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Clinical Trial Summary

The effectiveness of breathing exercise on anxiety in women during the first period of labor.


Clinical Trial Description

The groups will be randomized into intervention groups, which will be held ventilatory patterns while the control group will receive routine care service. The measurements will be made during the admission, and every 2 hours until the final phase of dilation. ;


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Health Services Research


Related Conditions & MeSH terms


NCT number NCT02164227
Study type Interventional
Source Universidade Federal de Pernambuco
Contact
Status Recruiting
Phase N/A
Start date March 2014
Completion date April 2015

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