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Study of Having a Female Friend as Labor Support

Evaluation of Continuous Support in Labor

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00127361
Enrollment
600
Registered
2005-08-05
Start date
1998-01-31
Completion date
2003-02-28
Last updated
2005-08-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Delivery, Obstetric, Pregnancy

Keywords

doula, caregivers, labor support, being with woman, continuous labor support, maternal outcomes, Parturition

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).

Interventions

BEHAVIORALdoula training

Sponsors

Saint Peters University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
16 Years to 45 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frame
Length of labor
type of delivery
type and timing of analgesia/anesthesia

Secondary

MeasureTime frame
Birthweight
neonatal Apgar score at 1 and 5 minutes after birth

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026