Frailty, Geriatric Syndromes and Care Pathways of Older Adults Living With HIV in West Africa

January 14, 2026 updated by: ANRS, Emerging Infectious Diseases

With currently available antiretroviral therapy, people living with HIV (PLWHIV) are living longer. This exposure to HIV and combination antiretroviral therapy may accelerate the aging of this population, thus increasing the prevalence of premature frailty.

There are few data on the prevalence of frailty and geriatric syndromes among older people living with HIV (OpHIV) in sub-Saharan Africa (SSA) and the screening and diagnostic tools to identify them.

The initiation contract financed by the ANRS-MIE in 2021 whose objective was to 1) carry out an inventory and evaluate the feasibility of a project for monitoring OpHIV in Burkina-Faso in Côte d'Ivoire and Togo and 2) to select the collection tools adapted to the description of geriatric syndromes in these elderly people has allowed to highlight the following (i) The collection of data on geriatric conditions and syndromes is almost non-existent in the daily care and management practice (ii) there is a significant proportion (10,6%) of PLWHIV aged 60 years and over in the active files of the PLWHIV care centers that participated in the survey (iii) Adapted screening tools have been selected and will allow documentation of the above-mentioned syndromes. This research project, which follows on from this initiation contract, will therefore make it possible to obtain data from the geriatric evaluation, to identify the specificities of PLWHIV by comparing them to a population not infected with HIV and to propose geriatric management adapted to PLWHIV. Its innovative nature also lies in its mixed approach combining quantitative and qualitative methods, which will make it possible to document the needs and resources for the care of PLWHIV in a global and holistic manner.

600 participants, aged 60 years and over (300 living with HIV and 300 not living with HIV), in three West African countries (Burkina Faso, Côte d'Ivoire, Togo) will be included in this study whose primary objective is to compare the prevalence of frailty among people aged 60 years and over (PA60) between HIV-infected and non-HIV-infected; the secondary objective is to estimate the prevalence of frailty among PA60 according to HIV status. A population-based matching will be performed on sex and age class (threshold 70 years), during the recruitment of HIV- PA60.

This will be a mixed study combining:

  • A "clinical" component comprising a stratified, comparative, international, multicenter cross-sectional study;
  • A "health systems strengthening" component combining a quantitative cross-sectional survey and a qualitative survey;
  • A qualitative socio-anthropological component including individual interviews and focus groups with people living with HIV60, their families and caregivers.

The 3 components will be conducted with a time lag between the different components due to the overlapping constitution of the source populations.

Most research on aging with HIV in the context of SSA has been very clinically focused (e.g., frailty or cognitive impairment). This research will provide a more comprehensive approach that takes into account the different levels of factors influencing health (individual, health system, social environment).

Study Overview

Status

Not yet recruiting

Conditions

Detailed Description

Methodology:

This is a mixed study combining:

  • a "clinical" component comprising a comparative, international, multicenter, two-strata (HIV+ and HIV-) cross-sectional study;
  • a "social sciences" component combining a quantitative cross-sectional survey and a qualitative survey involving individual interviews and focus groups with PA60, their families and caregivers.

Interventions:

  • Screening for several comorbidities (high blood pressure, diabetes, dyslipidemia, kidney failure, undernutrition, depression).
  • Comprehensive management including prevention strategies adapted to the various comorbidities mentioned above and their complications.

Statistical method:

Use of mixed approaches. For quantitative indicators, descriptive analysis techniques, bivariate analysis (Student t test or Wilcoxon test for quantitative variables, Chi² or Fisher test for categorical variables) and multivariate analysis (logistic regression).

Study Type

Observational

Enrollment (Estimated)

600

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

      • Bobo-Dioulasso, Burkina Faso
        • Hôpital de jour du CHU Sourou Sanou
    • Abidjan Autonomous District
      • Treichville, Abidjan Autonomous District, Côte d’Ivoire
        • Centre Médical de Suivi des donneurs de sang (CMSDS)
      • Treichville, Abidjan Autonomous District, Côte d’Ivoire
        • Service des Maladies Infectieuses et Tropicales (SMIT)
      • Yopougon, Abidjan Autonomous District, Côte d’Ivoire
        • Centre de Prise en Charge de Formation et de Recherche (CEPREF)
      • Lomé, Togo
        • ONG Espoir Vie Togo
      • Lomé, Togo
        • Service des Maladies Infectieuses et Tropicales-CHU Sylvanus Olympio

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Clinical component

The targets of this component of the study are two specific populations:

  • People over the age of 60 (PA60) infected with HIV who are receiving treatment at HIV care centers in Abidjan (Ivory Coast), Bobo-Dioulasso (Burkina Faso), and Lomé (Togo), or who have recently been infected with HIV;
  • People over the age of 60 who are not infected with HIV.

Social science component:

  • PA60 HIV+/HIV-
  • Caregivers
  • Healthcare providers

Description

Inclusion Criteria:

  • HIV+ Group

    • Person 60 years of age and older
    • Infected with HIV-1 and/or 2
    • Able to move around the data collection site
    • Having given free and informed consent
  • HIV- Group

    • Person 60 years of age and older
    • HIV-uninfected
    • Able to move around the data collection site
    • Having given free and informed consent

Exclusion Criteria:

Person deprived of liberty (guardianship, curatorship, judicial safeguard) Karnofsky Index 50≤50% Hospitalized

-

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
HIV positive group
Individuals aged 60 years and over living with HIV-1 and/or HIV-2 attending HIV care centers in Abidjan, Bobo-Dioulasso and Lomé.
HIV negative group
Individuals aged 60 years and over without HIV, matched by sex and age group.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Prevalence of frailty by HIV status among people aged 60 years and older (PA60) in West Africa
Time Frame: At 12 months
At 12 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Prevalence of frailty in AP60
Time Frame: At 12 months
At 12 months
Number and proportion of AP60 with geriatric syndrome
Time Frame: At 12 months
Including cognitive, visual and hearing disorders, depression, undernutrition, dehydration, pain, urinary and fecal continence disorders, gait and balance disorders, according to HIV status
At 12 months
Number and proportion of AP60 with at least one comorbidity
Time Frame: At 12 months
Including cancer, dyslipidemia, diabetes, hypertension, history of myocardial infarction or stroke, osteoarticular disease, renal failure, according to HIV status
At 12 months
Factors associated with the presence of geriatric syndromes
Time Frame: At t12 months
At t12 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Clotilde ALLAVENA, Nantes University Hospital
  • Principal Investigator: Raoul MOH, Programme PAC-CI CHU de Treichville

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

March 1, 2026

Primary Completion (Estimated)

March 1, 2026

Study Completion (Estimated)

March 1, 2029

Study Registration Dates

First Submitted

January 6, 2026

First Submitted That Met QC Criteria

January 14, 2026

First Posted (Actual)

January 21, 2026

Study Record Updates

Last Update Posted (Actual)

January 21, 2026

Last Update Submitted That Met QC Criteria

January 14, 2026

Last Verified

January 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • ANRS 0496s FraGericare-WA

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Older Adults

Subscribe