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Does the Implementation of Nurse-driven HIV Screening for Key Populations in the Emergency Departments Limit Undiagnosed Infections in the Paris Metropolitan Area? DEPIST Trial (ANRS 14055) (DEPIST)

Primary Purpose

Hiv, Nurse's Role

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Nurse-driven HIV screening for key populations combined with usual physician-directed diagnostic testing
Physician-directed diagnostic testing
Sponsored by
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional screening trial for Hiv focused on measuring Emergency service, Hospital, HIV, Mass screening, Nurses, Prevention and control, Key populations, Targeted screening

Eligibility Criteria

18 Years - 64 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

- Patients aged 18 to 64 years and visiting a participating ED for reasons other than a potential exposure to HIV within less than 48 hours

Exclusion Criteria:

- Not applicable

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    Nurse-driven HIV screening for key populations+UD

    Physician-directed diagnostic testing alone

    Arm Description

    Nurse-driven HIV screening for key populations combined with usual physician-directed diagnostic testing (UD)

    Outcomes

    Primary Outcome Measures

    Proportion of new HIV diagnoses among included patients.

    Secondary Outcome Measures

    Feasibility of the screening strategy and its implementation
    Feasibility of the screening strategy and its implementation based on: proportion of distributed and completed self-administered questionnaires among the patients included and among the patients able to participate who were not known to be HIV positive, the proportion of rapid tests offered by nurses among patients belonging to key populations, the proportion of patients screened by nurses among patients who were offered a rapid test and among patients belonging to high-risk groups .
    Effectiveness of the screening processes used by the caregivers, particularly the integration of the electronic questionnaire, and used by the patients as well as acceptability
    Proportions of patients with a new diagnosis
    Proportions of patients with a new diagnosis who had: a follow up visit with an infectious disease specialist within 1 month, a CD4 cell count greater or equal to 500 or 350/µL and no HIV-related symptoms, an acute HIV infection.
    Estimation through modelling of the number of new HIV diagnoses for different levels of coverage of the screening strategy in the Paris metropolitan area.

    Full Information

    First Posted
    March 4, 2020
    Last Updated
    March 4, 2020
    Sponsor
    Assistance Publique - Hôpitaux de Paris
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04298801
    Brief Title
    Does the Implementation of Nurse-driven HIV Screening for Key Populations in the Emergency Departments Limit Undiagnosed Infections in the Paris Metropolitan Area? DEPIST Trial (ANRS 14055)
    Acronym
    DEPIST
    Official Title
    Does the Implementation of Nurse-driven HIV Screening for Key Populations in the Emergency Departments Limit Undiagnosed Infections in the Paris Metropolitan Area?
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    March 2020
    Overall Recruitment Status
    Unknown status
    Study Start Date
    June 2020 (Anticipated)
    Primary Completion Date
    June 2021 (Anticipated)
    Study Completion Date
    June 2021 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Assistance Publique - Hôpitaux de Paris

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    In France, 40% of newly diagnosed HIV infections are concentrated in the Paris metropolitan area. Two key populations are mainly concerned: persons born in a foreign country and men who have sex with men. The randomized trial ANRS DICI-VIH (2014-2015) showed that nurse-driven HIV screening for key populations, supported by research staff, in 8 emergency departments (EDs) of the region, was effective in addition to diagnostic testing. The strategy advocated by the WHO and the recent French recommendations support the proposal of screening for key populations in the EDs. Thus, it is important to evaluate the impact and the feasibility of the implementation of this strategy on a large scale. The aim is to evaluate the impact of a wide implementation of nurse-driven HIV screening by rapid test in key populations combined with usual physician-directed diagnostic testing (intervention strategy) compared to diagnostic testing alone (control strategy) in the usual practice of the EDs. The strategies will be compared during two periods in 18 EDs of Paris metropolitan area following a stepped-wedge cluster randomized trial. During intervention period, nurses will suggest performing an HIV rapid test to patients belonging to key populations according to the answers to a self-administered questionnaire.
    Detailed Description
    Background: In France, 40% of newly diagnosed HIV infections are concentrated in the Paris metropolitan area. Two key populations are mainly concerned: persons born in a foreign country and men who have sex with men. The randomized trial ANRS DICI-VIH (2014-2015) showed that nurse-driven HIV screening for key populations, supported by research staff, in 8 emergency departments (EDs) of the region, was effective in addition to diagnostic testing. The strategy advocated by the WHO and the recent French recommendations of the National Health Authority (HAS) and expert group support the proposal of screening for key populations in the EDs. Thus, it is important to evaluate the impact and the feasibility of the implementation of this strategy on a large scale in a context where local institutions are taking initiatives to curb the epidemic ("Pour une Ile-de-France sans sida", "Vers Paris sans sida"). Our hypothesis is that nurse-driven HIV screening for key populations can be integrated to the consultants' care pathway as usual practice of the ED and assured over the long term in the Paris metropolitan area; this strategy combined with physician-directed diagnostic testing could reduce undiagnosed infections and help control the epidemic. Primary objective: The primary objective is to evaluate the impact of a wide implementation of nurse-driven HIV screening by rapid test in key populations combined with usual physician-directed diagnostic testing (intervention strategy) compared to diagnostic testing alone (control strategy) in the usual practice of the EDs. Patients aged 18 to 64 years and visiting a participating ED for reasons other than a potential exposure to HIV within less than 48 hours will be included. The primary outcome is the proportion of new HIV diagnoses among included patients. Secondary objectives are to : evaluate the feasibility of nurse-driven screening and its long-term implementation, evaluate the effectiveness of the screening process used by the caregivers, particularly the use of an electronic questionnaire, and by the patients as well as the acceptability, compare newly diagnosed HIV+ patients in the two groups in terms of : linkage to follow up care, proportions of patients who had a CD4 cell count greater or equal to 500 or 350 cells/µL and no HIV-related symptoms and proportions of patients with acute HIV infection. estimate through modelling the number of new HIV diagnoses for different levels of coverage of the screening strategy in the Paris metropolitan area. Methods The strategies will be compared in 18 EDs of Paris metropolitan area during two periods. The start of the intervention strategy will be randomly allocated for each ED following a stepped-wedge cluster randomized trial. EDs are selected according to the proportion of patients belonging to key populations in the patients they receive (data from two previous studies). During intervention period, nurses will suggest performing an HIV rapid test to patients belonging to key populations according to the answers to a self-administered questionnaire. The intervention period will last 3 to 11 months and the control period 0 to 8 months. Patients will participate up to 1 month if a follow-up is needed.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Hiv, Nurse's Role
    Keywords
    Emergency service, Hospital, HIV, Mass screening, Nurses, Prevention and control, Key populations, Targeted screening

