This study seeks to develop and test a novel digital pill system (DPS) that measures real-time medication ingestion and pairs it with a cognitive behavioral therapy (CBT)-based intervention to provide personalized, data-driven adherence support, with the long-term goal of providing new and improved personalized support and increase medication adherence for people with AUD and ALD.
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Ability to enroll participants- Feasibility
Timeframe: Baseline and 30 days
Retention- Feasibility
Timeframe: Baseline and 30 days
Feasibility of Intervention Measure (FIM)- Feasibility
Timeframe: Baseline and 30 days
Acceptability of Intervention (AIM)- Acceptability
Timeframe: Baseline and 30 days
Mean score Post-Study System Usability Questionnaire (PSSUQ)- Acceptability
Timeframe: Baseline and 30 days
Mean score Health Information Technology Usability Evaluation Scale (Health-ITUES) - Acceptability
Timeframe: Baseline and 30 days
Mean System Usability Scale (SUS) score- Usability
Timeframe: Baseline and 30 days