← Eichor
Study identifier: NCT06296797 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Patient-centered Information on Permanent Contraception

Condition: Contraception · Reproductive Behavior · Contraception Behavior  ·  Sponsor: University of California, San Francisco

PhaseNA
Planned participants650
Who can joinFemale, 21 Years to 45 Years
Healthy volunteersYes

About this 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.

This description comes directly from the study's public registry record.

Talk to the study team

Eleanor Schwarz, MD, MS  ·  415-502-1826  ·  eleanor.schwarz@ucsf.edu

Agatha Okobi  ·  (510) 660-0915  ·  agatha.okobi@ucsf.edu

Always discuss trial participation with your own doctor first.

Locations (1)

University of California, San FranciscoSan Francisco, California, United StatesRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06296797