RECRUITING

IV Ensure in Patients Receiving OPAT

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The purpose of remote therapeutic monitoring is to provide oversight and evaluation of patients receiving IV medications in the home setting post-acute. The goal is to improve patient outcomes and decrease re-admission rates for related diagnoses due to poor adherence. Remote therapeutic monitoring provides data used in the determination of dates, times, and duration of doses administered in the home setting to support real-time intervention by dedicated care managers to support improved adherence with prescribed dosing regiments. The objectives of the study are to: 1. Determine adherence rates for IV medications administered in the home. 2. Assess re-admission against adherence rates.

Official Title

IV Ensure in Patients Receiving OPAT

Quick Facts

Study Start:2023-08-23
Study Completion:2024-11
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06623318

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Adult patients enrolled in OPAT (IV antibiotic therapy) discharged to the home setting will be included in the study.
  1. * Patients enrolled in OPAT (IV antibiotic therapy) discharged to nursing homes, SNF (Skilled Nursing Facility), and pediatric patients will be excluded from the study.

Contacts and Locations

Study Contact

Mitchell T Berenson, MPH
CONTACT
214-924-6951
mitchell@ivensure.com
Jacob K Dozier, BGS
CONTACT
903-244-4842
jacob.dozier@ivensure.com

Principal Investigator

Joseph Sassine, MD, FACP
PRINCIPAL_INVESTIGATOR
The University of Oklahoma Health Sciences Center

Study Locations (Sites)

The University of Oklahoma Health Sciences Center
Oklahoma City, Oklahoma, 73104
United States

Collaborators and Investigators

Sponsor: IV Ensure

  • Joseph Sassine, MD, FACP, PRINCIPAL_INVESTIGATOR, The University of Oklahoma Health Sciences Center

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-08-23
Study Completion Date2024-11

Study Record Updates

Study Start Date2023-08-23
Study Completion Date2024-11

Terms related to this study

Keywords Provided by Researchers

  • OPAT
  • IV antibiotic
  • Adherence
  • home infusion
  • readmission

Additional Relevant MeSH Terms

  • Determine If Adherence Rates with IV Antibiotics in OPAT Have a Correlation to Hospital Readmission Rates