Information on permanent contraception options for women
Disseminating PCOR Findings to Reduce Racial Disparities in Surgical Sterilization
This study is testing if giving women better information about permanent birth control options can help them feel more confident in their choices for avoiding future pregnancies.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 650 (estimated) |
| Ages | 21 Years to 45 Years |
| Sex | Female |
| Sponsor | University of California, San Francisco Academic / other |
| Locations | 1 site (San Francisco, California) |
| Trial ID | NCT06296797 on ClinicalTrials.gov |
What this trial studies
This study aims to evaluate whether providing women who wish to avoid future pregnancies with information about tubal sterilization and long-acting reversible contraceptives (LARC) can improve their perceived access to contraceptive options. Participants will complete surveys before and after accessing web-based educational resources that summarize recent patient-centered outcomes research. The study compares outcomes between those using a new educational website and those using an existing resource. The goal is to enhance patient-centered contraceptive care and align contraceptive choices with personal preferences.
Who should consider this trial
Good fit: Ideal candidates are women who have a strong desire to avoid future pregnancies and can communicate in English or Spanish.
Not a fit: Patients who are currently pregnant, have undergone prior sterilization, or are experiencing infertility may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could empower women to make informed decisions about their contraceptive options, potentially reducing regret associated with permanent procedures.
How similar studies have performed: Other studies have shown that providing educational resources can improve patient decision-making and satisfaction regarding contraceptive choices.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Self-reported fertility * Have a strong desire to avoid future pregnancy * Speak English or Spanish Exclusion Criteria: * Current pregnancy * The inability to speak English or Spanish * Prior tubal sterilization or "Essure" procedure * Menopause * Infertility * Hysterectomy
Where this trial is running
San Francisco, California
- University of California, San Francisco — San Francisco, California, United States (Recruiting)
Study contacts
- Principal investigator: Eleanor Schwarz, MD, MS — University of California, San Francisco
- Study coordinator: Eleanor Schwarz, MD, MS
- Email: eleanor.schwarz@ucsf.edu
- Phone: 415-502-1826
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.