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
45 participants
INTERVENTIONAL
2009-03-31
2009-06-30
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
PREVENTION
SINGLE
Study Groups
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Avaliation
This group will have 15 women in puerperium and will be realize an interview to avalide the cesarean discomforts in immediate puerperium. These dates will be use for elaborate the orientations guide.
Avolition
\- avolition for cesarean discomforts
Orientation
In this group will be realize an interview to avalide the cesarean discomforts in immediate puerperium or in the first post operatory and in the second post operatory wil be realize a new interview.
Orientation
* avolition of cesarean discomfort
* physiotherapy orientation
Guide
in This group wiil be realize an interview to avalide the cesarean discomforts in immediate puerperium or in the first post operatory, will be realize the orientations and the guide will be give, and in the second post operatory will be realize a new interview.
Guide
* avolition of cesarean discomfort
* physiotherapy orientation
* guide orientation
Interventions
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Avolition
\- avolition for cesarean discomforts
Orientation
* avolition of cesarean discomfort
* physiotherapy orientation
Guide
* avolition of cesarean discomfort
* physiotherapy orientation
* guide orientation
Eligibility Criteria
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Inclusion Criteria
* has realize an emergency or elective cesarean
* being in immediate puerperium and did not have receive any orientation
Exclusion Criteria
* complications with the baby
* physicologics disease
15 Years
35 Years
FEMALE
No
Sponsors
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Sao Marcos University
OTHER
Responsible Party
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São Marcos University
Principal Investigators
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Patricia Batista
Role: PRINCIPAL_INVESTIGATOR
São Marcos University
Locations
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Sepaco Hospital
São Paulo, São Paulo, Brazil
Countries
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Other Identifiers
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Unimarco
Identifier Type: -
Identifier Source: org_study_id