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The Separate and Combined Effects of Vivitrol and Opiate Abstinence Reinforcement in the Treatment of Opioid Dependence

The Separate and Combined Effects of Vivitrol and Opiate Abstinence Reinforcement in the Treatment of Opioid Dependence

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01556425
Enrollment
84
Registered
2012-03-16
Start date
2012-05-31
Completion date
2017-08-06
Last updated
2018-03-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Opioid Dependence

Keywords

opioid use disorder, treatment, heroin, extended-release naltrexone, incentives, cotningency management, employment-based reinforcement, therapeutic workplace

Brief summary

In this 5-year study, the investigators propose to evaluate the separate and combined effects of the FDA-approved formulation of extended release naltrexone (Vivitrol®) and employment-based reinforcement of opiate abstinence in promoting opiate abstinence and reducing risky injection behavior in recently detoxified, opioid-dependent, injection drug users.

Detailed description

Injection heroin use is a chronic problem that fuels the transmission of HIV/AIDS through risky injection behaviors. Methadone and buprenorphine can reduce heroin use and risky injection behavior; however, they have abuse potential, produce physical dependence, can produce lethal overdose, are highly regulated, and some patients simply do not want agonist treatment. Opiate detoxifications can serve as an alternative to agonist treatment, but many injection drug users relapse to heroin use and resume risky injection behaviors after detoxification. Vivitrol®, an extended release formulation of naltrexone, was recently approved by the FDA for the treatment of opioid dependence, but its clinical utility is uncertain given the reluctance of many opioid-dependent adults to maintain its long-term use, and the fact that some patients continue to use opiates while under naltrexone blockade. The investigators research in the first period of this grant showed that employment-based reinforcement can be highly effective in promoting long-term adherence to Vivitrol®. Employment-based reinforcement may be ideally suited to address the limitations of extended release naltrexone by capitalizing on its potential to simultaneously reinforce naltrexone adherence and opiate abstinence. This grant will evaluate the effectiveness of employment-based reinforcement to simultaneously promote high rates of Vivitrol® adherence and increase opiate abstinence. After an opioid detoxification and induction onto oral naltrexone, participants will be invited to attend the Therapeutic Workplace for 24 weeks (where they can work and earn wages) and will be randomly assigned to one of four groups that will differ in whether they receive Vivitrol®, employment-based opiate abstinence reinforcement, both or neither. Participants in Vivitrol® conditions will be required to take scheduled injections to work and earn wages. Participants exposed to opiate abstinence reinforcement will receive a temporary decrease in their workplace pay if they fail to provide an opiate-free urine sample. The study will assess the effects of the interventions on weekly opiate urinalysis results, and on measures of injection drug use and cocaine use. If this study shows that the combined use of Vivitrol® and employment-based reinforcement of adherence and opiate abstinence is effective in maintaining long-term opiate abstinence, this model of employment-based addiction pharmacotherapy could be integrated into community workplaces to disseminate the effective use of Vivitrol®; it could be used to enhance the utility of other new antagonist-like addiction medications; and it could provide an effective means of reducing injection drug use in individuals who persist in injecting heroin and exposing themselves and others to the risk of acquiring or transmitting HIV infection due to their continued injection drug use and risky injection behaviors.

Interventions

Participants receiving this intervention will receive the FDA-approved dose, route, and schedule of administration of VIVITROL. The dose of VIVITROL of 380 mg will be delivered intramuscularly every 4 weeks.

BEHAVIORALEmployment-based opiate abstinence reinforcement

This intervention will require participants to provide opiate-negative urine samples on Monday, Wednesday and Friday to maintain their maximum pay. If a participant provides an opiate-positive urine sample, or fails to provide a scheduled sample, their base pay will be reset from $8 per hour to $1 per hour. On each day after the reset that the participant provides a urine sample that meets the opiate abstinence criteria and attends the workplace for at least 5 minutes, their base pay will increase by $1 per hour until it reaches the maximum of $8 per hour.

Participants receiving this intervention will be invited to attend the workplace and outpatient drug abuse counseling.

