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Search / Trial NCT06664034

Intervening on Women's Health for Rural Young Cancer Survivors

Launched by UNIVERSITY OF CALIFORNIA, SAN DIEGO · Oct 27, 2024

Trial Information

Current as of June 27, 2025

Recruiting

Keywords

Reproductive Health Oncofertility

ClinConnect Summary

This clinical trial is looking at ways to help young women who have survived cancer better manage their reproductive health. The study aims to see if a special program can help these women connect more with healthcare that aligns with their personal goals regarding fertility and contraception. Researchers believe that this program will encourage young cancer survivors to take a more active role in their reproductive health care.

To be part of this study, women must be between the ages of 18 and 26, have been diagnosed with any stage of cancer, and be receiving treatment in a rural area of California, specifically Imperial County. Participants should speak either English or Spanish. However, women who are pregnant cannot join the study. Those who participate can expect to take part in helpful activities and discussions designed to improve their understanding and management of reproductive health after cancer treatment.

Gender

FEMALE

Eligibility criteria

  • Inclusion Criteria:
  • Cancer (Stages 0-IV) diagnosis
  • Primary language English or Spanish
  • Receiving oncology care at rural oncology clinical participating site
  • Living in Imperial County, California
  • Exclusion Criteria:
  • - Women who are pregnant at recruitment

About University Of California, San Diego

The University of California, San Diego (UCSD) is a leading academic institution renowned for its commitment to advancing healthcare through innovative research and clinical trials. With a robust focus on translational medicine, UCSD leverages its interdisciplinary approach to explore groundbreaking therapies and interventions across a wide range of medical fields. The university's state-of-the-art facilities and collaboration with top-tier faculty and researchers ensure a comprehensive and ethical framework for conducting clinical trials, ultimately aiming to enhance patient outcomes and contribute to the global body of medical knowledge.

Locations

El Centro, California, United States

El Centro, California, United States

Brawley, California, United States

La Jolla, California, United States

Patients applied

0 patients applied

Trial Officials

H. Irene Su, MD, MSCE

Principal Investigator

University of California, San Diego

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported