Adherence Monitoring For Substance Abuse Clinical Trials

California Pacific Medical Center Research Institute

Status: Completed

Conditions: Medication Adherence

Treatments: Other: Automated Adherence Monitoring System

Study type: Observational

Funder types: Other; Industry

Identifiers

NCT01867476

2012.075EXP

Details and patient eligibility

About

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.

Enrollment: 8 patients

Sex: All

Ages: 18 to 60 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• 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.

Exclusion criteria

• 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.

Trial design

8 participants in 1 patient group

Healthy Normals

Treatment:

Other: Automated Adherence Monitoring System