NCT06677541 Vibrator Use to Improve Sexual and Pelvic Floor Function Among Urogynecology Patients
| NCT ID | NCT06677541 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Albany Medical College |
| Condition | Pelvic Floor Dysfunction |
| Study Type | INTERVENTIONAL |
| Enrollment | 84 participants |
| Start Date | 2024-11-01 |
| Primary Completion | 2025-11-01 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 84 participants in total. It began in 2024-11-01 with a primary completion date of 2025-11-01.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
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.
Eligibility Criteria
Inclusion Criteria: * • Women aged 18 and over presenting to the urogynecology clinic. * Women diagnosed with one of the following urogynecologic conditions o Pelvic organ prolapse, urgency incontinence, overactive bladder, stress urinary incontinence, fecal incontinence, recovering from a urogynecologic surgery over 6 weeks following surgery and clear for intercourse. Patients post op who continue to have pelvic floor dysfunction can be candidates for the study if they continue to have one of the pelvic floor dysfunctions listed. * Patient will be screened with the FSFI and will be eligible if they score less than 26.55 * Patient's must be willing to use a vibrator. * Able to provide informed consent. * Not currently using a vibrator or has not used a vibrator in the past 3 months. * Able to read and write in English Exclusion Criteria: * • Patients with cognitive impairment. * Patients with refusal or discomfort with vibrator use. * Currently using a vibrator or has used a vibrator in the past 3 months. * Patients unable to provide informed consent. * Patients not clear for intercourse following their surgery * Patients with surgery within 2 months of recruitment.
Contact & Investigator
Frequently Asked Questions
Who can join the NCT06677541 clinical trial?
This trial is open to female participants only, aged 18 Years or older, studying Pelvic Floor Dysfunction. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06677541 currently recruiting?
Yes, NCT06677541 is actively recruiting participants. Contact the research team at robertsbrittanylee@gmail.com for enrollment information.
Where is the NCT06677541 trial being conducted?
This trial is being conducted at Albany, United States.
Who is sponsoring the NCT06677541 clinical trial?
NCT06677541 is sponsored by Albany Medical College. The trial plans to enroll 84 participants.