Study of Having a Female Friend as Labor Support

This study has been completed.
Sponsor:
Information provided by:
Saint Peters University Hospital
ClinicalTrials.gov Identifier:
NCT00127361
First received: August 4, 2005
Last updated: August 22, 2005
Last verified: April 2005

August 4, 2005
August 22, 2005
January 1998
Not Provided
  • Length of labor
  • type of delivery
  • type and timing of analgesia/anesthesia
Same as current
Complete list of historical versions of study NCT00127361 on ClinicalTrials.gov Archive Site
  • Birthweight
  • neonatal Apgar score at 1 and 5 minutes after birth
Same as current
Not Provided
Not Provided
 
Study of Having a Female Friend as Labor Support
Evaluation of Continuous Support in Labor

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.

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).

Interventional
Not Provided
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
  • Pregnancy
  • Delivery, Obstetric
Behavioral: doula training
Not Provided
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
600
February 2003
Not Provided

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
Female
16 Years to 45 Years
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00127361
DAC-1998
Not Provided
Not Provided
Saint Peters University Hospital
Not Provided
Principal Investigator: Della A Campbell, PhDc Saint Peters University Hospital
Saint Peters University Hospital
April 2005

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