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Package of Resources for Assisted Contact Tracing: Implementation, Costs, and Effectiveness (PRACTICE)

University of North Carolina (UNC) logo

University of North Carolina (UNC)

Status

Completed

Conditions

Human Immunodeficiency Virus

Treatments

Behavioral: Enhanced implementation package
Behavioral: Standard implementation package

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT05343390
R01MH124526 (U.S. NIH Grant/Contract)
20-1810

Details and patient eligibility

About

Having health workers assist HIV-infected persons with the recruitment and testing of their sexual contacts and biological children is an effective and efficient way of identifying additional HIV-infected persons in need of HIV treatment and HIV-uninfected persons in need of HIV prevention. However, in Malawi, a country with a generalized HIV epidemic, health workers lack the counseling and coordination skills to routinely assist their HIV-infected clients with these services. This study will determine how to help health workers to effectively and efficiently provide these services to their patients through a set of digital capacity-building tools.

Full description

Voluntary assisted contact tracing (ACT) is an evidence-based approach that efficiently identifies persons in need of HIV treatment and prevention. Malawi, like many countries in sub-Saharan Africa, has adopted ACT policies to support its "95-95-95" targets for HIV testing, treatment, and viral suppression.

However, Malawi's ACT implementation has been poor due to deficits in health worker capacity and clinical coordination. Through preliminary work, our team has 1) developed a set of implementation strategies (theory-based health worker training and continuous quality improvement processes) that address these barriers; 2) packaged these strategies into a blended learning platform that combines digital and face-to-face modalities; and 3) field-tested the package in Malawi with promising preliminary results. In this proposal, the package will be rigorously evaluated in Malawi for implementation, service uptake, and cost-effectiveness outcomes.

Through a two-arm pragmatic cluster randomized implementation trial, the proposed research will address these gaps through three specific aims. Twenty Malawian facilities in two districts will be randomized to receive the blended learning implementation package (enhanced) versus standard implementation package (standard). In the first aim, ACT implementation outcomes will be compared between the enhanced and standard arms. Health worker fidelity to ACT procedures will be assessed through audio-recorded ACT encounters. In the second aim, HIV service uptake outcomes will be compared between the enhanced and standard arms. In the third aim, cost and cost-effectiveness outcomes will be examined.

The findings will offer important insights and innovations into how to bridge the gap between ACT research and practice, a critical step towards achieving the 95-95-95 targets.

Enrollment

841 patients

Sex

All

Ages

15+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Health worker inclusion criteria:

  • 18 years of age or older
  • working full-time at one of the health facilities included in the study
  • staff in Malawi's Assisted Contact Tracing program.

Health worker exclusion criteria:

  • conditions that would compromise ability of participant to provide informed consent, undergo study procedures safely, or prevent proper conduct of study

Patient (index or contact) inclusion criteria:

->=15 years

-potential index, contact, or parent or guardian of a potential index or contact

Patient (index or contact) exclusion criteria:

  • conditions that would compromise ability of individual to provide informed consent, undergo study procedures safely, or prevent proper conduct of study

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

841 participants in 2 patient groups

Enhanced implementation strategy
Experimental group
Description:
digitally guided training and continuous quality improvement
Treatment:
Behavioral: Standard implementation package
Behavioral: Enhanced implementation package
Standard implementation strategy
Active Comparator group
Description:
standard training and clinical support
Treatment:
Behavioral: Standard implementation package

Trial documents
2

Trial contacts and locations

33

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Central trial contact

Nora Rosenberg, PhD; Tapiwa Tembo, MSc

Data sourced from clinicaltrials.gov

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