Repeated-dose Brief Intervention to Reduce Overdose and Risk Behaviors Among Naloxone Recipients
Status: | Active, not recruiting |
---|---|
Conditions: | Gastrointestinal |
Therapuetic Areas: | Gastroenterology |
Healthy: | No |
Age Range: | 18 - 65 |
Updated: | 4/21/2016 |
Start Date: | July 2014 |
End Date: | December 2016 |
REBOOT is a pilot randomized trial of a repeated-dose brief intervention to reduce overdose
and risk behaviors among naloxone recipients (REBOOT). It includes an established overdose
education curriculum within an Informational-Motivation-Behavior (IMB) model. This study
will test the feasibility of an efficacy trial of REBOOT vs treatment as usual (information
and referrals) that will evaluate overdose events (non-fatal or death), drug use cessation,
and overdose and HIV risk behaviors, among opioid-dependent persons who have previously
overdosed and already received take-home naloxone (the opioid antagonist used to reverse
overdose).
and risk behaviors among naloxone recipients (REBOOT). It includes an established overdose
education curriculum within an Informational-Motivation-Behavior (IMB) model. This study
will test the feasibility of an efficacy trial of REBOOT vs treatment as usual (information
and referrals) that will evaluate overdose events (non-fatal or death), drug use cessation,
and overdose and HIV risk behaviors, among opioid-dependent persons who have previously
overdosed and already received take-home naloxone (the opioid antagonist used to reverse
overdose).
Inclusion Criteria:
- age 18-65 years;
- current opioid dependence by SCID
- urine positive for opioids during screening, excluding prescribed agonist maintenance
therapy
- history of prior opioid overdose
- previously received take-home naloxone
- no serious illnesses likely to progress clinically during trial
- able and willing to provide informed consent, provide locator information,
communicate in English, adhere to visit schedule
Exclusion Criteria:
- suicidal ideation by concise health risk tracking (CHRT)
- currently participating in another interventional research study that could possible
impact the study's outcomes of interest
- any condition that, in the Principal Investigator's judgment, interferes with safe
study participation or adherence to study procedures
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