Opioid UseNCT03933345
Overdose Risk Management and Naloxone
An observational study of Opioid Use, run by National Development and Research Institutes, Inc. at 2 sites in United States.
Trial summary
A growing body of research underscores the life- and cost-saving advantages of equipping people who use opioids with naloxone, but very little is known about: 1) barriers to naloxone awareness and access, and 2) the potential psychosocial and behavioral impacts of being "protected" by naloxone while engaging in… Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Opioid Use
- How many people
- 600 participants
- Where
- 2 sitesUnited States
- Study dates
- 5 Apr 2019to 31 Aug 2023
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- Adult, Older adult
Study population: Study population will consist of 600 people who use illicit opioids in New York City.
Who may be able to join
- Adult-age (18+)
- Current illicit opioid use (verified by rapid urine screen)
- Speak English
- Willing to participate
Who cannot join
- Unable to comprehend informed consent and/or study procedures.
Trial locations and contacts
2 sites in 1 country.
United States2 sites, 2 recruiting
- Recruiting
270 West 25th Street
New York, New York, 10001
Gina Bonilla, BA, 917-736-3288, Bonilla@ndri.org
Bethany Medley, MSW, 804 551 1532, medley@ndri.org
- Recruiting
National Development and Research Institutes, Inc.
New York, New York, 10010
Alexander S Bennett, PhD, 917-470-7000, bennett@ndri.org
Luther Elliott, PhD, 3473266757, elliott@ndri.org
About this study
Official title: Overdose Risk Management and Compensation in the Era of Naloxone
A growing body of research underscores the life- and cost-saving advantages of equipping people who use opioids with naloxone, but very little is known about: 1) barriers to naloxone awareness and access, and 2) the potential psychosocial and behavioral impacts of being "protected" by naloxone while engaging in overdose risk behaviors, of using naloxone on someone else, and of surviving an overdose in which naloxone is used. This research will provide insight into both of these domains to yield a richly contextualized understanding of the processes and mechanisms underlying changes in overdose risk behaviors related to naloxone access and use and will illuminate the disparities that may limit access to naloxone for some or result in compensatory behavior following naloxone exposure for others. Findings from this study will provide an empirical basis to strengthen and refine existing overdose prevention efforts and to design tailored interventions to engage opioid users who have recently survived or reversed an overdose.
Read the detailed description
Drug overdose (OD) deaths in the United States nearly tripled between 1999 and 2014. During 2015 more than 50,000 people died from overdose nationwide, and almost two thirds (63.1%) involved opioids.1 In response, the number of opioid OD prevention programs offering naloxone has ballooned.2 Many states have sought to expand access through provision of the medication to EMT and police first-responders, over-the-counter availability at pharmacies, and emergency legislation providing for lay prescribing, largely within the context of opioid OD prevention programs serving people who use heroin or diverted prescription opioids (henceforth, people who use illicit opioids; PWUIO). As naloxone has become more commonplace, however, OD rates have continued to rise, and critical viewpoints about the failure of OD reversal efforts to deter subsequent high-risk behavior have begun to emerge from police,3 firefighers,4 EMS personnel,5 and news media,6-8 especially following the recent loss of pop-artist, Prince, to an opioid OD only days after being administered naloxone in an Illinois hospital.9 This study is responsive to a recent NIDA and FDA mandate for foundational naloxone research among active users of illicit opioids.10 Specifically, it assesses two main concerns at the heart of current policymaking related to opioid OD and naloxone. 1) Disparities in access to naloxone and obstacles to a willingness to be trained as a naloxone-carrying OD responder: Despite the critically important role PWUIO can play as OD responders,11-15 questions remain about differential awareness of and access to naloxone and OD response training among PWUIO. Even in NYC where city and state departments of health have led concerted and well-funded efforts to saturate the city with naloxone and OD reversal training, considerable limitations in coverage and training uptake still exist.16 Findings from our ongoing study of opioid OD risks among military veterans in NYC indicate that many PWUIO are still naloxone-naïve and, even after learning about its lifesaving utility, still decline no-cost naloxone and OD response training. 