At a glance

ClinicalIndex Comparison Record

N/ACompleted· 97 enrolled

Drug / intervention

Survey +1 moreother

Likely dose

Not stated in record

Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04530591

NCT04530591N/ACompleted

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A Proof of Concept, Randomized, Single Center Study on Frameworks for Wearable Devices to Sense and Respond to Opioid Overdoses

University of Pennsylvania·observational·Posted Aug 28, 2020·Updated Jul 7, 2021

In Brief

An observational study evaluating Survey and Interview for Opioid Overdose and 2 related conditions. Completed, enrolled 97 participants across 1 site.

Detailed 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.

Study Details

Study Typeobservational

Allocation--

Masking--

Primary Purpose--

ConditionsOpioid Overdose, Opioid-use Disorder, Substance Use Disorders

CountriesUnited States

Collaborators--

Timeline

N/ACompletedFinished

202120222023202420252026

Enrollment StartAug 2020

First PostedAug 2020

Primary CompletionSep 2020

TodayJul 2026

First PostedAug 28, 2020

Enrollment StartAug 25, 2020

Primary CompletionSep 15, 2020

TodayJul 2, 2026

Enrollment to primary: 20 daysPosted 5.8 years ago

Interventions

Surveyother

Participants will complete a survey about their opioid use history, its impact on their lives, their current strategies for preventing or reversing opioid overdoses, and their preferences for a device-based intervention.

Interviewother

Participants will participate in a semi-structured interview, during which they will provide feedback on non-functional, "looks-like" prototypes of a naloxone delivery device.