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Improving Sexual Health in Gynecological Cancer Patients

NCT07144566 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 35

Last updated 2025-08-27

No results posted yet for this study

Summary

The goal of this clinical trial is to test whether a nurse-led program can improve screening and referral rates for sexual dysfunction and improve sexual health care in individuals with gynecological cancer. The main questions it aims to answer are:

Does participation in a nurse-led program improve the treatment of sexual dysfunction in individuals with gynecological cancer?

Does the program increase the frequency of screenings and referrals for sexual dysfunction?

Participants will:

Complete a visit with an advanced practice provider.

Fill out the Female Sexual Function Index survey.

Allow the research team to review medical records.

Conditions

  • Gynaecologic Cancer

Interventions

OTHER

Nurse Led Sexual Health Clinical Program Intervention

In person visit with Advanced Practice Provider (APP) whom is an Advanced Practice Nurse Practitioner in Oncology. Visit will include a focused pelvic exam, sexual health treatment plan, sexual health education, and referrals that follow the current Sexual Health Survivorship NCCN guidelines. A post visit telephone will be provided by the APP 8 weeks after APP visit for follow up questions and further education if needed.

Sponsors & Collaborators

  • Cedars-Sinai Medical Center

    lead OTHER

Principal Investigators

  • Leah Spiro, DNP · Cedars-Sinai Medical Center

Study Design

Allocation
NA
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
30 Years
Max Age
65 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-09-02
Primary Completion
2025-12-31
Completion
2026-04-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07144566 on ClinicalTrials.gov