RECRUITING

Vibrator Use to Improve Sexual and Pelvic Floor Function Among Urogynecology Patients

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Limited data exist describing the use and role of vibrators in a urogynecology population and no randomized controlled trials investigating the use of vibrators as a therapeutic tool to enhance sexual and pelvic floor function in urogynecology patients has been conducted. This study aims to evaluate the efficacy of vibrator use in improving sexual and pelvic floor function in urogynecology patients who report sexual dysfunction.

Official Title

Vibrator Use to Improve Sexual and Pelvic Floor Function Among Urogynecology Patients

Quick Facts

Study Start:2024-11-01
Study Completion:2026-01-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06677541

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * • Women aged 18 and over presenting to the urogynecology clinic.
  2. * Women diagnosed with one of the following urogynecologic conditions
  3. * Patient will be screened with the FSFI and will be eligible if they score less than 26.55
  4. * Patient's must be willing to use a vibrator.
  5. * Able to provide informed consent.
  6. * Not currently using a vibrator or has not used a vibrator in the past 3 months.
  7. * Able to read and write in English
  1. * • Patients with cognitive impairment.
  2. * Patients with refusal or discomfort with vibrator use.
  3. * Currently using a vibrator or has used a vibrator in the past 3 months.
  4. * Patients unable to provide informed consent.
  5. * Patients not clear for intercourse following their surgery
  6. * Patients with surgery within 2 months of recruitment.

Contacts and Locations

Study Contact

Brittany Roberts, MD
CONTACT
3057908544
robertsbrittanylee@gmail.com
Erin Deverdis, MD
CONTACT
3152540263
deverde@amc.edu

Study Locations (Sites)

Albany Medical Center
Albany, New York, 12207
United States

Collaborators and Investigators

Sponsor: Albany Medical College

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-11-01
Study Completion Date2026-01-31

Study Record Updates

Study Start Date2024-11-01
Study Completion Date2026-01-31

Terms related to this study

Additional Relevant MeSH Terms

  • Pelvic Floor Dysfunction
  • Sexual Dysfunction Female
  • Vibrator