SPARCS: Structured Peer-delivered ART and Reentry Community Strategy

Sponsor
Johns Hopkins University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06027671
Collaborator
Aurum Institute (Other), Seoul National University (Other), National Institute of Mental Health (NIMH) (NIH)
640
4
54

Study Details

Study Description

Brief Summary

The overarching goal of this study is to implement both a transition community adherence club strategy (Group-SPARCS) and an ART provision strategy (ART-SPARCS) for HIV-positive individuals transitioning from correctional to community settings in South Africa. The current proposal will allow for a fully powered effectiveness randomized clinical trial (RCT).

  • To compare the effectiveness of Full-SPARCS, ART-SPARCS, and Group-SPARCS to care as usual and to each other to achieve HIV RNA suppression 6 months following correctional facility release

  • To assess determinants of implementation of Full-SPARCS, ART-SPARCS, and Group-SPARCS.

  • To assess the scalability through costing and cost effectiveness analysis of Full-SPARCS, ART-SPARCS, and Group-SPARCS.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Structured Peer-delivered ART and Reentry Community Strategy
N/A

Detailed Description

Background: The South African government has devoted resources towards HIV care in correctional facilities that have resulted in antiretroviral therapy (ART) coverage of >90% and viral load (VL) suppression of >80% among incarcerated people living with HIV (PLWH). However, despite free post-release care, the investigators previously observed that only an estimated 34% were in care three months post-release. The investigators developed, tested, and manualized the Structured Peer-delivered ART and Re-entry Community Strategy (SPARCS) to overcome post-incarceration barriers specific to PLWH returning to the community.8-10 In the investigators randomized controlled pilot of SPARCS, 6-month post-release, continuity of care was 61% in the intervention arm compared to 36% in the usual care arm (p=0.001), demonstrating effectiveness. Full-SPARCS, has two distinct components spanning six months post-release: direct provision of ART (ART-SPARCS) and 12 biweekly peer facilitator-led group sessions (Group-SPARCS). ART-SPARCS is designed to overcome clinic-level barriers through bimonthly distribution of ART without a group component. Group-SPARCS is designed to increase self-efficacy, social support, and life skills through facilitated group discussion and curriculum including planning, problem solving, financial literacy, and living with HIV without ART distribution. The current usual care is a supply of ART and a referral letter at the time of release from incarceration.

Methods: This research study will be conducted in Gauteng Province. Recruitment will occur within correctional facilities of the Department of Correctional Services (DCS) - Modderbee, Kgosi Mampuru II, and Johannesburg. All study interventions will occur following release in either Ekurhuleni District, Tshwane District or Johannesburg District. The study population will be comprised of adult (≥18 years old) corrections inmates, either male or female, with known HIV infection and are receiving ART within the correctional facility and are expected to be released back into the community within 3 months of study enrollment Participants will be randomized 1:1:1:1 to either the standard of care, Full-SPARCS, Group-SPARCS, or ART-SPARCS using sequential envelopes with study arm determination sealed inside. Study staff will contact participants to ascertain care status and update contact information at one week, one month, three months, six months, nine months, and twelve months from release. Participants assigned to Group-SPARCS or ART-SPARCS will be asked to attend biweekly sessions. Group-SPARCS activities will include - structured curriculum, symptom screening, and routine laboratory monitoring. ART-SPARCS will include the distribution of pre-packed medication and routine laboratory monitoring. Full-SPARCS includes all components of Group-SPARCS and ART-SPARCS.

Study sample: A total of 640 participants will be randomized to one of the four arms. Sixty of the participants will be selected for participation in qualitative in-depth interviews. An additional 25 staff involved in Transition community adherence club (TCAC) referral, ART provision, implementation, coordination will be enrolled for qualitative in-depth interviews.

Significance: The proposed study is consistent with NIH HIV/AIDS highest priority research and the South African National Strategic Plan on HIV, Tuberculosis (TB), and Sexually Transmitted Infections (STIs) 2017-2022. The research addresses the HIV/AIDS Research Priority of "retention and engagement in these services, and achievement and maintenance of optimal prevention and treatment responses." It also addresses "health disparities" through a focus on recently released inmates, a marginalized population. The proposal also fits with the South African National Strategic Plan prioritizing inmates as a key population for HIV services.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
640 participants
Allocation:
Randomized
Intervention Model:
Factorial Assignment
Intervention Model Description:
This is a hybrid type 1 effectiveness-implementation study with a factorial design to compare care as usual, Full-SPARCS, ART-SPARCS, or Group-SPARCS. We will recruit participants from correctional facilities in the Department of Correctional Services (DCS) Gauteng Region, South Africa. Study activities for the intervention arm will be delivered in community venues near to where participants live in Tshwane District, Ekurhuleni District, and City of Johannesburg.This is a hybrid type 1 effectiveness-implementation study with a factorial design to compare care as usual, Full-SPARCS, ART-SPARCS, or Group-SPARCS. We will recruit participants from correctional facilities in the Department of Correctional Services (DCS) Gauteng Region, South Africa. Study activities for the intervention arm will be delivered in community venues near to where participants live in Tshwane District, Ekurhuleni District, and City of Johannesburg.
Masking:
Double (Investigator, Outcomes Assessor)
Masking Description:
We will perform individual randomization blocked by the correctional facility. Study staff will open numbered envelopes with the allocation following enrolment. Participants will be randomized 1:1:1:1 to one of the study arms using sequential envelopes with study arm determination sealed inside. Randomization will be stratified by study site and by sex. The randomization lists for each site/sex combination will be generated through randomly permuted blocks of four and eight study assignments with an equal number of group assignments within each block. Study assignments will be masked to staff performing outcome assessments (in-person and telephonic interviews) and the investigators until all outcome data have been collected.
Primary Purpose:
Treatment
Official Title:
Structured Peer-delivered Antiretroviral Therapy (ART) and Reentry Community Strategy to Overcome Barriers to HIV Care Continuity During Community Re-entry From Incarceration in South Africa
Anticipated Study Start Date :
Feb 1, 2024
Anticipated Primary Completion Date :
Feb 1, 2028
Anticipated Study Completion Date :
Aug 1, 2028

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Care-as-usual (CAU) arm

Per DCS routine, at release, participants will receive a referral letter form the DCS health services and, in most cases, will be provided with a 28-day supply of ART.

