Patient-centered Information on Permanent Contraception

Recruiting now · Not applicable

Conditions studied: Contraception, Reproductive Behavior, Contraception Behavior

In brief

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.

Key facts

Study ID

NCT06296797

Run by

University of California, San Francisco

People needed

650

Starts

2024-04-01

Expected to finish

2026-08-01

Last updated by the study team

2026-01-26

Who can join

Age: 21 and older, up to 45. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Self-reported fertility
• Have a strong desire to avoid future pregnancy
• Speak English or Spanish

You may not qualify if…

• Current pregnancy
• The inability to speak English or Spanish
• Prior tubal sterilization or "Essure" procedure
• Menopause
• Infertility
• Hysterectomy

Where it is running

• University of California, San Francisco — San Francisco, California, United States (enrolling)

Full record on ClinicalTrials.gov

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