- Open Access
Community-based malaria control in southern Malawi: a description of experimental interventions of community workshops, house improvement and larval source management
Malaria Journal volume 17, Article number: 266 (2018)
Increased engagement of communities has been emphasized in global plans for malaria control and elimination. Three interventions to reinforce and complement national malaria control recommendations were developed and applied within the context of a broad-based development initiative, targeting a rural population surrounding a wildlife reserve. The interventions, which were part of a 2-year research trial, and assigned to the village level, were implemented through trained local volunteers, or ‘health animators’, who educated the community and facilitated collective action.
Community workshops on malaria were designed to increase uptake of national recommendations; a manual was developed, and training of health animators conducted, with educational content and analytical tools for a series of fortnightly community workshops in annual cycles at village level. The roll-back malaria principle of diagnosis, treatment and use of long-lasting insecticidal nets was a central component of the workshops. Structural house improvement to reduce entry of malaria vectors consisted of targeted activities in selected villages to mobilize the community into voluntarily closing the eaves and screening the windows of their houses; the project provided wire mesh for screening. Corrective measures were introduced to respond to field challenges. Committees were established at village level to coordinate the house improvement activities. Larval source management (LSM) in selected villages consisted of two parts: one on removal of standing water bodies by the community at large; and one on larviciding with bacterial insecticide Bacillus thuringiensis israelensis by trained village committees. Community workshops on malaria were implemented as ‘core intervention’ in all villages. House improvement and LSM were implemented in addition to community workshops on malaria in selected villages.
Three novel interventions for community mobilization on malaria prevention and control were described. The interventions comprised local organizational structure, education and collective action, and incorporated elements of problem identification, planning and evaluation. These methods could be applicable to other countries and settings.
In the face of substantial advancements made in malaria control in sub-Saharan Africa since 2000 , there are strong indications that the active involvement of communities within malaria control and elimination programmes has not been fully realized [2, 3]. Community engagement is critical to the uptake of prevention, diagnosis and treatment, and helps elucidate how local knowledge, beliefs and practices affect the acceptability of interventions by the community [4, 5]. A review of studies on the impact of community participation concluded that the use of locally selected, and trained, volunteers was a common and important element of the success of interventions .
Now that bold new global targets have been set for further reduction of malaria case incidence and mortality by 2030 , a long-term commitment to community engagement is emphasized in the Roll Back Malaria (RBM) action plan that places malaria within the broader development agenda of the sustainable development goals (SDG), instead of a focus on disease alone . Recommended interventions cover vector control, chemoprevention, diagnostic testing, treatment and surveillance. Insecticide-treated nets (ITNs) and indoor residual spraying (IRS) are core vector control interventions for endemic settings, but challenges with insecticide resistance and residual transmission (including outdoor transmission) suggest that supplemental interventions will be needed to enhance and sustain transmission reduction [8,9,10].
Structural house improvement and larval source management are existing vector control methods that have demonstrated an epidemiological impact in specific settings [11,12,13,14]. These methods have different modes of action from ITNs and IRS and, when they show incremental impact on disease, they could be implemented in addition to the core interventions. Active engagement of communities and local partners is considered appropriate for implementing house improvement and larval source management on a large scale.
In Malawi, malaria continues to be a major public health burden, with over 6 million presumed and confirmed cases reported in 2015 in a population of 17 million , although the malaria mortality rate has shown a steady decline over the past 15 years . Insecticide-treated nets are the primary intervention for malaria prevention, but problems have been reported with net use and the development of insecticide resistance [17,18,19,20,21]. Moreover, challenges remain in adherence to case management policy and prompt treatment seeking [21, 22].
This paper describes three interventions that were implemented through trained community volunteers: community workshops on malaria, structural house improvement and larval source management. The interventions were part of a cluster-randomized controlled trial, described in a separate paper . The descriptions of these intervention methods may inspire other vector-borne disease control initiatives in developing their community-based interventions.
The study area is a zone, on average 10 km wide, surrounding the 70,000 ha of the Majete Wildlife Reserve in the Lower Shire Valley in Chikhwawa District, southern Malawi (Fig. 1). This zone, which is inhabited by approximately 90,000 people, will be referred to as the Majete perimeter. Within this zone, three focal areas (indicated as A, B and C), spaced roughly evenly around the perimeter were selected for the intervention trial . These focal areas had a population of 24,153 (enumeration results as of 2014) living in 65 villages, including some recently split-up villages. Average household size was 4.5.
