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
56 participants
INTERVENTIONAL
2019-07-24
2024-03-29
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
HEALTH_SERVICES_RESEARCH
NONE
Study Groups
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Telemedicine Support
Weekly telemedicine breastfeeding support visits for four weeks, delivered via telemedicine
Telemedicine Support
Telemedicine intervention
Control
Standard of care
Standard of Care
Standard of Care
Interventions
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Telemedicine Support
Telemedicine intervention
Standard of Care
Standard of Care
Eligibility Criteria
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Inclusion Criteria
* late preterm delivery (34-37 6/7 weeks)
* enrollment up to 1 week postpartum
* breastfeeding initiated
* access to a smartphone, tablet, or laptop computer in their home
Exclusion Criteria
* inability to communicate in English
* infant with medical condition compromising breastfeeding (e.g. cleft lip and/or palate).
ALL
No
Sponsors
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National Institutes of Health (NIH)
NIH
University of California, Davis
OTHER
Responsible Party
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Principal Investigators
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Laura Kair, MD
Role: PRINCIPAL_INVESTIGATOR
University of California, Davis
Locations
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University of California-Davis
Sacramento, California, United States
Countries
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Related Links
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Learn more or sign up for the study here!
Other Identifiers
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1382496
Identifier Type: -
Identifier Source: org_study_id
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