DengueNCT06648603
Citizen Action for Sustainable Dengue Control in Sub-Saharan Africa
A study testing Community-based larval source management, Enhanced Aedes adults trapping (BG-GAT) and Community-based larval source management with Enhanced Aedes adults trapping (BG-GAT) in people with Dengue, run by Swiss Tropical & Public Health Institute at 1 site in Côte d’Ivoire.
Trial summary
This project focuses on addressing arboviral outbreaks in Ivory Coast by involving local communities in the sustainable control of Aedes mosquitoes, utilizing scientific advice and environmental interventions. Read more about this study
- Who is it for?
- Any ageHealthy volunteers can take part
- Conditions the study is for
- Dengue
- What is being tested?
- Community-based larval source management, Enhanced Aedes adults trapping (BG-GAT) and Community-based larval source management with Enhanced Aedes adults trapping (BG-GAT)
- Type of treatment
- Medical device, Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 40 participants
- Where
- 1 siteCôte d’Ivoire
- Study dates
- 15 Jul 2023to 30 Sep 2024
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Any age
- All sexes
- Healthy volunteers accepted
- Child, Adult, Older adult
Who may be able to join
- Geographical location: households must be located within the designated clusters in the two districts involved in the trial.
- Participation in cluster arms: households must belong to a cluster that is assigned to one of the four arms (1. Control, 2. Community-based larval source management, 3 Enhanced Aedes adults trapping (BG-GAT), 4. Enhanced Aedes adults trapping (BG-GAT) + Community-based larval source management).
- Willingness to participate: households agreed to allow researchers to place mosquito traps and conduct larval and adult mosquito surveys.
- Socio-Environmental Data: households must agree and provide consent to participate to the socio-environmental questionnaire.
Who cannot join
- Outside of trial clusters: households located outside the designated clusters in the two districts were excluded.
- Refusal to participate: households that do not consent to mosquito trap placement or surveys
- Inaccessibility: households that are not accessible for regular visits or data collection (e.g., due to relocation or difficult terrain).
Trial locations and contacts
1 site in 1 country.
Côte d’Ivoire1 site
Centre Suisse de Recherches Scientifiques en Côte d'Ivoire
Abidjan
About this study
This project focuses on addressing arboviral outbreaks in Ivory Coast by involving local communities in the sustainable control of Aedes mosquitoes, utilizing scientific advice and environmental interventions. It will evaluate the impact of a participatory strategy on decreasing mosquito populations and the risk of virus transmission, aiming to provide insights for policy development on disease prevention.
Read the detailed description
This project targets the growing threat of Aedes mosquito-borne diseases such as dengue in Africa, focusing on the Anono and Gbagba communities in Abidjan, Ivory Coast, by transitioning from traditional control approaches to a community-driven strategy. It focuses on educating and involving communities in the design of sustainable mosquito management measures, such as breeding site eradication and adult mosquito capturing, with scientific experts guiding the efforts. The approach will entail conducting sociocultural surveys and interactive workshops while also encouraging local participation and multi-sectoral collaboration. A randomized controlled trial (RCT) will test this effectiveness of this novel integrated community-based participatory intervention approach in reducing the transmission of Aedes mosquito and other arboviruses. This effort seeks to develop a scalable model for arboviral disease control, promote community resilience, and inform policy recommendations for better public health outcomes in resource-constrained urban settings.
- Conditions
- Dengue
- Being tested
- Community-based larval source management, Enhanced Aedes adults trapping (BG-GAT), Community-based larval source management with Enhanced Aedes adults trapping (BG-GAT)
- Keywords
- Aedes Aegypti, Vector control, Community based intervention, Participatory research, Dengue, Africa, Ivory Coast
- Medical subject headings
- Dengue
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Community-based larval source managementBehavioural
This project will foster active engagement with community stakeholders, including healthcare workers, community leaders, and other key informants, through participatory meetings aimed at co-creating and developing larval source reduction measures tailored to community's needs. This method emphasizes a participatory framework, ensuring that interventions are both community-informed and culturally relevant.
