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Studies inflammation and thinking skills in teens living with HIV in Eswatini

Compares inflammation markers and thinking speed in teens aged 13 to 19 with HIV.

Plain-language title generated from the registry record
Registry title: The Eswatini Study on Neurocognitive Performance in Adolescents Living With HIV

Key facts

Where
Manzini, EswatiniSee the site

AI summary: who the study is looking for

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adolescents aged 13-19 years. Some are living with HIV and on antiretroviral therapy at Baylor Clinic, and some are HIV-negative controls.

Age
13-19 years
Sex
All sexes can join.
Earlier treatment
People living with HIV must be on antiretroviral therapy at Baylor Clinic.
Biomarker or test result
HIV-positive (cases) or HIV-negative (controls).

Main reasons for not taking part

  • Recent (within 2 months) influenza, COVID-19, TB or acute gastroenteritis
  • Diabetes, hypertension or asthma
  • Epilepsy, cerebrovascular accident or neurodegenerative disease
  • History of significant cranial trauma or perinatal complications

Read by machine on 12 November 2026.

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 13 and 19 years old?

Source: NCT07165639, who can take part

Where in Eswatini

  • Eswatini Nazarene Health Institution, Baylor College of Medicine Children's Foundation-Eswatini (Centers of Excellence in Mbabane and satellite clinic in Manzini in Raleigh Fitkin Memorial Hospital)Manzini, EswatiniContact: Phathizwe M Eswatini Nazarene Health Institution, BScNo longer taking part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Trial details

Who runs it
Eswatini Nazarene Health Institutions
Trial code
NCT07165639
Record updated
15 September 2025
Original description
This study explores the link between inflammatory biomarkers and neurocognitive performance in adolescents living with HIV (ALHIV) in Eswatini. Persistent HIV infection during adolescence has been associated with ongoing systemic inflammation and subsequent neurocognitive dysfunction. However, the exact nature of this relationship is not well-defined, especially in resource-limited settings where epidemiological and mechanistic data are scarce.Read full original descriptionShow less

Association Between Inflammation Biomarkers and Neurocognitive Performance Among Adolescents Living With HIV in Eswatini

This study explores the link between inflammatory biomarkers and neurocognitive performance in adolescents living with HIV (ALHIV) in Eswatini. Persistent HIV infection during adolescence has been associated with ongoing systemic inflammation and subsequent neurocognitive dysfunction. However, the exact nature of this relationship is not well-defined, especially in resource-limited settings where epidemiological and mechanistic data are scarce.

objectives

* To determine the prevalence of cognitive impairment among a sample of adolescents living with HIV, compared to HIV-negative adolescents in Eswatini * To assess the relationship between neurocognitive performance and current viral load status in adolescent living with HIV (ALHIV). * To examine the association between inflammation biomarkers and viral load suppression status in ALHIV. * To investigate whether adolescents with HIV experiencing neurocognitive decline exhibit a high inflammatory status.

A case-control design will be employed, involving 80 adolescents aged 13-19 years: 50 who are HIV-positive and 30 HIV-negative controls. Participants will be recruited from Baylor Manzini and Mbabane, as well as Raleigh Fitkin Memorial Hospital. Neurocognitive function will be evaluated using the Symbol Digit Modalities Test, focusing on areas such as processing speed, motor coordination, attention, and visual scanning.

Blood samples will be collected to measure key inflammatory biomarkers, including C-reactive protein (CRP), soluble CD14 (sCD14), lipopolysaccharide (LPS), soluble CD163 (sCD163), and monocyte chemoattractant protein-1 (MCP-1). Sociodemographic and clinical data will be gathered through questionnaires and medical record reviews.

Primary outcomes will include neurocognitive performance scores, while secondary outcomes will involve biomarker levels and their correlation with cognitive function. Multivariate regression models will assess associations, adjusting for confounders such as age, sex, education, and HIV disease severity. Structural equation modeling will be used to explore potential mediators in the inflammation-cognition pathway.

Inclusion: Cases; Adolescents aged 13-19 years; HIV-positive; Undergoing antiretroviral therapy at Baylor Clinic; Providing consent or assent to participate; Controls; Adolescents aged 13-19 years; HIV-negative; Providing consent or assent to participate.

Exclusion: Exclusion Criteria; Recent (within 2 months) acute conditions: influenza, COVID-19, TB, acute gastroenteritis (as these conditions elevate CRP levels); Chronic conditions: diabetes, hypertension, asthma; Neurological disorders: epilepsy, cerebrovascular accident, neurodegenerative diseases; History of significant cranial trauma or perinatal complications; All the aforementioned conditions will be identified through self-reported data and medical records.

ClinicalTrials.gov NCT07165639