The objective of the trial was to determine the incremental impact of house improvement and larval source management on malaria parasite transmission, when added to nationally recommended interventions . The trial was implemented from May 2016 through April 2018, preceded by a 1-year baseline period. After the end of the trial, the best interventions will be rolled out to the remainder of Majete perimeter. Out of the 65 villages covered by the trial, seven were allocated as ‘control’, twelve as ‘buffer’, thirteen as ‘house improvement’, 24 as ‘larval source management’, and nine as ‘house improvement plus larval source management’. Community workshops on malaria were implemented in all villages, as ‘core intervention’ to enhance uptake of nationally recommended tools and guidelines.
During the baseline data collection in 2015/16 preceding the trial, a 34% malaria prevalence rate and a clinical malaria incidence rate of 1.2 cases per child-year at risk in U5′s were measured in the three focal areas [24, 25], indicating high parasite transmission and burden. Malaria control is implemented by the District Health Office following national guidelines and coverage targets, using long-lasting insecticidal nets (LLINs) and IPTp for prevention, microscopy or malaria rapid diagnostic tests (RDT) for diagnosis, and artemisinin-based combination therapy (ACT) for treatment; however, these interventions are often challenged by field realities . The District Health Office employs community health workers who were in 2015 upgraded and trained to conduct malaria diagnosis and treatment at community level.
From 2003, Majete Wildlife Reserve has, after a period of being devoid of most wildlife due to poaching, been rehabilitated, restocked and managed by African Parks Majete (Ltd), with the goal to develop an environmentally and financially sustainable park by 2028. A 144 km-long predator-proof perimeter fence was constructed to surround the entire reserve, and law enforcement officers and scouts patrol the Reserve to deter poaching . In order to advance the role of the people living in Majete perimeter as partner in wildlife conservation, various initiatives for employment, education and development have been created during the past decade, through a series of community projects, and construction of schools, boreholes and health clinics.
The main development project in Majete perimeter is operated by international non-governmental organization The Hunger Project. This organization uses the so-called ‘epicentre’ strategy, whereby an epicentre is an introduced social infrastructure covering proximate villages with a 4000–20,000 population per epicentre. An epicentre actively engages with existing local government structures and services, and initiates a number of development programmes to address acute problems in rural livelihoods . As of 2018, there are 5 existing and 3 planned epicentres in Majete perimeter. Four phases are identified in the development of an epicentre: (i) 1 year of activities to mobilize the community and establish thematic committees; (ii) a 2-year period in which a large epicentre building is constructed together with the community and during which development programmes are established; (iii) a 3-year period of implementation of development programmes; and (iv) a 2-year period to establish self-reliance of the epicentre, whereby external support is retracted but monitoring continues.
The Hunger Project uses participatory methods at village-level to initiate a change in people’s mindset—from resignation and dependency towards vision and commitment—to help overcome livelihood challenges. Selected villagers are trained to become ‘animators’, which are local volunteers who facilitate educational programmes, such as on nutrition and HIV/AIDS prevention, within their own village. Other epicentre development programmes each with their dedicated committee and core members include: water and sanitation, adult literacy, improved farming, food security, and microfinance. The epicentre building accommodates a health facility, nursery school, library, food processing room, microcredit bank, meeting hall, and sanitary facilities. The health facility, with outpatient department and often with maternity facility, is operated by the District Health Office, which provides personnel and commodities.
The research project took an early decision to embed its malaria control interventions within the ‘context’ of The Hunger Project’s epicentres, rather than implementing malaria control as a stand-alone package. The rationale was that the uptake of the malaria interventions could be enhanced through the community approach introduced by The Hunger Project. The project entered into a collaborative agreement with The Hunger Project and African Parks. Hence, malaria control effectively became an additional development programme of the epicentre. In accordance, the ‘animator approach’ was adopted, whereby ‘health animators’ facilitated activities on malaria in each village at regular intervals.
In total, 77 health animators (1 or 2 per village) were selected, covering the 65 trial villages. The selection was conducted by village leaders and guided by The Hunger Project using criteria of literacy skills, leadership potential and level of motivation. Health animators operated as volunteers, without remuneration, but during their training they received a standard upkeep cash allowance, and branded T-shirts, caps and bags; they also received a bicycle for attending coordination meetings . The community health workers operating for the District Health Office in the focal areas were given orientation training on the project’s interventions and attended some of the training courses for health animators, so as to stimulate active linkages with health animators.
Intervention 1: Community workshops on malaria
Community workshops on malaria, led by trained health animators, were the core intervention implemented in all 65 villages covered by the trial (Fig. 2A). The objective of this intervention was to reach a meaningful proportion of the population with education, situation analysis and discussion on malaria prevention and control. The aim was to increase people’s compliance with nationally recommended malaria control measures and to encourage collective action. The intervention was through training-of-trainers, training of health animators, monitoring and support. The community workshops were delegated to the health animators.
In consultation with various stakeholders, and based on available information about the target population , a manual was developed with a number of topics designed for a series of fortnightly community workshops for an annual cycle (see Additional file 1); all project manuals were translated into the local language Chichewa. Visual aids were provided. Each community workshop session addressed a topic (Table 1), group discussion and self-reporting on malaria cases. Self-reporting on malaria cases involved the counting new cases since the previous workshop among participating households, and noting health services received; the results were then to be used in group discussion .
After a 2-day training-of-trainers, the health animators received a total of 7 days of training to build technical, organizational and group facilitation skills, using participatory methods. Also, drama and songs were developed and practiced on a range of issues, for example on the malaria transmission cycle, or in relation to the health system. Following the initial training September–October 2014, health animators received 3-day refresher trainings at the end of the year in 2015, 2016 and 2017. Health animators made initial arrangements with the village head and informed villagers about a launch event, coinciding with the first community workshop. Community workshops were then to be held at village level, or cluster village level, whereby the communities from one or, in some cases, more villages met in a central place, typically under a landmark tree.
Monitoring and support was given through monthly coordination meetings, conducted at focal-area level, under the leadership of an epicentre project officer. Participants were health animators, and sometimes also the village leaders and community health workers. Community workshops were also monitored through spot checks and self-monitoring.
The implementation and outputs of the community workshops have been reported in a separate contribution . The results indicated feasibility of the malaria workshops with reasonable attendance of communities in the malaria workshops; 10–17% of the population participated per workshop (average 46 adult participants per workshop), with 23.5 workshops held per village per year. The community workshops were found appropriate and acceptable in rural communities, but the support from village leaders and community health workers was critical for success.
Intervention 2: Structural house improvement
Structural house improvement was implemented in 22 selected villages of the trial (total of 2344 houses) in addition to intervention 1. Prior observations had indicated a high proportion of houses with eaves (including gables) and windows (including vent holes) being open, thus allowing entry of malaria vectors. The intervention consisted of targeted activities for mobilizing the community into making adequate house improvements; the project itself did not conduct house improvements.
The project provided locally-procured mosquito wire mesh and some basic hand tools; the community provided bricks, mud, wood, nails and tools. A manual was developed for a series of community workshops on house improvement, including learning units, community organizing and action planning, for implementation in 2015 (see Additional file 2A). Each community workshop session covered a specific topic (Table 2A) and group discussion. There was no material provision for the doors, but the curriculum encouraged villagers to improve the door or doorframe, and keep the door closed after dark.
After a 1-day training-of-trainers, 29 health animators representing the villages selected for house improvement in the three focal areas took part in a 3-day training workshop in July 2015; half-day refresher courses were given in 2016 and 2017. During the training, health animators conducted a simple house survey, to understand people’s perceptions regarding house improvement, and a practical exercise to gain hands-on experience in developing best practices of house improvement. The training was interactive in that some outcomes of discussions were subsequently adopted in the training curriculum. The group decided that best practices of house improvement in the local setting were to begin with closing of eaves with bricks and mud, after which wire mesh would be made available to households for screening the windows. There was consensus that open eaves were generally not intended to provide ventilation, which was confirmed by a survey conducted in one of the focal areas, indicating 97% willingness to close eaves (Mburu, unpublished data, 2015). The group further decided that the best strategy for house improvement (HI) would be to establish a HI committee at village level, tasked with the distribution of wire mesh, coordination and monitoring. Committee members would be gender balanced and democratically elected, with the village head and community health worker having advisory roles.
