User Acceptability of a Device-Based Opioid Overdose Intervention

Status Completed

Clinical Trial Summary

This pilot study evaluates the needs of opioid users for a device-based intervention for opioid overdoses. The results of this one-time short questionnaire will inform development of a novel naloxone delivery device.

Clinical Trial Description

All opioid overdose related deaths can be prevented with the timely delivery of Naloxone. This study is a one-time, preliminary survey of participants with opioid use disorder to assess the need for, and community attitudes towards, a wearable device capable of autonomously detecting and responding to an opioid overdose. The results of this survey will be used to guide ongoing development of a de novo device. This study will be conducted over a 3 month period and survey participants from the Kensington Neighborhood in North Philadelphia. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04530591
Study type	Observational
Source	University of Pennsylvania
Contact
Status	Completed
Phase
Start date	August 25, 2020
Completion date	September 15, 2020

View Details

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