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Intermittent Preventive Treatment With Dihydroartemisinin-piperaquine in Papua, Indonesia (STOPMiP-2)

Primary Purpose

Malaria in Pregnancy

Status
Active
Phase
Phase 4
Locations
Indonesia
Study Type
Interventional
Intervention
Intermittent preventive treatment in pregnancy (IPTp) with dihydroartemisinin-piperaquine
Sponsored by
Liverpool School of Tropical Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Malaria in Pregnancy

Eligibility Criteria

15 Years - 49 Years (Child, Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

Health facilities (pilot implementation)

  • Antenatal services must be operational and accessible
  • Midwives/nurses have been trained to prescribe IPTp-DP

Healthcare providers

  • Healthcare providers responsible for providing antenatal care services, and facility managers
  • District and provincial health managers

Pregnant women

  • Pregnant women aged 15-49 years
  • Women in 2nd/3rd trimester of pregnancy
  • HIV negative (where status is known)

Exclusion Criteria:

Health facilities (pilot implementation)

  • Health facilities which have accessibility issues and will not be enrolled in the pilot.

Healthcare providers

  • Health workers providing ANC and IPTp-DP services in health facilities who have provided services for <1 month.

Pregnant women

  • Women with communication or language problems including not being able to speak Indonesian.
  • Pregnant women who are unwell during interview
  • Pregnant women who move outside the pilot implementation areas.

Sites / Locations

  • Yayasan Pengembangan Kesehatan dan Masyarakat Papua

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

IPTp-DP

Arm Description

Pregnant women attending routine antenatal care visits in their second and third trimester are given a monthly, presumptive treatment dose of dihydroartemisinin-piperaquine of three tablets daily for three days (9 tablets). The first dose is given by directly observed therapy (DOT), and the remaining doses given to the women to take at home.

Outcomes

Primary Outcome Measures

Adherence in pregnant women
The proportion of pregnant women who receive the first dose of IPTp-DP by DOT at ANC clinic and have the correct number of DP tablets for subsequent doses on exiting, who when visited at home verify they have completed the treatment (self report and pill counts)

Secondary Outcome Measures

Delivery effectiveness
The proportion of women attending ANC clinic treated appropriately according to the IPTp-DP guidelines, defined as the first dose given by directly observed therapy (DOT) on day-1 plus adequate doses to take home for days 2 and 3. Women's understanding of the treatment regimens given during that ANC visit will also be assessed.

Full Information

First Posted
March 9, 2022
Last Updated
March 23, 2022
Sponsor
Liverpool School of Tropical Medicine
Collaborators
Gadjah Mada University, Indonesia-MoH, Yayasan Pengembangan Kesehatan dan Masyarakat Papua (Timika Research Facility)
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1. Study Identification

Unique Protocol Identification Number
NCT05294406
Brief Title
Intermittent Preventive Treatment With Dihydroartemisinin-piperaquine in Papua, Indonesia
Acronym
STOPMiP-2
Official Title
Evaluation of a Pilot Implementation of Intermittent Preventive Treatment With Dihydroartemisinin-piperaquine to Prevent Adverse Birth Outcomes in Papua, Indonesia
Study Type
Interventional

2. Study Status

Record Verification Date
March 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
February 7, 2022 (Actual)
Primary Completion Date
March 31, 2023 (Anticipated)
Study Completion Date
August 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Liverpool School of Tropical Medicine
Collaborators
Gadjah Mada University, Indonesia-MoH, Yayasan Pengembangan Kesehatan dan Masyarakat Papua (Timika Research Facility)