    7. Study Design

    Primary Purpose
    Screening
    Study Phase
    Not Applicable
    Interventional Study Model
    Crossover Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    487000 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Nurse-driven HIV screening for key populations+UD
    Arm Type
    Experimental
    Arm Description
    Nurse-driven HIV screening for key populations combined with usual physician-directed diagnostic testing (UD)
    Arm Title
    Physician-directed diagnostic testing alone
    Arm Type
    Active Comparator
    Intervention Type
    Procedure
    Intervention Name(s)
    Nurse-driven HIV screening for key populations combined with usual physician-directed diagnostic testing
    Intervention Description
    A self-administered questionnaire on HIV exposure factors will be offered to all patients of ages 18-64 able to complete it. This questionnaire will be available in a paper-based format, electronic format on the patient phone or can be conducted verbally by the nurse. According to the answers, the nurses will suggest performing a rapid test to patients belonging to key populations. A finger-stick rapid HIV test will be performed and results will be disclosed by the nurse assisted by a physician if necessary. If needed, a follow-up visit with an infectious disease specialist will be scheduled within 72 hours.
    Intervention Type
    Other
    Intervention Name(s)
    Physician-directed diagnostic testing
    Intervention Description
    Throughout the intervention, physicians will prescribe HIV tests to patients with HIV-related symptoms, following usual practice.
    Primary Outcome Measure Information:
    Title
    Proportion of new HIV diagnoses among included patients.
    Time Frame
    At the end of the expected total duration of the inclusion period: 11 months in each ED
    Secondary Outcome Measure Information:
    Title
    Feasibility of the screening strategy and its implementation
    Description
    Feasibility of the screening strategy and its implementation based on: proportion of distributed and completed self-administered questionnaires among the patients included and among the patients able to participate who were not known to be HIV positive, the proportion of rapid tests offered by nurses among patients belonging to key populations, the proportion of patients screened by nurses among patients who were offered a rapid test and among patients belonging to high-risk groups .
    Time Frame
    At the end of the expected total duration of the inclusion period: 11 months in each ED
    Title
    Effectiveness of the screening processes used by the caregivers, particularly the integration of the electronic questionnaire, and used by the patients as well as acceptability
    Time Frame
    At the end of the expected total duration of the inclusion period: 11 months in each ED
    Title
    Proportions of patients with a new diagnosis
    Description
    Proportions of patients with a new diagnosis who had: a follow up visit with an infectious disease specialist within 1 month, a CD4 cell count greater or equal to 500 or 350/µL and no HIV-related symptoms, an acute HIV infection.
    Time Frame
    At the end of the expected total duration of the inclusion period: 11 months in each ED
    Title
    Estimation through modelling of the number of new HIV diagnoses for different levels of coverage of the screening strategy in the Paris metropolitan area.
    Time Frame
    At the end of the expected total duration of the inclusion period: 11 months in each ED

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    64 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: - Patients aged 18 to 64 years and visiting a participating ED for reasons other than a potential exposure to HIV within less than 48 hours Exclusion Criteria: - Not applicable
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Judith LEBLANC, RN, PhD
    Phone
    00 33 1 49 28 22 02
    Email
    judith.leblanc@aphp.fr
    First Name & Middle Initial & Last Name or Official Title & Degree
    Anne-Claude CREMIEUX, Md, PhD
    Phone
    00 33 1 49 28 22 02
    Email
    anne-claude.cremieux@aphp.fr
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    judith LEBLANC
    Organizational Affiliation
    Assistance Publique - Hôpitaux de Paris
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    Undecided

    Learn more about this trial

    Does the Implementation of Nurse-driven HIV Screening for Key Populations in the Emergency Departments Limit Undiagnosed Infections in the Paris Metropolitan Area? DEPIST Trial (ANRS 14055)

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