Sponsors

National Institute on Drug Abuse (NIDA)
CollaboratorNIH
Johns Hopkins University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

1. meet the DSM-IV criteria for opioid dependence, 2. report using heroin at least 21 of the last 30 days while living in the community, 3. are unemployed, 4. are 18-65 years old, 5. are medically approved for naltrexone, 6. live in or near Baltimore, MD.

Exclusion criteria

1. have current DSM-IV major Axis I disorders 2. have current suicidal or homicidal ideation 3. express interest in methadone treatment 4. are required to use opioids for medical purposes 5. earned over $200 in taxable income over the previous 30 days while living in the community 6. have physical limitations that prevent them from using a keyboard 7. are pregnant or breastfeeding 8. have serum aminotransferase levels over three times normal 9. have known intolerance and/or hypersensitivity to naltrexone, carboxymethylcellulose, or poly (lactide-co-glycolide) (PLG) or any other components of the diluents; 10. are participating in any other clinical study.

Design outcomes

Primary

MeasureTime frameDescription
Percent of Weekly Urine Samples Negative for Opiates24 weeksWas the participant's urine sample negative for opiates at each of the 24 weekly assessments scheduled after random assignment (Y/N)? The outcome measure was the percentage of weekly urine samples that was negative for opiates.

Secondary

MeasureTime frameDescription
Percent of Weekly Urine Samples Negative for Cocaine24 weeksWas the participant's urine sample negative for cocaine at each of the 24 weekly assessments scheduled after random assignment (Y/N)? The outcome measure was the percentage of weekly urine samples that was negative for cocaine.

Countries

United States

Participant flow

Participants by arm

ArmCount
Vivitrol Only
The VIVITROL group will be offered one injection of VIVITROL every 4 weeks. Participants in the VIVITROL group will be required to take their scheduled injections to work and earn wages. If a participant misses a scheduled VIVITROL injection (more than 3 days from the scheduled date of administration), the participant will not be allowed to work until the injection is accepted. Additionally, missing a scheduled injection will result in a base pay reset from $8 per hour to $1 per hour. After the reset, the participant's base pay will increase by $1/hour to the maximum of $8/hour for every day that the participant works at least 5 minutes. Vivitrol: Participants receiving this intervention will receive the FDA-approved dose, route, and schedule of administration of VIVITROL. The dose of VIVITROL of 380 mg will be delivered intramuscularly every 4 weeks.
25
VIVITROL&Opiate Abstinence Reinforcement
This group will be offered VIVITROL and will be required to take it to attend the workplace and to maintain maximum pay. This group will also receive employment-based opiate abstinence reinforcement. This contingency will require participants to provide opiate-negative urine samples on M,W, and F to maintain their maximum pay. If a participant in this group provides an opiate-positive urine sample, or fails to provide a scheduled sample, their base pay will be reset from $8 per hour to $1 per hour. On each day after the reset that the participant provides a urine sample that meets the opiate abstinence criteria and attends the workplace for at least 5 minutes, their base pay will increase by $1 per hour until it reaches the maximum of $8 per hour.
23
Opiate Abstinence Reinforcement Only
This group would receive employment-based opiate abstinence reinforcement, but this group will not receive VIVITROL. Employment-based opiate abstinence reinforcement: This intervention will require participants to provide opiate-negative urine samples on Monday, Wednesday and Friday to maintain their maximum pay. If a participant provides an opiate-positive urine sample, or fails to provide a scheduled sample, their base pay will be reset from $8 per hour to $1 per hour. On each day after the reset that the participant provides a urine sample that meets the opiate abstinence criteria and attends the workplace for at least 5 minutes, their base pay will increase by $1 per hour until it reaches the maximum of $8 per hour.
18
Usual Care Control
This group will receive neither abstinence reinforcement nor VIVITROL injections, but they will be invited to attend the workplace and outpatient drug abuse counseling. Usual Care Control: Participants receiving this intervention will be invited to attend the workplace and outpatient drug abuse counseling.
18
Total84

