UnityPhilly Response App for Overdose Reversal

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorDrexel University

About this trial

The goal of this clinical trial is to discover if an overdose prevention app (UnityPhilly) can encourage citizen responders to respond and prevent opioid overdoses using the UnityPhilly app. The main hypotheses to answer are:

Hypothesis 1: UnityPhilly signal rates relative to EMS calls will increase over time. The primary outcome will be assessed as the total number of overdoses signaled by participants relative to all overdose-related EMS calls, per year.

Hypothesis 2: The number of cases where a nearby UnityPhilly participant successfully reverses an overdose with naloxone will increase over time. The primary outcome will be assessed as the number of successful reversals relative to the total number of responder arrivals, per year.

Participants will be supplied with the UnityPhilly app, training on how to use the app and respond to an opioid overdose using naloxone, and respond to follow up surveys about their experiences.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

owning a smartphone with a data package;

living or working in one of three identified Philadelphia neighborhoods;

aged 18 or older.

Disqualifiers

persons aged under 18 years of age

Trial design

Design model

Single group

Treatments tested in this trial

  • UnityPhilly app

    Other intervention

    UnityPhilly automatically connects bystanders and victims of opioid overdose with nearby community members who can respond immediately with naloxone.

Treatment groups

450 Participants
are divided into 5 treatment groups
Group A: Active non-medical opioid userOther 1 intervention
Group B: Active prescription medical opioid userOther 1 intervention
Group C: Person in recovery from opioid misuseOther 1 intervention
Group D: Caregiver/family members of groups 1, 2, 3Other 1 intervention
Group E: Concerned community memberOther 1 intervention

Trial outcomes

Primary outcomes

1

Rate of Overdoses Signaled

\# events signaled by participants vs. # all overdose-related EMS calls, per year

Time frame
2 year period
2

Rate of Overdoses Reversed

\# successful opioid reversals vs. # all arrivals, per year

Time frame
2 year period

Secondary outcomes

Other outcomes

Sponsors and contacts

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Drexel University

Lead sponsor

University of Michigan

Collaborator