Plain English Summary
Background and study aims
Malaria is the world’s most important vector-borne disease, infecting millions and causing over 400,000 deaths, mainly in sub-Saharan Africa. The Plasmodium parasites that cause malaria are transmitted by Anopheles mosquitoes, which in African countries most often bite indoors at night. Sleeping under a bed net, especially if treated with insecticide is a proven way to reduce malaria, and much of the decrease in malaria over the past 10-15 years has been attributed to massive increases in treated net distribution campaigns. After a decade of decline, malaria rates have begun to increase; one major reason for which is widespread mosquito resistance to the pyrethroid insecticides used to treat bednets. For safety reasons only pyrethroids are currently approved as the main insecticide for net treatment, but other compounds can be added which may improve their effectiveness. For example, bednets are available co-treated with both pyrethroid and a molecule called PBO which blocks mosquito enzymes that can cause pyrethroid resistance. These PBO co-treated nets have been demonstrated in a single large-scale clinical trial in Tanzania to be more effective than pyrethroid only nets, but more evidence is required from a range of different countries to justify the greater cost of their distribution when health budgets are often very limited. Such evidence is extremely expensive to accumulate from multiple formal clinical trials but an alternative approach is to monitor the relative effectiveness of PBO and standard nets when both are distributed in the same area as part of an ongoing programme. The aim of this study is to determine which type of net works better, and for how long any benefits last, in the province of Sud Ubangi in the northern Democratic Republic of Congo, which is receiving both types of bednet. The study also aims to increase cost efficiency by monitoring malaria rates in women (living in areas receiving the different net types) as they attend routine ante-natal clinic appointments.
Who can participate?
Women visiting antenatal clinics and households in villages around some of the antenatal clinics included in the study
What does the study involve?
All 16 of the health zones in Sud Ubangi province are involved in the study, with 8 receiving only standard bednets, 7 receiving only PBO co-treated bednets and 1 receiving both; determined at random. The number of pregnant women tested at antenatal clinics and found to carry malaria infections will be compared between the zones with each net type. Measures of mosquito abundance and resistance will also be compared, along with the durability/quality of nets over time from first distribution.
What are the possible benefits and risks of participating?
There are no significant benefits or risks involved in participating.
Where is the study run from?
The study will be run from the University of Kinshasa School of Public Health in collaboration with health services in Sud Ubangi province, based in Gemena (province capital).
When is study starting and how long is it expected to run for?
November 2019 to November 2022
Who is funding the study?
Against Malaria Foundation (UK)
Who is the main contact?
Dr David Weetman
david.weetman@lstmed.ac.uk
Trial website
Contact information
Type
Scientific
Primary contact
Dr David Weetman
ORCID ID
http://orcid.org/0000-0002-5820-1388
Contact details
Liverpool School of Tropical Medicine
Pembroke Place
Liverpool
L3 5QA
United Kingdom
+44 (0)1517053225
david.weetman@lstmed.ac.uk
Additional identifiers
EudraCT number
Nil known
ClinicalTrials.gov number
Nil known
Protocol/serial number
SU-ITN_1
Study information
Scientific title
Comparative evaluation of standard insecticide-treated bednets and co-treated bednets on malaria prevalence in Sud Ubangi, Democratic Republic of Congo: a cluster-randomised trial
Acronym
Sud Ubangi ITN study
Study hypothesis
The primary study hypothesis is that parasite prevalence will be lower in intervention clusters (health zones receiving PBO co-treated bednets), than in control clusters (health zones receiving standard insecticide only bednets) in Sud Ubangi, Democratic Republic of Congo.
Ethics approval
1. Approved 24/09/2019, Liverpool School of Tropical Medicine: Research Ethics Committee (Pembroke Place, Liverpool, L3 5QA, UK; Tel: +44(0)151 705 3100), ref: 19-072
2. Approval pending, University of Kinshasa Research Ethics Committee (Ecole de Sante Publique
Comite d'Ethique, Ministere de 1'Enseignement Superieur et Universitaire, Unlversite de Kinshasa Faculte de Medecine: B.P 11850 Kin I, Republique Democratique du Congo)
Study design
Cluster randomised trial
Primary study design
Interventional
Secondary study design
Cluster randomised trial
Trial setting
Home
Trial type
Prevention
Patient information sheet
See additional files
Condition
Malaria
Intervention
A total of 16 clusters (provincial health zones) are involved in the study; clusters were randomised to receive a different type of treated bednet by a member of LSTM staff, who will not be directly involved in the study. All houses within the eight zones allocated to group 1 will receive standard (pyrethroid only) bednet; within the seven zones allocated to group 2 will receive a PBO co-treated bednet. Within the remaining zone, the distribution will be mixed with one part receiving each bednet, as dictated by different numbers of bednets available within the distribution programme.
