Patient-centered Information on Permanent Contraception (NCT06296797)
Disseminating PCOR Findings to Reduce Racial Disparities in Surgical Sterilization
๐ฉบ Plain-English Summary (8th-Grade Level)
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.
Who can join: Review the eligibility criteria below.
Location: University of California, San Francisco โ San Francisco, California
Age range: 21 Years to 45 Years
๐งช Interventions in This Study
- Control arm: Existing educational website (BEHAVIORAL)
- Advancing Access Website (BEHAVIORAL)
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (1 Sites)
- University of California, San Francisco โ San Francisco, California
๐ Contact the Study Coordinator
Phone: (415) 502-1826
Email: eleanor.schwarz@ucsf.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
๐ฐ Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Contraception
- Casea S Contraceptive Implants (Casea S) Trial โ Santo Domingo, DN
- Family Planning Elevated: Initiative Evaluation โ Salt Lake City, Utah
- Birth Control to Improve Birth Spacing โ Boston, Massachusetts
- FemBlocยฎ Permanent Contraception - Confirmation Feasibility Trial โ Chandler, Arizona
- The Over The Counter Pill National Study โ Portland, Oregon
- Evaluation of the Efficacy, Safety, and Tolerability of LevoCept โ Berkeley, California
Explore by condition: All Contraception clinical trials
๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.