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Potency and Precision Investigation — PAPI  

Depression, Anxiety Clinical Trial

Official title:
An Exploratory Open-Label Potency and Precision Investigation of a Relational Agent Intervention

Clinical Trial Summary

The overarching goal of this study is to establish initial proof of mechanism for precision interventions in an adult population.

Clinical Trial Description

This exploratory single-arm trial will provide initial learning on the current implementation of precision interventions and generate data and hypotheses to inform the exploration of future interventions by identifying mechanisms and moments in the user journey to target. The DISC-MA app uses a relational agent (Woebot) to engage users in conversations. Eligible participants will be assigned to use DISC-MA, in which Woebot selects from a list of responses based on natural language processing. Participants will receive instructions on downloading and using the DISC-MA app in order to access the intervention. Participants will use the app as instructed and will complete assessments for the primary endpoint as Week 4 (EOT) with additional measures being collected as Baseline, Week 1, and Week 2. Results from this study will provide data on baseline participant clinical and psychological characteristics and their engagement with DISC-MA, and associations between the two. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06240091
Study type Interventional
Source Woebot Health
Contact
Status Completed
Phase N/A
Start date March 13, 2024
Completion date May 9, 2024
View Details
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