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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COMPLETED
NA
132 participants
INTERVENTIONAL
2011-01-31
2013-02-28
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Usual contraceptive counseling
subjects received usual contraceptive counseling
Usual contraceptive counseling
all subjects recieved usual contraceptive counseling
Physician self-disclosure of IUC use
subjects received usual contraceptive counseling plus intervention which was Physician self-disclosure of personal IUC use during the counseling
Physician self-disclosure of personal IUC use
Physicians self-disclosed personal intrauterine contraceptive use to subjects in intervention arm of study during contraceptive counseling
Interventions
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Physician self-disclosure of personal IUC use
Physicians self-disclosed personal intrauterine contraceptive use to subjects in intervention arm of study during contraceptive counseling
Usual contraceptive counseling
all subjects recieved usual contraceptive counseling
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* currently sexually active
* scheduled for benign gynecology visit, annual exam, or family planning visit
Exclusion Criteria
* currently using IUC
* prior sterilization procedure
* currently pregnant
18 Years
44 Years
FEMALE
No
Sponsors
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University of Michigan
OTHER
Responsible Party
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Mya Zapata
Clinical Lecturer
Locations
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University of Michigan Medical Center
Ann Arbor, Michigan, United States
Countries
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Other Identifiers
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N014264
Identifier Type: OTHER_GRANT
Identifier Source: secondary_id
IUC Disclosure
Identifier Type: -
Identifier Source: org_study_id