Experimental: Group-SPARCS intervention arm

The Group-SPARCS component comprises one individual pre-release session, one individual post-release session, and 12 every-other-week (every two weeks) post-release group sessions extending six months post-release. Each session will be led by two trained individuals: a peer (history of criminal justice involvement and living with HIV) and a social worker.30 Within 14 days of release, participants will have one-on-one contact with a facilitator to update locator information, continue rapport building, review disclosure plans, provide a reminder of SPARCS logistics, and assign or remind the participant to a SPARCS group based on their location of residence and timing of release (depending on whether this occurred pre-release). Each Group-SPARCS meeting lasts approximately 2 hours, and the sessions occur in a private space in a community venue (e.g., community centre or church).

Behavioral: Structured Peer-delivered ART and Reentry Community Strategy
The intervention aims to circumvent clinic barriers by directly providing ART and build behavioral skills (planning, self-efficacy) through peer-facilitator led group sessions to improve care continuity following release from incarceration.

Experimental: ART-SPARCS intervention arm

ART delivery will follow Department of Health (DoH) procedures for differentiated models of care, in particular the Community Adherence Club model. Similar to community adherence clubs, the ART provision in SPARCS will be affiliated with a 'home clinic" that will provide ART supplies for the participants. Routine community adherence club activities include: ART will be provided every two months from correctional facility release to 6 months post-release (months 2, 4, and 6). Participants with less than two months of ART at release will receive a top-off to reach two months. ART will be pre-packaged by the DoH "home clinic", collected by the facilitators, and distributed to the participants. At the time of distribution, the facilitators will conduct a standard DoH differentiated care symptom screen. Participants who report specific symptoms will be referred to the "home clinic" for further assessment per routine with Community Adherence Clubs.

Behavioral: Structured Peer-delivered ART and Reentry Community Strategy
The intervention aims to circumvent clinic barriers by directly providing ART and build behavioral skills (planning, self-efficacy) through peer-facilitator led group sessions to improve care continuity following release from incarceration.

Experimental: Full-SPARCS arm

Full-SPARCS combines Group-SPARCS and ART-SPARCS with ART delivery during SPARCS group meetings.

Behavioral: Structured Peer-delivered ART and Reentry Community Strategy
The intervention aims to circumvent clinic barriers by directly providing ART and build behavioral skills (planning, self-efficacy) through peer-facilitator led group sessions to improve care continuity following release from incarceration.

Outcome Measures

Primary Outcome Measures

  1. HIV RNA (viral load) suppression at 6 months [6 months]

    HIV RNA suppression will be defined as a viral load <1000 copies/mL. Participants without viral load data will be assumed to have a viral load >1000 c/mL.

Secondary Outcome Measures

  1. HIV RNA (viral load) suppression at 12 months [12 months]

    HIV RNA suppression will be defined as a viral load <1000 copies/mL. Participants without viral load data will be assumed to have a viral load >1000 c/mL.

  2. Cost-effectiveness [up to 12 months]

    Cost effectiveness will be measured by combining standardized data collection tools and an analytic framework developed from prior studies to document and classify resources used (e.g. direct human resources, consumables, capital assets) for all intervention-related activities from design, coordination, to direct delivery.

  3. Percentage of participants receiving ART at 6 months [6 months]

    Participants receiving ART by 6 months post-release.

  4. Percentage of participants receiving ART at 12 months [12 months]

    Participants receiving ART by 12 months post-release.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Incarcerated at one of the participating study enrolment sites, awaiting trial (un-sentenced) and sentenced individuals.

  • Diagnosed with HIV and ART at the time of enrolment.

  • Anticipated release or trial date within three months of study enrolment.

  • Self-report expected to reside in an unrestricted environment within Ekurhuleni, Tshwane, or Johannesburg districts of Gauteng Province and within proximity to one of the SPARCS intervention sites (i.e., within 20km, 45-minute travel time, or two local taxi minibus rides)

  • Willing to participate in study post-release follow-up activities and provide contact information for post-release follow-up.

Exclusion Criteria:
  • <18 years of age.

  • Condition (severe cognitive dysfunction or mental illness) rendering the individual unable to provide informed consent.

  • Unable to provide informed consent to participate in the study.

  • Assessment by DCS health staff indicating that the individual requires a high intensity of care exceeding that which can be provided in a differentiated model of care setting.

  • Not released from the correctional facility during the period of intervention delivery.

  • Release to a region outside of Gauteng.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Johns Hopkins University
  • Aurum Institute
  • Seoul National University
  • National Institute of Mental Health (NIMH)

Investigators

  • Principal Investigator: Christopher Hoffmann, Johns Hopkins School of Medicine

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Johns Hopkins University
ClinicalTrials.gov Identifier:
NCT06027671
Other Study ID Numbers:
  • IRB00386911
First Posted:
Sep 7, 2023
Last Update Posted:
Sep 7, 2023
Last Verified:
Aug 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Keywords provided by Johns Hopkins University

Study Results

No Results Posted as of Sep 7, 2023