Enhanced Aedes adults trapping (BG-GAT)Device
Furthermore, the project intends to determine whether the addition of cost-effective, gravid female mosquito-targeting traps, specifically two Biogents Gravid Aedes Traps (BG-GAT) per household, can improve the overall success of these community-based intervention.
Community-based larval source management with Enhanced Aedes adults trapping (BG-GAT)Combination product
The community-based interventions and the BG-GAT deployment will be evaluated in combination to assess their individual and synergistic effects on vector control. This dual strategy combines local participation and practical, evidence-based solutions to address mosquito-borne illness transmission.
| Study group | Role | What they receive |
|---|---|---|
| Control | No intervention | Non-intervened control arm: no community-based larval source management (LSM) or BG-GAT intervention |
| Community-based larval source management | Experimental | LSM intervention arm: Aedes larval source reduction carried out by trained and supervised local community members Receives: Behavioral: Community-based larval source management |
| Enhanced Aedes adults trapping (BG-GAT) | Experimental | BG-GAT intervention arm: Aedes adult mass trapping by BG-GAT set up and maintained by trained and supervised local community members Receives: Device: Enhanced Aedes adults trapping (BG-GAT) |
| Community-based larval source management + Enhanced Aedes adults trapping (BG-GAT) | Experimental | Combined LSM and BG-GAT intervention arm: simultaneous Aedes larval source reduction and Aedes adult mass trapping by BG-GAT carried out by trained and supervised local community members Receives: Combination Product: Community-based larval source management with Enhanced Aedes adults trapping (BG-GAT) |
What is being measured
The primary outcome is the main question the study is designed to answer.
Aedes aegypti mean number per trap per day
Biting rate is the mean number of Aedes females per trap and per day. The proportion of unfed, fed, half-gravid and gravid females will be estimated.
Measured: Continuously during months 1-4 (baseline) and months 5-17 (trial)
Secondary outcomes (7)
House index
House index: proportion of houses with at least one larva
Measured: Before (month 1), twice during (month 4, 8) and once at the end of the trial (month 12)
Pupal indices: pupae per person index, pupa index and pupae per hectare index
Pupae per person index: number of pupae per person Pupa index: number of pupae per house Pupae per hectare index: number of pupae per ha
Measured: Before (month 1), twice during (month 4, 8) and once at the end of the trial (month 12)
Adults: parity rate
The parity rate (PR) (proposition of parous females) will be calculated to estimate vector longevity.
Measured: Continuously during months 1-4 (baseline) and months 5-17 (trial)
Knowledge, attitudes, and practices on Dengue prevention among the population of Cocody-Bingerville
A Knowledge, Attitudes, and Practices (KAP) study will be conducted to assess the communities' understanding, attitudes, practices, and beliefs related to dengue. This will be done using a structured questionnaire developed specifically for this trial. The questionnaire comprises both multiple-choice and open-ended questions, allowing for a comprehensive assessment of: 1) Knowledge: Understanding of dengue transmission, symptoms, and prevention, 2) Attitudes: Perceptions of dengue risk and confidence in prevention methods, 3) Practices: Reported behaviors to prevent dengue, such as mosquito control measures. This structured tool will be used at both baseline and endline to measure changes and assess the effectiveness of the intervention."
Measured: Before (month 1) the start of the trial and at the end of the trial (month 12)
Mapping and describe Aedes aegypti breeding sites, focusing on their geographic and ecological characteristics. This mapping will be used to enhance targeted larval control efforts in these areas.
The geographic survey will collect household and environmental data, including demographic details, public space quality, water provision, sanitation access, and waste management practices. It will map housing conditions, examining building types, construction materials, and key features like water storage and solid waste management. The survey will also assess local built environments to inform interventions for improving living conditions and controlling mosquito breeding sites.
