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PLOS One logoLink to PLOS One
. 2022 Dec 1;17(12):e0274656. doi: 10.1371/journal.pone.0274656

Malaria prevention knowledge, attitudes, and practices (KAP) among adolescents living in an area of persistent transmission in Senegal: Results from a cross-sectional study

Fassiatou Tairou 1,*, Saira Nawaz 2, Marc Christian Tahita 3, Samantha Herrera 4, Babacar Faye 1, Roger C K Tine 1
Editor: Sammy O Sam-Wobo5
PMCID: PMC9714833  PMID: 36454893

Abstract

Introduction

While malaria morbidity has sharply declined in several areas in Senegal, it remains an important problem in the southern part of the country, particularly among adolescents. Understanding adolescents’ knowledge, attitudes, prevention and care-seeking practices is important to inform more targeted interventions aimed at optimizing adolescents’ uptake of malaria prevention and control measures. This study assessed malaria-related knowledge, attitudes, and practices (KAP) among adolescents living in a highly persistent transmission area in Senegal.

Methods

A community-based cross-sectional survey was conducted among 391 adolescents living in the Saraya health district. A multistage random sampling technique was used to select households. An electronic questionnaire developed on Open Data Kit (ODK), was used to collect data on socio-demographic characteristics, household assets, adolescents’ knowledge of malaria, as well as their attitudes with regards to malaria prevention, and care-seeking behaviors. Bivariate and multivariate analyses were performed to assess factors associated with adolescents’ KAP towards malaria.

Results

Nearly, one-third of the participants had good knowledge of malaria (34.4%) and good practice in regards to malaria preventive measures (32.8%) while 59.0% had a positive attitude and 73.8% had good care-seeking behavior regarding malaria. Multivariate analysis revealed that a primary (aOR = 5.43, p = 0.002) or secondary level of education (aOR = 10.41, p = 0.000) was associated with good knowledge of malaria transmission, signs, and prevention measures. Male individuals had lower knowledge compared to female ones (aOR = 0.40, p = 0.001). Individuals belonging to households from the highest wealth quintile were more likely to have a positive attitude towards malaria compared to those from households in the lowest wealth quintile (aOR = 3.49, p = 0.004). The odds of positive attitude towards malaria decreased among participants with koranic and primary education level, respectively (aOR = 0.14, p = 0.005) and (aOR = 0.24, p = 0.019). A positive attitude was 1.89 more likely to be (aOR = 1.89, p = 0.026) associated with good practice of prevention measures compared to adolescents who demonstrated negative attitudes. Individuals from households in the fourth (aOR = 0.42, p = 0.024), middle (aOR = 0.34, P = 0.005), and second (aOR = 0.42, p = 0.027) wealth quintiles were less likely to use malaria prevention measures compared to those from households in the highest wealth quintile.

Conclusion

The study revealed that adolescents, generally have poor levels of malaria knowledge and low uptake of malaria prevention and control interventions. Targeted interventions for high-risk adolescents are needed, that focus on improving their knowledge of the disease and effective preventive measures, and on increasing their access to health care services and LLINs.

Introduction

Malaria remains a severe global public health problem, despite important efforts to control the disease. Malaria cases declined globally from 238 million in 2000 to 229 million in 2019 [1], while the incidence rate decreased from 80 per 1000 population at risk in 2000 to 57 in 2019 [1]. However, the Coronavirus (COVID-19) pandemic has disrupted malaria control activities, threatening progress in the fight against the disease [2, 3], leading in 2020 to an increase in malaria morbidity and mortality worldwide, with an estimated 241 million cases and 627 000 deaths [4]. The incidence rate (per 1000 population at risk) increased from 57 in 2019 to 59 in 2020 [1]. Most of these cases occurred in Sub-Saharan Africa (SSA), with an estimated 228 million cases and 602 000 deaths in 2020 [4]. In recent years, multiple studies reported increased risk or higher prevalence of malaria among old children and adolescents across several SSA countries, including Kenya [5], Malawi [6, 7], Tanzania [8], Democratic Republic of Congo [9] and Senegal [10], suggesting a shift of the disease burden from children under five years old to older children and adolescents.

In Senegal, malaria is endemic in most of the country, with an upsurge during the rainy season [11]. Malaria control relies on prompt and accurate diagnosis, treatment using artemisinin-based combination therapy combined with preventive measures such as use of long-lasting insecticide-treated nets (LLINs), indoor residual spraying (IRS), intermittent preventive treatment in pregnant women and children. The scaling-up of these interventions has led to a substantial reduction in the malaria burden in the country. Proportional morbidity has decreased from 4.9% in 2015 to 3.3% in 2019, and proportional mortality from 3.5% in 2015 to 1.7% in 2019 [12]. However, an increase in malaria burden was observed in 2020, the proportional morbidity and mortality increased to a level close to the observed trends in 2015; respectively 3.8% and 2.1% [13, 14]; and the majority of these malaria cases occurred in the three southern regions of Kolda, Tambacounda, and Kedougou [13, 14]. In addition, the Senegalese National Malaria Control program (NMCP) through longitudinal routine data has shown an important increase in malaria cases among older children (15 to 19 years) compared to children under-five years old. The observed upward trend in malaria risk among older children and adolescents could be due to suboptimal use of preventive measures [15, 16] and their behavioral patterns, such as staying outdoors in the evening hours when mosquitos are most active [16, 17].

Given this shift in the malaria burden, it has become increasingly important to develop strategies to improve the use of malaria prevention measures among this population. Appropriation of any control program by the population and their willingness to act is largely influenced by their level of understanding, attitude, and perception towards the disease and existing control measures [18, 19]. Hence, to promote the use of malaria interventions among adolescents, it is necessary to understand their knowledge, attitudes, and perceptions of the disease. Knowledge, attitudes, and practices (KAP) surveys are common tools that can capture critical information to guide the design of control interventions, in order to ensure community involvement, acceptance, and adherence [20, 21]. Malaria KAP surveys have been conducted in many African countries [19, 2230]; however, to our knowledge, there is a scarcity of data on malaria knowledge, attitudes, and practices among adolescents in Senegal, specifically those living in rural areas with high malaria transmission. Therefore, the present study sought to assess malaria related knowledge (causes, symptoms, prevention methods), attitudes towards the disease, uptake of control and prevention practices and care-seeking behaviors among adolescents living in areas with persistent malaria transmission in Senegal. In addition, the study explored factors associated with adolescent knowledge, attitudes, and practices towards malaria. The main objective of this study was to generate evidence that can guide the NMCP to design social and behavior change interventions tailored to adolescents, in order to raise their awareness and improve their uptake of malaria control and prevention measures.

