Cedars Sinai Medical Center
Los Angeles, California, 900048, United States
Location contact
Corina P Hernandez, MSN
CONTACT
Leah Spiro, DNP
PRINCIPAL_INVESTIGATOR
Not Yet Recruiting
NCT Number: NCT07144566
Improving Sexual Health in Gynecological Cancer Patients
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.
Not Yet Recruiting
Trial opening soon.
Get NotifiedKey information
Conditions
Age range
30 year–65 year
Sex eligibility
Female
Study type
Interventional
Phase
Not applicable
Primary location
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
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
Treatment and study plan
Nurse Led Sexual Health Clinical Program Intervention
OtherIn 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.
Other names: Sexual health education, Sexual health treatment plan, Sexual Health Referrals, Sexual health focused pelvic exam
Primary outcomes
-
Effectiveness of the nurse led clinical sexual health dysfunction program
Time frame: 12 weeks
Assess improvement in sexual dysfunction in gynecologic cancer survivors via the Female Sexual Function Index (FSFI).
-
Effectiveness of the nurse led clinical sexual health dysfunction program
Time frame: 12 weeks
Assess effectiveness of the nurse led clinical sexual dysfunction program via number of referrals and treatments in the chart before and after the intervention in gynecologic cancer patients.
Study contacts
Contact information is provided by the study sponsor or research team.
Sponsors and collaborators
Lead sponsor
Cedars-Sinai Medical Center
Other
Registry information
Official study title
Implementation of a Nurse-Led Clinical Program to Decrease Sexual Dysfunction Among Gynecological Cancer Patient
Important dates
- Study start
- 2025
- Primary completion
- 2025
- Study completion
- 2026
- First posted
- Aug 27, 2025
- Registry last updated
- Aug 27, 2025
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Related clinical trials
Published trials that share one or more normalized conditions with this study.
Not Yet Recruiting
Benefits of Early Collaboration Between Oncologists and Palliative Care Physicians in Cases of Unplanned Hospitalization for Patients With Metastatic Cancer
NCT07490106
Cancer, Digestive Cancers
Lille, France
View Trial Details
Not Yet Recruiting
GCCC 2578 Randomized Photon vs Proton RT for Newly Diagnosed Gynecologic Primaries
NCT07415681
Cervical Cancer, Female Urogenital Diseases
Baltimore, Maryland, United States
View Trial Details
Not Yet Recruiting
More Representative Vaginal Temperature Measurements With a Hyperthermia Pelotte During Hyperthermia Treatments for Gynaecological Cancer.
NCT07235540
Body Temperature Changes, Gynaecologic Cancer
Rotterdam, South Holand, Netherlands
View Trial Details
Recruiting
Holistic Acupuncture for Patients With Chemotherapy Induced Nausea
NCT07201194
Breast Cancer, Breast Diseases
Vejle, Denmark
View Trial Details