N/A
N=130
Measuring and Monitoring Adherence to ART With Pill Ingestible Sensor System
HIV/AIDS · Medication Adherence
Bottom Line
View on ClinicalTrials.gov: NCT02797262 ↗Enrolled (actual)
130
Serious AEs
0.0%
Results posted
Dec 2021
Primary outcome: Primary: Adherence Measured by Sensor by Percentage of Prescribed Medications Taken — 87.5 percentage of prescribed medication
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Proteus digital health feedback (PDHF) system (Device)
- Age
- Pediatric, Adult, Older Adult · 17+ yrs
- Sex
- All
- Sponsor
- University of California, Los Angeles
- Primary completion
- Oct 2020
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Adherence Measured by Sensor by Percentage of Prescribed Medications Taken |
87.5 | — |
| PRIMARY Pharmacokinetic Adherence by Integrated Pharmacokinetic Adherence Score |
0.817; 0.798 | 0.57 |
| PRIMARY Self-Reported Medication Adherence and "Change" Over Time |
90.7; 87.4; 91.1; 87.4; 90.6; 91.6 | — |
| SECONDARY Viral Load |
2.273; 2.061; 1.916; 1.906; 1.851; 1.916 | 0.08 |
| SECONDARY Cluster of Differentiation 4 (CD4) |
526.17; 542.78; 531.02; 553.08; 522.00; 582.25 | — |
Summary
Introduction of antiretroviral therapy (ART) has transformed HIV-infection from a fatal to manageable disease but adherence to ART remains critical to optimize outcomes. Existing measures of ART adherence provide only inferred measures of actual drug intake and most offer no real-time notification capability. Directly observed therapy measures actual drug intake but is not practical. These limitations constrain research into medication adherence and more importantly, limit our ability to develop real-time interventions based on feasible, in vivo monitoring of adherence among HIV-infected people to facilitate medication-taking. The Proteus digital health feedback (PDHF) system, a pill ingestible sensor based adherence measuring and monitoring system developed by Proteus Digital Health, addresses these limitations. It involves use of an ingestible sensor, a tiny edible material that is over-encapsulated along with prescribed medication. The sensor is activated by ingestion and is sensed by a patch worn by the patient with an embedded monitor and sensor. The monitor sends a Bluetooth signal to a mobile device, which in turn sends an encrypted message to a central server, thus effecting real-time monitoring that a dose has been taken. The investigators propose to develop a data receiving hub and add to these components an automated text message that is sent to the patient when a dose is missed. The investigators will evaluate the feasibility, acceptability and sustainability of using the PDHF system; assess the accuracy of the PDHF system in measuring adherence to ART; and evaluate the efficacy of the PDHF system for monitoring and leveraging adherence to ART.
Eligibility Criteria
Inclusion Criteria
- HIV-infected individuals in HIV care
- greater than 17 years of age
- demonstrated ability to take over-encapsulated ARVs at time of screening; able to provide informed consent
- On ART with sub-optimal adherence estimated by either patient (self-reports < 90% adherence over last 28 days) or treating clinician (e.g., based on gaps in treatment (e.g., missed appointments) or viral load elevations within last 6 months)
Exclusion Criteria
- Inability to follow the study procedures manifested during the intake, as evidenced by mental confusion, disorganization, intoxication, withdrawal, risky or threatening behavior
Data sourced from ClinicalTrials.gov (NCT02797262). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.