Actively Recruiting

Phase Not Applicable
Age: 21Years - 45Years
FEMALE
Healthy Volunteers
ID06296797

Disseminating Patient-Centered Outcomes Research to Reduce Racial Disparities in Surgical Sterilization and Improve Contraceptive Access

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

650

Participants Needed

1

Research Sites

N/A

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

Researchers are evaluating whether providing women who strongly want to avoid future pregnancy with detailed information comparing tubal sterilization to long-acting reversible contraceptives (LARC) improves their perceived access to different contraceptive options. The study aims to support patient-centered contraceptive care by increasing knowledge and access to all long-acting contraceptives. This research also seeks to reduce the number of women who regret permanent sterilization and address racial disparities in surgical sterilization. Participants are randomly assigned to one of two groups: one group accesses a new website that compares tubal sterilization and LARC based on recent patient-centered outcomes research, while the other group views an existing Planned Parenthood webpage focused on tubal sterilization. These web-based resources serve as educational interventions to help patients prepare for discussions with their healthcare providers about contraception. During the study, participants complete a baseline survey, explore their assigned website, and then complete a brief follow-up survey immediately afterward. They also complete another follow-up survey three months later. Researchers measure outcomes such as perceived access to long-acting contraceptives, contraceptive counseling quality, patient-provider interactions, knowledge about contraceptive methods, use of preferred contraception, and willingness to recommend the website. The study includes safety and adherence monitoring through surveys and lasts at least three months from enrollment.

CONDITIONS

Brief 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
  • Speak English or Spanish
  • Female aged 21 to 45 years
Not Eligible

You will not qualify if you...

  • Current pregnancy
  • Unable 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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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person or remote) for eligibility assessment

Treatment

Duration - Single session

Participants are introduced to one of two educational websites to provide information on tubal sterilization and long-acting reversible contraceptives to support contraceptive decision-making.

1 visit (online introduction to website)

Follow-up

Duration - 3 months

Participants complete follow-up assessments to evaluate perceived access, knowledge, counseling experience, contraceptive use, and satisfaction with the educational websites.

1 follow-up visit (online or remote) at 3 months

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

A

Agatha Okobi

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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