Household Engagement


We are aiming to enroll a total of 50 households into this study, including 10 households with existing municipal sewer connections, 30 households from Phase III, and 10 households from Phase IV.

As of 2024-08-18, 8 households have been enrolled into this study, including:

Sample Collection and Processing


From each household, at each of the six visits, we will collect:

All samples will be cultured for E. coli and enterococci. A portion of these samples will be extracted for total nucleic acids and analyzed for pathogenic targets by TaqMan Array Cards.

As of 2024-08-18,

Preliminary Data

---
title: "CWP Project Tracking: Evaluation of the Alabama Wastewater Demonstration"
output: 
  flexdashboard::flex_dashboard:
    storyboard: true
    social: menu
    source: embed
    theme:
      primary: "#7BAFD4"
      navbar-bg: "#13294B"
---

```{r setup}
#Load libraries
library(tidyverse)
library(readxl)
library(openxlsx)
library(purrr)
library(ggpubfigs)
library(flexdashboard)
library(epoxy)
```

```{r color palettes}
#Load color palettes

primary_palette = c("#7BAFD4", "#13294B", "#151515", "#FFFFFF", "#F8F8F8")
secondary_palette = c("#4F758B", "#00594C", "#EF426F", "#00A5AD", "#FFD100", "#C4D600","#F4E8DD")
```


```{r load data}

#Load data

#Read in the excel file names 
raw_files = fs::dir_ls("./data/", glob="*.xlsx")

#Read in the data from the excel files and sheets 

for(i in 1:length(raw_files)){
my_sheet_names <- excel_sheets(raw_files[i])
my_sheets <- lapply(my_sheet_names, function(x) read_excel(raw_files[i], sheet = x))
names(my_sheets) <- my_sheet_names
list2env(my_sheets, envir=.GlobalEnv)
}

```


```{r}

todays_date = Sys.Date()

```




### Household Engagement


```{r participant engagement, fig.width = 10, fig.height = 6}


participant_engagement = enrollment_recruitment_visits %>% 
  pivot_longer(cols = c("Enrollment", "V01", "V02", "V03", "V04", "V05", "V06"), 
               names_to = "benchmark", values_to = "date") %>%
  mutate(date = as.Date(date)) %>%
  mutate(tally = case_when(is.na(date) == TRUE ~ 0, 
                            TRUE ~ 1))

households_enrolled = 
  participant_engagement %>%
  filter(benchmark == "Enrollment") %>%
  tally()

n_enrolled = as.numeric(households_enrolled$n)


households_arm =
  participant_engagement %>%
    filter(benchmark == "Enrollment") %>%
  group_by(study_arm) %>%
  tally()

n_sewerage = as.numeric(households_arm[households_arm$study_arm == "sewerage",2])
n_intervention = as.numeric(households_arm[households_arm$study_arm == "intervention",2])
n_intervention_phaseIV = 0


participant_engagement %>%
  ggplot() + 
  geom_col(aes(x = benchmark, y = tally, fill = study_arm)) + 
  ylim(0,50) + 
  ylab("Number of Households") + 
  xlab("Stage")+
  labs(fill = "Study Arm") + 
  scale_fill_manual(values = secondary_palette) +
  theme_big_grid() + 
  theme(legend.position = "right")

```

***

We are aiming to enroll a total of 50 households into this study, including 10 households with existing municipal sewer connections, 30 households from Phase III, and 10 households from Phase IV.


As of `r todays_date`, `r n_enrolled` households have been enrolled into this study, including: 

- `r n_sewerage` households with existing municipal sewer connections

- `r n_intervention` households connecting to the demonstration system in Phase III

- `r n_intervention_phaseIV` households connecting to the demonstration system in Phase IV.




### Sample Collection and Processing

```{r sample collection and processing, fig.width = 10, fig.height = 8}

#How many samples have been collected and cultured? 
Cultured = 
  Colilert %>% 
  group_by(HouseholdNo, Type, Status) %>% 
  tally() %>%
  group_by(Type, Status) %>% 
  tally() %>%
  ungroup() %>%
  mutate(Type = as.factor(Type), 
         Type = fct_recode(Type, 
                           "Septic Tank Influent" = "SLS", 
                           "Sewage Lagoon Influent" = "SGLN", 
                           "Soil - Impacted" = "IS", 
                           "Soil - Unimpacted" = "US", 
                           "Drinking Water" = "DW")) %>%
  filter(Status != "C") %>%
  select(Type, n) %>%
  mutate(benchmark = "Cultured")


#How many samples have been archived for extraction?
archive = rbind(`BOX-DWA-HH01-`, `BOX-SOILA-HH01-`, `BOX-WWA-HH01-`) #Only the "A" boxes. "B" is for backup.

Archived = archive %>%
  drop_na() %>%
  separate(sample_id, into = c("household_id", "visit_no", "Type", "replicate"), sep = "-") %>%
  mutate(Type = as.factor(Type), 
         Type = fct_recode(Type, 
                           "Septic Tank Influent" = "SLS", 
                           "Sewage Lagoon Influent" = "SLL", 
                           "Soil - Impacted" = "IS", 
                           "Soil - Unimpacted" = "US", 
                           "Drinking Water" = "DW")) %>%
  filter(Type != "CW") %>%
  group_by(Type) %>%
  summarise(n = n()) %>%
  mutate(benchmark = "Archived")

#How many samples have been extracted? 

Extracted = 
  data.frame(Type = c("Septic Tank Influent", 
                           "Sewage Lagoon Influent", 
                           "Soil - Impacted", 
                           "Soil - Unimpacted", 
                           "Drinking Water"), 
             n = 0, 
             benchmark = "Extracted")

#How many samples have been analyzed by TAC? 

TAC = 
  data.frame(Type = c("Septic Tank Influent", 
                           "Sewage Lagoon Influent", 
                           "Soil - Impacted", 
                           "Soil - Unimpacted", 
                           "Drinking Water"), 
             n = 0, 
             benchmark = "TAC")

sample_processing = rbind(Cultured, Archived, Extracted, TAC)


#Generate a figure

sample_processing %>%
 ggplot(aes(x = reorder(benchmark, -n), y = n, fill = Type)) + 
  geom_col() + 
  ylab("No. Samples") + 
  xlab("Processing Stage")+
  theme_big_grid() +
  theme(legend.position = "right") + 
  scale_fill_manual(values = secondary_palette) + 
  ylim(0,50)


#Add details to the caption

n_collected = 
  sample_processing %>%
  group_by(benchmark) %>%
  summarize(n = sum(n))

n_cultured = as.numeric(n_collected[n_collected$benchmark == "Cultured",2])
n_archived = as.numeric(n_collected[n_collected$benchmark == "Archived",2])
n_extracted = as.numeric(n_collected[n_collected$benchmark == "Extracted",2])
n_TAC = as.numeric(n_collected[n_collected$benchmark == "Extracted",2])

```

***

From each household, at each of the six visits, we will collect: 

- Drinking water 

- Soil, undisturbed

- Soil, impacted by raw sewage (if relevant)

- Septic sludge or influent wastewater from municipal sewer


All samples will be cultured for E. coli and enterococci. A portion of these samples will be extracted for total nucleic acids and analyzed for pathogenic targets by TaqMan Array Cards. 


As of `r Sys.Date()`, 

- `r n_cultured` total samples have been collected.

- `r n_cultured` total samples have been cultured for E. coli and enterococci. 

- `r n_archived` total samples have been archived in duplicate. 

- `r n_extracted` total samples have been extracted for total nucleic acids. 

- `r n_TAC` total samples have been analyzed by TaqMan Array Card.


### Preliminary Data