Improving Sexual Health in Gynecological Cancer Patients
ConditionGynaecologic Cancer
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age30-65
SponsorCedars-Sinai Medical Center
About this trial
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.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
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
Disqualifiers
None
Trial design
Design model
Single group
Treatments tested in this trial
Nurse Led Sexual Health Clinical Program Intervention
Other interventionIn 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.
Treatment groups
35 Participants
are divided into 1 treatment groupGroup A: Nurse Led Sexual Health InterventionExperimental treatment 1 intervention
Trial outcomes
Primary outcomes
1
Effectiveness of the nurse led clinical sexual health dysfunction program
Assess improvement in sexual dysfunction in gynecologic cancer survivors via the Female Sexual Function Index (FSFI).
Time frame
12 weeks2
Effectiveness of the nurse led clinical sexual health dysfunction program
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.
Time frame
12 weeksSponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov
This trial is not recruiting at the moment. You can still explore other options: