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Vibrator Use for Sexual and Pelvic Floor Function in Urogynecology Patients

This study is looking at whether using a vibrator can help improve sexual and pelvic floor function in women who have certain urogynecological conditions and are experiencing sexual difficulties. You would receive an instructional handout and an FDA-approved vibrator device. The researchers want to see if these interventions can improve your sexual function, which will be measured using a tool called the Female Sexual Function Index. This study plans to include 84 women aged 18 and older who are patients in a urogynecology clinic and have conditions like pelvic organ prolapse or incontinence. The current recruitment status is unclear.

Study design
This is an interventional study, meaning participants will receive a specific intervention. It plans to enroll 84 participants.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Your sexual function will be measured for up to 12 weeks.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT06677541

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

Recruiting
NAAges 18+InterventionalTreatment
Albany Medical College
~84 participants
Updated 2025-01-15 on ClinicalTrials.gov
What's tested:Instructional handoutVibrator

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Female Sexual Function Index
Measured over up to 12 weeks

Conditions

Pelvic Floor Dysfunction
Sexual Dysfunction Female
Vibrator

Explore related trials

Fecal IncontinenceGenuine stress incontinenceIdiopathic fecal incontinenceOveractive BladderPelvic Organ Prolapse

Where it's being run

1 sites across 1 states
New York1

Who to contact

Brittany Roberts, MD
[email protected]
3057908544
Email the study team

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Do you actually qualify for this trial?

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Eligibility criteria

Inclusion

• Women aged 18 and over presenting to the urogynecology clinic.
Women diagnosed with one of the following urogynecologic conditions
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

• 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.

What this trial measures

  • Female Sexual Function Indexup to 12 weeks

    A 19 question validated survey on sexual function with lower scores indicating worse outcome