Evaluation of a new alcohol monitoring device
Lay Description
We will examine the accuracy, precision, and reproducibility of the ION, a non-invasive and wearable wristband-style alcohol monitoring device by performing in-situ, on-human-skin, compared to (1) SCRAM transdermal ankle monitors and (2) BAC measurements inside the laboratory.
Category
- Substance Abuse
- IRB Number
- 20190490HU
- NCT Number
- ct.gov registration not required
- Open to Enrollment
- Yes
Eligibility
- Eligible Ages
- 21-55
- Eligible Genders
- Both
- Accepts Healthy Volunteers
Inclusion Criteria
a) are 21 to 55 years old;
(b) consumed 5 or more alcohol on at least one day in past month
(c) demonstrate understanding of consent procedures and instructions.
Exclusion Criteria
(a) presence of DSM-5 psychiatric disorder (including alcohol or other substance dependence);
(b) self-reported psychoactive medication use (last 3 months);
(c) pregnancy or lactation;
(d) a positive urine-drug test for metabolites of drugs of abuse (i.e., cocaine, amphetamines, methamphetamines, MDMA, opiates, or benzodiazepines);
(e) respondents who show evidence of alcohol withdrawal (Clinical Institute Withdrawal Assessment for Alcohol scores > 10).
Study Design
Arm Groups
Study Contact
Regulatory Point of Contact
Donald Dougherty
(210) 567-2726
doughertyd@uthscsa.edu
Regulatory Point of Contact
Nathalie Hill-Kapturczak
(210) 567-2725
hillkapturcz@uthscsa.edu
Regulatory Point of Contact
Tae Moon
(210) 567-2711
moontj@uthscsa.edu
Regulatory Point of Contact
Tara Wright
+1 (210) 450-3903
wrightt3@uthscsa.edu
Local Recruitment Point of Contact
Nathalie Hill-Kapturczak
(210) 567-2725
hillkapturcz@uthscsa.edu
Principal Investigator
Tae Moon