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Adaptive Interventions for Optimizing Malaria Control: A Cluster-Randomized SMART Trial

Primary Purpose

LLIN, PBO LLIN, IRS, Larviciding

Status
Recruiting
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Regular long-lasting insecticidal nets
LLIN plus Piperonyl butoxide-treated LLIN
Long-lasting microbial larvicide
Indoor residual spraying with micro-encapsulated pirimiphos-methyl
Sponsored by
University of California, Irvine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for LLIN, PBO LLIN, IRS, Larviciding focused on measuring Adaptive intervention, Multiple assignment randomized trial (SMART), Cluster-randomized SMART trial, Optimal intervention strategy, Clinical malaria incidence, Cost-effectiveness

Eligibility Criteria

6 Months - undefined (Child, Adult, Older Adult)All SexesAccepts Healthy Volunteers

Household inclusion criteria:

  • Households with residents at the time of survey
  • Agreement of the adult resident to provide informed consent for the intervention and survey

Study subjects inclusion criteria:

  • Passive case detection by health facilities will include all residents in the study clusters; active case detection will include residents of >6 months
  • Agreement of parent/guardian to provide informed consent and minors to provide assent.

Household exclusion criteria:

  • Household vacant
  • No adult resident home on more than 3 occasions

Study subjects exclusion criteria:

• Participants not home on day of survey

Sites / Locations

  • Program in Public Health
  • Tom-Mboya University College, Maseno UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm 6

Arm 7

Arm Type

Placebo Comparator

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Arm Label

Regular long-lasting insecticidal nets

Piperonyl butoxide-treated LLIN

PBO-LLIN plus larval source management

PBO-LLIN plus enhanced methods

LLIN plus indoor residual spraying

LLIN+IRS+LSM

LLIN+IRS plus enhanced method

Arm Description

All participants will have LLIN coverage through routine MoH distribution of long-lasting insecticidal nets (LLINs), no other interventions will be applied. Regular LLIN: Olyset nets containing 2% permethrin or PermaNet 2.0 containing 1.8 and 1.4 g/kg, respectively, for 75 and 100 denier yarn.

All participants will received piperonyl butoxide-treated LLINs (PBO-LLINs) at Stage 1 and Stage 2 interventions provided that PBO-LLINs are effective at Stage 1 interventions. Each household will be provided on PBO-LLIN per two people with appropriate eduction. PBO-LLIN: Olyset Plus, containing 2% permethrin and 1% PBO.

All participants will received piperonyl butoxide-treated LLINs (PBO-LLINs) at Stage 1, however, Stage 1 intervention is not effective. All participants will received PBO-LLINs plus larval source management (LSM) at Stage 2. LSM will be implemented in selected clusters, including both physical and chemical methods by physical filling or removal of temporary larval habitats and larviciding of semi-permanent and permanent habitats, per the National Malaria Strategic Plan of Kenya. We will use the long-lasting microbial larvicides manufactured by Central Life Sciences. Semi-permanent and permanent habitats will be treated with FourStar® 180-day Briquets using the recommended dosage of 100 ft2 water surface per briquet.

All participants will received piperonyl butoxide-treated LLINs (PBO-LLINs) at Stage 1, however, Stage 1 intervention is not effective. All participants will received PBO-LLINs plus an enhanced intervention at Stage 2. The enhanced intervention is determined by machine learning method.

All participants will received regular LLINs plus indoor residual spraying (IRS) (LLIN+IRS) at Stage 1 and Stage 2 interventions provided that LLIN+IRS is effective at Stage 1 interventions. For LLIN+IRS clusters, each dwelling's interior walls and ceilings will be sprayed with micro-encapsulated pirimiphos-methyl (Actellic 300CS) at the recommended dosage of 1g/m² and at the recommended frequency of once a year.

All participants will received regular LLINs plus IRS at Stage 1, provided that LLIN+IRS is not effective. LSM will be added on these clusters at Stage 2 interventions. LSM at Stage 2 will be the long-lasting microbial larvicides manufactured by Central Life Sciences. Semi-permanent and permanent habitats will be treated with FourStar® 180-day Briquets using the recommended dosage of 100 ft2 water surface per briquet.

