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NCT05826977Completed

CASI-Plus mHealth for Ukraine's APS Program (Aim 2)

CASI-Plus: A Mobile Health (mHealth) Tool for Client Engagement to Improve Ukraine's Assisted Partner Services (APS) Program Workflow and HIV Testing Outcomes (Aim 2)

Source: ClinicalTrials.gov · Last updated 10 Jun 2025

Brief summary (registry, in English)

The CASI-Plus mHealth intervention seeks to improve partner elicitation and testing as part of assisted partner services (APS) in Ukraine, through a mHealth client engagement tool using computer-assisted self-interview (CASI). APS is a strategy for contact tracing and HIV testing for the high-risk sexual and needle-sharing partners of patients known to be living with HIV. This implementation science research will provide useful evidence on whether CASI-Plus can improve partner elicitation and HIV testing in a routine APS program operating at scale, toward the ultimate goal of linkage to HIV prevention and treatment services among those at highest risk of HIV. The aim of the study is to assess adoption of CASI-Plus and its impact on contact elicitation in a randomized controlled trial (RCT). Participants will integrate CASI-Plus as part of the APS services workflow to collect information from clients on sexual partners, needle-sharing partners, and biological children with risk of HIV exposure, and on self-reported partner notification and partner HIV testing outcomes. The investigators will compare APS clients using CASI-Plus to APS clients receiving standard APS services, to see if the contact index (number of partners named per index client enrolled in APS services) and the HIV testing index (number of partners with unknown HIV status tested per index client enrolled in APS services) increase with use of CASI-Plus.

Status (registry)
Completed
Study type
Interventional
Enrollment
178 (actual)
First submitted
24 Mar 2023
Start date
7 Aug 2024
Primary completion date
31 Jan 2025
Lead sponsor
University of Washington
Diseases
HIV
NCT number
NCT05826977

What you commit to

  • Study type: Interventional
  • Participants enrolled: 178
  • From 7 Aug 2024 to the primary completion date, 31 Jan 2025
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • \-

Who the study is looking for

  • consent to participate in APS services and the study;
  • are 18 years or older;
  • have been diagnosed with HIV and enrolled in care;
  • have not previously participated in APS services at another health facility; and
  • have access to a personal cell phone and internet.

Age in the registry: 18 years to 75 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
• Municipal Enterprise "Chernihiv Regional Hospital" of the Chernihiv Regional Council "Center for HIV/AIDS and Hepatitis Prevention"
Coordinator of this site? Confirm its status
ChernihivUkraineUnknown status
• Municipal Enterprise "Dnipropetrovsk Regional Medical Center for Socially Significant Diseases" of the Dnipropetrovsk Regional Council
Coordinator of this site? Confirm its status
DniproUkraineUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.