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NCT07075536

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

Enrolling by Invitation
NAAges 18–49InterventionalTreatment
University of Michigan
~795 participants
Updated 2026-06-15 on ClinicalTrials.gov
What's tested:My Health, My Choice Web-Based Contraceptive Decision ToolUsual Contraceptive Care

At a glance

Recruiting sites
0 of 19 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Proportion of participants who report contraceptive nonuse at 3 months
Measured over Baseline, 1 month, and 3 months after the clinic visit

Conditions

Contraceptive Usage
Contraceptive Behavior
Chronic Disease
Chronic Condition
Chronic Conditions, Multiple

Explore related trials

Chronic Disease

Where it's being run

19 sites across 13 states
Michigan6
New Jersey2
Arizona1
California1
Idaho1
Kansas1
Maine1
Massachusetts1

Study leadership

  • Justine P Wu, MD, MPH · PRINCIPAL_INVESTIGATOR · Department of Family Medicine, University of Michigan

Who to contact

This trial hasn't published a contact. View it on ClinicalTrials.gov

Do you actually qualify for this trial?

Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.

Check eligibility for this trial ~2 min · HIPAA-protected · delete anytime
Eligibility criteria

Inclusion

Between the ages of 18 and 49
Assigned female sex at birth, regardless of gender identity
Presumed to be fertile (have an intact uterus/tube/ovary; premenopausal)
Have at least one index health condition, characteristic or medication usage (full list of 60+ eligible conditions, characteristics, and 50+ medications available upon request); and want to talk about birth control at an upcoming clinic visit with their clinician
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

Exclusion

Trying to get pregnant in the next 12 months
Presumed infertile for any surgical or medical reason (e.g., postmenopausal, hysterectomy, chemotherapy)

What this trial measures

  • Proportion of participants who report contraceptive nonuse at 3 monthsBaseline, 1 month, and 3 months after the clinic visit

    This is a binary outcome (yes/no) that will be assessed at baseline, 1 month, and 3 months after the clinic visit. Participants will report use or nonuse of a contraceptive method in the last month. Contraceptive methods include all non-prescription methods, prescription methods, intrauterine devices (IUDs), the implant, tubal ligation/surgery, and vasectomy of their partner. If patients report use of the cervical cap, condoms, diaphragm, spermicides, vaginal gel, or withdrawal, their outcome will be determined by whether they used the method at last intercourse in the prior month. Only patients who did not want to get pregnant in the last month will be included in the calculation of this outcome.