All participants will received regular LLINs plus IRS at Stage 1, provided that LLIN+IRS is not effective. Enhanced method will be added on these clusters at Stage 2 interventions.The enhanced intervention is determined by machine learning method.

Outcomes

Primary Outcome Measures

Annual clinical malaria incidence rate
To compare clinical malaria incidence rates among different intervention arms

Secondary Outcome Measures

Malaria infection prevalence
To compare infection prevalence rates among different intervention arms using microscopic, RDT and molecular diagnostic methods
Malaria vector density
To compare malaria vector densities between different intervention arms
Malaria transmission intensity
To compare entomological inoculation rates between different intervention arms

Full Information

First Posted
November 25, 2019
Last Updated
February 1, 2023
Sponsor
University of California, Irvine
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1. Study Identification

Unique Protocol Identification Number
NCT04182126
Brief Title
Adaptive Interventions for Optimizing Malaria Control: A Cluster-Randomized SMART Trial
Official Title
Environmental Modifications in Sub-Saharan Africa: Changing Epidemiology, Transmission and Pathogenesis of Plasmodium Falciparum and P. Vivax Malaria
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
December 1, 2019 (Actual)
Primary Completion Date
March 31, 2024 (Anticipated)
Study Completion Date
March 31, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of California, Irvine

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
In the past decade, massive scale-up of long-lasting insecticidal nets (LLINs) and indoor residual spraying (IRS) have led to significant reductions in malaria mortality and morbidity. Nonetheless, malaria burden remains high, and a dozen countries in Africa show a trend of increasing malaria incidence over the past several years. The high malaria burden in many areas of Africa underscores the need to improve the effectiveness of intervention tools by optimizing first-line intervention tools and integrating newly approved products into control programs. Vector control is an important component of the national malaria control strategy in Africa. Because transmission settings and vector ecologies vary among countries or among districts within a country, interventions that work in one setting may not work well in all settings. Malaria interventions should be adapted and re-adapted over time in response to evolving malaria risks and changing vector ecology and behavior. The central objective of this application is to design optimal adaptive combinations of vector control interventions to maximize reductions in malaria burden based on local malaria transmission risks, changing vector ecology, and available mix of interventions approved by the Ministry of Health in each target country. The central hypothesis is that an adaptive approach based on local malaria risk and changing vector ecology will lead to significant reductions in malaria incidence and transmission risk. The aim of this study is to use a cluster-randomized sequential, multiple assignment randomized trial (SMART) design to compare various vector control methods implemented by the Ministry of Health of Kenya in reducing malaria incidence and infection, and develop an optimal intervention strategy tailored toward to local epidemiological and vector conditions.
Detailed Description
In the past decade, massive scale-up of long-lasting insecticide-treated nets (LLINs) and indoor residual spraying (IRS) in Africa have led to significant reductions in malaria mortality and mobility. However, current first-line interventions are not sufficient to eliminate malaria in most countries. The widespread use of pyrethroid insecticides has resulted in resistant vector populations, and high coverage of LLINs and IRS has led to increased outdoor human feeding behavior and resting behavior. These changes in vector ecology and behaviors have significantly limited the effectiveness of current first-line interventions that target indoor biting and resting mosquitoes. Furthermore, as a result of ecological changes and intervention measures, malaria risk in a locality is dynamic, and the utility of malaria intervention tools may vary as new tools are being approved and introduced and the cost of each tool differs among locations and over time. Such variations in malaria risk, vector ecology, and utility of intervention tools exemplify the need to develop optimal adaptive interventions tailored to local malaria risks, vector ecology and supply chains. The central objective of this application is to design optimal adaptive combinations of vector control interventions to maximize reductions in malaria burden based on local malaria transmission risks, changing vector ecology, and available mix of interventions approved by the Ministry of Health in each target country. The central hypothesis is that an adaptive approach based on local malaria risk and changing vector ecology will lead to significant reductions in malaria incidence and transmission risk. To accomplish this objective, we propose the following three specific aims: Measure malaria incidence and predict risk using environmental, biological, social, and climatic features with machine learning approaches. Hypothesis: Malaria risk prediction can be improved through the use of machine