Improving Sexual Health in Gynecological Cancer Patients

Implementation of a Nurse-Led Clinical Program to Decrease Sexual Dysfunction Among Gynecological Cancer Patient

Status

Not yet recruiting

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT07144566

Enrollment

Registered

2025-08-27

Start date

2025-09-02

Completion date

2026-04-30

Last updated

2025-08-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gynaecologic Cancer

Keywords

Survivorship, Sexual Health, Sexual Dysfunction, Gynecologic Cancer

Brief 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.

Interventions

OTHERNurse 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.

Study design

Allocation

Intervention model

SINGLE_GROUP

Primary purpose

SUPPORTIVE_CARE

Masking

NONE

Eligibility

Sex/Gender

FEMALE

Age

30 Years to 65 Years

Healthy volunteers

Inclusion criteria

Inclusion: * Patients with a gynecologic cancer history * Patients ages 30-65 years old * Patients must have completed cancer treatment within the past 12 months * Patients may be on maintenance therapy Exclusion: * Any records flagged break the glass or research opt-out. * Patients with severe psychiatric disorders that would impair consent or participation * Patients with neurological disorders affecting sexual function * Patients with a history of sexual violence or sexual assault

Design outcomes

Primary

Measure	Time frame	Description
Effectiveness of the nurse led clinical sexual health dysfunction program	12 weeks	Assess improvement in sexual dysfunction in gynecologic cancer survivors via the Female Sexual Function Index (FSFI).

Countries

United States

Contacts

Primary ContactCorina P Hernandez, MSN

corina.hernandez@cshs.org310-423-6074

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026