ClinicalTrials.gg
CompletedNCT05510973Updated Sep 10, 2026

Evaluation of Advanced HIV Disease Differentiated Care Model in Malawi

An interventional study of Enhanced package for AHD care in Opportunistic Infections, HIV-Related, Cryptococcal Infections and AIDS With Tuberculosis, sponsored by Elizabeth Glaser Pediatric AIDS Foundation. Completed at 13 sites in Malawi. Per ClinicalTrials.gov, last updated 2026-09-10.

Primary conditionAIDS-related Kaposi sarcomaRegistry: AIDS-Related Opportunistic InfectionsReclassifiedWhy we changed it
Registry
AIDS-Related Opportunistic Infections — the first condition term the registry derived for this study.
ClinicalTrials.gg
AIDS-related Kaposi sarcoma
Why
  1. The study's listed conditions name AIDS-related Kaposi sarcoma, a narrower term within AIDS-Related Opportunistic Infections.
Confidence
High: the new condition is named in the study's own listed conditions. Of 351 hand-checked studies reclassified this way, 68% were exactly right and 84% in the right disease family; the registry's first term was right for 5% (measured 2026-10-21). How we classify →
Wrong?
Tell us the study's main condition →

Sponsored by Elizabeth Glaser Pediatric AIDS Foundation · Not applicable, Interventional, and Other

From the registry’s dates

  • Registered 1 year 2 months after the study started (first participant enrolled Jun 2021, registered Aug 2022).
Phase
Not applicable
Study type
Interventional
Enrollment
700
Allocation
Non-randomized
Sex
All
01

Study summary

This study will evaluate the implementation of an enhanced package of care, CD4 and tuberculosis lipoarabinomannan (TB-LAM) tests and the initiation of patients on TB prophylaxis [TPT and CPT], on retention in care and viral suppression ((\<50 copies/ml) at 6 and 12 months after AHD care and treatment enrollment. The study will also assess the change in AHD screening, management and service uptake indicators among PLHIV clients before and after implementation of the QI collaborative implementation (QICI) project, evaluate the acceptability and feasibility of the AHD package of care among patients and HCWs providing related health services, and conduct a cost analysis of implementing the enhanced AHD package of care in a hub-and-spoke implementation of care model.

Read the detailed description

Background Despite significant advances in the diagnosis of human immunodeficiency virus (HIV) and expanded access to anti-retroviral therapy (ART), recent data suggest that a third of people living with HIV/AIDS (PLHIV) starting ART do so with advanced HIV disease (AHD), and an increasing number of patients require advanced HIV disease care following a period of disengagement. Despite considerable effort to implement the AHD model in Malawi and bring it to scale, several challenges regarding AHD implementation and outcomes still exist.

Description of Study Intervention:

To optimize the package of care offered to HIV-infected clients with advanced HIV disease in Malawi, a hub-and-spoke model will be designed and implemented to bring AHD services geographically closer to patients. An enhanced package of AHD interventions such as decentralized cluster of differentiation 4 (CD4) tests, Tuberculosis lipoarabinomannan (TB-LAM) and initiation of patients on prophylaxis [TPT and CPT] will be implemented [system strengthening through quality improvement (QI)]. A client and systems focus will identify challenges experienced by providers and clients while at the same time describing the contextual factors that affect the delivery of AHD services. These lessons learnt will be used to optimize client flow, enhance sample transportation regulation and increase client engagement.

Evaluation Description The evaluation will be a mixed method design study: (1) the quantitative component which will be a non-randomized cluster design based on control of intervention vs control sites for outcomes evaluation (2) the qualitative component that will aim at evaluating acceptability and feasibility of the strengthened AHD service provision (3) cost evaluation that will use quantitative methods.

Specific Objectives

  1. To determine the effect of implementation of enhanced AHD package of care in intervention sites versus control sites on the proportion of PLHIV with AHD who are alive and retained in care at 6 and 12 months after diagnosis of AHD and enrolment into AHD care.
  2. To determine the effect of implementation of enhanced AHD package of care in intervention sites versus control sites on the proportion of PLHIV with AHD, who achieve viral suppression (\<50 copies/ml) at 6 and 12 months after AHD care and treatment enrollment
  3. To estimate the change in AHD screening, management and service uptake indicators among PLHIV clients before and after implementation of the QI collaborative implementation (QICI) project
  4. To evaluate the acceptability and feasibility of the AHD package of care among patients utilizing AHD services and HCWs providing related health services
  5. To conduct a cost analysis of implementing the hub and spoke enhanced AHD package of care to improve AHD differentiated care in selected sites in Malawi.

Endpoints

  1. Proportion of PLHIV with advanced disease who will be alive and retained in care at 6 and 12 months after antiretroviral therapy (ART) initiation and after diagnosis of AHD.
  2. Proportion of PLHIV with AHD enrolled in care and treatment who are virally suppressed at 6 and 12 months.

Study Population:

The study population for quantitative study component will include children, adolescents and adults of all ages in all the intervention and control sites identified for the project evaluation who are diagnosed with AHD. The study population for the qualitative component will include PLHIV, HCWs and lay cadre supporting the health facility 18 years of age and above available and willing to participate.

Description of Sites/Facilities Enrolling Participants:

The project will be implemented in twenty-two intervention sites in Malawi three selected districts and thirteen control sites in other districts where the intervention is not implemented.

Study duration: The study will take a period of 18 months, including 4 to 6 months enrolment and up to 12 months follow-up.

02

Conditions studied

  • Opportunistic Infections, HIV-Related
  • Cryptococcal Infections
  • AIDS With Tuberculosis
  • AIDS-related Kaposi Sarcoma
  • AIDS and Infections
03

In context

AIDS-related Kaposi sarcoma Reclassified

43 studies on the registry are indexed under AIDS-related Kaposi sarcoma; 2 are open to participants now.

This study's enrollment of 700 is above the median of 30 across 28 interventional studies indexed under AIDS-related Kaposi sarcoma.

Browse AIDS-related Kaposi sarcoma studies →

Lead sponsor

Elizabeth Glaser Pediatric AIDS Foundation is the lead sponsor of 30 studies on the registry; none are open to participants now.

Compared within AIDS-related Kaposi sarcoma, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is AIDS-Related Opportunistic Infections. The counts are of registry records indexed under each term, refreshed daily. How we classify →

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

-infected clients (all ages) meeting the WHO definition for AHD:

  • of \<200c/mm3
  • or WHO clinical stage 3 or 4
  • or children under the age of 5 on treatment for less than 12 months or unstable on treatment after 12 months

Exclusion criteria

Exclusion Criteria:

  • None
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

CD4 count

The number of CD4 cells, a type of white blood cell, in a given amount of blood. It is used to follow how well the immune system is doing in HIV.

05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
700 participants (actual)

Study arms

  • No intervention
    Control

    standard of care

  • Experimental
    Intervention

    Enhanced package of AHD care

    Other: Enhanced package for AHD care

Interventions

  • OtherEnhanced package for AHD care

    The enhanced package of AHD care includes CD4 and tuberculosis lipoarabinomannan (TB-LAM) tests and the initiation of patients on TB prophylaxis \[TPT and CPT\], offered through a hub-and-spoke facility system, with continuous quality improvement (QI)

06

What researchers measure

Primary outcomes

  1. Proportion of AHD patients alive and retained in care

    Number of AHD patients alive and retained in care divided by the number of AHD patients initiated on antiretroviral therapy (ART) after diagnosis of AHD

    Time frame: 6 and 12 months after initiation on ART after AHD diagnosis

  2. Proportion of AHD patients in care and treatment virally suppressed

    Number of AHD patients in care and treatment virally suppressed (\<50 cells/ml) divided by the number of AHD patients in care and treatment

    Time frame: 6 and 12 months after initiation of ART after AHD diagnosis

Secondary outcomes

  1. Cost analysis of implementing the hub and spoke enhanced AHD package of care

    Estimation of total costs, costs per patients with the intervention, and cost drivers

    Time frame: 12 months after intervention implementation

07

Study locations

13 sites
  • Mlambe Mission Hospital
    Mlambe, Blantyre, Malawi
  • Chiradzulu District Hospital
    Chiradzulu, Chiradzulu, Malawi
  • Dedza district hospital
    Dedza, Dedza, Malawi
  • Lobi rural hospital
    Lobi, Dedza, Malawi
  • Mua Mission Hospital
    Mtakataka, Dedza, Malawi
  • Kapiri Mission Hospital
    Kapiri, Mchinji, Malawi
  • St Michael's Guilleme Community Hospital
    Mchinji, Mchinji, Malawi
  • Malamulo Mission Hospital
    Thyolo, Thyolo, Malawi
  • Domasi Rural Hospital
    Domasi, Zomba, Malawi
  • Saint Luke's Mission Hospital
    Zomba, Zomba, Malawi
  • Mchinji District Hopsital
    Mchinji, Malawi
  • Ntcheu District Hospital
    Ntcheu, Malawi
  • Sister Theresa Community Hospital
    Ntcheu, Malawi
08

References and documents

Publications

  • Katirayi L, Maphosa T, Chilikutali L, Chamanga RK, Petersson J, Khatib S, Munthali B, Nyirenda R, Matiya E, Nyirenda L, Tiam A, Denoeud-Ndam L. Understanding gender differences of people with HIV newly diagnosed or returning to care with advanced HIV disease in Malawi: a qualitative study. BMC Public Health. 2023 Dec 1;23(1):2382. doi: 10.1186/s12889-023-17384-y. PubMed 38041058 ↗
09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Jun 2021 to primary completion in Oct 2024, 40 months.

How these figures are worked out, and which studies are left out of them.

Registered
Aug 15, 2022
First posted
Aug 22, 2022
StartActual
Jun 1, 2021
Primary completionActual
Oct 31, 2024
CompletionActual
Dec 30, 2024
Last update
Sep 10, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 10, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05510973
Lead sponsor
Elizabeth Glaser Pediatric AIDS Foundation
Collaborators
Bill and Melinda Gates Foundation
Responsible party
Sponsor
First posted
Aug 22, 2022
Start date
Jun 1, 2021
Primary completion
Oct 31, 2024
Completion
Dec 30, 2024
Last update
Sep 10, 2026

Study contacts

Thulani Maphosa, PhD
principal investigator · Elizabeth Glaser Pediatric AIDS Foundation
Appolinaire Tiam, MBChB, MMed, PhD
principal investigator · Elizabeth Glaser Pediatric AIDS Foundation
Rose Nyirenda, MPH, PhD
principal investigator · Ministry of Health, Malawi

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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