Immediately after the training, health animators organized a launch event in their respective villages to elect committee members (average 10/village) and initiate need-based brick making. Community workshops on house improvement were implemented at monthly intervals (Table 2A). In October 2015, progress monitoring suggested that the majority of households had made a voluntary effort to close their eaves, in response to which the wire mesh was distributed to the community (Fig. 3A–C). In May 2016, field visits indicated reasonably good implementation of window screening (including vent holes; Fig. 3C), but a poor quality of closure of eaves. In response, a plan for corrective voluntary measures was made (Table 2B; see Additional file 2B), which emphasized the preparation of demonstration houses in each HI village and the launch of the next stage in the house improvement campaign by HI committees. By September 2016, all villages had at least one demonstration house with properly sealed eaves and screened windows.
Concurrently, the wire mesh started to show signs of corrosion in some locations; a magnet-test confirmed that the mesh contained iron. By February 2017, corrosion had led to broken screens in a number of houses, implying the need for replacement. To address this challenge, 1-day training sessions were held covering all 22 HI committees, their health animators, community health workers and village leaders, to identify local gaps, and to discuss monitoring and response action by the committees (Table 2C; see Additional file 2C). In June 2017, field monitoring indicated that replacement of wire mesh with a non-corrosive aluminium mesh had been largely completed, with some exceptions. The quality of house improvement was measured using coverage indicators in randomly selected houses during the trial period, which will be reported separately.
Intervention 3: Larval source management
Larval source management (LSM) was implemented in 33 selected villages of the trial, and in the 400-m buffer zone surrounding each selected village ; LSM was in addition to intervention 1. The intervention consisted of activities aiming to mobilize the community to conduct LSM; the project itself did not directly carry out LSM. In the context of the trial, LSM refers to removal or larviciding of larval habitats .
Removal of larval habitats (draining, filling) can be implemented by the community without external material support (Fig. 3D, E). However, larviciding depends on equipment and supplies that were provided by the project, namely manual compression knapsack sprayers, goggles, gloves, rubber boots, and a supply of the bacterial insecticide Bacillus thuringiensis israelensis (VectoBac WDG, Valent Biosciences, Libertyville IL, USA), referred to as ‘Bti’. Hence, the training was developed in two parts: the first part with focus on removal of standing water bodies by the community at large; the second part on larviciding with Bti by community representatives (Fig. 3F). A flowchart was developed to facilitate the efficient use of Bti (Fig. 4).
Regarding the removal of larval habitats, a manual was developed for a series of community workshops, including learning units and action planning (Table 3; see Additional file 3). In November 2015, after a 2-day training-of-trainers, 43 health animators representing the villages selected for LSM in the three focal areas took part in a 3-day training workshop; 1-day refresher courses were given in 2016 and 2017. The curriculum included practical sessions on identification of larvae of Anopheles and Culex, use of LSM planning tools (e.g. participatory mapping; community work plan), and field sampling of various larval habitats (Fig. 2B) to discuss options for control. As for house improvement, the health animators agreed on the need to establish LSM committees to run LSM activities in each selected village (in some cases, the committee covered several adjoining villages).
Regarding larviciding with Bti, a training manual was developed for LSM committee members, as community representatives who would do the spraying. The curriculum covered basics (e.g. surveying larval habitats), practical aspects (e.g. how to conduct a spray operation), and organizational and management aspects (e.g. record keeping) (Table 4; see Additional file 4). In May 2016, a 3-day training-of-trainers was succeeded by 3-day practical training sessions conducted in nine locations, to cover all 266 LSM committee members, their health animators, community health workers and village leaders. After these trainings, the LSM committees were monitored and supported regarding technical issues (e.g. preparing spray mix; systematic surveying). In addition, the monthly coordination meetings held in each focal area for intervention 1, provided a forum for discussion and support on LSM. The quality of LSM was measured by the project using coverage indicators, which will be reported separately.
