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Community-based Screening and Treatment of Malaria in Pregnancy: a Cluster-randomized Trial (COSMIC)

Primary Purpose

Malaria, Antepartum, Maternal Malaria During Pregnancy - Baby Not Yet Delivered, Small for Gestational Age (Disorder)

Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
community based screening and treatment
Sponsored by
Royal Tropical Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Malaria, Antepartum focused on measuring malaria, placenta, pregnancy, plasmodium falciparum, screening and treatment, rapid diagnostic test, coartem, artemether-lumefantrine, community health worker

Eligibility Criteria

16 Years - undefined (Child, Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Residence in the study area and intention to stay in the area for the duration of the pregnancy and for delivery.
  • Aged at least 16 years (pregnant adolescents younger than 16 years will be considered only if they are accompanied by a responsible adult (in the Gambia) or married (considered an adult by marriage in Burkina Faso and Benin.)
  • Willing to provide biological samples as and when required during the study period (blood and placental biopsy)
  • Informed consent

Exclusion Criteria:

  • A history of sensitivity to sulphonamides.
  • Already participating in another research study

Sites / Locations

  • Centre de Recherches Entomologiques de Cotonou (CREC)
  • Clinical Research Unit of Nanoro URCN/CMA, Centre Muraz (CM)
  • Medical Research Council (MRC)

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

No Intervention

Arm Label

community based screening and treatment

Control

Arm Description

CHWs will identify pregnant women in the village and encourage to go to the antenatal care clinic, furthermore, once a month the community health worker will screen the pregnant women for malaria with a rapid diagnostic test and treat with artemether-lumefantrine in case of a positive test result.

All pregnant women will be identified in the study area and asked for participation to the study. No intervention will take place.

Outcomes

Primary Outcome Measures

Placental malaria
Placental malaria will be diagnosed by microscopy of placental biopsies and polymerase chain reaction (PCR) on placental blood.

Secondary Outcome Measures

Birth weight
Babies of mothers included in the study will be weighed after delivery.

Full Information

First Posted
September 10, 2013
Last Updated
October 3, 2016
Sponsor
Royal Tropical Institute
Collaborators
Medical Research Council Unit, The Gambia, Centre Muraz, Imperial College London, World Health Organization, European Union
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1. Study Identification

Unique Protocol Identification Number
NCT01941264
Brief Title
Community-based Screening and Treatment of Malaria in Pregnancy: a Cluster-randomized Trial
Acronym
COSMIC
Official Title
Community-based Scheduled Screening and Treatment of Malaria in Pregnancy for Improved Maternal and Infant Health: a Cluster-randomized Trial in The Gambia, Burkina Faso and Benin
Study Type
Interventional

2. Study Status

Record Verification Date
November 2015
Overall Recruitment Status
Completed
Study Start Date
October 2013 (undefined)
Primary Completion Date
May 2016 (Actual)
Study Completion Date
May 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Royal Tropical Institute
Collaborators
Medical Research Council Unit, The Gambia, Centre Muraz, Imperial College London, World Health Organization, European Union

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Malaria is a common disease in Africa and a major health problem. Pregnant women are also at risk of malaria. Malaria in pregnancy is life threatening to both the mother and the baby she is carrying. It can result in the destruction of the mother's blood and in babies with a lower birth weight than normal, making them less healthy in their first years of life. These risks are even higher in women having their first pregnancy. When a woman is pregnant she should go to the Antenatal clinic (ANC) for care. Usually the ANC health staff gives the woman intermittent preventable treatment (IPTp-SP) against malaria. This drug helps protect the woman against getting malaria. Each pregnant woman should receive at least 2 doses of this drug during their pregnancy; thus, they should go the ANC at least 2 times during their pregnancy. However, many women still do not go often to the ANC for health care during their pregnancy. This study would like to see whether community health workers (CHW) can work with pregnant women to encourage them to attend ANC more often. Also, the CHW will test a pregnant woman every month for malaria with a rapid test. If a woman has malaria, the CHW will treat her in her home instead of the woman having to go a health clinic for treatment. The woman will be treated with a different drug than the drug that is given at the ANC visits. Our hypothesis is that this will improve the care and management of malaria during pregnancy and this will improve the health of women and their newborns. To see whether this strategy improved the health of women and their newborns, we will take a small piece of the placenta at delivery to test for malaria and we will weigh the baby. We will test this strategy in multiple communities. We will compare this to pregnant women in communities where this strategy was not followed, thus where pregnant women received standard care. Participants will be pregnant women. There are no direct benefits for participating in the study, except the outcome of our research question that is possible health benefits in the intervention group. The drugs involved are tested safe in pregnant women from second trimester on.
Detailed Description
Community health workers (CHWs) that will be working in intervention villages will be trained on community-based case management of malaria by monthly testing of pregnant women using a rapid diagnostic test (RDT). They will also be taught the benefit of pregnant women visiting the antenatal clinics (ANC) and that women should receive intermittent preventive treatment with sulphadoxine-pyrimethamine (SP) at the ANC according to WHO guidelines. The CHWs will try to identify all pregnant women in their villages and encourage them to visit the ANC as early as possible in their pregnancy. The CHW will check after one week if the ANC was visited. For women who do not attend the ANC, the CHW will further encourage and discuss reasons for non-attendance. Subsequently the CHW will visit the woman's house every month to test for malaria with a RDT.The CHW will give a full course of AL to any woman with a positive RDT. The CHW will also collect a blood slide and a blood spot on filter paper for later analysis in the laboratory. The CHWs will return to women who were treated for malaria to check uptake and compliance by using a short questionnaire and checking the empty packaging of the treatment at the end of the course. In control communities, CHW will not be trained to do RDTs and give AL to pregnant women. The only data collection will occur during ANC visits. All women are asked to deliver in collaborating health centres. Peripheral blood will be tested for hemoglobin, malaria infection and resistance against SP. A placenta biopsy will be collected and all babies will be weighed and examined.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Malaria, Antepartum, Maternal Malaria During Pregnancy - Baby Not Yet Delivered, Small for Gestational Age (Disorder)
Keywords
malaria, placenta, pregnancy, plasmodium falciparum, screening and treatment, rapid diagnostic test, coartem, artemether-lumefantrine, community health worker