Methods

Study area and design

A community-based cross-sectional survey was conducted in the health district of Saraya in November 2021. The health district of Saraya is located in the Kedougou region in the south-eastern part of Senegal, 800 km from the capital, Dakar. The district shares a border with Mali to the east, Guinea to the south, the region of Tambacounda to the north, and the health district of Kedougou to the west. The health district occupies a land area of 6,837 sq km. The population was estimated to be around 66,017 inhabitants in 2021 [31] and the district has 1 health center, 22 health posts, 28 health huts, and 78 villages with a village volunteer for malaria case management (“DSDOM”, Dispensateur de soins à domicile). The climate is Sudano-Guinean with a dry season and a rainy season. Malaria is meso-endemic and stable in Saraya, with a long transmission season lasting 4 to 6 months from July to December. Transmission intensity remains high during the rainy season, with a high biting rate (25 bites/person/night) [32] and high morbidity during the transmission period. The major vectors are Anopheles gambiae, An. arabiensis sl, An. funestus and An. nili [33]. Malaria incidence (per 1000 population at risk) has steadily increased from 379.8 in 2019, to 607.6 in 2020, and up to 744.7 in 2021 [13, 14].

Study population and sampling technique

A multistage random sampling technique was used to select study participants. We first selected the four health posts (out of 22 total) that reported the highest number of malaria cases in 2020 (Diakhaling, Khossanto, Mamakhono, Sambrambougou) in the Saraya health district. In the second stage, thirty clusters, representing fifteen villages in the catchment areas of the targeted health posts, were selected using a random sampling process with probability proportional to the village’s population size (PPS). The third stage consisted of selecting households to be surveyed in each village using the compact segment sampling method. A map of each village was drawn and then was divided into segments so that each segment included approximately 13 adolescents. Segments were numbered and then one segment was randomly selected. All the households in the segment were selected for inclusion in the survey [34, 35]. Households were visited by surveyors, and in each household, all resident adolescents aged 10 to 19 years old were enrolled in the study after consenting.

Data collection method

The study questionnaire adapted from previous studies [22, 25, 26, 3638] was developed using the Open Data Kit (ODK) platform, and was reviewed by malaria experts and field epidemiologists for accuracy and validity. The questionnaire was first designed in French then translated into Malinké, the local language in the study area. The questionnaire included closed questions that focused on the following topics: i) socio-demographic information of the participant and the household head, ii) household assets, iii) knowledge on malaria transmission, signs and symptoms of malaria, and how to prevent malaria, iv) prevention practices, v) attitudes toward malaria and, vi) care seeking practices for malaria. The questionnaire was pretested in Saraya city, which was not one of the study sites, to check for accuracy and the questionnaire was modified based on the pilot study results. Cronbach’s coefficient alpha was calculated to check the reliability of each construct of the questionnaire, including knowledge, attitude, and practices. The coefficient was respectively 0.78, 0.80, 0.58, and 0.53 for knowledge, attitude, prevention, and care seeking.

Data were collected by trained field workers, using android tablets. The study team was trained on the study protocol, the questionnaire, and on the consent process. During the data collection phase, monitoring visits were performed for data quality checks and to assess compliance with the study protocol including informed consent requirements. Eligible participants included adolescents aged 10–19 years old who had lived in the selected households for at least six months.

Outcome variables

The main outcomes assessed in this study were: malaria knowledge, attitudes, uptake of malaria prevention and control practices, and care-seeking practices for fever.

Three items were used to assess participants’ knowledge on malaria: (1) correct identification of the mode of transmission, identification of the signs and symptoms of malaria, and knowledge of methods to prevent malaria. A knowledge score was calculated by summing the participant’s score across the three knowledge questions. A participant who described a mosquito bite as the mode of transmission for malaria was given a score of one, otherwise the participant was assigned a score of zero. For knowledge on malaria symptoms, a score of one was granted for each correct answer for the main symptoms of malaria: fever, headache, chills, abdominal pain, and vomiting. For knowledge of how to prevent malaria, a score of one was given to participants who correctly reported a bed net as a means to prevent malaria, and half point was given if the participant identified any of the other following prevention measures: mosquito coils, wearing long clothes, insecticide spray, weeding, or sewage disposal. Malaria knowledge was categorized into two levels using the median of the total score as cut off. Participants were classified as having a poor (below or equal to the median) or a good (above the median) level of knowledge on malaria.

To assess malaria attitudes, six items related to the population at risk of malaria, prevention, and treatment were used. The responses, based on Likert’s scaling technique had five possible levels, ranging from strongly agree (score 5), agree (score 4), undecided (score 3), disagree (score 2), to strongly disagree (score 1) [25, 39]. The scale was reversed for one item (malaria can be cured without medical treatment). An attitude score was estimated by adding up each participant ‘score across the six variables. Participants that scored the median of the total score or above were considered having a positive attitude, and the others as having a negative attitude.

A variable to assess the practice of the participant with regard to malaria prevention was defined considering bed net ownership and use of a bed net more than three times in a week or every night [26, 27]. Participants who own a bed net and use this more than three times in a week or every night, are categorized as having a good prevention practice, whereas bad prevention practices were considered those who do not have a bed net, and those who possess a net but do not use it at least 3 times a week.

Care-seeking practices for malaria was assessed as whether the adolescent sought care at a health facility (specifically a health center, health post, health hut, or DSDOM) for recent malaria within 24 hours at the onset of the symptoms. Adolescents who sought care at a health facility within 24 hours were considered to have good care-seeking practice, otherwise, they were considered as having bad care-seeking practice.

Other covariates assessed included socio-demographic factors of the adolescent and the household head (age, sex, education level, occupation, ethnicity, marital status, wealth index). Wealth index was calculated based on household assets (water source, type of toilet, ownership of radio, TV, bicycle, fridge, combustible) and household material characteristics (type of wall, type of floor, type of roof) using a principal component analysis [40, 41]. The index was categorized into five levels (highest, fourth, middle, second, and lowest).

Sample size calculation

With 391 adolescents sampled, the study was powered at 90%, to detect 8% variation in knowledge, assuming a prevalence of knowledge on malaria cause, symptoms and preventive methods at 50%, with alpha at 0.05 (two sided).

Data management and analysis

A unique identifier is attributed to each participant for confidentiality. The data collected were extracted from the server and checked for the completeness and consistencies. Cleaned data were analyzed using STATA software (Stata Corp 2016). Continuous variables were described as mean, standard deviation. Categorical variables were presented as frequency and percentage. Bivariate and multivariate logistic regressions were performed to assess factors that are related to adolescents’ malaria-related knowledge, attitudes, and practices with cluster robust standard error to account for the study design. Variables with a p < = 0.25 in the bivariate analysis, were introduced in the multivariable regression models [36, 40]. Odds ratios of these models were derived from the final model with 95% confidence interval (CI). Akaike’s Information Criteria (AIC) and Bayesian Information Criteria (BIC) were used for model selection. The significance level for the final models was set at 5% (two sided). The goodness fit of the model was assessed using Hosmer- Lemeshow test.