Baseline characteristics

CharacteristicVivitrol OnlyTotalUsual Care ControlOpiate Abstinence Reinforcement OnlyVIVITROL&Opiate Abstinence Reinforcement
Age, Continuous43.9 years
STANDARD_DEVIATION 10.3
42.7 years
STANDARD_DEVIATION 10.5
42.2 years
STANDARD_DEVIATION 11.4
41.1 years
STANDARD_DEVIATION 11.1
43.1 years
STANDARD_DEVIATION 10
Race (NIH/OMB)
American Indian or Alaska Native
1 Participants1 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
0 Participants1 Participants0 Participants1 Participants0 Participants
Race (NIH/OMB)
Black or African American
19 Participants68 Participants15 Participants13 Participants21 Participants
Race (NIH/OMB)
More than one race
0 Participants0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
White
5 Participants14 Participants3 Participants4 Participants2 Participants
Region of Enrollment
United States
25 Participants84 Participants18 Participants18 Participants23 Participants
Sex: Female, Male
Female
10 Participants24 Participants3 Participants4 Participants7 Participants
Sex: Female, Male
Male
15 Participants60 Participants15 Participants14 Participants16 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
EG002
affected / at risk
EG003
affected / at risk
deaths
Total, all-cause mortality
0 / 250 / 231 / 180 / 18
other
Total, other adverse events
6 / 253 / 233 / 189 / 18
serious
Total, serious adverse events
2 / 251 / 232 / 184 / 18

Outcome results

Primary

Percent of Weekly Urine Samples Negative for Opiates

Was the participant's urine sample negative for opiates at each of the 24 weekly assessments scheduled after random assignment (Y/N)? The outcome measure was the percentage of weekly urine samples that was negative for opiates.

Time frame: 24 weeks

ArmMeasureValue (MEAN)
Vivitrol OnlyPercent of Weekly Urine Samples Negative for Opiates64.5 percentage of negative urine samples
VIVITROL&Opiate Abstinence ReinforcementPercent of Weekly Urine Samples Negative for Opiates81.3 percentage of negative urine samples
Opiate Abstinence Reinforcement OnlyPercent of Weekly Urine Samples Negative for Opiates71.1 percentage of negative urine samples
Usual Care ControlPercent of Weekly Urine Samples Negative for Opiates66.7 percentage of negative urine samples
p-value: 0.4895% CI: [0.2, 21.6]General Estimating Equation (GEE)
p-value: 0.6195% CI: [0.1, 4.6]General Estimating Equation (GEE)
p-value: 0.1195% CI: [0.7, 54.9]General Estimating Equation (GEE)
p-value: 0.3995% CI: [0.3, 24.9]General Estimating Equation (GEE)
p-value: 0.0395% CI: [1.3, 85.5]General Estimating Equation (GEE)
Secondary

Percent of Weekly Urine Samples Negative for Cocaine

Was the participant's urine sample negative for cocaine at each of the 24 weekly assessments scheduled after random assignment (Y/N)? The outcome measure was the percentage of weekly urine samples that was negative for cocaine.

Time frame: 24 weeks

ArmMeasureValue (MEAN)
Vivitrol OnlyPercent of Weekly Urine Samples Negative for Cocaine60.8 percentage of cocaine negative samples
VIVITROL&Opiate Abstinence ReinforcementPercent of Weekly Urine Samples Negative for Cocaine68.1 percentage of cocaine negative samples
Opiate Abstinence Reinforcement OnlyPercent of Weekly Urine Samples Negative for Cocaine56.3 percentage of cocaine negative samples
Usual Care ControlPercent of Weekly Urine Samples Negative for Cocaine68.3 percentage of cocaine negative samples
p-value: 0.395% CI: [0.1, 2.4]General Estimating Equation (GEE)
p-value: 0.0895% CI: [0.03, 1.2]General Estimating Equation (GEE)
p-value: 0.9195% CI: [0.1, 5.8]General Estimating Equation (GEE)
p-value: 0.3495% CI: [0.4, 15.8]General Estimating Equation (GEE)
p-value: 0.0995% CI: [0.8, 26.1]General Estimating Equation (GEE)

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026