Actively Recruiting

Phase Not Applicable
Age: 21Years - 45Years
FEMALE
Healthy Volunteers
NCT06296797

Patient-centered Information on Permanent Contraception

Led by University of California, San Francisco · Updated on 2026-01-26

650

Participants Needed

1

Research Sites

121 weeks

Total Duration

On this page

Sponsors

U

University of California, San Francisco

Lead Sponsor

E

Essential Access Health

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Patient-centered Information on Permanent Contraception

Who Can Participate

Age: 21Years - 45Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Self-reported fertility
  • Strong desire to avoid future pregnancy
  • Ability to speak English or Spanish
Not Eligible

You will not qualify if you...

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

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of California, San Francisco

San Francisco, California, United States, 94143

Actively Recruiting

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Research Team

E

Eleanor Schwarz, MD, MS

CONTACT

A

Agatha Okobi

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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Patient-centered Information on Permanent Contraception | DecenTrialz