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Clinical Trials/NCT05414812
NCT05414812
Completed
Not Applicable

Intervening on Women's Health for Rural Young Breast Cancer Survivors

University of California, San Diego4 sites in 1 country81 target enrollmentOctober 15, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Breast Cancer
Sponsor
University of California, San Diego
Enrollment
81
Locations
4
Primary Endpoint
Medical record review of engagement in goal-concordant oncofertility care
Status
Completed
Last Updated
last year

Overview

Brief Summary

The purpose of this study is to evaluate the effectiveness of a multi-component intervention to improve young breast cancer survivors' engagement in goal-concordant oncofertility care, concurrently with observing and gathering information on how the intervention is implemented. The investigators hypothesize that implementation of the intervention will result in increased young breast cancer survivors' engagement in goal-concordant oncofertility care.

Registry
clinicaltrials.gov
Start Date
October 15, 2021
End Date
April 30, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Sequential
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Hui-Chun Irene Su

Professor

University of California, San Diego

Eligibility Criteria

Inclusion Criteria

  • Breast cancer (Stages 0-IV) diagnosis
  • Primary language English or Spanish
  • Receiving oncology care at participating clinical sites
  • Living in Imperial County, California

Exclusion Criteria

  • Women who are pregnant at recruitment

Outcomes

Primary Outcomes

Medical record review of engagement in goal-concordant oncofertility care

Time Frame: 12 weeks after oncology visit

Study staff will be trained to abstract the primary outcome of engagement in goal-concordant oncofertility care from the patient's medical records using standardized case report forms. Engagement in goal-concordant oncofertility care will be assigned to young breast cancer survivors who undergo: 1) oncofertility needs screen, complete a navigation session, receive the women's health survivorship care plan (SCP), and thereafter have no oncofertility needs; OR 2) oncofertility needs screen, complete a navigation session, receive the SCP, have an oncofertility need, undergo telehealth oncofertility consultation, and thereafter have no oncofertility services needs; OR 3) oncofertility needs screen, complete a navigation session, receive the SCP, have an oncofertility need, undergo telehealth oncofertility consultation, have an oncofertility services need, and thereafter uptake appropriate services.

Study Sites (4)

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