RECRUITING

Shared Decision for Drug Interactions in Oral Anticoagulation

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 this project is to implement and evaluate a shared-decision making (SDM) tool called DDInteract that was developed to support decision making for drug-drugs interactions while on oral anticoagulants. DDInteract will be implemented in clinics at the University of Utah, University of Colorado and University of Vanderbilt. DDInteract will be launched from within the electronic health record (EHR) retrieving patient-specific risk factors, will calculate the risk of harm, and will allow providers and patients to dynamically explore "what if" scenarios to optimize treatment and minimize risk. DDInteract will enable shared-decision making using individually-tailored information on the potential benefits and harms of drug interactions in anticoagulated patients.

Official Title

Implementation of DDInteract A Shared-decision Making Tool for Anticoagulant Drug-Drug INTERACTions (DDinteract)

Quick Facts

Study Start:2023-10-01
Study Completion:2026-07-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06401863

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:21 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Be at least 21 years of age or older
  2. * Receive more than one prescription of an oral anticoagulant (i.e. warfarin, apixaban, edoxaban, dabigatran, rivaroxaban)
  1. * Individuals not able to speak English or Spanish

Contacts and Locations

Study Contact

Daniel C Malone, PhD
CONTACT
801 581 8054
dan.malone@utah.edu
Ainhoa Gomez Lumbreras, MD, PhD
CONTACT
8015853201
Ainhoa.Gomez-Lumbreras@pharm.utah.edu

Principal Investigator

Daniel C Malone, PhD
PRINCIPAL_INVESTIGATOR
College of Pharmacy. University of Utah

Study Locations (Sites)

University of Colorado. School of Medicine
Denver, Colorado, 80045
United States
Vanderbilt University
Nashville, Tennessee, 37235
United States
University of Utah
Salt Lake City, Utah, 84112
United States

Collaborators and Investigators

Sponsor: University of Utah

  • Daniel C Malone, PhD, PRINCIPAL_INVESTIGATOR, College of Pharmacy. University of Utah

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 Date2023-10-01
Study Completion Date2026-07-31

Study Record Updates

Study Start Date2023-10-01
Study Completion Date2026-07-31

Terms related to this study

Keywords Provided by Researchers

  • Oral anticoagulants
  • Drug interactions
  • Gastrointestinal hemorrhage
  • Shared Decision Making

Additional Relevant MeSH Terms

  • Anticoagulants
  • Drug Interactions