Bednets, supplied by Against Malaria Foundation, will be distributed in Sud Ubangi by IMA World Health in partnership with SANRU (DRC rural health programme). All households in Sud Ubangi will receive sufficient nets to permit coverage of one net per two occupants. At the time of distribution, nets will be hung over sleeping spaces by the distribution team partners with an accompanying education programme to increase correct usage, care and maintenance of nets by householders. The study team have no role in the distribution or hanging of bednets or the bednet-related education programme.
The study involves:
1. Determination of parasite prevalence in women visiting monthly antenatal clinics
2. Entomological collections for surveillance of insecticide resistance and mosquito abundance and parasite infection
3. Assessment of bednet durability (physical and chemical analysis) and bioefficacy (against mosquitoes) over time
The intervention is not under control of the trial but it is planned by the Ministry of Health to replace the nets after a minimum of 36 months, which could be viewed as the end of the intervention. The follow up is planned to be 36 months, subject to continuation of funding (guaranteed for 12 months as present from start of the trial period).
Intervention type
Other
Phase
Drug names
Primary outcome measure
Parasite prevalence (defined as the proportion of positive malaria rapid diagnostic tests) in pregnant women assessed at 0, 6 months, 12 months, 18 months, 24 months, 30 months, 36 months after bednet distribution
Secondary outcome measures
1. Frequency of molecular markers associated with insecticide resistance in the primary malaria vector mosquito (Anopheles gambiae) is measured from DNA extracted from mosquitoes collected in one half of the study clusters at 0, 6 months, 12 months, 18 months, 24 months, 30 months, 36 months after bednet distribution
2. Mosquito abundance and parasite infection rate (with the infectious sporozoite stage) will be measured in one half of the study clusters at 0, 6 months, 12 months, 18 months, 24 months, 30 months, 36 months after bednet distribution
3. Prevalence and intensity of phenotypic insecticide resistance, assessed using World Health Organization (WHO) tests of insecticide, in 4 study clusters at 0, 6 months, 12 months, 18 months, 24 months, 30 months, 36 months after bednet distribution
4. Bednet durability and bio-efficacy assessed will be measured using WHO guidelines for physical assessment of the area of holes, chemical analysis of insecticide (and PBO) concentrations and capacity of the net material to kill locally-caught mosquitoes in controlled experiments in nets collected from 4 study clusters at 0, 6 months, 12 months, 18 months, 24 months, 30 months, 36 months after bednet distribution
Overall trial start date
01/11/2019
Overall trial end date
30/11/2022
Reason abandoned (if study stopped)
Eligibility
Participant inclusion criteria
Women attending first ANC appointment at a clinic that is taking part in the study and who consent to be enrolled in the study
Participant type
Patient
Age group
Adult
Gender
Female
Target number of participants
20 visitors per month in each of 7 antenatal clinics (held monthly) in each of 17 study clusters, which gives a total of approximately 2400 participants per month; 28500 per year and 86000 in total.
Participant exclusion criteria
1. Young adolescents (<15 years)
2. Women presenting with symptoms of severe malaria
3. Women suffering from other illness requiring prompt treatment
Recruitment start date
01/12/2019
Recruitment end date
30/10/2022
Locations
Countries of recruitment
Congo, Democratic Republic
Trial participating centre
University of Kinshasa
School of Public Health
Kinshasa
H8Q3+2H Kinshasa
Congo, Democratic Republic
Sponsor information
Organisation
Liverpool School of Tropical Medicine
Sponsor details
Pembroke Place
Liverpool
L3 5QA
United Kingdom
+44 (0)151 705 3100
info@lstmed.ac.uk
Sponsor type
University/education
Website
Funders
Funder type
Charity
Funder name
Against Malaria Foundation
Alternative name(s)
Funding Body Type
Funding Body Subtype
Location
Results and Publications
Publication and dissemination plan
Results will be published as soon as feasible at dates to be determined. Results will be disseminated on a biannual basis to the funders and other key stakeholders.
IPD sharing statement
The datasets generated and/or analysed during the current study will be available upon request from Dr David Weetman (david.weetman@lstmed.ac.uk). The participant level data is basic and involves only a short questionnaire with the addition of the malaria test result. The unanonymised data represent a patient medical record so will be maintained at the Sud Ubangi records office in Gemena Hospital. These data sheets are not intended to be publicly available, but access could be possible with an appropriate (separate) ethical/data protection application, which could be sent to Dr Weetman in the first instance for communication to the local health authority. In anonymised format the data could be made available by the trial team (via Dr Weetman), who will retain (anonymised) records for 5 years from the end of the trial. The trial team will also maintain consent forms for the same 5 year period.
Intention to publish date
01/06/2023
Participant level data
Available on request
Basic results (scientific)
Publication list
Publication citations
Additional files
- ISRCTN99611164_PROTOCOL_v4.1_26Oct19.pdf Uploaded 08/11/2019
- ISRCTN99611164_PIS_v1.2.pdf Uploaded 08/11/2019