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Early ART Initiation Among HIV-positive Pregnant Women in Central Mozambique

Primary Purpose

HIV

Status
Completed
Phase
Not Applicable
Locations
Mozambique
Study Type
Interventional
Intervention
Adherence and retention package
Sponsored by
University of Washington
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for HIV focused on measuring HIV, Mozambique, antenatal care, adherence, retention, pregnancy, HIV-positive mothers retained in ART after 90 days

Eligibility Criteria

14 Years - 50 Years (Child, Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Pregnant women who test HIV-positive in antenatal care services at target health facilities

Exclusion Criteria:

  • Pregnant women who arrived at health facilities who already have tested positive
  • HIV-positive pregnant women who cannot start ART

Sites / Locations

  • Beira Operations Research Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Adherence and retention intervention

Control

Arm Description

Implementation of adherence and retention package

Clusters continue without intervention package

Outcomes

Primary Outcome Measures

Retention at 30 days
The primary outcome measure for Aim 3 is the proportion of HIV-positive pregnant women tested at the participating ANC sites that successfully initiates appropriate ART and returns for their scheduled 30-day visit for pharmacy refill and evaluation within 45 days.
Adherence at 90 days
The primary outcome measure for Aim 4 is the ART adherence rate through 90 days after ART initiation.

Secondary Outcome Measures

Full Information

First Posted
February 18, 2015
Last Updated
May 8, 2023
Sponsor
University of Washington
Collaborators
Health Alliance International, Beira Operations Research Center, Mozambique Ministry of Health
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1. Study Identification

Unique Protocol Identification Number
NCT02371265
Brief Title
Early ART Initiation Among HIV-positive Pregnant Women in Central Mozambique
Official Title
Early ART Initiation Among HIV-positive Pregnant Women in Central Mozambique
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Completed
Study Start Date
April 2012 (undefined)
Primary Completion Date
August 2015 (Actual)
Study Completion Date
August 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Washington
Collaborators
Health Alliance International, Beira Operations Research Center, Mozambique Ministry of Health

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The overall objective of the study is to develop and test a pilot intervention in central Mozambique to implement the new WHO "Option B+" guidelines that seek to increase the proportion of HIV-positive pregnant women in six antenatal care clinics who start antiretroviral therapy (ART) prior to delivery, and are retained in care after 90- days.
Detailed Description
For over 10 years, services to prevent maternal to child HIV-1 transmission (PMTCT) have been scaled-up and integrated into antenatal care (ANC) in the national health system across Mozambique. In 2004, scale-up of anti-retroviral treatment (ART) also began in Mozambique and is now provided at hundreds of health units. In 2010, the World Health Organization developed new treatment guidelines, termed "Option B" that emphasized early initiation of ART in antenatal care for all HIV-positive pregnant women. In 2012, the WHO issued a programmatic update endorsing a third option termed "Option B+" in which HIV positive pregnant women initiate ART during pregnancy regardless of disease progression and continue treatment for life. The new "Option B+" approach has been adopted by the Ministry of Health (MoH) in Mozambique and is in the early phases of implementation. As in many African settings, numerous health system factors present major challenges to successful adoption of the guidelines. In Mozambique, ANC and HIV testing coverage is high but there is substantial loss-to-follow-up (LTFU) at successive stages in the treatment cascade, limited counseling for women and many barriers to actively tracking those women lost to follow-up. Early Ministry of Health data suggests significant challenges remain for long-term adherence for women started on ART via the new Option B+ framework in Manica and Sofala provinces and throughout Mozambique. The successful implementation of new WHO guidelines therefore requires major streamlining of links among ANC, PMTCT, and ART services. The overall objective of this study is to develop and test a pilot intervention in central Mozambique to implement the new WHO guidelines, and increase the proportion of HIV-positive pregnant women in target ANC clinics who start ART prior to delivery, without reducing ART adherence in the first 3 months of therapy. The intervention will emphasize a WHO defined "Option B+" approach; HIV-positive mothers will be referred for ART at the time they receive a positive HIV test result in their first ANC visit. The project utilizes an innovative formative research process, which has already been completed, and a stepped wedge implementation science design to evaluate the intervention. The entire study is being conducted in close collaboration with the Center for Operations Research in Beira (known by its Portuguese acronym as CIOB) that is one of three research centers in Mozambique managed by the MOH National Institute of Health (the research arm of the MoH).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV
Keywords
HIV, Mozambique, antenatal care, adherence, retention, pregnancy, HIV-positive mothers retained in ART after 90 days

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
761 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Adherence and retention intervention
Arm Type
Experimental
Arm Description
Implementation of adherence and retention package
Arm Title
Control
Arm Type
No Intervention
Arm Description
Clusters continue without intervention package
Intervention Type
Other
Intervention Name(s)
Adherence and retention package
Intervention Description
Based on formative research findings, the following core components of the B+ study intervention have been designed and will be stepped in at the study sites to improve early retention in care and adherence: Workflow modification: 1) Redefinition of key roles of MCH nurses and task shifting to community health workers (CHW's), and 2) enhanced patient tracking via improved management of registries/charts; Adherence and retention package: 1) Creation of "Adherence Committees" at each site to coordinate and systematize patient follow-up, 2) active patient follow-up and home visits by community health workers (CHWs or activistas), 3) use of text messaging to patients by MCH nurses, 4) improved and intensified counseling coordinated with active CHW and text follow-up, and 5) intensified and improved Option B+ training and supportive supervision.
Primary Outcome Measure Information:
Title
Retention at 30 days
Description
The primary outcome measure for Aim 3 is the proportion of HIV-positive pregnant women tested at the participating ANC sites that successfully initiates appropriate ART and returns for their scheduled 30-day visit for pharmacy refill and evaluation within 45 days.
Time Frame
45 days
Title
Adherence at 90 days
Description
The primary outcome measure for Aim 4 is the ART adherence rate through 90 days after ART initiation.
Time Frame
90 days

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
14 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Pregnant women who test HIV-positive in antenatal care services at target health facilities Exclusion Criteria: Pregnant women who arrived at health facilities who already have tested positive HIV-positive pregnant women who cannot start ART
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rachel Chapman, PhD
Organizational Affiliation
University of Washington
Official's Role
Principal Investigator
Facility Information:
Facility Name
Beira Operations Research Center
City
Beira
State/Province
Sofala
Country
Mozambique

12. IPD Sharing Statement

Citations:
PubMed Identifier
25924668
Citation
Cowan JF, Micek M, Cowan JF, Napua M, Hoek R, Gimbel S, Gloyd S, Sherr K, Pfeiffer JT, Chapman RR. Early ART initiation among HIV-positive pregnant women in central Mozambique: a stepped wedge randomized controlled trial of an optimized Option B+ approach. Implement Sci. 2015 Apr 30;10:61. doi: 10.1186/s13012-015-0249-6.
Results Reference
derived

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Early ART Initiation Among HIV-positive Pregnant Women in Central Mozambique

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