RECRUITING

Pre-operative Education Modalities to Decrease Opioid Use

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

This is a triple-armed, randomized, controlled, non-blinded trial to study the effect of preoperative patient education in conjunction with a limited opioid peri-operative analgesia program on post-operative opioid use following radical prostatectomy. Patients will be randomized into three education arms: usual care (variable provider-dependent education), text handout, or text handout and pre-recorded video. The impact of patient education on outcomes of in-hospital, post-discharge, and persistent opioid use will be studied.

Official Title

Evaluation of Pre-operative Education Modalities to Decrease Opioid Use in Prostate Cancer Patients: A Prospective Randomized Control Trial

Quick Facts

Study Start:2021-09-16
Study Completion:2024-05
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04933084

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:MALE
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Age \> 18
  2. * Undergoing RARP at VMMC
  3. * Consent to participate in the study
  1. * Long-term opioid use defined as use of opioids on most days for \>3 months
  2. * History of drug or alcohol dependence
  3. * Concurrent surgery during radical prostatectomy
  4. * History of allergy to opioid analgesics, NSAIDs, acetaminophen or local anesthetics
  5. * Inability or unwillingness to give written informed consent

Contacts and Locations

Study Contact

Eyal Kord, MD
CONTACT
206-223-6772
Eyal.Kord@virginiamason.org

Principal Investigator

Una Lee, MD
PRINCIPAL_INVESTIGATOR
Virginia Mason Medical Center

Study Locations (Sites)

Virginia Mason Medical Center
Seattle, Washington, 98101
United States

Collaborators and Investigators

Sponsor: Benaroya Research Institute

  • Una Lee, MD, PRINCIPAL_INVESTIGATOR, Virginia Mason Medical 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 Date2021-09-16
Study Completion Date2024-05

Study Record Updates

Study Start Date2021-09-16
Study Completion Date2024-05

Terms related to this study

Keywords Provided by Researchers

  • Opioid Education
  • Post-operative Opioid Use

Additional Relevant MeSH Terms

  • Prostatectomy
  • Opioid-Related Disorders