RECRUITING

AvertD Post-Approval Study

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

A Prospective Post-Approval Study of AvertD to Evaluate Device Performance, Prescribing Impact, and Labeling Comprehension in the Intended Use Population

Official Title

AvertD Post-Approval Study

Quick Facts

Study Start:2024-11-15
Study Completion:2031-11
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT07135323

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:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * ≥18 years of age
  2. * Prior to first opioid prescription
  3. * Being considered for first oral opioid prescription (4-30 days)
  4. * Prescribed AvertD as part of care
  5. * Willing and able to complete yearly assessments for 5 years
  6. * Signed informed consent
  1. * Planned opioid prescription \<4 or \>30 days
  2. * Any condition making participation unsafe or infeasible per investigator judgment

Contacts and Locations

Study Contact

Amanda Smith, MD
CONTACT
800-800-5525
amanda.smith@concentricsresearch.com

Study Locations (Sites)

Concentrics Research
Indianapolis, Indiana, 46240
United States

Collaborators and Investigators

Sponsor: Prescient Medicine Holdings, Inc.

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 Date2024-11-15
Study Completion Date2031-11

Study Record Updates

Study Start Date2024-11-15
Study Completion Date2031-11

Terms related to this study

Additional Relevant MeSH Terms

  • Opioid Use Disorder