Recent studies on vector control have highlighted the value of community participation from various angles. Studies from Rwanda, Uganda and Kenya showed the critical importance of engaging communities in the formulation of appropriate measures towards malaria reduction [30, 31], and in the design of a suitable implementation strategy for a new vector control technology [32, 33]. Other studies demonstrated the community’s role in implementation of larval control. Surveillance and microbial larviciding of malaria vectors in Dar es Salaam, Tanzania, has been successfully implemented through trained, modestly-paid community members, recruited via the local government, resulting in reduced malaria prevalence [34, 35]. In Sri Lanka, farmer field schools in irrigated rice systems led to improved knowledge and an increase in environmentally sound mosquito control measures [36, 37].
The methods of community participation described in this paper resemble those of studies on dengue vector control, which comprised local organizational structure, education and collective action. In Cuba, community working groups of trained volunteers at the neighbourhood level engaged the community and stakeholders in decision making, leading to effective dengue vector control [38, 39]. In Vietnam, committees of volunteers at commune level received education and carried out surveillance and use of biological control agents, resulting in local elimination of dengue [40, 41]. Comparably, this paper describes methods of establishing ‘nodes’ at village level, whereby animators and committees educated the community on malaria prevention and control, and instigated village-wide action.
The economic and financial costs of the described interventions, the outcomes in terms of a change in knowledge, attitudes and practices, and impact on malaria prevalence and transmission, will be presented in separate publications.
There are several reasons why the described methods have prospect for increasing the community’s role in malaria control. The decision to operate through trained local unpaid volunteers (health animators; village-level committees) allowed the interventions to be carried out at scale, despite the time-consuming character of the methods (e.g. conducting community workshops). Moreover, the methods included elements that have been associated with community ownership and empowerment; these elements are: problem identification, adult education, priority setting, planning, action, and participatory monitoring and evaluation [2, 38, 42, 43]. For example, problem analysis was included as topic for community workshops on malaria, and a form of evaluation during community workshops was through self-reporting on malaria cases.
The interventions were introduced through the existing structures of local government and epicentres in order to foster acceptability and sustainability, whereby village leaders and community health workers played a supportive role. Also, the core intervention of community workshops provided momentum through fortnightly malaria-related activities at village level during annual cycles. The Hunger Project envisages to sustain the community workshops for epicentres that have become self-reliant, as a continuous forum for villagers to tackle malaria or other (emerging) health issues.
It has been advocated that strategies of vector-borne disease control need to be complemented by actions in other sectors to address the determinants of malaria, thus increasing effectiveness and sustainability [44,45,46]. The partnership with The Hunger Project and African Parks—agencies with long-term strategies that aim towards self-reliance and sustainability—had several benefits, as compared to a stand-alone malaria package. Harnessing the epicentre’s existing infrastructure with its mechanisms of support, feedback and non-fiscal incentives can render participatory malaria control interventions more effective, by raising motivation and volunteerism. Moreover, the epicentre’s development programmes, and income generated from tourism from Majete Wildlife Reserve, potentially improve local socio-economic conditions, thus complementing malaria control .
Despite these prospects for increasing the demand for, and uptake of, interventions by the community, the provision of health services in the targeted areas remains a challenge, with inadequate personnel, frequent stock-outs of anti-malaria commodities, and inconsistent case recording . Consequently, systematic strengthening of the rural health services deserves urgent attention.
A limitation of the intervention methods described in this paper was that the investment in training and field support during the trial period was moderately costly. Nevertheless, it is planned that during the roll-out phase after the trial, in which all villages within the Majete perimeter will receive malaria interventions based on the trial’s outcome, inputs will be gradually reduced by handover of tasks of training, monitoring and field support from project staff to health animators, in line with the epicentre strategy, resulting in reduced expenses for personnel and transport. Regarding the provision of supplies, a system of local entrepreneurship could be developed, in which the community makes financial contributions for purchase of wire mesh or Bti. Also, future trials could consider the use of botanical insecticide products such as Neem oil (Azadirachta indica, Meliaceae) as locally-available alternatives to Bti.
There may be further options for using community-based interventions such as described in this paper—other than through a partnership with development agencies. One approach could be by expanding the reach of the health system, whereby local field staff are assigned with tasks similar to those of a health animator, under supervision of the community health worker. However, the question will remain to be studied whether the approach would be feasible if not imbedded within a broader development programme like the epicentre strategy.
