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Same-Day Antiretroviral Therapy as a Behavioral Design Intervention to Reduce Stigma in Key Affected Populations (Peru SD-ART)

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Yale University

Status

Begins enrollment in a year or more

Conditions

Hiv

Treatments

Behavioral: SD-ART

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT07053514
R01TW013180 (Other Grant/Funding Number)
2000040491

Details and patient eligibility

About

The goal of this study is to develop and implement a same-day ART (SD-ART) protocol for key affected populations with HIV in Peru. The development of the protocol will be guided by asynchronous online focus groups with HIV experts to define eligibility criteria and essential components of the protocol, as well as nominal group technique focus groups and in-depth interviews to identify barriers and facilitators to SD-ART implementation. Finally, investigators will pilot the SD-ART protocol with patients and clinicians using a prospective, longitudinal design integrated into routine HIV care.

Full description

The proposed study has 3 aims:

  1. Conduct asynchronous online focus groups (AOFGs) and flowcharting to map the current ART initiation process and design a streamlined same-day antiretroviral therapy (SD-ART) protocol as a behavioral design.
  2. Assess the multi-level barriers and facilitators to refine and implement an SD-ART protocol from the perspectives of patients, clinicians, and administrators, considering the high levels of stigma and suboptimal HIV treatment outcomes. Findings from Aims 1 and 2 will guide Aim 3.
  3. Pilot-test the protocol-concordant SD-ART strategy in newly diagnosed People with HIV where investigators will assess and follow multi-level stigma constructs in patients and providers, analyzed through longitudinal dyadic analyses, to provide the evidence for SD-ART as a behavioral design intervention that reduces stigma.

The focus of this registration is the trial in aim 3.

Enrollment

139 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Aim 1:

HIV experts will be selected from National Societies of HIV experts according to the following criteria: 1) 18 years old or older; 2) Be an HIV expert, including those from NGOs providing HIV care, and international specialists; 3) Provide informed consent.

  • Aim 2:

    • NGT Focus Groups (FG)

      • Staff members

        1. 18 years old or older.
        2. Be a clinical staff member at Hospital Dos de Mayo or Patrucco Primary Health Center.
        3. Provide informed consent.
      • PWH receiving HIV care

        1. 18 years old or older.
        2. Identify as member of a KAP.
        3. Receive HIV care at Hospital Dos de Mayo or Patrucco Primary Health.
        4. Provide informed consent.
      • PWH who dropped out of HIV care

        1. 18 years old or older.
        2. Identify as a member of a KAP.
        3. Previously received HIV care at Hospital Dos de Mayo or Patrucco Primary Health but dropped out of care, as identified through patient registries.
        4. Provide informed consent.
    • In-depth interviews

        1. 18 years old or older.
        1. Be the director of Hospital Dos de Mayo or Patrucco primary health center or the HIV director at the Ministry of Health
        1. Provide informed consent
  • Aim 3:

    • Clinical Staff Dyadic Surveys

        1. 18 years old or older.
        1. Be an HIV provider at Hospital Dos de Mayo or Raul Patrucco Primary Health Center.
        1. Provide HIV care to one of the 125 PWH
        1. Provide informed consent.
    • Patient Dyadic Surveys

        1. 18 years old or older.
        1. Identify as a member of a KAP.
        1. Be newly diagnosed with HIV and eligible for SD-ART based on clinical criteria identified from Aims 1 and 2.
        1. Provide informed consent.

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

139 participants in 2 patient groups

People With HIV (PWH)
Experimental group
Description:
SD-ART protocol for PWH prescribed by their HIV clinicians
Treatment:
Behavioral: SD-ART
Clinicians prescribing ART
No Intervention group

Trial contacts and locations

2

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Central trial contact

David Oliveros, MPH

Data sourced from clinicaltrials.gov

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