Scripted Sexual Health Informational Intervention in Improving Sexual Function in Patients With Gynecologic Cancer

Completed · Not applicable

Conditions studied: Anxiety Disorder, Cervical Cancer, Endometrial Cancer, Female Reproductive Cancer, Gestational Trophoblastic Tumor, Ovarian Epithelial Cancer, Ovarian Germ Cell Tumor, Sexual Dysfunction, Uterine Sarcoma, Vaginal Cancer, Vulvar Cancer

In brief

This randomized pilot clinical trial studies the feasibility of a pre-operative and/or post-operative scripted sexual health informational intervention and how well it works in improving sexual function in patients with gynecologic cancer. Discussing sexual outcomes and counseling options with patients may help improve sexual outcomes and/or anxiety after primary gynecologic cancer treatment.

Key facts

Study ID

NCT02096783

Run by

University of Wisconsin, Madison

People needed

15

Starts

2014-09-01

Expected to finish

2016-06-01

Last updated by the study team

2019-11-18

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Patients with a new suspected or confirmed gynecologic malignancies
• Patients plan to have primary surgery at either the University of Chicago Hospital or the University of Wisconsin Hospital
• Patients must be English speaking

You may not qualify if…

• Previous treatment of any cancer excluding skin cancer
• Patients with a suspected benign gynecologic process
• Patients who are prisoners or incarcerated

Where it is running

• University of Wisconsin, Madison — Madison, Wisconsin, United States

Full record on ClinicalTrials.gov

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