2) The poorly understood impacts of possessing naloxone, using naloxone on someone else, or having it used on oneself on PWUIO's subsequent OD rates and risk behaviors: An increasing number of studies seek to track the uses to which naloxone kits are put, but the broader behavioral impacts of exposure to naloxone on actual opioid-related risk behaviors have seen almost no empirical investigation since 2003 when a study of street-recruited PWUIO in San Francisco reported that 35% indicated that they intended to use more heroin than usual after receiving naloxone.17 Building on our current studies of naloxone use and related attitudes among opioid-using military veterans and other drug users we propose to recruit 600 adult-age (18+) people who use illicit opioids (i.e., heroin and/or diverted pharmaceutical opioids) in New York City using Respondent Driven Sampling. At enrollment, participants will complete a detailed survey instrument establishing histories of substance use, naloxone exposure, and other potential barriers to the uptake of naloxone training. Because extant research establishes a clear public health and ethical imperative to provide PWUIO with naloxone, we will also offer all participants training to become naloxone-equipped OD responders at enrollment. We will follow the sample for two years using a mixed-methods approach involving text-message-based exposure tracking, monthly surveys using a state-of-the-art online data collection portal, and a qualitative subsample to ensure that naloxone exposures and changes in OD risk behavior are carefully tracked and contextualized by ethnographic data about the psychosocial and sociocultural mechanisms underlying participant experiences.
Aim A - Describe factors associated with: 1) lifetime history of access to and use of naloxone and 2) uptake of no-cost naloxone and OD response training. We will test the following hypotheses:
HypA1 - Naloxone knowledge and exposure history will vary at enrollment, potentially revealing disparities based on background factors (e.g., SES, ethnicity, age, neighborhood) and individual level factors (e.g., mental health diagnoses, opioid use disorder severity, duration of opioid use) HypA2 - Interest in OD response training and naloxone at baseline will vary by background and individual-level factors.
Aim B - Describe longitudinal relationships between naloxone exposure (access to and use of naloxone) and overdose risk behaviors. We will test the following hypothesis:
HypB1 - Naloxone access and use exposures will have measurable impacts on opioid OD-related risk behaviors over time, potentially varying in degree and direction across subgroups of PWUIO.
Aim C (Qualitative) - Explore barriers to naloxone uptake and any identified secondary impacts (e.g., compensatory risk taking, positive change after a naloxone exposure such as risk reduction or treatment-seeking) in terms of opioid users' own experiences and perceptions.
By employing a longitudinal and mixed-methods design capable of detecting naloxone exposure impacts and also illuminating the various mechanisms that may undergird them in participants' own terms, this project holds serious policy and direct service implications for the refinement of naloxone training programs and OD risk interventions that target PWUIO. This research also holds the potential to identify varying naloxone impacts among PWUIO of different social and behavioral groups-such as people who inject drugs (PWID) vs. prescription opioid misusers, older vs. younger (or shorter- vs. longer-term) PWUIO, and male vs. female users-and can inform future efforts to tailor prevention and education to these distinct subpopulations.
- Conditions
- Opioid Use
- Being tested
- Study provides naloxone to participants who wish to have it. Not required to accept naloxone and no control.
- Keywords
- Overdose Risk Behaviors, Opioids, Naloxone, Overdose
- Medical subject headings
- Drug Overdose
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Study provides naloxone to participants who wish to have it. Not required to accept naloxone and no control.Other
At enrollment, participants will complete a detailed survey instrument establishing histories of substance use, naloxone exposure, and other potential barriers to the uptake of naloxone training. Because extant research establishes a clear public health and ethical imperative to provide PWUIO with naloxone, we will also offer all participants training to become naloxone-equipped OD responders at enrollment. We will follow the sample for two years using a mixed-methods approach involving text-message-based exposure tracking, monthly surveys using a state-of-the-art online data collection portal, and a qualitative subsample to ensure that naloxone exposures and changes in OD risk behavior are carefully tracked and contextualized by ethnographic data about the psychosocial and sociocultural mechanisms underlying participant experiences.