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
Malaria in pregnancy is a major cause of maternal and neonatal death in Papua, Indonesia. A recent trial in Papua showed that monthly intermittent preventive treatment (IPTp) with the long-acting artemisinin-based combination dihydroartemisinin-piperaquine (DP) among pregnant women in the second and third trimester was safe, tolerable and more efficacious than the current policy of single screening at antenatal care (ANC) booking and treatment of rapid diagnostic test (RDT)-positive cases. The Ministry of Health (MOH) Indonesia now plans to pilot the strategy in the routine health system in Papua, Indonesia. This study will assess the programme effectiveness of IPTp-DP delivery through antenatal care services and women's adherence to the monthly 3-day DP treatment regimen in a 'real life' setting. The study will be undertaken in ten community health centres in the lowlands and their associated health posts in Timika city. In the first 18 months, MOH will be trained to implement the intervention using quality improvement (QI) approaches to continuously strengthen service delivery, uptake and adherence through plan-do-study-act cycles. The MOH will also be supported to collect safety data for pharmacovigilance. A mixed-methods evaluation will be conducted towards the end of the pilot using exit interviews to assess delivery effectiveness, home visits to assess adherence, and qualitative research to explore provider perceptions of the drivers of successful integration and scalability, and user acceptability. The primary outcome is adherence, defined as the proportion of pregnant women who receive the first dose of IPTp-DP by directly observed therapy (DOT) at ANC, have received the correct number of DP tablets for subsequent doses, and when visited at home have verified they completed the course. The net cost-effectiveness of implementing IPTp-DP and of the current policy of single screening and treatment (SST) in the routine health system will be assessed and compared. Net cost-effectiveness means that cost savings from averted malaria will be deducted from the intervention costs. The incremental financial cost of implementing IPTp-DP from the provider (MOH) perspective at scale in Papua, Indonesia, will also be estimated.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Malaria in Pregnancy

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
1420 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
IPTp-DP
Arm Type
Experimental
Arm Description
Pregnant women attending routine antenatal care visits in their second and third trimester are given a monthly, presumptive treatment dose of dihydroartemisinin-piperaquine of three tablets daily for three days (9 tablets). The first dose is given by directly observed therapy (DOT), and the remaining doses given to the women to take at home.
Intervention Type
Drug
Intervention Name(s)
Intermittent preventive treatment in pregnancy (IPTp) with dihydroartemisinin-piperaquine
Intervention Description
Pregnant women attending routine antenatal care visits in their second and third trimester are given monthly IPTp consisting of a treatment dose of dihydroartemisinin-piperaquine (3 tablets per day for 3 days, 9 tablets total)
Primary Outcome Measure Information:
Title
Adherence in pregnant women
Description
The proportion of pregnant women who receive the first dose of IPTp-DP by DOT at ANC clinic and have the correct number of DP tablets for subsequent doses on exiting, who when visited at home verify they have completed the treatment (self report and pill counts)
Time Frame
At study completion, an average of 10 months
Secondary Outcome Measure Information:
Title
Delivery effectiveness
Description
The proportion of women attending ANC clinic treated appropriately according to the IPTp-DP guidelines, defined as the first dose given by directly observed therapy (DOT) on day-1 plus adequate doses to take home for days 2 and 3. Women's understanding of the treatment regimens given during that ANC visit will also be assessed.
Time Frame
At study completion, an average of 10 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
15 Years
Maximum Age & Unit of Time
49 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Health facilities (pilot implementation) Antenatal services must be operational and accessible Midwives/nurses have been trained to prescribe IPTp-DP Healthcare providers Healthcare providers responsible for providing antenatal care services, and facility managers District and provincial health managers Pregnant women Pregnant women aged 15-49 years Women in 2nd/3rd trimester of pregnancy HIV negative (where status is known) Exclusion Criteria: Health facilities (pilot implementation) Health facilities which have accessibility issues and will not be enrolled in the pilot. Healthcare providers Health workers providing ANC and IPTp-DP services in health facilities who have provided services for <1 month. Pregnant women Women with communication or language problems including not being able to speak Indonesian. Pregnant women who are unwell during interview Pregnant women who move outside the pilot implementation areas.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jenny Hill, MSc, PhD
Organizational Affiliation
LSTM
Official's Role
Principal Investigator
Facility Information:
Facility Name
Yayasan Pengembangan Kesehatan dan Masyarakat Papua
City
Timika
State/Province
Papua
ZIP/Postal Code
99910
Country
Indonesia

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Intermittent Preventive Treatment With Dihydroartemisinin-piperaquine in Papua, Indonesia

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