Adherence Monitoring For Substance Abuse Clinical Trials

Completed

Conditions studied: Medication Adherence

In brief

The purpose of this study is to determine the feasibility and accuracy of an automated adherence monitoring system, and to compare the variance between urine and oral fluid riboflavin levels when specimens are obtained 'as usual' and after a one-hour inter specimen interval.

Key facts

Study ID

NCT01867476

Run by

California Pacific Medical Center Research Institute

People needed

8

Starts

2013-01-01

Expected to finish

2013-02-01

Last updated by the study team

2013-06-04

Who can join

Age: 18 and older, up to 60. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Male or female, aged 18 to 60
• Ability to give informed consent.
• Be willing and able to use the study-provided phone for taking and transmitting capsule photos.

You may not qualify if…

• Unwilling or unable to use a cell phone.
• Any medical, psychiatric, or other condition that, in the opinion of the investigator, would preclude safe, consistent, or useful participation in the study.

Where it is running

• Addiction & Pharmacology Research Lab, St. Luke's Hospital — San Francisco, California, United States

Full record on ClinicalTrials.gov

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