| Study group | Role | What they receive |
|---|---|---|
| People who use illicit opioids | The study will recruit an adult-age (18+) sample of 600 people who use illicit opioids (either heroin or prescription opioid analgesics without a doctor's prescription) in New York City using Respondent Driven Sampling. Receives: Other: Study provides naloxone to participants who wish to have it. Not required to accept naloxone and no control. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Naloxone access
Number of times offered naloxone
Measured: Lifetime (at baseline)
Naloxone uptake
Number of times accepted naloxone when offered
Measured: Lifetime (at baseline)
Naloxone use
Number of times used naloxone
Measured: Lifetime (at baseline)
Naloxone access
Number of times offered naloxone
Measured: 24 months
Naloxone use
Number of times used naloxone
Measured: 24 months
Overdose risk behaviors
Overdose Risk Behavior Scale - a 22 item validated scale that measures past 30-day overdose risk behaviors. See (Development of an Overdose Risk Behavioral Scale: ORBS; Pouget et al., 2017).
Measured: 24 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted1 May 2019
- Study start5 Apr 2019
- Primary completion1 Aug 2022 (estimated)
- Study completion31 Aug 2023 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Opioid UseStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 600 participants (estimated)
Sponsor and investigators
- Lead sponsor
- National Development and Research Institutes, Inc.
- Sponsor type
- University, hospital or other
- Collaborators
- Brandeis University, Drexel University, New York University, Rhode Island Hospital
- Responsible party
- Principal investigator, Alexander Bennett, National Development and Research Institutes, Inc.
- Investigators
- Andrew Rosenblum, Study director, National Development & Research Institutes (NDRI)
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03933345
- Sponsor's protocol ID
- 660
- Status last verified
- Apr 2019
- First submitted
- 23 Apr 2019
- Last updated
- 1 May 2019
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Publications
Pouget ER, Bennett AS, Elliott L, Wolfson-Stofko B, Almenana R, Britton PC, Rosenblum A. Development of an opioid-related Overdose Risk Behavior Scale (ORBS). Subst Abus. 2017 Jul-Sep;38(3):239-244. doi: 10.1080/08897077.2017.1282914. Epub 2017 Jan 23.
PubMed 28113004
Study at a glance
From the registry record, last updated by the sponsor on 1 May 2019. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Overdose Risk Management and Compensation in the Era of Naloxone
- ClinicalTrials.gov ID
- NCT03933345
- Acronym / sponsor ID
- 660
- Conditions
- Opioid Use
- Keywords
- Overdose Risk Behaviors, Opioids, Naloxone, Overdose
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 600 participants (estimated)
- Lead sponsor
- National Development and Research Institutes, Inc.University, hospital or other
- Collaborators
- Brandeis University, Drexel University, New York University, Rhode Island Hospital
- Study start
- 5 Apr 2019 (actual)
- Primary completion
- 1 Aug 2022 (estimated)
- Study completion
- 31 Aug 2023 (estimated)
- First posted
- 1 May 2019 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
A growing body of research underscores the life- and cost-saving advantages of equipping people who use opioids with naloxone, but very little is known about: 1) barriers to naloxone awareness and access, and 2) the potential psychosocial and behavioral impacts of being "protected" by naloxone while engaging in overdose risk behaviors, of using naloxone on someone else, and of surviving an overdose in which naloxone is used. This research will provide insight into both of these domains to yield a richly contextualized understanding of the processes and mechanisms underlying changes in overdose risk behaviors related to naloxone access and use and will illuminate the disparities that may limit access to naloxone for some or result in compensatory behavior following naloxone exposure for others. Findings from this study will provide an empirical basis to strengthen and refine existing overdose prevention efforts and to design tailored interventions to engage opioid users who have recently survived or reversed an overdose.
