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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01822132
Other study ID # ALKIIT-KOR-034
Secondary ID 1R21DA033182-01A
Status Completed
Phase N/A
First received
Last updated
Start date May 2013
Est. completion date March 2015

Study information

Verified date February 2019
Source Oregon Health and Science University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this protocol is to learn more about impulsive decision making in people who use methamphetamines. The investigators would like to know if a medication called naltrexone changes how people make decisions. The investigators would also like to know whether changes in decision making can be observed by MRI (magnetic resonance imaging).

The research is conducted in Portland, OR.


Recruitment information / eligibility

Status Completed
Enrollment 76
Est. completion date March 2015
Est. primary completion date March 2015
Accepts healthy volunteers No
Gender All
Age group 18 Years to 55 Years
Eligibility Summary Inclusion Criteria:

- Diagnostic and Statistical Manual (DSM)-IV Methamphetamine Dependence

- Deemed healthy enough to participate by study physician

- Age 18-55

- Right handed

- English-speaking

Summary Exclusion Criteria:

- Current opioid use in the last 30 days; opioid abuse or dependence within past 5 years

- Pregnancy

- MRI contraindications (e.g. metal in head).

The research is conducted in Portland, OR.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Extended release naltrexone

Placebo


Locations

Country Name City State
United States Oregon Health & Science University Portland Oregon
United States Portland VA Medical Center Portland Oregon

Sponsors (2)

Lead Sponsor Collaborator
Oregon Health and Science University National Institute on Drug Abuse (NIDA)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Discounting Tasks: Sexual Probability Discounting (SexPD) In the SexPD task, subjects are asked to choose between having sex with a more appealing partner with a varying chance of having a sexually transmitted infection (STI) or a less appealing partner with no STI.
A hyperbolic decay model was used to calculate h, a free parameter that indexes the rate of probabilistic discounting. Smaller h values indicate a preference for probabilistic (i.e., riskier) outcomes. To normalize the data, the natural log of h values were calculated and reported here.
28 days post drug intervention
Primary Discounting Tasks: Standard Delay Discounting (DD) Monetary delay discounting task consisted of choosing between a larger, delayed and a smaller, immediate reward. A hyperbolic decay model was used to calculate k, a free parameter that indexes the rate of delay discounting. As k values are typically skewed across subjects, the distribution of k was normalized by using a natural log transformation. The normalized values are reported here. If k typically ranges between 0.5 and 10^-5, then the natural log of k will range between -0.69 and -11.5. Larger normalized k values indicate a preference for smaller sooner outcomes (i.e., more impulsive decision-making). 28 days post drug intervention
Primary Barrat Impulsiveness Scale (BIS) The Barrat Impulsiveness Scale (BIS) is a 30 item questionnaire to measure a persons impulsiveness. Items are answered on a 4-point scale and scored 1-4 then summed across responses. Total scores range from 30-120 with a higher summed score indicating higher impulsivity. 28 days post drug intervention
Primary Risk Assessment Battery (RAB) The Risk Assessment Battery (RAB) is a 26 question self-administered assessment focusing on drug use, injection and sexual risk during the past 30 days.
Three composite HIV risk scores (drug, sex, and total score) are calculated. The questions have different numbers of items, and scores for a single question can range from 0 to 7, with higher values reflecting more instances of risk behavior. The drug risk score has a range of 0 to 22 and is calculated from 8 questions that address recent substance use, including frequency, needle sharing, and cleaning of the "works." 9 questions are used to calculate a sex risk score that has a range of 0 to 18, and these questions address the frequency and types of sexual behavior, HIV status of sexual partners, and type of protection that was used (if any). Total score is calculated by adding drug and sex scores and dividing by 40, the maximum score possible, and ranges from 0 to 40 where higher scores indicate greater risk behavior.
28 days post drug intervention
Secondary Methamphetamine Use Participants were asked "How many days in the past 30 days did you use methamphetamine?". This is a self-report measure. 28 days post drug intervention
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