Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
2000 participants
OBSERVATIONAL
2025-02-12
2027-03-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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In-person via established clinic
People seeking or who have received in-person medication abortion care through an established clinic.
No interventions assigned to this group
Telehealth via established clinic
People seeking or who have received telehealth medication abortion care through an established clinic. A telehealth medication abortion involves a remote clinical consultation to confirm medical eligibility with medications delivered by mail
No interventions assigned to this group
Telehealth through other online services or searches
People seeking or who have received telehealth medication abortion care through an online service
No interventions assigned to this group
In-person through online search
People seeking or who have received in-person abortion services through online searches
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
14 Years
64 Years
ALL
Yes
Sponsors
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Ibis Reproductive Health
OTHER
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
NIH
University of California, San Francisco
OTHER
Responsible Party
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Principal Investigators
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Ushma Upadhyay, PhD, MPH
Role: PRINCIPAL_INVESTIGATOR
University of California, San Francisco
Locations
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Advancing New Standards in Reproductive Health (ANSIRH)
Oakland, California, United States
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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23-39122
Identifier Type: -
Identifier Source: org_study_id
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