Detailed description
Drug overdose (OD) deaths in the United States nearly tripled between 1999 and 2014. During 2015 more than 50,000 people died from overdose nationwide, and almost two thirds (63.1%) involved opioids.1 In response, the number of opioid OD prevention programs offering naloxone has ballooned.2 Many states have sought to expand access through provision of the medication to EMT and police first-responders, over-the-counter availability at pharmacies, and emergency legislation providing for lay prescribing, largely within the context of opioid OD prevention programs serving people who use heroin or diverted prescription opioids (henceforth, people who use illicit opioids; PWUIO). As naloxone has become more commonplace, however, OD rates have continued to rise, and critical viewpoints about the failure of OD reversal efforts to deter subsequent high-risk behavior have begun to emerge from police,3 firefighers,4 EMS personnel,5 and news media,6-8 especially following the recent loss of pop-artist, Prince, to an opioid OD only days after being administered naloxone in an Illinois hospital.9 This study is responsive to a recent NIDA and FDA mandate for foundational naloxone research among active users of illicit opioids.10 Specifically, it assesses two main concerns at the heart of current policymaking related to opioid OD and naloxone. 1) Disparities in access to naloxone and obstacles to a willingness to be trained as a naloxone-carrying OD responder: Despite the critically important role PWUIO can play as OD responders,11-15 questions remain about differential awareness of and access to naloxone and OD response training among PWUIO. Even in NYC where city and state departments of health have led concerted and well-funded efforts to saturate the city with naloxone and OD reversal training, considerable limitations in coverage and training uptake still exist.16 Findings from our ongoing study of opioid OD risks among military veterans in NYC indicate that many PWUIO are still naloxone-naïve and, even after learning about its lifesaving utility, still decline no-cost naloxone and OD response training. 2) The poorly understood impacts of possessing naloxone, using naloxone on someone else, or having it used on oneself on PWUIO's subsequent OD rates and risk behaviors: An increasing number of studies seek to track the uses to which naloxone kits are put, but the broader behavioral impacts of exposure to naloxone on actual opioid-related risk behaviors have seen almost no empirical investigation since 2003 when a study of street-recruited PWUIO in San Francisco reported that 35% indicated that they intended to use more heroin than usual after receiving naloxone.17 Building on our current studies of naloxone use and related attitudes among opioid-using military veterans and other drug users we propose to recruit 600 adult-age (18+) people who use illicit opioids (i.e., heroin and/or diverted pharmaceutical opioids) in New York City using Respondent Driven Sampling. At enrollment, participants will complete a detailed survey instrument establishing histories of substance use, naloxone exposure, and other potential barriers to the uptake of naloxone training. Because extant research establishes a clear public health and ethical imperative to provide PWUIO with naloxone, we will also offer all participants training to become naloxone-equipped OD responders at enrollment. We will follow the sample for two years using a mixed-methods approach involving text-message-based exposure tracking, monthly surveys using a state-of-the-art online data collection portal, and a qualitative subsample to ensure that naloxone exposures and changes in OD risk behavior are carefully tracked and contextualized by ethnographic data about the psychosocial and sociocultural mechanisms underlying participant experiences.
Aim A - Describe factors associated with: 1) lifetime history of access to and use of naloxone and 2) uptake of no-cost naloxone and OD response training. We will test the following hypotheses:
HypA1 - Naloxone knowledge and exposure history will vary at enrollment, potentially revealing disparities based on background factors (e.g., SES, ethnicity, age, neighborhood) and individual level factors (e.g., mental health diagnoses, opioid use disorder severity, duration of opioid use) HypA2 - Interest in OD response training and naloxone at baseline will vary by background and individual-level factors.
Aim B - Describe longitudinal relationships between naloxone exposure (access to and use of naloxone) and overdose risk behaviors. We will test the following hypothesis:
HypB1 - Naloxone access and use exposures will have measurable impacts on opioid OD-related risk behaviors over time, potentially varying in degree and direction across subgroups of PWUIO.
