Decreasing Patient Dissatisfaction With Unplanned Cesarean Sections
NCT ID: NCT02472327
Last Updated: 2018-01-12
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
208 participants
INTERVENTIONAL
2015-06-30
2017-05-31
Brief Summary
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Detailed Description
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Two weeks after the cesarean section, patients participating in the study are called on the phone by one of the investigators. A patient satisfaction survey, using a Likert scale is administered. This investigator is blinded as to whether the patient has received the additional counseling or not. Comparison of these scores will be used to determine whether pre-operative counseling can reduce dissatisfaction in patients undergoing unplanned cesarean sections.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
SINGLE
Study Groups
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Typical Care
These patients will receive normal peripartum care and support.
No interventions assigned to this group
Pre-operative support
These patients will receive additional emotional support prior to undergoing an unplanned cesarean section during labor.
Pre-operative support
Interventions
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Pre-operative support
Eligibility Criteria
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Inclusion Criteria
* Faculty group patient
Exclusion Criteria
FEMALE
No
Sponsors
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Albany Medical College
OTHER
Responsible Party
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Paul Burcher Md, PhD
Paul Burcher MD, PhD
Locations
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Albany Medical College
Albany, New York, United States
Countries
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Other Identifiers
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AlbanyMC
Identifier Type: -
Identifier Source: org_study_id
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