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Clinical Trials/NCT02478385
NCT02478385
Completed
Not Applicable

Birth Environment of the Future - a Randomised Controlled Study

Herning Hospital1 site in 1 country680 target enrollmentMay 2015
ConditionsPregnancy

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pregnancy
Sponsor
Herning Hospital
Enrollment
680
Locations
1
Primary Endpoint
No. of women receiving oxytocin stimulation during Labour
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

The main purpose of this study is to explore the impact of the birth environment on women's birth experience and relevant birth outcomes in the experimental Labour room compared to a standard Labour room.

Detailed Description

In the last decade, there has been an increased interest in exploring the impact of the birth environment on midwifery practice and the women's birth experiences. Results from these studies show that a home-like birth environment has positive effects on both midwifery practice and the birth experience. The hormone oxytocin that causes contractions during labour may play an important role in this context. The hormone is released when being in a safe, secure and confident environment. Therefore, it is a reasonable assumption that the birth environment also has an impact on birth outcomes. To investigate this assumption one traditional labour room was transformed to an experimental labour room. The design of the room is inspired by knowledge from evidence-based healthcare design, which describes bringing nature into the room. Furthermore, it is possible for the parents to design their own birth setting by choosing atmosphere through sound, light and nature scenes.

Registry
clinicaltrials.gov
Start Date
May 2015
End Date
August 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Herning Hospital
Responsible Party
Principal Investigator
Principal Investigator

Iben Lorentzen

Midwife, Master in Health Hummanities (MHH)

Herning Hospital

Eligibility Criteria

Inclusion Criteria

  • primiparas with a singleton pregnancy
  • Gestational age 37-42
  • speaks and understands Danish

Exclusion Criteria

  • Inducted delivery

Outcomes

Primary Outcomes

No. of women receiving oxytocin stimulation during Labour

Time Frame: From allocation at delivery ward (date, hour and minute) to delivery (date, hour, minute). Duration is recorded time in hours and minutes

No of women augmented with oxytocin drip. The intervention is registered in the electronic patient journal. The duration in time (date,hours,minutes) of oxytocin treatment is registered in the electronic journal log

Secondary Outcomes

  • Pain relieving interventions(From allocation at delivery ward (date, hour and minute) to delivery (date, hour, minute). Duration is recorded time in hours and minutes)
  • Duration of labour(From allocation at delivery ward (date, hour and minute) to delivery (date, hour, minute). Duration is recorded time in hours and minutes)

Study Sites (1)

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