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User Acceptability of a Device-Based Opioid Overdose Intervention

NCT04530591 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 97

Last updated 2021-07-07

Study results available
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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.

Conditions

Interventions

OTHER

Survey

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.

OTHER

Interview

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.

Sponsors & Collaborators

Principal Investigators

  • Jacob Brenner, MD/PhD · University of Pennsylvania

Eligibility

Min Age
21 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-08-25
Primary Completion
2020-09-15
Completion
2020-09-15

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04530591 on ClinicalTrials.gov