The ENHANCE Project Toolkit (NCT07649278) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
The ENHANCE Project Toolkit
United States40 participantsStarted 2026-06
Plain-language summary
This study will examine the feasibility, appropriateness, and acceptability of a bundle of smartphone-based tools for lowering overdose risk. 40 participants will be enrolled and can expect to be on study for up to 9 months.
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria (Pilot Participant):
* Be at least 18 years old
* Be able to read and write in English
* Report drug use in the past 30 days, defined as
* Any use of illicit stimulants, opioids, OR
* Use of prescription opioids by a route other than "by mouth/swallowed"
* Additionally report recent drug use of at least twice in the past 7 days
* Have NOT used any of the following harm reduction services in the past 6 months:
* In-person community-based prevention services for people who use drugs
* Overdose crisis hotlines
* Online mail-order prevention supply delivery
* Apps for supporting addiction treatment or recovery
Inclusion Criteria (Peer Mentor Participant):
* Be at least 18 years old
* Be able to read and write in English
* Have served as a member of the existing Community Leadership Team.
Exclusion Criteria:
* Are under the age of 18
* Have impaired decision making capacity at the time of screening
* Do not have the ability to participate in screening and enrollment activities in any one of the following ways:
* Traveling to their nearest participating Vivent Health health center
* Coordinating a visit with the Vivent Health harm reduction mobile unit
* Accessing and completing the online screening survey on a personal wifi/internet enabled device
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.