This paper described novel interventions for community mobilization on malaria prevention and control through involvement of local volunteers as health animators in 65 villages. The interventions were embedded within the context of a broad-based development programme, thus, harnessing existing mechanisms of support, feedback, non-fiscal incentives. The interventions incorporated elements of problem identification, planning and evaluation, which could lead to empowerment effects in individuals and communities.
Community workshops on malaria provided a platform for basic education on malaria, aiming to increase demand for and uptake of health services by the community. Interventions of house improvement and larval source management were introduced in addition to the community workshops on malaria, as two introduced methods with potential to complement national malaria control recommendations; both were implemented by the community.
artemisinin-based combination therapy
Bacillus thuringiensis israelensis
intermittent preventive treatment in pregnancy
indoor residual spraying
long-lasting insecticidal nets
larval source management
malaria rapid diagnostic test
National Malaria Control Programme
Roll Back Malaria Partnership
sustainable development goals
water dispersible granule
Bhatt S, Weiss DJ, Cameron E, Bisanzio D, Mappin B, Dalrymple U, et al. The effect of malaria control on Plasmodium falciparum in Africa between 2000 and 2015. Nature. 2015;526:207–11.
Atkinson JA, Vallely A, Fitzgerald L, Whittaker M, Tanner M. The architecture and effect of participation: a systematic review of community participation for communicable disease control and elimination. Implications for malaria elimination. Malar J. 2011;10:225.
Chilaka MA. Ascribing quantitative value to community participation: a case study of the Roll Back Malaria (RBM) initiative in five African countries. Public Health. 2005;119:987–94.
Whittaker M, Smith C. Reimagining malaria: five reasons to strengthen community engagement in the lead up to malaria elimination. Malar J. 2015;14:410.
Heggenhougen HK, Hackethal V, Vivek P. The behavioural and social aspects of malaria and its control: an introduction and annotated biliography. TDR/STR/SEB/VOL/03.1. Geneva: World Health Organization; 2003.
World Health Organization. Global Technical Strategy for malaria. Geneva: World Health Organization; 2015.
World Health Organization. Action and investment to defeat Malaria 2016–2030. For a malaria-free world. Geneva: World Health Organization on behalf of the Roll Back Malaria Partnership Secretariat; 2015.
Ranson H, Lissenden N. Insecticide resistance in African Anopheles mosquitoes: a worsening situation that needs urgent action to maintain malaria control. Trends Parasitol. 2016;32:187–96.
Durnez L, Coosemans M. Residual transmission of malaria: an old issue for new approaches. In: Manguin S, editor. Anopheles mosquitoes—new insights into malaria vectors. Rijeka: InTech; 2013. p. 671–704.
Benelli G, Beier JC. Current vector control challenges in the fight against malaria. Acta Trop. 2017;174:91–6.
Tusting LS, Ippolito MM, Willey BA, Kleinschmidt I, Dorsey G, Gosling RD, et al. The evidence for improving housing to reduce malaria: a systematic review and meta-analysis. Malar J. 2015;14:209.
RBM. Housing and malaria consensus statement. Vector Control Working Group. New York: Roll Back Malaria Partnership, UNDP and UN Habitat; 2015.
Tusting LS, Thwing J, Sinclair D, Fillinger U, Gimnig J, Bonner KE, et al. Mosquito larval source management for controlling malaria. Cochrane Database Syst Rev. 2013;8:CD008923.
WHO. Larval source management: a supplementary measure for malaria vector control: an operational manual. Geneva: World Health Organization; 2013.
PMI. Malaria Operational Plan FY 2017. Washington DC: President’s Malaria Initiative; 2016.
WHO. World malaria report 2016. Geneva: World Health Organization; 2016.
Zamawe COF, Nakamura K, Shibanuma A, Jimba M. The effectiveness of a nationwide universal coverage campaign of insecticide-treated bed nets on childhood malaria in Malawi. Malar J. 2016;15:505.
Riveron JM, Chiumia M, Menze BD, Barnes KG, Irving H, Ibrahim SS, et al. Rise of multiple insecticide resistance in Anopheles funestus in Malawi: a major concern for malaria vector control. Malar J. 2015;14:344.