Ethical considerations

The study protocol was approved by the Institutional Ethics Committee of University Cheikh Anta Diop of Dakar (CER/UCAD/AD/MSN /039/2020). The protocol was presented to the staff of the health district to seek authorization to conduct the study. Authorization to conduct the study was also sought from community leaders in the study area. Participation in the study was voluntary. Written informed consent was sought from the parents/guardians of all adolescents aged 10–17 years old. In addition, written assent was sought from adolescents aged 15–17 years old. Furthermore, older adolescents, aged from 18–19 years old were invited to provide a written consent for their participation. No personal identifiable data was collected in the study. A unique identifier was attributed to each participant. All the data collected for the study was kept confidential, with restricted access to the study staff, only for the study purpose.

Results

Study participants characteristics

Overall, 391 participants, aged 10 to 19 years old [mean (SD) age = 13.8(3.1)] were enrolled in the study. Most of the participants (56.0%) were female and had (60.6%) primary school level of education. The majority of the participants belonged to the Malinke ethnic group (78.3%) and forty-eight percent (48.1%) of them were students (Table 1).

Table 1. Socio-demographic characteristics of the study participants.

Variable Category Frequency Percentage
Characteristics of the participants
Age (in years) 10–14 232 59.3%
15–19 159 40.7%
Sex Female 219 56.0%
Male 172 44.0%
Ethnicity Malinke 306 78.3%
Pular 62 15.9%
Other 23 5.9%
Educational level No education 68 17.4%
Koranic school 52 13.3%
Primary 237 60.6%
Secondary 34 8.7%
Occupation No occupation 89 22.8%
Student 188 48.1%
Household maid 24 6.1%
Farmer 14 3.6%
Gold digger 45 11.5%
Vendor 13 3.3%
Workers 13 3.3%
Other* 5 1.3%
Wealth index Highest 78 19.9%
Fourth 78 19.9%
Middle 79 20.2%
Second 78 19.9%
Lowest 78 19.9%
Characteristics of the household’s head
Age (in years) <29 34 8.7%
30–39 40 10.2%
40–49 40 10.2%
50–59 49 12.5%
60–69 40 10.2%
> = 70 14 3.6%
Missing 174 44.5%
Sex Female 25 6.4%
Male 363 92.8%
Missing 3 0.7%
Educational level No education 164 41.9%
Koranic school 135 34.5%
Primary school 80 20.5%
Secondary school 9 2.3%
Missing 3 0.8%
Occupation None 17 4.3%
Farmer 169 43.2%
Gold digger 135 34.5%
Vendor 21 5.4%
Workers 22 5.6%
Others** 24 6.1%
Missing 3 0.8%
Marital status Married 382 97.7%
Others*** 6 1.5%
Missing 3 0.8%

Dialounke, Bambara, Dogon, Bosso and Mossi.

* Community health worker and apprentice.

** Commhealthealth worker, imam, head of the village, shepherd, apprentice, housewife.

*** divorced and widower.

Knowledge about malaria causes, symptoms, and prevention

Out of the 391 adolescents included in the study, 317 (81.1%) reported that they had heard of malaria and of those, 87.7% (n = 278), reported that malaria is transmitted by mosquito bites. However, some participants reported other factors as possible means of malaria transmission, including sleeping with a sick person (12.9%, n = 41), through an insect bite (5.7%, n = 18), lack of body hygiene (6.3%, n = 20). Overall, 7.3% (n = 23) of the participants did not know how malaria is transmitted. The most commonly reported symptoms of malaria by adolescents were headache (89.3%, n = 283), vomiting (52.4%, n = 166), abdominal pain (30.3%, n = 96), chills (10.4%, n = 33), fatigue (6.0%, n = 19), and loss of appetite (5.1%, n = 16).

The majority of the adolescents (84.5%, n = 268) mentioned mosquito nets as a preventive measure against malaria. Other preventive measures noted by adolescents included mosquito’s coils (8.8%, n = 28), weeding (7.9%, n = 25), insecticide spray (4.7%, n = 15), antimalarial drugs (5.1%, n = 16), sewage disposal (4,7%, n = 15), wearing of long cloves (3.8%, n = 12). Six percent (n = 19) of adolescents did not know any malaria preventive measures. Approximately, one-third (34.4%, n = 109) [95%CI: 29.3%–39.8%] of adolescents had good knowledge of the cause, signs and symptoms, and preventive measures of malaria (Table 2).

Table 2. Participant knowledge of malaria transmission, signs and symptoms, and prevention methods.

Variable Category Frequency Percentage
Have you heard about malaria? No 74 18.9%
Yes 317 81.1%
How is malaria transmitted? Sleep with a sick person 41 12.9%
Mosquito bite 278 87.7%
Insect bite 18 5.7%
Lack of body hygiene 20 6.3%
Oil consummation 1 0.3%
Contaminated food 8 2.5%
Dirt 3 0.9%
Don’t know 23 7.3%
Other 3 0.9%
Malaria signs and symptoms Headache 283 89.3%
Abdominal pain 96 30.3%
Chills 33 10.4%
Fatigue 19 6.0%
Loss of appetite 16 5.1%
Vomiting 166 52.4%
Fever 6 1.9%
Don’t know 10 3.2%
other* 4 1.3%
Malaria prevention Mosquito net 268 84.5%
Spray insecticide 15 4.7%
Mosquito coils 28 8.8%
Antimalarial drug 16 5.1%
Weeding 25 7.9%
Long cloves 12 3.8%
Sewage disposal 15 4.7%
Don’t know 19 6.0%
Other** 8 2.5%
Knowledge *** Poor 208 65.6%
Good 109 34.4%

water and non-use of net.

*aches and body swelling.

** go to hospital, traditional treatment, cleanliness, cannot be prevented.

*** knowledge score calculated by summing up the score of knowledge on malaria transmission, signs and prevention, then categorized in accordance to the median of the total score.

Participants were mostly (87.1%, n = 276) informed about malaria by health workers, specifically by community health workers (CHWs) (53.3%, n = 169) and nurses (33.7%, n = 107). Other sources of information included school (19.8%, n = 63), radio (16.4%, n = 52), television (16.1%, n = 51), and neighborhood (community members) (12.0%, n = 38) (Fig 1).

Fig 1.

Fig 1

Attitude towards malaria

Overall, 88.0% (n = 279) of the study participants believe that everybody can contract malaria and 92.1% (n = 292) perceived the disease as deadly. The majority of the participants (85.5%, n = 271) perceived malaria as a preventable disease. Furthermore, participants indicated the necessity to be tested prior to malaria treatment initiation (86.7%, n = 275) and the necessity to complete a full course of treatment when given (84.5%, n = 268). However, 46.7% (n = 148) believed that malaria could be cured without medical treatment. Considering the total score of attitude, 59.0% (n = 187) [95% CI: 53.5%–64.3%] of the participants had a positive attitude (Table 3).

Table 3. Attitudes of the study participants towards malaria.