learning techniques that include environmental, biological, socio-economic, and climatic features. Approach: Each site will measure malaria incidence, prevalence and social economic factors through community surveys. Classification-based and regression-based approaches will be used to develop malaria risk predictive models, and model performance will be validated. Outcome: This Aim will establish improved malaria risk prediction models and lay an important foundation for developing intervention strategies adaptive to local vector ecology and future malaria risks using reinforced machine learning approaches. Use a cluster-randomized sequential, multiple assignment randomized trial (SMART) design to develop an optimal adaptive intervention strategy. Hypothesis: Malaria control interventions that are adapted to local malaria risk and vector ecology and are cost effective can be identified using a cluster-randomized SMART design. Approach: Cluster-randomized SMART design will be used in a high transmission areas in Kenya to evaluate the impact of adaptive interventions that involve sequential and combinational use of next-generation nets, indoor spraying of non-pyrethroid insecticides, and larval source management for malaria control. Evaluate the cost-effectiveness and impact of an adaptive intervention approach on secondary endpoints related to malaria risk and transmission. Hypothesis: Intervention strategies adapted to local malaria risk and vector ecology will be more cost-effective in reducing malaria incidence and transmission risk than the currently-used LLIN intervention. Approach: The economic costs of individual interventions or combinations thereof will be assessed from both a provider and societal perspective using standard economic evaluation methodologies. Cost-effectiveness will be measured in terms of cost per person protected. The study will examine changes in drug and insecticide resistance and infection prevalence attributable to the adaptive interventions. Malaria interventions adapted to rapidly changing malaria risk and vector ecologies are critically needed to improve the effectiveness of malaria control measures. This study will use new techniques, including machine learning and a novel cluster-randomized SMART design, to develop optimal adaptive malaria intervention strategies. We will use 84 clusters in Kisumu County in Western Kenya to conduct the trial. Since it is a sequential multiple assignment randomized trail, the trial will include several intervention stages. At each stage there will be different interventions. If an intervention is effective (i.e., yields an above threshold reduction in malaria incidence) at Stage 1, the intervention will be continued, otherwise, the intervention will be replaced by another one at Stage 2. The replacement intervention may be decided by different ways, e.g., an known effective intervention or an intervention determined by a machine learning algorithm. Since interventions in some clusters may be continued (i.e., effective) by next stage, other interventions may be replaced by different interventions, the number of interventions arms can vary from stage to stage. This is very different from ordinary cluster randomized trials. In this trial, we planned to start with piperonyl butoxide (PBO) treated long-lasting insecticidal nets (PBO LLIN), indoor residual spraying with Actellic(R) insecticide, and using the routine LLIN intervention as control. Both Actellic IRS and PBO LLIN have been tested to be effective against pyrethroid resistant Anopheles malaria vectors and reduce clinical malaria. Therefore, the initial stage will have three arms, i.e., regular LLIN, PBO LLIN, and regular LLIN plus Actellic IRS. Since we don't know if the effectiveness of these interventions in different clusters, the stage 2 interventions may include up to 7 arms, i.e., some arms may be split into two arms, based on the evaluation at the end of Stage 1 intervention. We will begin the trial with a two-year smaller scale trial using 36 cluster and randomly assign the three interventions, i.e., regular LLIN, PBO LLIN and regular LLIN plus Actellic IRS, into these 36 cluster, with 12 clusters for each intervention. This pre-trial trial is to determine the optimal way for conducting the full-scale 84 cluster trial, including operational and effectiveness evaluation procedures, as well as cost-effectiveness analysis. The full scale 84 cluster trial will be started by Year 3. The full trial will be started from fresh, i.e., the same three interventions will be randomly assigned to the 84 clusters with 28 clusters for each interventions. Clinical malaria will be monitored using a cohort active case surveillance, parasite prevalence and vector density will be monitored using cross-sectional samplings. The results of these surveillance at the end of Stage 1 trial will be used to evaluate the effectiveness of interventions at each cluster for the Stage 1 interventions. Stage 2 interventions will be determined for each cluster based on the above evaluations, e.g., continue the same intervention or replace the intervention with different ones.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
LLIN, PBO LLIN, IRS, Larviciding
Keywords
Adaptive intervention, Multiple assignment randomized trial (SMART), Cluster-randomized SMART trial, Optimal intervention strategy, Clinical malaria incidence, Cost-effectiveness

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Sequential Assignment
Model Description
This study will use a longitudinal sequential multiple assignment randomized trial design. It will include multiple stages, at each stage, clusters are assigned to different arms (interventions) using an adaptive strategy. Therefore, number of arms vary from stage to stage.
Masking
Care ProviderInvestigatorOutcomes Assessor
Masking Description
This study partially masking participants, because by design some participants will receive PBO treated long-lasting insecticidal nets (LLINs) and others will not receive such bed nets, therefore, those who receives the PBO LLINs can not be masked.
Allocation
Randomized
Enrollment
122872 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Regular long-lasting insecticidal nets
Arm Type
Placebo Comparator
Arm Description
All participants will have LLIN coverage through routine MoH distribution of long-lasting insecticidal nets (LLINs), no other interventions will be applied. Regular LLIN: Olyset nets containing 2% permethrin or PermaNet 2.0 containing 1.8 and 1.4 g/kg, respectively, for 75 and 100 denier yarn.
Arm Title
Piperonyl butoxide-treated LLIN
Arm Type
Experimental
Arm Description
All participants will received piperonyl butoxide-treated LLINs (PBO-LLINs) at Stage 1 and Stage 2 interventions provided that PBO-LLINs are effective at Stage 1 interventions. Each household will be provided on PBO-LLIN per two people with appropriate eduction. PBO-LLIN: Olyset Plus, containing 2% permethrin and 1% PBO.
Arm Title
PBO-LLIN plus larval source management
Arm Type
Experimental
Arm Description
All participants will received piperonyl butoxide-treated LLINs (PBO-LLINs) at Stage 1, however, Stage 1 intervention is not effective. All participants will received PBO-LLINs plus larval source management (LSM) at Stage 2. LSM will be implemented in selected clusters, including both physical and chemical methods by physical filling or removal of temporary larval habitats and larviciding of semi-permanent and permanent habitats, per the National Malaria Strategic Plan of Kenya. We will use the long-lasting microbial larvicides manufactured by Central Life Sciences. Semi-permanent and permanent habitats will be treated with FourStar® 180-day Briquets using the recommended dosage of 100 ft2 water surface per briquet.
Arm Title
PBO-LLIN plus enhanced methods
Arm Type
Experimental
Arm Description
All participants will received piperonyl butoxide-treated LLINs (PBO-LLINs) at Stage 1, however, Stage 1 intervention is not effective. All participants will received PBO-LLINs plus an enhanced intervention at Stage 2. The enhanced intervention is determined by machine learning method.
Arm Title
LLIN plus indoor residual spraying
Arm Type
Experimental
Arm Description
All participants will received regular LLINs plus indoor residual spraying (IRS) (LLIN+IRS) at Stage 1 and Stage 2 interventions provided that LLIN+IRS is effective at Stage 1 interventions. For LLIN+IRS clusters, each dwelling's interior walls and ceilings will be sprayed with micro-encapsulated pirimiphos-methyl (Actellic 300CS) at the recommended dosage of 1g/m² and at the recommended frequency of once a year.
Arm Title
LLIN+IRS+LSM
Arm Type
Experimental
Arm Description
All participants will received regular LLINs plus IRS at Stage 1, provided that LLIN+IRS is not effective. LSM will be added on these clusters at Stage 2 interventions. LSM at Stage 2 will be the long-lasting microbial larvicides manufactured by Central Life Sciences. Semi-permanent and permanent habitats will be treated with FourStar® 180-day Briquets using the recommended dosage of 100 ft2 water surface per briquet.
Arm Title
LLIN+IRS plus enhanced method
Arm Type
Experimental
Arm Description
All participants will received regular LLINs plus IRS at Stage 1, provided that LLIN+IRS is not effective. Enhanced method will be added on these clusters at Stage 2 interventions.The enhanced intervention is determined by machine learning method.
Intervention Type
Other
Intervention Name(s)
Regular long-lasting insecticidal nets
Other Intervention Name(s)
LLIN
Intervention Description
Olyset nets: containing 2% permethrin or PermaNet 2.0 containing 1.8 and 1.4 g/kg, respectively, for 75 and 100 denier yarn
