Feasibility of Addressing Sexual Dysfunction in Women with Breast and Gynecologic Cancers with a Novel Mobile Application

The University of Texas System (UT)

Status: Not yet enrolling

Conditions: Sexual Dysfunction

Treatments: Behavioral: Rosy app

Study type: Interventional

Funder types: Other

Identifiers

NCT06694142

HSC-MS-24-0817

Details and patient eligibility

About

The purpose of this study is to identify breast and gynecologic cancer patients with sexual dysfunction, to measure sexual dysfunction with the Female Sexual Function Index (FSFI) and to provide Patients with the opportunity during this six-month period to follow up with a healthcare provider to discuss the sexual dysfunction needs and to see if a medical intervention can be of aid.

Enrollment: 20 estimated patients

Sex: Female

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patient with a current or historic diagnosis of breast cancer or gynecologic cancer (uterine ovarian, fallopian tube, peritoneal, cervical, vulva, or vaginal cancers)
• Agree to participate in the study with completion of survey and use of ROSY mobile application

Exclusion criteria

• Currently pregnant
• Non-English speaking (ROSY is currently is only available is in English).

Trial design

Primary purpose: Supportive Care

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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20 participants in 1 patient group

Rosy app

Experimental group

Treatment:

Behavioral: Rosy app