- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02164227
Effective Use of Respiratory Patterns in the First Period of Labor in Control of Maternal Anxiety
June 12, 2014 updated by: Alessandra da Boaviagem Freire, Universidade Federal de Pernambuco
EFFECTIVE USE OF RESPIRATORY PATTERNS IN THE FIRST PERIOD OF LABOR IN CONTROL OF MATERNAL ANXIETY: A CLINICAL TRIAL
The effectiveness of breathing exercise on anxiety in women during the first period of labor.
Study Overview
Detailed 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 Type
Interventional
Enrollment (Anticipated)
30
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Pernambuco
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Recife, Pernambuco, Brazil, 50770-400
- Recruiting
- Maternidade Professor Bandeira Filho
-
Contact:
- Maria Lima
- Phone Number: 3355-2230
- Email: humanizadora@hotmail.com
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Principal Investigator:
- Alessandra Freire
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
12 years to 40 years (Child, Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- Primiparous
- First stage of labor
Exclusion Criteria:
- Multiple gestation;
- Eclampsia;
- Pregnancy with a dead fetus;
- Use of analgesia;
- Pregnant women with clinical instability;
- Psychiatric disorders;
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Single Group Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: respiratory pattern
Deep and slow inspiration is used in the initial and active stages, at which time the contractions vary from uncomfortable to strong, lumbosacral pain and cervical dilation may occur between 3 and 8 cm in this case the mother is driven to inspire slowly and the level of inspiratory reserve volume followed by slow exhalation to functional residual capacity; Sigh with post-expiratory pause that corresponds to a small spontaneous exhalation to relax occurs in tidal volume; Expiratory delay that corresponds to a prolonged propelled with the lips during the lull and expiration in the expiration time that corresponds to a slow inspiration followed by two or three puffs with the short lips will be used propelled.
|
|
No Intervention: Control
Follows the service routine
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Anxiety
Time Frame: 2 hours
|
The anxiety of patients will be assessed using IDATE questionnaire
|
2 hours
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
March 1, 2014
Primary Completion (Anticipated)
July 1, 2014
Study Completion (Anticipated)
April 1, 2015
Study Registration Dates
First Submitted
May 21, 2014
First Submitted That Met QC Criteria
June 12, 2014
First Posted (Estimate)
June 16, 2014
Study Record Updates
Last Update Posted (Estimate)
June 16, 2014
Last Update Submitted That Met QC Criteria
June 12, 2014
Last Verified
June 1, 2014
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 025972/2013
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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