Intervention Type
Other
Intervention Name(s)
LLIN plus Piperonyl butoxide-treated LLIN
Other Intervention Name(s)
PBO-LLIN
Intervention Description
Olyset Plus: containing 2% permethrin and 1% PBO
Intervention Type
Other
Intervention Name(s)
Long-lasting microbial larvicide
Other Intervention Name(s)
FourStar® 180-day Briquets
Intervention Description
Semi-permanent and permanent habitats will be treated with FourStar® 180-day Briquets using the recommended dosage of 100 ft2 water surface per briquet
Intervention Type
Other
Intervention Name(s)
Indoor residual spraying with micro-encapsulated pirimiphos-methyl
Other Intervention Name(s)
Actellic 300CS
Intervention Description
each dwelling's interior walls and ceilings will be sprayed with micro-encapsulated pirimiphos-methyl at the recommended dosage of 1g/m² and at the recommended frequency of once a year
Primary Outcome Measure Information:
Title
Annual clinical malaria incidence rate
Description
To compare clinical malaria incidence rates among different intervention arms
Time Frame
Clinical malaria will be monitored for up to 60 months
Secondary Outcome Measure Information:
Title
Malaria infection prevalence
Description
To compare infection prevalence rates among different intervention arms using microscopic, RDT and molecular diagnostic methods
Time Frame
Infection prevalence will be monitored for up to 60 months
Title
Malaria vector density
Description
To compare malaria vector densities between different intervention arms
Time Frame
Vector density will be monitored for up to 60 months
Title
Malaria transmission intensity
Description
To compare entomological inoculation rates between different intervention arms
Time Frame
Entomological inoculation rate will be examined for up to 60 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Months
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Household inclusion criteria: Households with residents at the time of survey Agreement of the adult resident to provide informed consent for the intervention and survey Study subjects inclusion criteria: Passive case detection by health facilities will include all residents in the study clusters; active case detection will include residents of >6 months Agreement of parent/guardian to provide informed consent and minors to provide assent. Household exclusion criteria: Household vacant No adult resident home on more than 3 occasions Study subjects exclusion criteria: • Participants not home on day of survey
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Guiyun Yan, Ph.D.
Phone
19498240175
Email
guiyuny@uci.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Guiyun Yan
Phone
19498240175
Email
guiyuny@uci.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Guiyun Yan, Ph.D.
Organizational Affiliation
University of California at Irvine
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
John Githure, Ph.D.
Organizational Affiliation
Tom-Mboya University, Kenya
Official's Role
Study Director
Facility Information:
Facility Name
Program in Public Health
City
Irvine
State/Province
California
ZIP/Postal Code
92697
Country
United States
Individual Site Status
Active, not recruiting
Facility Name
Tom-Mboya University College, Maseno University
City
Homa Bay
State/Province
Homa Bay County
Country
Kenya
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Harrysone E Atieli, Ph.D.
Phone
+254 721 347 437
Email
etemesi2012@yahoo.com
First Name & Middle Initial & Last Name & Degree
John Githure, Ph.D.
Email
jgithure@gmail.com
First Name & Middle Initial & Last Name & Degree
Andrew K Githeko, Ph.D.
First Name & Middle Initial & Last Name & Degree
Gordon Okomo, Ph.D.

12. IPD Sharing Statement

Citations:
PubMed Identifier
32690063
Citation
Zhou G, Lee MC, Atieli HE, Githure JI, Githeko AK, Kazura JW, Yan G. Adaptive interventions for optimizing malaria control: an implementation study protocol for a block-cluster randomized, sequential multiple assignment trial. Trials. 2020 Jul 20;21(1):665. doi: 10.1186/s13063-020-04573-y.
Results Reference
derived

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Adaptive Interventions for Optimizing Malaria Control: A Cluster-Randomized SMART Trial

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