Fact CheckerSign in

NCT07021092Active, not recruiting

PERSON-CENTERED APPROACHES TO VIREMIA: CONNECTION, RAPPORT, AND ENGAGEMENT STUDY

Source: ClinicalTrials.gov · Last updated 10 Aug 2026

Brief summary (registry, in English)

The study aims to increase the reach of the person-centred interpersonal practices by developing and accessing a tailored, scalable, and sustainable approach that meets the distinctive needs of populations identified as most disproportionately affected by viremia in Zambia. The study population include pregnant and breastfeeding women, children, adolescents and adult that are more than thirty -30 days late for their next hospital appointments.The study will be implemented over a period of 36 months in 24 facilities in Lusaka and Central province, Zambia.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
3000 (estimated)
First submitted
25 Mar 2025
Start date
1 Apr 2025
Primary completion date
28 Feb 2027
Lead sponsor
Centre for Infectious Disease Research in Zambia
Diseases
HIV
NCT number
NCT07021092

What you commit to

  • Study type: Interventional
  • Planned participants: 3000
  • From 1 Apr 2025 to the primary completion date, 28 Feb 2027
  • 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 illness

  • Participant who is NOT living with HIV/AIDS;

Other

  • Patients that are unable to provide consent or unwilling to participate in the study
  • Participant is too sick i.e., failing to talk, general discomfort and emergency cases);

Who the study is looking for

  • Patients that are lost to follow up (\[LTFU\] from HIV care i.e. confirmed \>30 days late for a scheduled appointment) at the time of sampling. (i.e. not people who were previously LTFU but then returned and have a documented VL.)
  • Individuals returning to care after being out of care and not taking ART with no VL measure (i.e., unmeasured viremia)
  • Patients that are 6 months late for a scheduled Viral Load (VL) according to Ministry of Health guidelines at the time of sampling (regardless of care status)
  • Patients that have a last documented VL that is elevated, \> 1000 copies/ml at time of sampling in current clinic population (CCP) (regardless of care status)
  • Participant that are willing to provide written informed consent in English, or any of the local languages that include Nyanja or Bemba.

Sex: All · Does not accept 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
Ministry of Health
Coordinator of this site? Confirm its status
LusakaZambiaUnknown status
Railway GRZ Urban Health Centre, Kafue District Health Hospital, Nangongwe OPD Urban Health Centre, Chawama 1st level hospital, Chipate 1st level hospital, Matero Reference Health Centre, Mtendere Health Centre, Lwiimba Rural Health Centre
Coordinator of this site? Confirm its status
LusakaZambiaUnknown status

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