Intervening on Women's Health for Rural Young Cancer Survivors
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Multi-component reproductive health care intervention.
- Who it may be relevant to
- Registry conditions: Cancer, Fertility Issues, Contraception. Basic parameters: 15 years — 50 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
The purpose of this pilot study is to evaluate the feasibility of a multi-component intervention to improve young female cancer survivors' engagement in goal-concordant reproductive health care. The investigators hypothesize that implementation of the intervention will result in increased young cancer survivors' engagement in goal-concordant reproductive health care.
Interventions
- Behavioral Multi-component reproductive health care intervention
The multi-component reproductive health care intervention includes: 1. Young cancer patients presenting to oncology visits will complete a clinic-based reproductive health needs screen with a member of the clinical team. This needs screen assesses i) desire to have a child in the future and ii) need for contraception. 2. Reproductive health patient navigation consists of one telehealth or in-person session with a social worker to: i) assess the patient's reproductive health needs, ii) provide i
Primary outcome measures
- Proportion of patient's engagement in goal-concordant reproductive health care [Time frame: 12 weeks after oncology visit]
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
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Supportive care
Study locations
United States · 4 centers
- San Diego State University - Imperial Valley/ School of Nursing — Brawley
- Cancer Resource Center of the Desert — El Centro
- El Centro Regional Medical Center — El Centro
- University of Califiornia San Diego — La Jolla
Identifiers
NCT: NCT06664034 · U54800646 · 5U54CA285115-02