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Recollection of Event Memory following Drugs, Alcohol, and Stress

Not Applicable
Conditions
memory impairment
Mental Health - Studies of normal psychology, cognitive function and behaviour
Registration Number
ACTRN12624000645550
Lead Sponsor
niversity of Sydney
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot yet recruiting
Sex
All
Target Recruitment
90
Inclusion Criteria

1) Self-reported previous experience with the substance of interest but not current regular use. Regular use is defined as taking amphetamines for non-medical purposes more than once a week.
2) Adequate cognition and English to consent and complete the study. This will be determined by the researcher who administers the phone screening.

Exclusion Criteria

1) Current, clinically significant physical disease (e.g., cardiac, liver). The nurse or doctor associated with the study will make this determination based on an examination of the potential participant.
2) Severe psychiatric illness (i.e., schizophrenia, suicide risk). The nurse or doctor associated with the study will make this determination based on an examination of the potential participant.
3) Current substance use disorder other than nicotine. The nurse or doctor associated with the study will make this determination based on an examination of the potential participant and the diagnostic tools.
4) Previous hypersensitivity/adverse reaction to the studied drugs. We will evaluate this based on the potential participant’s self-report.
5) Current medication use that is a contraindication for the study drug or interferes with drug absorption. The nurse or doctor associated with the study will make this determination based on an examination of the potential participant. Stable antidepressant use for > one month will be permitted.
6) Oral-contraceptive use in females. We will evaluate this based on the potential participant’s self-report.
7) Current pregnancy/lactation. We will evaluate this based on the potential participant’s self-report in the first instance (phone screen) but also via pregnancy testing prior to study session commencement.
8) Women of child-bearing capacity who are not prepared to use (non-pharmacological) contraception during the study. We will evaluate this based on the potential participant’s self-report.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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