Wondji CS, Coleman M, Kleinschmidt I, Mzilahowa T, Irving H, Ndula M, et al. Impact of pyrethroid resistance on operational malaria control in Malawi. Proc Natl Acad Sci USA. 2012;109:19063–70.
Mzilahowa T, Chiumia M, Mbewe RB, Uzalili VT, Luka-Banda M, Kutengule A, et al. Increasing insecticide resistance in Anopheles funestus and Anopheles arabiensis in Malawi, 2011–2015. Malar J. 2016;15:563.
National Malaria Control Programme (NMCP) and ICF. Malawi Malaria Indicator Survey 2017. Lilongwe and Rockville: NMCP and ICF; 2018. https://dhsprogram.com/pubs/pdf/MIS28/MIS28.pdf. Accessed 27 Jun 2018.
Steinhardt LC, Chinkhumba J, Wolkon A, Luka M, Luhanga M, Sande J, et al. Quality of malaria case management in Malawi: results from a nationally representative health facility survey. PLoS One. 2014;9:e89050.
McCann RS, van den Berg H, Diggle PJ, van Vugt M, Terlouw DJ, Phiri KS, et al. Assessment of the effect of larval source management and house improvement on malaria transmission when added to standard malaria control strategies in southern Malawi: study protocol for a cluster-randomised controlled trial. BMC Infect Dis. 2017;17:639.
Kabaghe AN, Chipeta MG, Terlouw DJ, McCann RS, Van Vugt M, Grobusch MP, et al. Short-term changes in anemia and malaria parasite prevalence in children under 5 years during one year of repeated cross-sectional surveys in rural Malawi. Am J Trop Med Hyg. 2017;97:1568–75.
Kabaghe AN, Chipeta MG, Gowelo S, Mburu M, Truwah Z, McCann RS, et al. Fine-scale spatial and temporal variation of clinical malaria incidence and associated factors in children in rural Malawi: a longitudinal study. Parasit Vectors. 2018;11:129.
African_Parks. About Majete. https://www.african-parks.org/the-parks/majete. Accessed 27 Jun 2018.
The-Hunger-Project. Malawi. http://www.thp.org/our-work/where-we-work/africa/malawi/. Accessed 27 Jun 2018.
Malenga T, Kabaghe AN, Manda-Taylor L, Kadama A, McCann RS, Phiri KS, et al. Malaria control in rural Malawi: implementing peer health education for behaviour change. Global Health. 2017;13:84.
Chungu H. Majete I baseline survey report. Blantyre: The Hunger Projec Malawi; 2012.
Ingabire CM, Alaii J, Hakizimana E, Kateera F, Muhimuzi D, Nieuwold I, et al. Community mobilization for malaria elimination: application of an open space methodology in Ruhuha sector, Rwanda. Malar J. 2014;13:167.
Lindsay SW, Egwang TG, Kabuye F, Mutambo T, Matwale GK. Community-based environmental management program for malaria control in Kampala and Jinja, Uganda. Final Report. Washington DC: Environmental Health Project; 2004.
Oria PA, Hiscox A, Alaii J, Ayugi M, Mukabana WR, Takken W, et al. Tracking the mutual shaping of the technical and social dimensions of solar-powered mosquito trapping systems (SMoTS) for malaria control on Rusinga Island, western Kenya. Parasit Vectors. 2014;7:523.
Homan T, Hiscox A, Mweresa CK, Masiga D, Mukabana WR, Oria P, et al. The effect of mass mosquito trapping on malaria transmission and disease burden (SolarMal): a stepped-wedge cluster-randomised trial. Lancet. 2016;388:1193–201.
Chaki PP, Dongus S, Fillinger U, Kelly A, Killeen GF. Community-owned resource persons for malaria vector control: enabling factors and challenges in an operational programme in Dar es Salaam, United Republic of Tanzania. Hum Resour Health. 2011;9:21.
Geissbühler Y, Kannady K, Chaki PP, Emidi B, Govella NJ, Mayagaya V, et al. Microbial larvicide application by a large-scale, community-based program reduces malaria infection prevalence in urban Dar es Salaam, Tanzania. PLoS One. 2009;4:e5107.
