Integrated Intervention
Behavioralsystems navigation, psychosocial counseling
NCT Number: NCT02935296
The purpose of this study is to determine the feasibility of a future trial that will assess whether an integrated intervention combining psychosocial counseling and supported referrals for antiretroviral therapy (ART) at any CD4 cell count and substance use treatment for HIV-infected people who inject drugs (PWID) will reduce HIV transmission to HIV-uninfected injection partners, as compared to routine care dictated by national guidelines for HIV-infected PWID.
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Notify Me18 year–45 year
All sexes
Interventional
Not applicable
CIPTO, Jakarta, Indonesia
This is a multi-site, two-arm, randomized, vanguard study. Network units will consist of an HIV-infected index participant and his/her HIV-uninfected network injection partner(s). Network units will be randomized to the intervention or standard of care arms in a 1:3 ratio, stratified by site. To assess feasibility of the intervention, additional interviews will be conducted with study staff (systems navigators and counselors) and clinic-based stakeholders at each study site.
Approximately 500 Index participants and their partners will be enrolled.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Index participants:
HIV uninfected injection partners:
Exclusion criteria
-
systems navigation, psychosocial counseling
Time frame: 18 months
Number of HIV seroconversions to partners to control arm Index participants
Time frame: 18 months
Number of participants enrolled, and number of participants with a final study visit.
Time frame: 18 months
Number of HIV seroconversions to partners of Intervention arm participants
Time frame: 18 months
Number of participants in both arms who report being in ART (case report forms) care, as well as testing stored plasma for HIV RNA suppression
Time frame: 18 months
self reported on case report forms
Time frame: 18 months
self reported data via questionnaire of drug sharing habits and partners at each study visit
Time frame: 18 months
self report via questionnaire
Time frame: 18 months
stored plasma samples from those persons who are HIV positive and those who become HIV positive during the study
HIV Prevention Trials Network
Network
Integrated Treatment and Prevention for People Who Inject Drugs: A Vanguard Study for a Network-based Randomized HIV Prevention Trial Comparing an Integrated Intervention Including Supported Antiretroviral Therapy to the Standard of Care
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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