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NCT03590106 · ClinicalTrials.gov registry record · NA

Cardiac Surgery Peer Recovery Support Program

A NA study, sponsored by University of Rochester.

Completed
Registry status
NA
Development phase
8
Enrollment target

NCT03590106: Completed NA study, sponsored by University of Rochester.

NCT03590106 is a NA study that has completed, run by University of Rochester. The registered enrollment target is 8 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03590106, a NA study, has completed, sponsored by University of Rochester.

COMPLETED
Registry status
NA
Development phase
8 participants
Enrollment target

Study Summary

The purpose of the study is to develop and implement an addiction recovery support program for cardiac surgery patients admitted with a diagnosis of infective endocarditis secondary to IV drug addiction. This is a single center/single unit (7-3600) exploratory study to examine the efficacy of three interventions on a subject's SOCRATES 8D score at time of discharge, at three months, and at six months. A convenience sample of all patients admitted to 7-3600 who meet the inclusion criteria for this study will be approached and provided information related to this study. Once entered into the study, the subjects will continue in the study through their hospitalizations and up to 60 days post hospitalization. This is a quality improvement study designed specifically for the cardiac surgery population. The unit is the primary unit that subjects who are admitted with IE are located. The study's objectives include: By date of discharge, subjects enrolled in the Peer Recovery Support Program will: 1. Actively engage in the program as defined by meeting with a Peer Support Volunteer at least two times prior to discharge, and or use of resilience journal, and or review of NA book. 2. Demonstrate negative drug screens done randomly during their hospitalization. 3. Actively contact at least one outpatient recovery program that they might enroll in prior to discharge (information about recovery programs to be provided by unit SW). 4. Demonstrate appropriate changes in their SOCRATES 8D survey scores from admission to program to post discharge. 5. Participate in follow up phone call with completion of SOCRATES 8D survey at 30 and 60 days post discharge.

Primary Outcome

Personal Drug Use Questionnaire

Interventions

  • BEHAVIORAL Peer Recovery Support Program

Trial Details

FieldValue
Enrollment Target 8 participants
Start Date 2018-09-03
Est. Completion 2019-10-07
Phase NA
University of Rochester

636 total trials

What the finished NCT03590106 record still lists

NCT03590106 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 8 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 1 intervention - of which Peer Recovery Support Program is the first listed.

NCT03590106 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03590106 about?

NCT03590106 is a clinical study titled "Cardiac Surgery Peer Recovery Support Program". The purpose of the study is to develop and implement an addiction recovery support program for cardiac surgery patients admitted with a diagnosis of infective endocarditis secondary to IV drug addiction. This is a single center/single unit (7-3600) exploratory study to examine the efficacy of three...

What is the current status of trial NCT03590106?

This trial is currently completed. It is a NA study. The enrollment target is 8 participants. The study started on 2018-09-03. Estimated completion is 2019-10-07.

What interventions are being tested in trial NCT03590106?

The interventions under investigation include: Peer Recovery Support Program (BEHAVIORAL).

Who is sponsoring clinical trial NCT03590106?

This trial is sponsored by University of Rochester, which has 636 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03590106's enrollment target sits among peer trials

8 1976th of 2000 higher than 19 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03590106, the US trial registry maintained by the National Library of Medicine. NCT03590106 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.