RECRUITING

PRISM Race and Communication Pilot RCT

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 pilot randomized trial of 60 patients to test feasibility, acceptability and efficacy of PRISM to improve resilience and facilitate improved patient-clinician communication in racially minorities patients with serious illness.

Official Title

Racial Inequities in End-of-life Healthcare: How Perceived Discrimination Affects Communication and Decision-making During Serious Illness

Quick Facts

Study Start:2023-07-19
Study Completion:2024-07
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04915079

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. * Seriously ill adults with median life expectancy of two years or less (e.g. metastatic cancer or inoperable lung cancer, chronic obstructive pulmonary disease (COPD) with forced expiratory volume in 1 second (FEV1) \<35% predicted or oxygen dependence, restrictive lung disease with total lung capacity (TLC) \<50% predicted, New York Heart Association (NYHA) class III or IV heart failure, or Child's class C cirrhosis or Model for End Stage Liver Disease(MELD) \>17)
  2. * Hospitalized at either Harborview Medical Center or University of Washington Medical Center-Montlake
  3. * At least 18 years of age
  4. * English-speaking
  5. * No cognitive impairment precluding completion of surveys or participation in the PRISM sessions
  1. * Younger than 18 years of age
  2. * Non-English speaking
  3. * Ccgnitive impairment that would preclude completion of surveys and participation in the PRISM sessions.

Contacts and Locations

Study Contact

Crystal E Brown, MD MA
CONTACT
206-744-5018
crysb@uw.edu

Principal Investigator

Crystal E Brown, MD, MA
PRINCIPAL_INVESTIGATOR
University of Washington

Study Locations (Sites)

University of Washington - Harborview Medical Center
Seattle, Washington, 98112
United States

Collaborators and Investigators

Sponsor: University of Washington

  • Crystal E Brown, MD, MA, PRINCIPAL_INVESTIGATOR, University of Washington

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 Date2023-07-19
Study Completion Date2024-07

Study Record Updates

Study Start Date2023-07-19
Study Completion Date2024-07

Terms related to this study

Additional Relevant MeSH Terms

  • Discrimination, Racial
  • Communication
  • Chronic Illness
  • Bias, Racial