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Physiotherapy in Postpartum After a Cesarean

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01020240
First Posted: November 25, 2009
Last Update Posted: November 26, 2009
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Sao Marcos University
November 24, 2009
November 25, 2009
November 26, 2009
March 2009
May 2009   (Final data collection date for primary outcome measure)
Analogic Visual Scale [ Time Frame: 6 months ]
Same as current
Complete list of historical versions of study NCT01020240 on ClinicalTrials.gov Archive Site
Analogic Visual Scale [ Time Frame: 6 months ]
Same as current
Not Provided
Not Provided
 
Physiotherapy in Postpartum After a Cesarean
Effectiveness of an Orientation Guide for Puerperal Women After Cesarean.
The purpose of this study is to promote a prevention of the complications using an elaborate guide effective and easy to understand.
The puerperium consists the period of pregnancy and postpartum cycle that the alterations provoked for pregnancy and delivery on the women organism return to your state before pregnancy. The physiotherapist can follow the puerperium since hospital phase until women has been recovered of pregnancy physiologist alterations.
Interventional
Not Provided
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Participant)
Primary Purpose: Prevention
Postpartum Period
  • Behavioral: Avolition
    - avolition for cesarean discomforts
  • Behavioral: Orientation
    • avolition of cesarean discomfort
    • physiotherapy orientation
  • Behavioral: Guide
    • avolition of cesarean discomfort
    • physiotherapy orientation
    • guide orientation
  • No Intervention: 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.
    Intervention: Behavioral: Avolition
  • No Intervention: 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.
    Intervention: Behavioral: Orientation
  • Experimental: 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.
    Intervention: Behavioral: Guide
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
45
June 2009
May 2009   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • have between 15 and 35 yeas old
  • has realize an emergency or elective cesarean
  • being in immediate puerperium and did not have receive any orientation

Exclusion Criteria:

  • complications in delivery and postpartum
  • complications with the baby
  • physicologics disease
Sexes Eligible for Study: Female
15 Years to 35 Years   (Child, Adult)
No
Contact information is only displayed when the study is recruiting subjects
Brazil
 
 
NCT01020240
Unimarco
Yes
Not Provided
Not Provided
Patricia Andrade Batista, São Marcos University
Sao Marcos University
Not Provided
Principal Investigator: Patricia Batista São Marcos University
Sao Marcos University
November 2009

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP