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Search / Trial NCT07075536

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

Launched by UNIVERSITY OF MICHIGAN · Jul 9, 2025

Trial Information

Current as of July 24, 2025

Enrolling by invitation

Keywords

Contraceptive Use Contraceptive Decision Making Shared Decision Making Person Centered Contraceptive Counseling Decisional Conflict Web Based Tool

ClinConnect Summary

Fourteen outpatient clinics in the United States that provide birth control services, including primary care and obstetrics and gynecology clinics, will be enrolled. Each clinic will be randomly assigned to the My Health My Choice Group (intervention group) or the Usual Care group. Only patients who receive health care at enrolled clinics are eligible for study participation.

Participants must be aged 18-49 years, read English, fertile (able to get pregnant), have at least one health condition or prior pregnancy complication and/or currently take a medicine that may interact with hormonal ...

Gender

FEMALE

Eligibility criteria

  • Patient Inclusion Criteria:
  • Between the ages of 18 and 49
  • Assigned female sex at birth
  • Presumed to be fertile (have an intact uterus/tube/ovary; premenopausal)
  • Have at least one health condition, prior adverse pregnancy outcome, taking a teratogenic medication, or taking a medication that has interactions with hormonal contraception
  • Able to read in English
  • Access to mobile phone, computer, or tablet with internet capabilities
  • Not currently pregnant
  • Desire to talk to their clinician about starting, switching, or adding a contraceptive method for the purpose of preventing pregnancy
  • Patient Exclusion Criteria:
  • Trying to get pregnant in the next 12 months
  • Presumed infertile for any surgical or medical reason (e.g., postmenopausal, hysterectomy, chemotherapy)
  • There are additional clarifications regarding patient eligibility, such as a full list of eligible medical diagnoses and medicines, that can be found in the protocol.
  • Clinician Inclusion Criteria:
  • • Any licensed clinician who provides contraceptive care at a participating clinic, including physicians, physician assistants, certified nurse midwives, nurse practitioners. (For clinicians, there are no restrictions based upon age, gender identify or sex).
  • Clinician Exclusion Criteria:
  • • Physician interns (PGY-1) are not eligible

About University Of Michigan

The University of Michigan, a leading academic institution renowned for its commitment to advancing healthcare and medical research, serves as a prominent clinical trial sponsor. With a robust infrastructure that supports innovative research initiatives, the university leverages its multidisciplinary expertise to conduct a wide array of clinical trials aimed at improving patient outcomes and advancing medical knowledge. Through its state-of-the-art facilities and collaborative environment, the University of Michigan fosters partnerships between researchers, clinicians, and industry leaders, ensuring the development of cutting-edge therapies and interventions that address pressing health challenges.

Locations

Pomona, California, United States

Phoenix, Arizona, United States

Kansas City, Kansas, United States

Sanford, Maine, United States

Boston, Massachusetts, United States

Ann Arbor, Michigan, United States

Kalamazoo, Michigan, United States

Ypsilanti, Michigan, United States

New Brunswick, New Jersey, United States

Cleveland, Ohio, United States

Salt Lake City, Utah, United States

Morgantown, West Virginia, United States

Patients applied

0 patients applied

Trial Officials

Justine P Wu, MD, MPH

Principal Investigator

Department of Family Medicine, University of Michigan

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported