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Virologic Treatment Failure and Drug Resistance in HIV-infected Kenyan Children (RESPECT)

Virologic Treatment Failure and Drug Resistance in HIV-infected Kenyan Children

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03120065
Acronym
RESPECT
Enrollment
499
Registered
2017-04-19
Start date
2017-04-24
Completion date
2018-08-30
Last updated
2020-07-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Treatment Failure, Viral Resistance

Keywords

adherence

Brief summary

The primary objective of this study is to use a well-characterized pediatric AMPATH cohort, with detailed medication-taking, drug level, and clinical data, to longitudinally evaluate treatment failure and drug resistance to improve long-term care for HIV-infected children in Kenya and other RLS. Examining treatment failure and drug resistance emergence in children on ART and what factors impact these negative outcomes, will provide needed data to critically evaluate the efficacy of current ART, weight-based pediatric drug dosing guidelines, and recommendations for subsequent therapies. The objective is to specifically characterize how non-adherence leads to a lack of viral suppression and to drug resistance evolution, and how this characterization can inform interventions to improve adherence and increase treatment success.

Detailed description

Resistance to antiretroviral therapy (ART) hampers effective treatment of pediatric HIV infection and can undermine long-term clinical care outcomes. In resource-limited settings (RLS), where 90% of the world's HIV-infected children live, the risk and impact of ART failure and resistance development are particularly significant due to limited treatment monitoring, restricted medication options and lifelong ART needs, from birth through adolescence and into adulthood. Children in RLS therefore face serious clinical consequences when their virus is not suppressed, but few longitudinal data are available to inform pediatric clinical guidelines or direct interventions to minimize those risks. How specific patterns of medication non-adherence or challenges with appropriate ART dosing might impact ART failure and the development of drug resistance are poorly understood for children in RLS. The primary objective of this study is to use a well-characterized pediatric AMPATH cohort, with detailed medication-taking, drug level, and clinical data, to longitudinally evaluate treatment failure and drug resistance to improve long-term care for HIV-infected children in Kenya and other RLS. Examining treatment failure and drug resistance emergence in children on ART and what factors impact these negative outcomes, will provide needed data to critically evaluate the efficacy of current ART, weight-based pediatric drug dosing guidelines, and recommendations for subsequent therapies. The objective is to specifically characterize how non-adherence leads to a lack of viral suppression and to drug resistance evolution, and how this characterization can inform interventions to improve adherence and increase treatment success. AMPATH cares for over 80,000 adult and pediatric HIV-infected patients in western Kenya, including over 2,800 children on ART. The research objective of this application will be accomplished by pursuing the following five specific aims: Aim 1: Determine prevalence of viral failure and examine resistance mutations among a retrospective study cohort of 685 perinatally HIV-infected Kenyan children on 1st-line ART; Aim 2: Investigate associations between specific adherence patterns, ART drug levels and other demographic and clinical factors, with viral failure and drug resistance; Aim 3: Study long-term immunologic, virologic and drug resistance outcomes and their associations in prospectively re-enrolled study participants; Aim 4: Enhance analyses of viral failure, drug resistance accumulation and associated demographic and clinical factors by examining the longitudinal banked samples available for a subset of the study cohort (n=327); Aim 5: Develop a data-driven intervention algorithm to identify children at risk for viral failure and resistance. The hypothesis of this study proposes that there will be high levels of treatment failure and drug resistance associated with patterns of non-adherence and inadequate drug levels.

Interventions

OTHERElectronic Dose Monitoring (MEMS)

The MEMS cap is an electronic bottle cap that records the time and date of a bottle being opened. The research personnel will extract the timing of the MEMS bottle opening events for adherence analysis.

Sponsors

Moi University
CollaboratorOTHER
Brown University
CollaboratorOTHER
Rachel Vreeman, MD, MS
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
4 Years to 19 Years
Healthy volunteers
No

Inclusion criteria

* Previous enrollment in CAMP study * Viable banked blood sample; HIV-infected documented by DNA-PCR (Amplicor, Roche, Basel, Switzerland) for children less than 18 months of age and by 2 parallel HIV rapid ELISA tests using Determine and Bioline for children older than 18 months of age. * \< 19 years of age

Exclusion criteria

Mental or physical incapacity of legal caregiver leading to inability to provide informed consent

Design outcomes

Primary

MeasureTime frameDescription
Viral Resistance18 monthsBlood samples will be analyzed for viral resistance testing, both for retrospective and prospective samples samples (TP1)

Secondary

MeasureTime frameDescription
Adherence CAMP3 monthsAdherence will be assessed via CAMP questionnaire
Clinical Data: WHO stage6 yearsWHO stage will be analyzed for associations with viral resistance and treatment failure in this cohort.
Clinical Data: Viral Load6 yearsLongitudinal viral loads will be analyzed for associations with viral resistance and treatment failure in this cohort.
Clinical Data: Weight6 yearsLongitudinal weight will be analyzed for associations with viral resistance and treatment failure in this cohort.
Adherence MEMS3 monthsAdherence will be monitored via MEMS bottle caps
Clinical Data: Regimen6 yearsLongitudinal regimen will be analyzed for associations with viral resistance and treatment failure in this cohort.
Clinical Data: Opportunistic Infections6 yearsLongitudinal opportunistic infections will be analyzed for associations with viral resistance and treatment failure in this cohort.
Clinical Data: Disclosure Status6 yearsLongitudinal disclosure status will be analyzed for associations with viral resistance and treatment failure in this cohort.
Clinical Data: Height6 yearsLongitudinal height will be analyzed for associations with viral resistance and treatment failure in this cohort.

Countries

Kenya

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026