RECRUITING

Patient-centered Information on Permanent Contraception

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Disseminating PCOR Findings to Reduce Racial Disparities in Surgical Sterilization

Quick Facts

Study Start:2024-04-01
Study Completion:2025-04-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06296797

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:21 Years to 45 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * Self-reported fertility
  2. * Have a strong desire to avoid future pregnancy
  3. * Speak English or Spanish
  1. * Current pregnancy
  2. * The inability to speak English or Spanish
  3. * Prior tubal sterilization or "Essure" procedure
  4. * Menopause
  5. * Infertility
  6. * Hysterectomy

Contacts and Locations

Study Contact

Eleanor Schwarz, MD, MS
CONTACT
415-502-1826
eleanor.schwarz@ucsf.edu
Hannah Begna, MS
CONTACT
(510) 660-0915
hannah.begna@ucsf.edu

Principal Investigator

Eleanor Schwarz, MD, MS
PRINCIPAL_INVESTIGATOR
University of California, San Francisco

Study Locations (Sites)

University of California, San Francisco
San Francisco, California, 94143
United States

Collaborators and Investigators

Sponsor: University of California, San Francisco

  • Eleanor Schwarz, MD, MS, PRINCIPAL_INVESTIGATOR, University of California, San Francisco

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-04-01
Study Completion Date2025-04-01

Study Record Updates

Study Start Date2024-04-01
Study Completion Date2025-04-01

Terms related to this study

Keywords Provided by Researchers

  • tubal sterilization
  • permanent contraception
  • intrauterine device
  • contraceptive implant
  • vasectomy

Additional Relevant MeSH Terms

  • Contraception
  • Reproductive Behavior
  • Contraception Behavior