FindMyKOL
Clinical trialNCT07075536Enrolling, by, invitationInterventional

A Web-Based Tool to Help People With Health Conditions Make Contraceptive Decisions

SponsorUniversity of MichiganEnrollment795Chronic ConditionChronic Conditions, MultipleChronic DiseaseContraceptive BehaviorContraceptive Usage
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

Among people who do not want to get pregnant, some do not use any birth control. This is also called contraceptive nonuse. Common reasons for contraceptive nonuse include concerns about birth control safety or side effects. People with health conditions, such as diabetes or high blood pressure, also report worries about how different birth control methods might affect their health condition or medicines. The goal of this clinical trial is to learn if a web tool called My Health, My Choice helps people with health conditions understand their birth control options and choose birth control that is right for them. The study will also look at the medical safety of birth control methods that participants decide to use. The main questions it aims to answer are: • Does the My Health My Choice tool lower the number of participants who do not use any birth control method? (contraceptive nonuse) In other words, does the My Health My Choice tool increase the number of participants who use any birth control method? (contraceptive use) Participants who use the My Health, My Choice tool before a clinic visit with their clinician (Intervention Group) will be compared to participants who only go to a clinic visit with their clinician (Usual Care Group). For this study, a "clinician" is any licensed health care provider who counsels about birth control, prescribes birth control, and/or inserts birth control devices. All participants will: * Complete 4-5 online surveys that take 5-10 minutes each, over a 3 month time period * Be asked to go to a scheduled clinic visit with their health care provider * A small group of participants (about 30) will be invited to a 1 hour exit interview Participants in the intervention arm will be asked to: • Use the My Health My Choice tool before their clinic visit

Investigators

The overall officials registered on this study. Names that resolve to a FindMyKOL profile link to it; the rest are shown as registered.

  • Justine P Wu, MD, MPH

    Department of Family Medicine, University of Michigan

    Principal Investigator

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

19 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

Puerto Rico
  • University of Puerto Rico Department of Obstetrics and Gynecology

    San Juan, Puerto Rico

United States
  • University of Arizona College of Medicine - Phoenix Department of Family, Community and Preventive Medicine - Research Division & Arizona Developing Experience With Practice-Based Research Network (pbrn) Studies

    Phoenix, Arizona, United States

  • Pomona Valley Hospital Medical Center Family Medicine Residency Program

    Pomona, California, United States

  • Full Circle Health Family Medicine Residency of Idaho - Nampa Program

    Nampa, Idaho, United States

  • University of Kansas Medical Center Department of Family Medicine & Community Health

    Kansas City, Kansas, United States

  • Mainehealth Primary Care - Family Medicine - Sanford

    Sanford, Maine, United States

  • Boston Medical Center'S Department of Family Medicine

    Boston, Massachusetts, United States

  • Department of Family Medicine Research Office

    Ann Arbor, Michigan, United States

  • Von Voigtlander Women'S Hospital Obstetrics and Gynecology Clinic University of Michigan Health Michigan Medicine

    Ann Arbor, Michigan, United States

  • Michigan State University Health Care Family Medicine

    East Lansing, Michigan, United States

  • Wmed Health Family Medicine - Crosstown Parkway

    Kalamazoo, Michigan, United States

  • Munson Healthcare

    Traverse City, Michigan, United States

  • Ypsilanti Health Center University of Michigan Health Michigan Medicine

    Ypsilanti, Michigan, United States

  • Rutgers Robert Wood Johnson Medical School - Family Medicine at Monument Square

    New Brunswick, New Jersey, United States

  • Capital Health Family Medicine

    Trenton, New Jersey, United States

  • Mountain Area Health Education Center (mahec) Family Health Center - Biltmore Site and Enka Site

    Asheville, North Carolina, United States

  • Cleveland Clinic - Complex Family Planning Clinic

    Cleveland, Ohio, United States

  • Ascent Center for Reproductive Health at the University of Utah

    Salt Lake City, Utah, United States

  • West Virginia University School of Medicine - Department of Family Medicine

    Morgantown, West Virginia, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study. It may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
15 Sept 2025
Primary completion
31 Aug 2028
Completion
31 Aug 2028
Last update posted
6 Oct 2026
Registered enrollment
795
Registry id
NCT07075536

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 11 Nov 2026. Registry facts are shown as registered by the study sponsor; FindMyKOL does not interpret them.