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Recruiting NCT06296797

Patient-centered Information on Permanent Contraception

Trial Parameters

Condition Contraception
Sponsor University of California, San Francisco
Study Type INTERVENTIONAL
Phase N/A
Enrollment 650
Sex FEMALE
Min Age 21 Years
Max Age 45 Years
Start Date 2024-04-01
Completion 2026-08-01
Interventions
Control arm: Existing educational websiteAdvancing Access Website

Brief Summary

The goal of this study is to understand whether providing information to women with a strong desire to avoid future pregnancy about how tubal sterilization compares to long-acting reversible contraceptives improves perceived access to available contraceptives. Participants will: * Complete a baseline survey * Receive access to web-based educational resources * Complete a brief follow up survey immediately after exploring these web-based resources * Complete a follow-up survey 3 months after enrolling The investigators will compare outcomes among participants provided with access to a new website (intervention) summarizing recent patient-centered outcomes research (PCOR) comparing interval laparoscopic tubal sterilization and long-acting reversible contraception (LARC) to control participants provided with access to the existing Planned Parenthood website on tubal sterilization.

Eligibility Criteria

Inclusion Criteria: * Self-reported fertility * Have a strong desire to avoid future pregnancy * Speak English or Spanish Exclusion Criteria: * Current pregnancy * The inability to speak English or Spanish * Prior tubal sterilization or "Essure" procedure * Menopause * Infertility * Hysterectomy

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