Measured: Before (month 1) the start of the trial and at the end of the trial (month 12)
Container index
Proportion of positive containers
Measured: before (month 1), twice during (month 4, 8) and once at the end of the trial (month 12)
Breteau index
Number of positive containers per 100 houses
Measured: Before (month 1), twice during (month 4, 8) and once at the end of the trial (month 12)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted18 Oct 2024
- Study start15 Jul 2023
- Primary completion31 Jul 2024
- Study completion30 Sep 2024
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for DengueStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Factorial
- Model description
- Cluster randomized trial with 2x2 factorial design - 40 clusters, 10 clusters per study arm (4 arms)
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 40 participants (actual)
Sponsor and investigators
- Lead sponsor
- Swiss Tropical & Public Health Institute
- Sponsor type
- University, hospital or other
- Collaborators
- Centre Suisse de Recherches Scientifiques en Cote d'Ivoire
- Responsible party
- Sponsor
- Investigators
- Pie Müller, PD, PhD, Principal investigator, Swiss Tropical & Public Health Institute
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06648603
- Sponsor's protocol ID
- C21047
- Status last verified
- Dec 2023
- First submitted
- 1 Jul 2024
- Last updated
- 22 Oct 2024
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 22 Oct 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Citizen Action for Sustainable Dengue Control in Sub-Saharan Africa
- ClinicalTrials.gov ID
- NCT06648603
- Acronym / sponsor ID
- C21047
- Conditions
- Dengue
- Keywords
- Aedes Aegypti, Vector control, Community based intervention, Participatory research, Dengue, Africa, Ivory Coast
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 40 participants (actual)
- Lead sponsor
- Swiss Tropical & Public Health InstituteUniversity, hospital or other
- Collaborators
- Centre Suisse de Recherches Scientifiques en Cote d'Ivoire
- Study start
- 15 Jul 2023 (actual)
- Primary completion
- 31 Jul 2024 (actual)
- Study completion
- 30 Sep 2024 (actual)
- First posted
- 18 Oct 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This project focuses on addressing arboviral outbreaks in Ivory Coast by involving local communities in the sustainable control of Aedes mosquitoes, utilizing scientific advice and environmental interventions. It will evaluate the impact of a participatory strategy on decreasing mosquito populations and the risk of virus transmission, aiming to provide insights for policy development on disease prevention.
Detailed description
This project targets the growing threat of Aedes mosquito-borne diseases such as dengue in Africa, focusing on the Anono and Gbagba communities in Abidjan, Ivory Coast, by transitioning from traditional control approaches to a community-driven strategy. It focuses on educating and involving communities in the design of sustainable mosquito management measures, such as breeding site eradication and adult mosquito capturing, with scientific experts guiding the efforts. The approach will entail conducting sociocultural surveys and interactive workshops while also encouraging local participation and multi-sectoral collaboration. A randomized controlled trial (RCT) will test this effectiveness of this novel integrated community-based participatory intervention approach in reducing the transmission of Aedes mosquito and other arboviruses. This effort seeks to develop a scalable model for arboviral disease control, promote community resilience, and inform policy recommendations for better public health outcomes in resource-constrained urban settings.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Factorial
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 4
- Model description
- Cluster randomized trial with 2x2 factorial design - 40 clusters, 10 clusters per study arm (4 arms)
| Arm | Type | Receives |
|---|---|---|
| Control | No intervention | –Non-intervened control arm: no community-based larval source management (LSM) or BG-GAT intervention |
| Community-based larval source management | Experimental | Behavioral: Community-based larval source managementLSM intervention arm: Aedes larval source reduction carried out by trained and supervised local community members |
| Enhanced Aedes adults trapping (BG-GAT) | Experimental | Device: Enhanced Aedes adults trapping (BG-GAT)BG-GAT intervention arm: Aedes adult mass trapping by BG-GAT set up and maintained by trained and supervised local community members |
| Community-based larval source management + Enhanced Aedes adults trapping (BG-GAT) | Experimental | Combination Product: Community-based larval source management with Enhanced Aedes adults trapping (BG-GAT)Combined LSM and BG-GAT intervention arm: simultaneous Aedes larval source reduction and Aedes adult mass trapping by BG-GAT carried out by trained and supervised local community members |
Who may qualify
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (4 listed)
- Geographical location: households must be located within the designated clusters in the two districts involved in the trial.