Aim C (Qualitative) - Explore barriers to naloxone uptake and any identified secondary impacts (e.g., compensatory risk taking, positive change after a naloxone exposure such as risk reduction or treatment-seeking) in terms of opioid users' own experiences and perceptions.
By employing a longitudinal and mixed-methods design capable of detecting naloxone exposure impacts and also illuminating the various mechanisms that may undergird them in participants' own terms, this project holds serious policy and direct service implications for the refinement of naloxone training programs and OD risk interventions that target PWUIO. This research also holds the potential to identify varying naloxone impacts among PWUIO of different social and behavioral groups-such as people who inject drugs (PWID) vs. prescription opioid misusers, older vs. younger (or shorter- vs. longer-term) PWUIO, and male vs. female users-and can inform future efforts to tailor prevention and education to these distinct subpopulations.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| People who use illicit opioids | – | Other: Study provides naloxone to participants who wish to have it. Not required to accept naloxone and no control.The study will recruit an adult-age (18+) sample of 600 people who use illicit opioids (either heroin or prescription opioid analgesics without a doctor's prescription) in New York City using Respondent Driven Sampling. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Age groups
- Adult, Older adult
- Study population
- Study population will consist of 600 people who use illicit opioids in New York City.
Key inclusion criteria (4 listed)
- Adult-age (18+)
- Current illicit opioid use (verified by rapid urine screen)
- Speak English
- Willing to participate
Key exclusion criteria (1 listed)
- Unable to comprehend informed consent and/or study procedures.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Study provides naloxone to participants who wish to have it. Not required to accept naloxone and no control.At enrollment, participants will complete a detailed survey instrument establishing histories of substance use, naloxone exposure, and other potential barriers to the uptake of naloxone training. Because extant research establishes a clear public health and ethical imperative to provide PWUIO with naloxone, we will also offer all participants training to become naloxone-equipped OD responders at enrollment. We will follow the sample for two years using a mixed-methods approach involving text-message-based exposure tracking, monthly surveys using a state-of-the-art online data collection portal, and a qualitative subsample to ensure that naloxone exposures and changes in OD risk behavior are carefully tracked and contextualized by ethnographic data about the psychosocial and sociocultural mechanisms underlying participant experiences. | Other | People who use illicit opioids |
Primary outcome
Naloxone access
Time frame: Lifetime (at baseline)
Number of times offered naloxone
Naloxone uptake
Time frame: Lifetime (at baseline)
Number of times accepted naloxone when offered
Naloxone use
Time frame: Lifetime (at baseline)
Number of times used naloxone
Naloxone access
Time frame: 24 months
Number of times offered naloxone
Naloxone use
Time frame: 24 months
Number of times used naloxone
Overdose risk behaviors
Time frame: 24 months
Overdose Risk Behavior Scale - a 22 item validated scale that measures past 30-day overdose risk behaviors. See (Development of an Overdose Risk Behavioral Scale: ORBS; Pouget et al., 2017).
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 1 May 2019.
- Results publication: PubMed 28113004Pouget ER, Bennett AS, Elliott L, Wolfson-Stofko B, Almenana R, Britton PC, Rosenblum A. Development of an opioid-related Overdose Risk Behavior Scale (ORBS). Subst Abus. 2017 Jul-Sep;38(3):239-244. doi: 10.1080/08897077.2017.1282914. Epub 2017 Jan 23.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Andrew Rosenblum study director
National Development & Research Institutes (NDRI)
2 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Opioid Use, run by National Development and Research Institutes, Inc. at 2 sites in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 1 May 2019. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 2 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Alexander Bennett, PhD (19174707000, bennett@ndri.org), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Naloxone access (time frame: Lifetime (at baseline)). The study lists 6 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT03933345, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 1 May 2019; AzTrials last refreshed its copy on 31 Oct 2026.