RESTORE Study R61 Phase: Recovery and Engagement for Stimulant Users on Re-entry

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of Texas Southwestern Medical Center

About this trial

Justice-involved individuals face disproportionately high rates of stimulant use disorder and HIV, along with disrupted access to HIV treatment and prevention services like ART and PrEP. Contingency management (CM) is the most effective intervention for stimulant use, but its use in justice-involved populations has been limited by logistical and structural barriers. DynamiCare is an FDA-approved mobile app that delivers behavioral CM and has shown promise in reducing stimulant use, but its impact on HIV-related outcomes remains unknown. The RESTORE study (Recovery and Engagement for Stimulant Users on Re-entry) will evaluate whether combining DynamiCare with patient navigation (DynamiCare-plus) improves PrEP/ART initiation and reduces stimulant use among individuals recently released from justice settings. The R61 phase will assess feasibility, acceptability, and preliminary effectiveness among 40 participants. If milestones are met, the R33 phase will scale to a randomized controlled trial with 252 participants to assess effectiveness, implementation, and cost. This scalable, mobile approach has the potential to address a critical gap in care for a highly vulnerable population.

Eligibility criteria

Qualifiers

Be 18 years of age or older

Have a DSM-5 diagnosis of stimulant use disorder (methamphetamine and/or cocaine)

Be at risk for or living with HIV

Be able to provide informed consent

Disqualifiers

Severe medical or psychiatric disability making participation unsafe

Unable to provide consent or engage with the intervention

Trial design

Treatments tested in this trial

  • DynamiCare
  • Patient Navigation (PN)

Treatment groups

40 Participants
are divided into 2 treatment groups