Multiparas Attitude to Outpatient Cesarean Section

August 26, 2021 updated by: Iben Lorentzen, Herning Hospital

Multiparas Attitude to Outpatient Care After Cesarean Section - A Qualitative Study

The main purpose of this study is to explore multiparas attitude to outpatient care after a planned cesarean section.

Study Overview

Status

Completed

Conditions

Detailed Description

This qualitative study should provide information about:

  • Multiparas reflections in relation to prefer inpatient care after a planned cesarean section
  • Womens anticipation of having inpatient care after cesarean section
  • The womens experiences in relation to a planned cesarean birth and the first postnatal weeks

Study Type

Observational

Enrollment (Actual)

10

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

  • Denmark
      • Aarhus, Denmark, 8000
        • Aarhus University

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

  • ADULT
  • OLDER_ADULT
  • CHILD

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Female

Sampling Method

Probability Sample

Study Population

Mulitparas having a planned cesarean section at the department of Obstetrics and Gynecology at Herning Hospital

Description

Inclusion Criteria:

  • Planned elective cesarean section of multiparous women
  • Singleton pregnancy
  • Age of at least 18
  • Gestational age between 37 and 42 weeks

Exclusion Criteria:

  • Lack of consent
  • Women with no or little understanding of Danish and ability to speak Danish.
  • Allergies to medicine included in the pain management regimes
  • Expected maternal or neonatal complications after delivery
  • Birth weight of less than 2500 grams

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

Cohorts and Interventions

Group / Cohort
Multiparas, planned cesarean section
Multiparas having a planned cesarean section at the departement of Obstetrics and Gynecology in Herning Hospital. Uncomplicated pregnancy that makes early discharge possible.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
womens attitude an reflections about based on interviews
Time Frame: october 2013- june 2014
october 2013- june 2014

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
womens attitude and reflections
Time Frame: october 2013- june 2014
this study is based on 20 interviews with 10 multiparas having a planned cesarean section. The first interview is performed about one month before term and the second interview about two weeks after the cesarean section.
october 2013- june 2014

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Herning Hospital

Investigators

  • Principal Investigator: Iben P Lorentzen, Midwife, Department of Obstetrics and Gynecology, Herning Hospital

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 (ACTUAL)

November 1, 2013

Primary Completion (ACTUAL)

May 1, 2014

Study Completion (ACTUAL)

June 1, 2014

Study Registration Dates

First Submitted

February 24, 2014

First Submitted That Met QC Criteria

August 26, 2021

First Posted (ACTUAL)

August 27, 2021

Study Record Updates

Last Update Posted (ACTUAL)

August 27, 2021

Last Update Submitted That Met QC Criteria

August 26, 2021

Last Verified

August 1, 2021

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • outpatientcesareanQual

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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