Variable Totally agree Agree Neutral Disagree Totally disagree
N % N % N % N % N %
Everybody can have malaria 214 67.5% 65 20.5% 13 4.1% 19 6.0% 6 1.9%
Malaria is deadly 197 62.1% 95 30.0% 16 5.1% 5 1.6% 4 1.3%
Malaria can be cured without medical treatment 115 36.3% 33 10.4% 42 13.3% 87 27.4% 40 12.6%
Malaria can be prevented 141 44.5% 130 41.0% 23 7.3% 14 4.4% 9 2.8%
It is important to be tested before taking malaria treatment 121 38.2% 154 48.6% 34 10.7% 5 1.6% 3 0.9%
It is necessary to finish malaria treatment 123 38.8% 145 45.7% 41 12.9% 5 1.6% 3 0.9%
Attitude *
Positive 187 (59.0%)
Negative 130 (41.0%)

*calculated by summing up the score across the items used to measure attitude and categorized based on the median of the total score.

Practice of malaria prevention

Forty-five percent (45.4%, n = 144) of the study participants reported that their households owned bed nets. The proportion of adolescents who reported using nets was 33.1% (n = 105) and those who declared having slept under a net the previous night of the survey was 27.8% (n = 88). Out of the 105 study participants who reported bed net usage, 31.4% (n = 33) stated using the bed nets in both the dry and rainy seasons and 71.4% (n = 75) reported using a bed net every night.

Forty-five percent of adolescents (45.1%, n = 143) reported using other preventive measures, including mosquito coils (60.1%, n = 86), insecticide spraying (30.8%, n = 44), and wearing of long cloves (27.3%, n = 39). Approximately one-third, 32.8% [95%CI: 27.8%-38.2%], (n = 104) of the participants have good practices in regard to malaria prevention (Table 4).

Table 4. Malaria prevention practices of the study participants.

Variable Category Frequency Percentage
Household owns a bed net (n = 317) Yes 144 45.4%
No 173 54.6%
Bed net use (n = 317) Yes 105 33.1%
No 212 66.9%
Bed net used the previous night (n = 317) Yes 88 27.8%
No 229 72.2%
Season of bed use (n = 105) Rainy season 71 67.6%
Dry season 1 0.9%
All seasons 33 31.4%
Frequency of bed net use (n = 105) Less than 3 times per week 1 0.9%
3–6 times per week 29 27.6%
Every night 75 71.4%
Use other measures? (n = 317) Yes 143 45.1%
No 174 54.9%
Other preventives measures used (n = 143) Mosquito coils 86 60.1%
Insecticide spray 44 30.8%
Grass cleaning 2 1.4%
Sewage cleaning 1 0.7%
Long cloves 39 27.3%
Hand cream 10 3.2%
Other* 6 1.9%
Prevention practice level** (n = 317) Good 104 32.8%
Bad 213 67.2%

* Topical repellent, traditional treatment, blanket, shea oil, personal hygiene.

** defined based on bed net ownership and usage.

n = number of respondents.

Twenty-seven percent (27,1%, n = 39) of adolescents reported not using the bed net. The main reason indicated was that they felt too hot when sleeping under a net (54.1%, n = 20). Other reasons included the smell of the net (16.2%, n = 6), “feeling trapped in the net” (10.8%, n = 4), “there is no mosquito” (10.8%, n = 4), “there is no malaria currently” (5.4%, n = 2), “don’t have access to a bed net” (5.4%, n = 2).

Care-seeking practices

Overall, 89.3% of the study participants (n = 283) reported having had a malaria episode, and among them, 86.2% (n = 244) have sought care for this episode. The majority (79.1%, n = 193) sought care at the health post, while 23.4% (n = 57) sought care at the health hut/ DSDOM. Of those that sought care, 76.6% (n = 187) sought care within 24 hours of the onset of symptoms. Altogether, 73.8% [95%CI: 68.4%–78.6%], (n = 209) of the participants demonstrated good care seeking practice for malaria (Table 5).

Table 5. Malaria care seeking practice among the study participants.

Variable Category Frequency Percentage
Have you ever experienced malaria? (n = 317) Yes 283 89.3%
No 34 10.7%
Have you sought care? (n = 283) Yes 244 86.2%
No 39 13.8%
Where did you seek care? (n = 244) Health post 193 79.1%
Health center 3 1.2%
Health hut/DSDOM 57 23.4%
Self-medication 3 1.2%
Timeliness of care seeking after disease onset (= 244) The same day 187 76.6%
One day after 24 9.8%
Two days after 29 11.9%
More than 2 days 2 0.8%
Don’t know 2 0.8%
Care seeking practice level* (n = 283) Good 209 73.8%
Bad 74 26.1%

*estimated based on care seeking in a health facility within 24 hours.

n = number of respondents.

Factors associated with malaria knowledge, attitude, and practices

Malaria causes, symptoms, and prevention knowledge

Table A in S1 Table presents the results of the logistic regression model looking at the determinants related to adolescents’ knowledge of the cause, signs and symptoms, and prevention methods for malaria. Male adolescents were 60% less likely to have good knowledge [aOR = 0.40(95%CI: 0.24–0.68)]; compared to female adolescents. The odds of having good knowledge increased with education level; the odds of having a good knowledge was 5 [aOR = 5.43(95%CI: 1.91–15.46)] and 10 times [aOR = 10.41(95%CI: 2.98–36.40)] higher among adolescents who had primary and secondary level of education, respectively, compared to those that had not received any education.

Attitude towards malaria

Household wealth and education level of the participants were significantly associated with participants’ attitudes towards malaria. Compared to adolescents from households in the lowest wealth quintile, those from households in the highest wealth quintile were 3.49 times [aOR = 3.49(95%CI: 1.48–8.28)] more likely to have positive attitude towards malaria. The odds of positive attitude regarding malaria was respectively 86% [aOR = 0.14(95%CI: 0.36–0.55)] and 76% [aOR = 0.24(95%CI: 0.70–0.79)] lower among participants with koranic and primary education, compared to those with secondary education level (Table B in S1 Table).

Malaria prevention practices

Adolescents who demonstrated a positive attitude towards malaria were 1.89 times [aOR = 1.89(95%CI: 1.08–3.30)] more likely to report engaging in good malaria prevention practices than those with a negative attitude. A significant association was found between household wealth and adolescent prevention practices: compared to adolescents from households in the highest wealth quintile, those from households in the fourth [aOR = 0.42(95%CI:0.19–0.89)], middle [aOR = 0.34(95%CI: 0.16–0.72)] and second wealth quintiles [aOR = 0.42(95%CI: 0.19–0.90)] were 58%, 66% and 58%, less likely, respectively, to practice good malaria prevention. Having a household head with a koranic school education was associated with good malaria prevention practice [(aOR = 1.85(95%CI: 1.04–3.28)] compared to adolescents from households where the household head received no education (Table C in S1 Table).

