Differentiated Service Delivery for Antiretroviral Therapy

  • STATUS
    Recruiting
  • End date
    Dec 15, 2025
  • participants needed
    5000
  • sponsor
    Thai Red Cross AIDS Research Centre
Updated on 19 February 2024
antiretroviral agents
antiretroviral therapy

Summary

This study is a prospective observational cohort. The target study population is PLHIV who receive ART at hospitals and community-based organizations (CBOs) in Chiang Mai, Ubon Ratchathani, Chonburi, and Songkhla. Participants will receive ART service in the same standard as in the hospital setting. Secondary data will be collected from the medical records already existed in the hospital and CBO systems.

Description

DSD-ART service at the Hospital

  • Medical examination: All clients who receive ART service at the hospital and agree to participate in the research project will be interviewed to collect personal information and receive physical and laboratory examination in order to assess eligibility in research participation. If ineligible, the clients will be referred to the standard of care.
  • Preparation and DSD-ART service offer: PLHIV who are eligible to participate in the research will receive counselling to assess the supports the clients need and will be offered various models of DSD-ART service. The clients may choose the model that is most suitable to their lifestyle.

Details
Condition HIV infection, Immunodeficiency
Age 18-100 years
Treatment questionnaires survey
Clinical Study IdentifierNCT04383769
SponsorThai Red Cross AIDS Research Centre
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

Thai citizenship
Age 18
HIV positive
Received ART for at least 6 months at a participating hospital (Except for After hour ART clinic model that will allow participants who receive ART less than 6 months into service)

Exclusion Criteria

N/A
Clear my responses

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  • You can expect the study team to contact you via email or phone in the next few days.
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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