects % coverage_effects_min1
  \item Prediction Interval (PI) coverage, \ie, the proportion of intervals
    containing the treatment effect of a newly simulated study. The newly
    simulated study has $n = 50$ and is not subject to publication bias. All
    other simulation parameters stay the same as for the simulation of the
    original studies (only for Harmonic mean, $k$-trials, REML, and HK methods)
    % coverage_prediction
  \item CI width (Corresponds to the sum the width of the individual intervals
    in case of more than one interval)%width
  \item Interval score \citep{Gnei:Raft:07} % score
  \item Number of CIs (only for Harmonic mean and $k$-trials methods). % n
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\end{enumerate}
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For the Harmonic mean and $k$-trials methods, we also investigate the
distribution of the lowest value of the $p$-value function between the lowest
and the highest treatment effect of the simulated studies. In order to do so,
we calculate the following measures:
\begin{itemize}
\item Minimum
\item First quartile
\item Mean
\item Median
\item Third quartile
\item Maximum
\end{itemize}

\vspace*{.5cm}

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As both methods, harmonic mean and $k$-trials, can result in more than one
CI for a given meta-analysis, we record the relative frequency of the number
of intervals $m$ over the 10'000 iterations for each of the different scenarios
mentioned in Section~\ref{sec:scenario}. However, we truncate the distribution
by summarising all events where the number of intervals is $> 9$.

\section{
  Estimates to be stored for each simulation and summary measures to
  be calculated over all simulations
}
For each simulated meta-analysis we construct CIs according to all methods
(Section~\ref{sec:method}) and calculate all available assessments
(Section~\ref{sec:meas}) for the respective method. For assessments 1-8 in
Subsection~\ref{sec:meas} we only store the mean value of all the 10'000
iterations in a specific scenario. Regarding the distribution of the lowest
value of the $p$-value function, we store the summary measures mentioned in
the respective paragraph of Subsection~\ref{sec:meas}. We calculate the relative
frequencies of the number of intervals $m=1, 2, \ldots, 9, >9$ in each
confidence set over the 10'000 iterations of the same scenario.

\section{Presentation of the simulation results}
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For each of the performance measures 1-8 in Subsection~\ref{sec:meas} we
construct plots with

\begin{itemize}
\item the number of studies $k$ on the $x$-axis
\item the performance measure on the $y$-axis
\item one connecting line and color for each value of $I^2$
\item one panel for each CI method
\end{itemize}

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Regarding the distribution of the $p$-value function for the harmonic mean
and $k$-trials methods, we will create plots that contain
\begin{itemize}
\item the number of studies $k$ on the $x$-axis
\item the value of the summary statistic on the $y$-axis
\item one connecting line and color for each summary statistic
\item one panel for each CI method
\end{itemize}

The plots for the relative frequencies of the number of intervals have
\begin{itemize}
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\item the category ($1$ to $9$ and $>9$) indicating the number of intervals
  $n$ on the $x$-axis
\item the relative frequency on the $y$-axis
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\item a bar for each category indicating the relative frequency for the
  respective category
\item one panel for each CI method
\end{itemize}


\newpage
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\end{document}