RECRUITING

Breast Cancer Patient Engagement With Patient Reported Outcome Measure Survey

Conditions

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 research protocol is to measure Patient Reported Outcome Measures (PROMs) in breast cancer patients. PROM results will be provided to patients and providers and the investigators will evaluate the relationship between patient engagement with PROM results and patient and clinicopathologic variables, utilization of supportive and hospital services, and patient satisfaction with patient-provider communication.

Official Title

A Randomized Study of Breast Cancer Patient Engagement With Patient Reported Outcome Measure Survey Results

Quick Facts

Study Start:2019-10-30
Study Completion:2026-06
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT03995082

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:Not specified
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:No
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. Age 18 years or older
  2. Willing and able to provide informed consent
  3. Able to understand and follow study procedures
  4. Stable medical condition
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Contact

Sarah Tevis
CONTACT
3037242731
sarah.tevis@ucdenver.edu

Principal Investigator

Sarah Tevis
PRINCIPAL_INVESTIGATOR
University of Colorado, Denver

Study Locations (Sites)

University of Colorado Hospital
Denver, Colorado, 80045
United States
Cherry Creek Medical Center
Denver, Colorado, 80206
United States
Lone Tree Medical Center
Lone Tree, Colorado, 80124
United States

Collaborators and Investigators

Sponsor: University of Colorado, Denver

  • Sarah Tevis, PRINCIPAL_INVESTIGATOR, University of Colorado, Denver

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 Date2019-10-30
Study Completion Date2026-06

Study Record Updates

Study Start Date2019-10-30
Study Completion Date2026-06

Terms related to this study

Additional Relevant MeSH Terms

  • Breast Cancer