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
4265 (Actual)

8. Arms, Groups, and Interventions

Arm Title
community based screening and treatment
Arm Type
Active Comparator
Arm Description
CHWs will identify pregnant women in the village and encourage to go to the antenatal care clinic, furthermore, once a month the community health worker will screen the pregnant women for malaria with a rapid diagnostic test and treat with artemether-lumefantrine in case of a positive test result.
Arm Title
Control
Arm Type
No Intervention
Arm Description
All pregnant women will be identified in the study area and asked for participation to the study. No intervention will take place.
Intervention Type
Other
Intervention Name(s)
community based screening and treatment
Other Intervention Name(s)
Rapid diagnostic test, Coartem, Artemether-lumefantrine, malaria village worker, village health worker, community case management
Intervention Description
Already described in intervention arm description.
Primary Outcome Measure Information:
Title
Placental malaria
Description
Placental malaria will be diagnosed by microscopy of placental biopsies and polymerase chain reaction (PCR) on placental blood.
Time Frame
After delivery
Secondary Outcome Measure Information:
Title
Birth weight
Description
Babies of mothers included in the study will be weighed after delivery.
Time Frame
After delivery
Other Pre-specified Outcome Measures:
Title
antenatal care clinic attendance
Description
A field worker will identify all eligible pregnant women and will follow-up on ANC attendance through lists at the antenatal care clinic
Time Frame
Throughout inclusion (+/- 6 months)
Title
Resistance to sulphadoxine-pyrimethamine (SP)
Description
Samples infected with P.falciparum will be checked for resistance profile for sulphadoxine-pyrimethamine
Time Frame
At delivery
Title
Peripheral malaria infection
Description
Each collected filter paper en microscopy slide (both in antenatal care clinics and from community health worker visits) will be checked for the presence of malaria parasites.
Time Frame
Throughout inclusion (+/- 6 months)
Title
hemoglobin
Description
Peripheral blood sample will be tested for hemoglobin
Time Frame
At delivery

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Residence in the study area and intention to stay in the area for the duration of the pregnancy and for delivery. Aged at least 16 years (pregnant adolescents younger than 16 years will be considered only if they are accompanied by a responsible adult (in the Gambia) or married (considered an adult by marriage in Burkina Faso and Benin.) Willing to provide biological samples as and when required during the study period (blood and placental biopsy) Informed consent Exclusion Criteria: A history of sensitivity to sulphonamides. Already participating in another research study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Henk Schallig, Dr
Organizational Affiliation
Royal Tropical Institute (KIT)
Official's Role
Study Director
Facility Information:
Facility Name
Centre de Recherches Entomologiques de Cotonou (CREC)
City
Cotonou
Country
Benin
Facility Name
Clinical Research Unit of Nanoro URCN/CMA, Centre Muraz (CM)
City
Nanoro
Country
Burkina Faso
Facility Name
Medical Research Council (MRC)
City
Fajara
Country
Gambia

12. IPD Sharing Statement

Citations:
PubMed Identifier
25169073
Citation
Scott S, Mens PF, Tinto H, Nahum A, Ruizendaal E, Pagnoni F, Grietens KP, Kendall L, Bojang K, Schallig H, D'Alessandro U. Community-based scheduled screening and treatment of malaria in pregnancy for improved maternal and infant health in The Gambia, Burkina Faso and Benin: study protocol for a randomized controlled trial. Trials. 2014 Aug 28;15:340. doi: 10.1186/1745-6215-15-340.
Results Reference
background
PubMed Identifier
30384846
Citation
Natama HM, Moncunill G, Rovira-Vallbona E, Sanz H, Sorgho H, Aguilar R, Coulibaly-Traore M, Some MA, Scott S, Valea I, Mens PF, Schallig HDFH, Kestens L, Tinto H, Dobano C, Rosanas-Urgell A. Modulation of innate immune responses at birth by prenatal malaria exposure and association with malaria risk during the first year of life. BMC Med. 2018 Nov 2;16(1):198. doi: 10.1186/s12916-018-1187-3.
Results Reference
derived
PubMed Identifier
29961848
Citation
COSMIC Consortium. Community-based Malaria Screening and Treatment for Pregnant Women Receiving Standard Intermittent Preventive Treatment With Sulfadoxine-Pyrimethamine: A Multicenter (The Gambia, Burkina Faso, and Benin) Cluster-randomized Controlled Trial. Clin Infect Dis. 2019 Feb 1;68(4):586-596. doi: 10.1093/cid/ciy522.
Results Reference
derived

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Community-based Screening and Treatment of Malaria in Pregnancy: a Cluster-randomized Trial

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