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Missed Opportunities to Pre-exposure Prophylaxis for HIV Infection on Person Newly Diagnosed With HIV

National Survey on Missed Opportunities to Pre-exposure Prophylaxis for Prevention of Human Immunodeficiency Virus-infection.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03671291
Enrollment
596
Registered
2018-09-14
Start date
2019-04-03
Completion date
2021-10-03
Last updated
2022-07-25

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

Conditions

Virus-HIV

Keywords

VIH, PrEP, risk factors, Prevention, Access to care

Brief summary

Missed opportunity to pre-exposure prophylaxis is a survey study that will be addressed to newly infected with human immunodeficiency virus (HIV) persons. The purposes of this study is to understand why despite the fact that pre-exposure prophylaxis exist, these persons have been contaminated with HIV.

Detailed description

Pre-exposure prophylaxis is a new strategy to prevent the occurrence of new cases of HIV. This prophylaxis strategy is based on taking antiretroviral drugs (ARV) before and after exposition to a risk of HIV infection which can reduce drastically the contamination with HIV. A certain groups of population based on their sexual orientation, for instance man who have sex with man (MSM), is among the groups that are highly exposed to this risk. To reduce this risk, French national regulatory authority (ANSM), firstly through temporary usage recommendation followed by a marketing authorization extension, allowed the prescription of these antiretroviral molecules to persons presenting eligibility criteria as defined by regulatory authority. Despite these preventive measures, the incidence of HIV such as the MSM group still high. The missed opportunity studies has as objectives to try to disentangle real obstacles of PrEP use in France and to optimize PrEP criteria if needed.

Interventions

Persons who the biological parameters or past screening show that they were recently infected with HIV cf. eligibility criteria, will, after obtaining his consent, answer a series of questions through a self-administrated questionnaire that will take approximately 40 minutes.

Sponsors

University Hospital, Marseille
CollaboratorOTHER
University Hospital, Grenoble
CollaboratorOTHER
Centre Hospitalier Universitaire de Nice
CollaboratorOTHER
University Hospital, Montpellier
CollaboratorOTHER
Hospital Purpan
CollaboratorOTHER
University Hospital, Bordeaux
CollaboratorOTHER
Hôpital de la Croix-Rousse
CollaboratorOTHER
Centre Hospitalier Universitaire Dijon
CollaboratorOTHER
University Hospital of Saint-Etienne
CollaboratorOTHER
University Hospital, Clermont-Ferrand
CollaboratorOTHER
Centre Hospitalier Universitaire de Besancon
CollaboratorOTHER
Tourcoing Hospital
CollaboratorOTHER
University Hospital, Strasbourg
CollaboratorOTHER
Nantes University Hospital
CollaboratorOTHER
Centre Hospitalier Régional d'Orléans
CollaboratorOTHER
Rennes University Hospital
CollaboratorOTHER
Saint Antoine University Hospital
CollaboratorOTHER
Tenon Hospital, Paris
CollaboratorOTHER
Saint-Louis Hospital, Paris, France
CollaboratorOTHER
Hôpital Necker-Enfants Malades
CollaboratorOTHER
Bicetre Hospital
CollaboratorOTHER
Pitié-Salpêtrière Hospital
CollaboratorOTHER
Bichat Hospital
CollaboratorOTHER
University Hospital Center of Martinique
CollaboratorOTHER
French National Agency for Research on AIDS and Viral Hepatitis
Lead SponsorOTHER_GOV

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 99 Years
Healthy volunteers
No

Inclusion criteria

* 18 years and older * Understanding and speaking French * Affiliated in or beneficiary of a Social Security (excluding State Medical Aid or AME that aren't considered as Social Security coverage) * Men and women with a diagnosis of HIV infection known for less than three months and with recent HIV infection established on: a diagnostic confirmation test by Western Blot (WB) or Immuno Blot showing incomplete pattern. OR Previous HIV negative screening test performed within 6 months of diagnosis.

Exclusion criteria

* Less than 18 years old * Unable to understand French * Not affiliated to a social security coverage * Under guardianship or under curatorship

Design outcomes

Primary

MeasureTime frameDescription
Percentage of patients eligible for PrEP at the time of HIV infectionThe needed time to answer to the questionnaire : 40 min to 1 hour.Quantify and describe among newly diagnosed people with HIV the missed opportunities for PrEP treatment for HIV infection prevention

Secondary

MeasureTime frameDescription
Taking a risky behaviour for HIV infectionThe needed time to answer to the questionnaire : 40 min to 1 hour.Better identify risk taking exposures to HIV contamination and determine the adequacy of the criteria for access to pre-exposure treatment with current practices. For this, questions concerning the frequency of unprotected sex, the number of partners and the type of sexual practices are collected in the self-questionnaire.
Awareness and level of knowledge of the PrEP strategyThe needed time to answer to the questionnaire : 40 min to 1 hour.Study the individual factors associated with the knowledge, representations, acceptance and prescription of PrEP in order to evaluate the hindrance to the establishment of PrEP and the persistence of infections despite the availability of this new strategy of preventive treatment. For this, the questionnaire asks about the knowledge of the existence of this prevention tool, the antecedent of PrEP intake, and the potential reasons for not taking PrEP.
Access to careThe needed time to answer to the questionnaire : 40 min to 1 hour.Evaluate the impact of healthcare professionals on missed opportunities for PrEP through the access to general or hospital physicians and screening history. Comparing percentage of new infections among new HIV diagnosis in order to study regional disparities in term of HIV screening access according to city/region and area. Access to care, meaning frequency of visit to, the nature of, health care facilities (hospital, urban doctor, anonymous screening center…), discussed items during consultation with physician etc. These kind of informations will help to appreciate if access to care in all its dimension is correlated to HIV infection risk. These different criteria will be compared by region to determine whether regional disparities in access to care occurred.
Availability of PrEPThe needed time to answer to the questionnaire : 40 min to 1 hour.Study the structural and demographic factors associated with missed opportunities for PrEP (regional disparities in access to PrEP). A questionnaire for each participating center asks about the type of consultations offered, the presence of specific consultations and support for PrEP, the active file of people under PrEP and will determine if there is a center and / or region effect for taking PrEP. Collected information will shed the light on potential relation between logistic means and availability of PrEP

Countries

France

Outcome results

None listed

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