Malaria care seeking behavior

The odds of a good care-seeking behavior for malaria was lower among adolescents from households in the second wealth quintile [aOR = 0.35(95 CI%: 0.15–0.80)] compared to those from the highest wealth quintile. In addition, the odds of good care-seeking behavior was lower among adolescents aged 15–19 years old [aOR = 0.57(95%CI: 0.32–1.02)] compared to those aged 10–14 years old, with a marginal effect (Table D in S1 Table).

Discussion

Many studies have been conducted to examine malaria control and prevention knowledge, attitudes, and practices; however, most studies have focused exclusively on adults [24, 2629, 36, 39, 42]. Adolescents, an emerging high-risk group, have received limited attention. To address this evidence gap, our study sought to assess malaria knowledge, attitudes, and practices and key determinants among adolescents living in an area of high malaria transmission in southern Senegal.

In general, most of the adolescents demonstrated awareness of malaria transmission, symptoms, and prevention methods. This result corroborates those reported by other studies conducted in Tanzania [22], in Nigeria [38, 4345], in India [46], and in Ethiopia [47]. The study participants reported CHWs and nurses as their main sources of malaria-related information, which was a similar finding to a study conducted in Nigeria among school adolescents [38]. This result could be explained by the fact that nurses and CHWs are often the primary points of contact for adolescent health care services in many remote settings, including in Senegal. Consequently, health care providers, such as nurses and CHWs, are well positioned to support implementation of malaria awareness strategies targeting adolescents. Conversely, in other studies conducted in Ethiopia [47] and India [46] among school-going adolescents, radio and television were reported as the main sources of information on malaria.

However, most of the adolescents did not report fever as a significant symptom, and 6–7% lacked knowledge on malaria transmission and prevention. This result highlights the need for improved health-related information among this group of population. Engaging and empowering adolescents to disseminate malaria-related information in order to sensitize their peers could be an approach to fill this gap [48]. School and community-based health education programs could be used to reach this goal. This will require a multisectoral approach involving different ministries and partners such as ministry of health, ministry of education, implementing partners, as it is the case for other disease program [49].

Overall, the level of malaria knowledge regarding the cause, symptoms, and prevention is poor for the majority of the participants. The present result is similar to the findings of a study conducted in Nigeria among in-school adolescents [43]. This finding is surprising, as most of the adolescents had a primary or secondary level of education and information on malaria and how to prevent transmission are integrated into the school curriculum in Senegal. In the current study, males were significantly less likely to possess a good knowledge of malaria compared to their female counterparts. Adolescents’ malaria knowledge was positively associated with their education level, with adolescents who possessed a primary and secondary level of education 5 and 10 times more likely to have a good malaria knowledge, compared adolescents who had received no education. This could be explained by the fact that educated people are more likely to access health information and have additional opportunities to be reached by messages on malaria control and prevention [50, 51].

In terms of attitude, most of the participants agreed that everyone is at risk of malaria and perceived the disease to be deadly. In addition, the majority of adolescents believe it is important to be tested for malaria before taking a malaria treatment and to complete the treatment when given. Similar findings were shown in a study conducted in Nigeria; participants also perceived malaria as deadly [38]. In our study, most adolescents believe malaria to be a preventable disease, a result that is consistent with another study conducted in Nigeria [44]. Despite many believe malaria to be preventable, just under half of the adolescents stated that malaria can be cured without any medical treatment. This finding justifies the important need to improve communication for social behavior change among adolescents. Adolescents’ attitudes toward malaria were associated with household wealth; with generally more positive attitudes among adolescents from wealthier households, and vice-versa, more negative attitudes were associated with adolescents from poorer households. In addition, positive attitude regarding malaria decreased with increase of education level, with lower odds of attitude among adolescents with koranic and primary education, in comparison to those with secondary education level. These findings could be explained by the fact that individuals from wealthier households, and those with high education level are more likely to access health information on malaria, and therefore could better understand the disease, its prevention methods as well as its seriousness [50, 51].

Regarding malaria prevention practices, less than half of the participants reported that their household own bed nets, around a third reported bed net usage, and nearly all of those who use a bed net, reported using the net between 3 to 6 times a week, or every night. The proportion of net utilization among adolescents in this study is lower compared to that indicated in studies conducted in Tanzania [22] and in Nigeria [52], but higher than the proportion reported in India [46], in other studies carried out in Nigeria [38, 53], and in Kenya [54]. Every three years in Senegal, free Long-Lasting Insecticide Nets (LLINs) are distributed to the population through mass campaigns to achieve universal coverage of LLIN, as recommended by WHO [55]. The latest campaign was carried out in 2019 and the next campaign scheduled for 2022 has not been conducted yet by the time of this study. The low proportion of bed net ownership reported in this study could be explained by the fact that the study was conducted several years after a mass LLIN campaign where the majority of the distributed nets are likely no longer being used or functional. Indeed, while LLIN are expected to last at least 3 years, studies on LLIN durability, revealed that under routine conditions LLIN can lose effectiveness because they are physically damaged, repurposed or discarded [56, 57]. Routine distribution of LLINs is also carried out at community level and in health facilities [14]. However, in the health-based routine distribution system, LLINs are only distributed free of charge for children under five and pregnant women. The low coverage of LLINs reported in this study, highlights the need for improved coverage and access. This could be achieved by expanding the target of the routine distribution to adolescents to keep them covered between mass campaigns [48]. Other channels should also be considered by the NMCP, to maintain continuous distribution and sustain LLIN coverage [58, 59].

The study revealed an important gap between LLIN ownership and LLIN usage with 25.7% of the participants reported not using the bed net, despite they have access to one. The main reason indicated was that they felt too hot when sleeping under a net. This finding justifies the necessity to reinforce sensitization to raise awareness among adolescents on the benefits of LLINs. This could be achieved through an adolescent-friendly health education program [48].

Overall, the level of good prevention practices was low. Factors associated with good prevention practice included positive attitude, adolescent education level, as well as the education level of the household head and household wealth. The odds of having a good prevention practice was 1.89 folds higher among adolescents with a positive attitude, as compared to those with a negative attitude. This finding is consistent with those indicated in studies conducted in Ethiopia [36, 51] and could be explained by the fact that the perception of the susceptibility and the threat related to malaria, and the belief in the effectiveness of the methods to avoid the disease can motivate the decision to act and adhere to prevention measures [60, 61]. This could also be explained as an increase in knowledge and favorable attitudes of an individual towards a disease, its risk factor, its seriousness, its mechanism of prevention, will lead to an increase in the probability of practicing preventive measures [36]. Furthermore, the odds of applying a good practice of prevention is 1.85 times higher in adolescents whose household head has a koranic education level compared to those with no education. Adolescents who belonged to households from the fourth, the middle, and the second wealth quintiles were less likely to engage in prevention practices compared to those from households in the highest wealth index. This result supports the findings of a study conducted in Nigeria, concluding that higher economic class is associated with LLIN use [44] and another one conducted in Cameroon showing that wealthier people are more likely to apply good practices of malaria prevention [50]. LLINs are distributed through mass campaign approach and this strategy has been shown to ensure equitable LLIN access [55, 62, 63]. Participants who belong to the highest wealth index may have more opportunities to access information on malaria prevention including the benefits of bed-net usage; this could increase their awareness and therefore lead to higher LLIN use compared to other wealth indexes. However, this result is not in line with findings from other studies that reported a decrease in net usage with the increase of the wealth index [64, 65].

