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Clinical Trials/NCT00127361
NCT00127361
Completed
Not Applicable

Evaluation of Continuous Support in Labor

Saint Peters University Hospital1 site in 1 country600 target enrollmentJanuary 1998

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pregnancy
Sponsor
Saint Peters University Hospital
Enrollment
600
Locations
1
Primary Endpoint
Length of labor
Status
Completed
Last Updated
20 years ago

Overview

Brief Summary

The purpose of this study was to compare labor outcomes in women accompanied by an additional support person (doula group) with outcomes in women who did not have this additional support person (control group).

The current study was designed with the benefits of continuous labor support in mind as well as the need for a cost-effective, affordable program to provide those services for low-income women. Its purpose was to evaluate the effects of continuous labor support provided by a female companion of the pregnant person's choosing who, with the mother, had participated in an educational program to teach her how to provide continuous labor support.

Detailed Description

The purpose of this study was to evaluate the influence of a female companion in labor who had been chosen by a nulliparous, underinsured, low-income woman and who had received brief training in supportive labor techniques. The objective was to compare labor outcomes, specifically cesarean section rates, in women accompanied by this additional support person (doula group) with outcomes in women who did not have this additional support person (control group).

Registry
clinicaltrials.gov
Start Date
January 1998
End Date
February 2003
Last Updated
20 years ago
Study Type
Interventional
Study Design
Single Group
Sex
Female

Investigators

Sponsor
Saint Peters University Hospital

Eligibility Criteria

Inclusion Criteria

  • Nulliparous (never given birth before)
  • Singleton pregnancy
  • Vertex presentation
  • Low risk pregnancy
  • Has a female friend willing to be a doula

Exclusion Criteria

  • Placenta previa
  • Abruptio placenta
  • Multiple pregnancy
  • Breech presentation
  • Planned operative delivery

Outcomes

Primary Outcomes

Length of labor

type of delivery

type and timing of analgesia/anesthesia

Secondary Outcomes

  • Birthweight
  • neonatal Apgar score at 1 and 5 minutes after birth

Study Sites (1)

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