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Patient-centered Information on Permanent Contraception
Disseminating PCOR Findings to Reduce Racial Disparities in Surgical Sterilization
Who can join
Ages 21 to 45 · Women · Healthy volunteers welcome
Full 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
About the study
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.
What is being tested
- Control arm: Existing educational website (behavioral)
- Advancing Access Website (behavioral)
Sponsor: University of California, San Francisco · Participants: 650 · Started: Apr 1, 2024
Contact the study team
- Eleanor Schwarz, MD, MS · Phone: 415-502-1826
- Agatha Okobi · Phone: (510) 660-0915
Official record on ClinicalTrials.gov — NCT06296797
Locations in the U.S.
| California | University of California, San Francisco, San Francisco |
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.