Overall, the level of care-seeking behavior was good for most of the study participants. The majority of adolescents reported having sought care for malaria in health facilities including a health center, a health post, a health hut, or from a CHW (DSDOM), within 24 hours of the start of the symptoms. This finding is similar to those of studies conducted in Nigeria [43], in Tanzania [22], and in India [46], in which most of the adolescents reported going to the hospital for malaria treatment. Regarding the associated factors, adolescents from the second wealth quintile are less likely to have good care-seeking behavior compared to those of the highest one. Since malaria treatment is free, financial resources for the transport to get to the health facilities and to pay the consultation fees may explain this difference between individuals from the second and the highest wealth indexes. This result highlights inequity in health care access among adolescents; efforts are thus needed, mainly among those from the lowest wealth households to ensure access to care.

Limitation of the study

The cross-sectional design of the study can lead to some bias including recall bias, and reflects information collected at a specific time point, and this information may be different in another period. However, the study has been conducted during the malaria transmission season to minimize this recall bias. In addition, the estimates could have been underestimated or overestimated due to the fact that certain information collected in the study were self-reported by the participants. For instance, the use of bed nets was self-reported and could have been overestimated by the participants for social desirability. It is shown that self-reports overestimate adherence of bed net [66, 67].

Conclusion

The study revealed that adolescents, generally have poor levels of malaria knowledge and low uptake of malaria prevention and control interventions. Targeted interventions for high-risk adolescents are needed, that focus on improving their knowledge of the disease and effective preventive measures, and on increasing their access to health care services and LLINs.

Supporting information

S1 File. English version of the study questionnaire.

(DOCX)

S2 File. French version of the study questionnaire.

(DOCX)

S3 File. Malinke version of the study questionnaire.

(DOCX)

S1 Dataset. KAP STATA dataset.

(DTA)

S1 Table. Tables presenting the results of logistic regression of the factors associated with knowledge, attitude, prevention, and care-seeking behaviors of the adolescent.

Tables are ordered as follows: Table A Logistic regression of the determinants related to malaria knowledge among adolescents; Table B Logistic regression of the factors associated with attitude of the participants towards malaria; Table C Logistic regression of the factors associated with malaria prevention practice; Table D Logistic regression of factors associated with malaria care-seeking behavior.

(DOCX)

Acknowledgments

The authors acknowledge Dr Baba Camara, Head of the District Health of Saraya, and his team who facilitated the conduct of the study in the health district, as well as the population of the study area for their participation in the study.

Data Availability

All relevant data are within the paper and its Supporting information files.

Funding Statement

The study was supported by the Senegalese National Malaria Control Program, through an agreement with the Department of Parasitology and Mycology of University Cheikh Anta Diop of Dakar (# funding number: NFM 2-SEN-M-PNLP 2018 - 2019 -2020). The funder had no role in the study design, data collection, and analysis, decision to publish, or preparation of the manuscript.

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Decision Letter 0

Sammy O Sam-Wobo

27 Sep 2022

PONE-D-22-24296Malaria prevention knowledge, attitudes, and practices (KAP) among adolescents living in an area of persistent transmission in Senegal: Results from a cross-sectional studyPLOS ONE

Dear Dr. TAIROU,

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Reviewer #1: Yes

Reviewer #2: Yes

**********

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Reviewer #1: Yes

Reviewer #2: Yes

**********

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Reviewer #1: Good and well written article.

I have few questions to the authors.

1) Why this study chose adolescents as the respondents, risk of transmission are in the community as a whole regardless their age group?Despite reason study have been done among adults group not in adolescents but I think study should include the all susceptible groups rather than separated agegroup.

2) Would you please explain on validity and reliability of the questionnaires used for this study.

3) Would you please explain on an academic basis why you measure attitude similar to how we measure knowledge? Any references? In my opinion, scope of attitude should be measured by psychometric assessment. There should be NO zero mark for the answer. Please kindly refer to the concept of Likert scale. Attitude questions were so superficial, but not much can be done as data already collected.

4) Please kindly explain the basis for sample size calculation. The formula you produced is valid if your objective is to determine prevalence of KAP level; but, if you need to have bivariate and multivariate analysis, some consideration of the power of the study should be done. Hope you can revise it, with a more appropriate formula for sample size.

5) Please check the presentation of your statistical data. As example in page 11 line 256, "Overall, 391 participants, aged 10 to 19 years old (mean age= 13. 8± 3.1) were enrolled in the..." should be written as Overall, 391 participants, aged 10 to 19 years old [mean (SD) age= 13. 8(3.1)] were enrolled in the...". 

In terms of discussion, please look into the reality in the field rather than detail of statistical findings. I would suggest if we can internalize detail if we can view it in general, what does this research tell us for us to do in detail therefore allow us preventing further transmission in the community. If you think schools are useful, how we can collaborate with all agencies to make this a reality .

Reviewer #2: This is an interesting and well written piece of work.

I have just a few minor comments.

1. Lines 202 - 206. It is stated that adolescents who did not seek care for malaria at a health facility were considered to have bad care-seeking practice. Was consideration given for adolescents who may have had limited access due to a variety of reasons. For example, requiring the permission of an adult, financial constraints, off hours' time at their local health facility etc?

2. A non-response rate of 8% was considered in calculating the sample size of the study. How was this figure arrived at?

3. The results section is rather lengthy.

4. The variables on tables 4 and 5 have numbers written in bracket beside them? What do these numbers represent? If they are not required here, they should be deleted.

5. The first line of the discussion (Lines 392-393) require references for the many studies the authors refer to.

6. Were the respondents given gifts for participating in the study? The limitation described on line 514 (under-reporting of bed nets if the respondents thought they would be given nets) should not have arisen if the respondents were not told they would be given nets.

**********

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Reviewer #1: No

Reviewer #2: No

**********

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PLoS One. 2022 Dec 1;17(12):e0274656. doi: 10.1371/journal.pone.0274656.r002

Author response to Decision Letter 0


10 Nov 2022

To PLOS ONE editor

Subject: Response to Reviewers

Ref: PONE-D-22-24296

Malaria prevention knowledge, attitudes, and practices (KAP) among adolescents living in an area of persistent transmission in Senegal: Results from a cross-sectional study

Dear Editor;

On behalf of the co-authors, I would like to thank the reviewers for the comments and submit the point-by-point responses to the concerns raised during the review process below:

1. Please ensure that your manuscript meets PLOS ONE's style requirements, including those for file naming. The PLOS ONE style templates can be found at

https://journals.plos.org/plosone/s/file?id=wjVg/PLOSOne_formatting_sample_main_body.pdf and

https://journals.plos.org/plosone/s/file?id=ba62/PLOSOne_formatting_sample_title_authors_affiliations.pdf"

Authors’ reply: The manuscript has been revised in accordance with PLOS ONE’s style requirements, including those for file naming

2. Thank you for providing an English version of your questionnaire. Please also provide the questionnaire in French and Malinké

Authors’reply: The French and the Malinké version of the questionnaire are submitted with the revised manuscript

3. Thank you for stating the following financial disclosure:

"The study was supported by the Department of Parasitology and Mycology through funding received from the Senegalese National Malaria Control Program. The funder had no role in the study design, data collection, analysis, decision to publish, or preparation of the manuscript."