- Participation in cluster arms: households must belong to a cluster that is assigned to one of the four arms (1. Control, 2. Community-based larval source management, 3 Enhanced Aedes adults trapping (BG-GAT), 4. Enhanced Aedes adults trapping (BG-GAT) + Community-based larval source management).
- Willingness to participate: households agreed to allow researchers to place mosquito traps and conduct larval and adult mosquito surveys.
- Socio-Environmental Data: households must agree and provide consent to participate to the socio-environmental questionnaire.
Key exclusion criteria (3 listed)
- Outside of trial clusters: households located outside the designated clusters in the two districts were excluded.
- Refusal to participate: households that do not consent to mosquito trap placement or surveys
- Inaccessibility: households that are not accessible for regular visits or data collection (e.g., due to relocation or difficult terrain).
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Community-based larval source managementThis project will foster active engagement with community stakeholders, including healthcare workers, community leaders, and other key informants, through participatory meetings aimed at co-creating and developing larval source reduction measures tailored to community's needs. This method emphasizes a participatory framework, ensuring that interventions are both community-informed and culturally relevant. | Behavioural | Community-based larval source management |
| Enhanced Aedes adults trapping (BG-GAT)Furthermore, the project intends to determine whether the addition of cost-effective, gravid female mosquito-targeting traps, specifically two Biogents Gravid Aedes Traps (BG-GAT) per household, can improve the overall success of these community-based intervention. | Device | Enhanced Aedes adults trapping (BG-GAT) |
| Community-based larval source management with Enhanced Aedes adults trapping (BG-GAT)The community-based interventions and the BG-GAT deployment will be evaluated in combination to assess their individual and synergistic effects on vector control. This dual strategy combines local participation and practical, evidence-based solutions to address mosquito-borne illness transmission. | Combination product | Community-based larval source management + Enhanced Aedes adults trapping (BG-GAT) |
Primary outcome
Aedes aegypti mean number per trap per day
Time frame: Continuously during months 1-4 (baseline) and months 5-17 (trial)
Biting rate is the mean number of Aedes females per trap and per day. The proportion of unfed, fed, half-gravid and gravid females will be estimated.
7 secondary outcomes
House index
Time frame: Before (month 1), twice during (month 4, 8) and once at the end of the trial (month 12)
Pupal indices: pupae per person index, pupa index and pupae per hectare index
Time frame: Before (month 1), twice during (month 4, 8) and once at the end of the trial (month 12)
Adults: parity rate
Time frame: Continuously during months 1-4 (baseline) and months 5-17 (trial)
Knowledge, attitudes, and practices on Dengue prevention among the population of Cocody-Bingerville
Time frame: Before (month 1) the start of the trial and at the end of the trial (month 12)
Mapping and describe Aedes aegypti breeding sites, focusing on their geographic and ecological characteristics. This mapping will be used to enhance targeted larval control efforts in these areas.
Time frame: Before (month 1) the start of the trial and at the end of the trial (month 12)
Container index
Time frame: before (month 1), twice during (month 4, 8) and once at the end of the trial (month 12)
Breteau index
Time frame: Before (month 1), twice during (month 4, 8) and once at the end of the trial (month 12)
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 22 Oct 2024.
- Individual participant dataSharing planned: No
Related trials for Dengue
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Pie Müller, PD, PhD principal investigator
Swiss Tropical & Public Health Institute
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Community-based larval source management, Enhanced Aedes adults trapping (BG-GAT) and Community-based larval source management with Enhanced Aedes adults trapping (BG-GAT) in people with Dengue, run by Swiss Tropical & Public Health Institute at 1 site in Côte d’Ivoire.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 22 Oct 2024. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Côte d’Ivoire. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Aedes aegypti mean number per trap per day (time frame: Continuously during months 1-4 (baseline) and months 5-17 (trial)). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 Oct 2024.