RECRUITING

Patient Priorities for Survivorship Care in Older Breast Cancer Survivors

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 objective of this study is to adapt the Patient Priorities Care (PPC) framework to breast cancer survivorship via a user-centered approach, through an iterative process in which patients and their physicians help to refine and modify the intervention. A second objective is to evaluate the feasibility and effectiveness of the adapted PPC framework in breast cancer survivorship for older adults.

Official Title

Patient Priorities for Survivorship Care in Older Breast Cancer Survivors

Quick Facts

Study Start:2025-01-02
Study Completion:2027-06-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06478589

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:65 Years to 100 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:No
Standard Ages:OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * able to write and speak English
  2. * Stage DCIS/I/II/III breast cancer diagnosis
  3. * 3 months from active cancer therapy (including first or second-line treatment chemotherapy, radiation and/or surgery, or multimodal treatment) up to 10 years since completing treatment
  4. * ≥3 documented comorbidities by chart review, or taking ≥10 medications, have ≥ 1 hospitalization over the past year, ≥ 2 emergency department visits over the past year, seen by \> 2 specialists over the past year
  5. * able to provide consent
  1. * currently on active cancer therapy (including first or second-line treatment chemotherapy, radiation and/or surgery, or multimodal treatment)

Contacts and Locations

Study Contact

Dana E. Giza, MD
CONTACT
(713) 500-6087
Dana.E.Giza@uth.tmc.edu

Principal Investigator

Dana E. Giza, MD
PRINCIPAL_INVESTIGATOR
The University of Texas Health Science Center, Houston

Study Locations (Sites)

UT Physicians Center for Healthy Aging Bellaire
Bellaire, Texas, 77401
United States
UT Physicians Family Medicine Bayshore
Houston, Texas, 77006
United States
Memorial Hermann Cancer Center
Houston, Texas, 77030
United States

Collaborators and Investigators

Sponsor: The University of Texas Health Science Center, Houston

  • Dana E. Giza, MD, PRINCIPAL_INVESTIGATOR, The University of Texas Health Science Center, Houston

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 Date2025-01-02
Study Completion Date2027-06-01

Study Record Updates

Study Start Date2025-01-02
Study Completion Date2027-06-01

Terms related to this study

Keywords Provided by Researchers

  • Patient priorities
  • Survivorship Care

Additional Relevant MeSH Terms

  • Breast Cancer Survivorship