At this time, please address the following queries:

a) Please clarify the sources of funding (financial or material support) for your study. List the grants or organizations that supported your study, including funding received from your institution.

Authors’reply: The study was supported by the Senegalese National Malaria Control Program, through an agreement with the Department of Parasitology and Mycology of University Cheikh Anta Diop of Dakar (# funding number: NFM 2-SEN-M-PNLP 2018 - 2019 -2020).

b) State what role the funders took in the study. If the funders had no role in your study, please state: “The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.”

Authors’reply: The funder had no role in the study design, data collection, and analysis, decision to publish, or preparation of the manuscript.

c) If any authors received a salary from any of your funders, please state which authors and which funders

Authors’reply: No one of the authors received a salary from the funder

d) If you did not receive any funding for this study, please state: “The authors received no specific funding for this work.”

Authors’reply: The source of funding is mentioned above (see a)

Please include your amended statements within your cover letter; we will change the online submission form on your behalf.

Authors’reply: The amended statements have been included in the cover letter.

4. Please review your reference list to ensure that it is complete and correct. If you have cited papers that have been retracted, please include the rationale for doing so in the manuscript text, or remove these references and replace them with relevant current references. Any changes to the reference list should be mentioned in the rebuttal letter that accompanies your revised manuscript. If you need to cite a retracted article, indicate the article’s retracted status in the References list and also include a citation and full reference for the retraction notice.

Authors’reply: No retracted reference was included in the manuscript. However, to address some of the reviewer’s comments, the following references have been added to the revised version (line 633 and 638):

Volkman HR, Walz EJ, Wanduragala D, Schiffman E, Frosch A, Alpern JD, et al. Barriers to malaria prevention among immigrant travelers in the United States who visit friends and relatives in sub-Saharan Africa: A cross-sectional, multi-setting survey of knowledge, attitudes, and practices. Carvalho LH, editor. PLoS ONE. 2020;15: e0229565

Munisi DZ, Nyundo AA, Mpondo BC. Knowledge, attitude and practice towards malaria among symptomatic patients attending Tumbi Referral Hospital: A cross-sectional study. Carvalho LH, editor. PLoS ONE. 2019;14: e0220501.

Reviewer #1:

1) Why this study chose adolescents as the respondents, risk of transmission are in the community as a whole regardless their age group? Despite reason study have been done among adults group not in adolescents but I think study should include the all susceptible groups rather than separated agegroup.

Authors’reply: We would like to thank the reviewer for the comment. The purpose of the current study is to generate evidence that will inform future programming and delivery of interventions to further reduce the malaria burden among adolescents. Routine data in Senegal as well as epidemiological studies have shown high performance in malaria control among the general population [1,2] but the disease burden remained high in some specific age groups such as adolescent [3]. These data call for an urgent need to design specific adolescent-oriented programs. This can only be done if malaria determinants among this specific population are well documented. Therefore, this study was designed to generate data that will contribute to filling the evidence gaps related to malaria determinants among new emerging high-risk populations including adolescents.

2) Would you please explain on validity and reliability of the questionnaires used for this study.

Authors’reply: The study questionnaire was adapted from previous studies [4–9], and was then reviewed by malaria experts and field epidemiologists for accuracy and validity. We have calculated Cronbach’s coefficient alpha to check the reliability of each construct of the questionnaire, including knowledge, attitude, and practices. The coefficient was respectively 0.78, 0.80, 0.58, and 0.53 for questions representing knowledge, attitude, prevention, and care seeking.

3) Would you please explain on an academic basis why you measure attitude similar to how we measure knowledge? Any references? In my opinion, scope of attitude should be measured by psychometric assessment. There should be NO zero mark for the answer. Please kindly refer to the concept of Likert scale. Attitude questions were so superficial, but not much can be done as data already collected.

Authors’reply: This comment is well acknowledged; consequently, we have executed the analysis to correct this inconsistency. In the methodology section, the description of outcomes variables has been revised in accordance (line 193-200), as well as the results related to attitude (line 46, line 50-57 in the abstract section, line 298-300 in the results section). The parameters significantly associated with attitude in adolescents were also slightly changed (352-358 in the results section). These results were also interpreted and explained in the discussion (line 427- 435 in the discussion section).

The questions related to attitude were adapted from previous similar studies [7,8]. However, we acknowledge that more in-depth questions would provide more accurate information regarding attitude of adolescents towards malaria.

4) Please kindly explain the basis for sample size calculation. The formula you produced is valid if your objective is to determine prevalence of KAP level; but, if you need to have bivariate and multivariate analysis, some consideration of the power of the study should be done. Hope you can revise it, with a more appropriate formula for sample size.

Authors’reply: We agree with this comment and have revised the sample size calculation using STATA software. The following section has been added to the manuscript (line 222-224): “With 391 adolescents sampled, the study was powered at 90%, to detect 8% variation in knowledge, assuming a prevalence of knowledge on malaria causes, symptoms and preventive methods at 50%, with alpha at 0.05 (two sided).

5) Please check the presentation of your statistical data. As example in page 11 line 256, "Overall, 391 participants, aged 10 to 19 years old (mean age= 13. 8± 3.1) were enrolled in the..." should be written as Overall, 391 participants, aged 10 to 19 years old [mean (SD) age= 13. 8(3.1)] were enrolled in the...".

Authors’reply: We have revised the presentation of statistical data regarding the mean age (line 251), and along the manuscript (Please see abstract and results section)

In terms of discussion, please look into the reality in the field rather than detail of statistical findings. I would suggest if we can internalize detail if we can view it in general, what does this research tell us for us to do in detail therefore allow us preventing further transmission in the community. If you think schools are useful, how we can collaborate with all agencies to make this a reality.

Authors’reply: The discussion section has been revised to account for this comment (line 399-405)

Reviewer #2:

1. Lines 202 - 206. It is stated that adolescents who did not seek care for malaria at a health facility were considered to have bad care-seeking practice. Was consideration given for adolescents who may have had limited access due to a variety of reasons. For example, requiring the permission of an adult, financial constraints, off hours' time at their local health facility etc?

