Actively Recruiting
Intervening on Women's Health for Rural Young Cancer Survivors to Improve Reproductive Health Engagement
Led by University of California, San Diego · Updated on 2025-09-04
64
Participants Needed
4
Research Sites
N/A
Total Duration
On this page
Sponsors
U
University of California, San Diego
Lead Sponsor
S
San Diego State University
Collaborating Sponsor
AI-Summary
What this Trial Is About
This research aims to test a multi-part approach to help young female cancer survivors in rural areas better engage with reproductive health care that matches their personal goals. The study focuses on females aged 15 to 50 who have been diagnosed with cancer and are receiving oncology care. The goal is to see if this supportive intervention can improve their involvement in reproductive health decisions and services. The intervention includes a reproductive health needs screening done during oncology visits to understand each patient's desire for children and contraception needs. Patients then have a session with a social worker for personalized education about infertility risks related to cancer and treatment, along with support to pursue care that fits their reproductive goals. Finally, a telehealth consultation with a reproductive specialist lasting about an hour is provided. All eligible patients at participating rural oncology clinics receive this multi-component intervention. Participants will be monitored for their engagement in goal-aligned reproductive health care 12 weeks after the oncology visit. The study will track how well patients follow through with recommended care and support their reproductive health choices. This trial is sponsored by the University of California, San Diego, and participation involves regular oncology visits where the intervention is delivered and assessed over the course of several weeks.
CONDITIONS
Brief Title
Intervening on Women's Health for Rural Young Cancer Survivors
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Female cancer patients diagnosed at any stage (0-IV)
- Primary language is English or Spanish
- Receiving oncology care at a rural clinical site
- Living in Imperial County, California
- Aged between 15 and 50 years
You will not qualify if you...
- Women who are pregnant at recruitment
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person or telehealth)
Duration - Up to 12 weeks
Participants receive a multi-component reproductive health care intervention including a needs screening during oncology visits, a patient navigation session by a social worker, and a telehealth consultation with a reproductive specialist.
1 oncology visit with needs screening, 1 patient navigation session (telehealth or in-person), and 1 telehealth reproductive health consultation
Trial Site Locations
Total: 4 locations
1
San Diego State University - Imperial Valley/ School of Nursing
Brawley, California, United States, 92227
Active, Not Recruiting
2
Cancer Resource Center of the Desert
El Centro, California, United States, 92243
Active, Not Recruiting
3
El Centro Regional Medical Center
El Centro, California, United States, 92243
Actively Recruiting
4
University of Califiornia San Diego
La Jolla, California, United States, 92093
Active, Not Recruiting
Research Team
S
Sally Romero, PhD, MPH
H
H. Irene Su, MD, MSCE
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
1
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