Yasuoka J, Mangione TW, Spielman A, Levins R. Impact of education on knowledge, agricultural practices, and community actions for mosquito control and mosquito-borne disease prevention in rice ecosystems in Sri Lanka. Am J Trop Med Hyg. 2006;74:1034–42.
van den Berg H, Knols BGJ. The farmer field school: a method for enhancing the role of rural communities in malaria control? Malar J. 2006;5:3.
Toledo ME, Vanlerberghe V, Baly A, Ceballos E, Valdes L, Searret M, et al. Towards active community participation in dengue vector control: results from action research in Santiago de Cuba, Cuba. Trans R Soc Trop Med Hyg. 2007;101:56–63.
Castro M, Sánchez L, Pérez D, Carbonell N, Lefèvre P, Vanlerberghe V, et al. A community empowerment strategy embedded in a routine dengue vector control programme: a cluster randomised controlled trial. Trans R Soc Trop Med Hyg. 2012;106:315–21.
Vu SN, Nguyen TY, Tran VP, Truong UN, Le QM, Le VL, et al. Elimination of dengue by community programs using Mesocyclops (Copepoda) against Aedes aegypti in central Vietnam. Am J Trop Med Hyg. 2005;72:67–73.
Kay B, Vu SN. New strategy against Aedes aegypti in Vietnam. Lancet. 2005;365:613–7.
Kaseje DCO, Sempebwa EKN. An integrated rural health project in Saradidi, Kenya. Soc Sci Med. 1989;28:1063–71.
van den Berg H, Velayudhan R, Ebol A, Catbagan BHG, Turingan R, Tuso M, et al. Operational efficiency and sustainability of vector control of malaria and dengue: descriptive case studies from the Philippines. Malar J. 2012;11:269.
RBM Partnership and UNDP. Multi-sectoral action framework for malaria. New York: United Nations Development Programme; 2013.
WHO. Global vector control response 2017–2030. Geneva: World Health Organization; 2017.
WHO. Handbook for integrated vector management. WHO/HTM/NTD/VEM/2012.3. Geneva: World Health Organization; 2012.
Tusting LS, Willey B, Lucas H, Thompson J, Kafy HT, Smith R, et al. Socioeconomic development as an intervention against malaria: a systematic review and meta-analysis. Lancet. 2013;382:963–72.
Kabaghe AN, Phiri MD, Phiri KS, van Vugt M. Challenges in implementing uncomplicated malaria treatment in children: a health facility survey in rural Malawi. Malar J. 2017;16:419.
Kabaghe AN, Chipeta MG, McCann RS, Phiri KS, Van Vugt M, Takken W, et al. Adaptive geostatistical sampling enables efficient identification of malaria hotspots in repeated cross-sectional surveys in rural Malawi. PLoS One. 2017;12:e0172266.
Conceived the study: HvdB, MvV, RM, KP, WT. Involved in development of manuals: HvdB, MvV, ANK, MN, RK, ZT, TM, AK, SB, TT, SG, MM, RM. Involved in training, field support and monitoring: HvdB, MvV, ANK, MN, ZT, TM, AK, SB, TT, SG, MM, RM. Drafted the manuscript: HvdB, RM. All authors read and approved the final manuscript.
The authors are grateful to Precious Magombo, Kennedy Kapulula, Joseph Mbalu, Carol Mateme, Amber Majidu, Gerald Nakoma, Seth Piriminta, John Mugawa, Ignatius Mtambalika for their valuable work in training and support of health animators, and to all the health animators for their relentless contribution to the project and to their communities. Henry Chungu, Grace Chikowi, Lucinda Manda-Taylor, Dianne J. Terlouw, Themba Mzilahowa, Doreen Ali, Mphatso Phiri, Tobias Kunkumbira, Samuel Kamoto, Craig Hay and Patricio Ndadzela are thanked for discussions that have contributed to the methods presented here.
The authors declare that they have no competing interests.
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Not applicable. Ethical considerations of the trial have been presented in the study’s protocol, published separately .
Majete Malaria Project is generously supported by Dioraphte Foundation, the Netherlands. The content is solely the responsibility of the authors and does not necessarily represent the official views of the funder.
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About this article
- Community participation
- Community workshops
- Health education
- House improvement
- Integrated vector management
- Larval source management
- Malaria transmission
- Vector control