Authors’reply: Adolescents who did not seek care for malaria at a health facility within 24 hours were considered to have bad care-seeking practices. We have not considered those who may have had limited access to health facility for variety of reasons, in the definition of “bad care-seeking practice” because in Senegal, the diagnosis and treatment of uncomplicated malaria are free of charge, and the geographic accessibility has significantly improved due to the presence in the community of “Dispensateurs de soins à domicile”, DSDOM (village volunteer trained to test for malaria with an RDT and treated with arthemeter Lumefantrine), living in the community, as well as functional health huts (“cases de santé”), managed by a community health worker, which are accessible for patients of all ages, at any time in case of fever.

2. A non-response rate of 8% was considered in calculating the sample size of the study. How was this figure arrived at?

Authors’reply: Based on previous studies conducted in the area, by the Department of medical parasitology (unpublished data), the non-response rate ranged between 8 and 10%, therefore we considered a non-response of 8% in this study.

3. The results section is rather lengthy.

Authors’reply: The authors acknowledge this comment and have revised the results section to reduce the length by combining the section of the results related to factors associated with knowledge, attitude, prevention, and care seeking behaviors of the adolescents; and present table 6, table 7, table 8 and table 9 describing the results of KAP’factors as supplementary materials (see S5 Table)

4. The variables on tables 4 and 5 have numbers written in bracket beside them? What do these numbers represent? If they are not required here, they should be deleted.

Authors’reply: The numbers written in bracket beside each variable on tables 4 and 5, represent the number of respondents. “n” has been added in bracket beside variable on these tables, and in the caption of the tables (line 319 for table 4 and line 336 for table 5).

5. The first line of the discussion (Lines 392-393) requires references for the many studies the authors refer to.

Authors’reply: The references have been added (lines 381-383)

6. Were the respondents given gifts for participating in the study? The limitation described on line 514 (under-reporting of bed nets if the respondents thought they would be given nets) should not have arisen if the respondents were not told they would be given nets.

Authors’reply: The respondents were not promised bed nets and they were not given any other gifts to participate in the study. The participation in the study was voluntary. To avoid misinterpretation, the section has been removed from the limitation

References

1. Programme National de Lutte contre le paludisme (PNLP). Bulletin Epidemiologique annuel 2021 du paludisme au Sénégal [Internet]. 2022 Mar p. 1–76. Available from: https://pnlp.sn/bulletin-epidemiologique-annuel/

2. Agence nationale de la Statistique et de la Démographie (ANSD), Programme National de Lutte contre le Paludisme (PNLP), l’Agence des Etats Unis pour le Développement international (USAID), Fond mondial et ICF. Enquête sur les Indicateurs du Paludisme au Sénégal, 2020-2021. Rockville, Maryland, USA : ANSD, PNLP, USAID, FM et ICF; 2021.

3. Wotodjo AN, Doucoure S, Diagne N, Sarr FD, Parola P, Gaudart J, et al. Another challenge in malaria elimination efforts: the increase of malaria among adults after the implementation of long-lasting insecticide-treated nets (LLINs) in Dielmo, Senegal. Malar J. 2018;17:384.

4. Sumari D, Dillip A, Ndume V, Mugasa JP, Gwakisa PS. Knowledge, attitudes and practices on malaria in relation to its transmission among primary school children in Bagamoyo district, Tanzania. MWJ. 2016;7:1–7.

5. Flatie BT, Munshea A. Knowledge, Attitude, and Practice towards Malaria among People Attending Mekaneeyesus Primary Hospital, South Gondar, Northwestern Ethiopia: A Cross-Sectional Study. Magalhães LG, editor. Journal of Parasitology Research. 2021;2021:1–14.

6. Tesfay K, Yohannes M, Mardu F, Berhe B, Negash H. Assessment of community knowledge, practice, and determinants of malaria case households in the rural area of Raya Azebo district, Northern Ethiopia, 2017. Carvalho LH, editor. PLoS ONE. 2019;14:e0222427.

7. Fikrie A, Kayamo M, Bekele H. Malaria prevention practices and associated factors among households of Hawassa City Administration, Southern Ethiopia, 2020. Di Gennaro F, editor. PLoS ONE. 2021;16:e0250981.

8. Munisi DZ, Nyundo AA, Mpondo BC. Knowledge, attitude and practice towards malaria among symptomatic patients attending Tumbi Referral Hospital: A cross-sectional study. Carvalho LH, editor. PLoS ONE. 2019;14:e0220501.

9. Eko J, Osonwa O, Offiong D. Practices of Malaria Prevention among School Adolescent within Calabar Metropolis, Southern Nigeria. Journal of Sociological Research. 2013;4:241.

Attachment

Submitted filename: Response to Reviewers.docx

Decision Letter 1

Sammy O Sam-Wobo

16 Nov 2022

Malaria prevention knowledge, attitudes, and practices (KAP) among adolescents living in an area of persistent transmission in Senegal: Results from a cross-sectional study

PONE-D-22-24296R1

Dear Dr. TAIROU,

We’re pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it meets all outstanding technical requirements.

Within one week, you’ll receive an e-mail detailing the required amendments. When these have been addressed, you’ll receive a formal acceptance letter and your manuscript will be scheduled for publication.

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Kind regards,

Sammy O. Sam-Wobo

Academic Editor

PLOS ONE

Additional Editor Comments (optional):

Reviewers' comments:

Acceptance letter

Sammy O Sam-Wobo

22 Nov 2022

PONE-D-22-24296R1

Malaria prevention knowledge, attitudes, and practices (KAP) among adolescents living in an area of persistent transmission in Senegal: Results from a cross-sectional study

Dear Dr. Tairou:

I'm pleased to inform you that your manuscript has been deemed suitable for publication in PLOS ONE. Congratulations! Your manuscript is now with our production department.

If your institution or institutions have a press office, please let them know about your upcoming paper now to help maximize its impact. If they'll be preparing press materials, please inform our press team within the next 48 hours. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information please contact onepress@plos.org.

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on behalf of

Dr. Sammy O. Sam-Wobo

Academic Editor

PLOS ONE

Associated Data

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

    Supplementary Materials

    S1 File. English version of the study questionnaire.

    (DOCX)

    S2 File. French version of the study questionnaire.

    (DOCX)

    S3 File. Malinke version of the study questionnaire.

    (DOCX)

    S1 Dataset. KAP STATA dataset.

    (DTA)

    S1 Table. Tables presenting the results of logistic regression of the factors associated with knowledge, attitude, prevention, and care-seeking behaviors of the adolescent.

    Tables are ordered as follows: Table A Logistic regression of the determinants related to malaria knowledge among adolescents; Table B Logistic regression of the factors associated with attitude of the participants towards malaria; Table C Logistic regression of the factors associated with malaria prevention practice; Table D Logistic regression of factors associated with malaria care-seeking behavior.

    (DOCX)

    Attachment

    Submitted filename: Response to Reviewers.docx

    Data Availability Statement

    All relevant data are within the paper and its Supporting information files.


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