CClinicalTrials.gg
CompletedNCT00826735Updated Jan 22, 2009

The Effect of Guided Imagery on the Third Stage of Labor

An interventional study of Guided imagery in Third Stage of Labor, Bleeding and Guided Imagery, sponsored by Vanderbilt University. Completed at 1 site in United States. Open to female participants aged 18 Years to 34 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2009-01-22.

Sponsored by Vanderbilt University · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Ages
18 Years to 34 Years
Sex
Female
01

Study summary

The purpose of this study was to evaluate the effect of guided imagery on the third stage of labor. Blood loss from hemorrhage during childbirth, most commonly due to uterine atony, is one of the leading causes of maternal mortality in the United States and the leading cause of maternal death worldwide. The hypothesis was that the use of physiologic guided imagery would reduce the amount of bleeding during the third stage of labor.

02

Conditions studied

  • Third Stage of Labor
  • Bleeding
  • Guided Imagery
  • Childbirth

Browse trials for

Keywords

  • third stage of labor
  • bleeding
  • guided imagery
  • childbirth
03

In context

Hemorrhage

3,000 studies on the registry are indexed under Hemorrhage; 474 are open to participants now.

Browse Hemorrhage studies →

Lead sponsor

Vanderbilt University is the lead sponsor of 508 studies on the registry; 19 are open to participants now.

Of its 7 completed or terminated interventional studies of FDA-regulated products, 5 (71%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 34 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes

Inclusion criteria

  • 18 years of age or older but less than 35 years
  • English as her primary language
  • fetus in a cephalic presentation
  • singleton pregnancy
  • 36 to 38 estimated gestational weeks
  • no contraindications to vaginal delivery
  • maternal weight less than 200 pounds prior to pregnancy

Exclusion criteria

Exclusion Criteria:

  • more than four previous children
  • a history of postpartum hemorrhage
  • bleeding disorder
  • seizure disorder
  • polyhydramnios
  • diabetes (including gestational)
  • hypertension
  • cardiac disease
  • uterine fibroids
  • anemia (hematocrit less than 30)
  • intrauterine fetal demise or tobacco use
05

Study design

Phase
Not applicable
Primary purpose
Prevention

Study arms

  • Experimental
    Guided imagery

    The experimental group received a relaxation focused guided imagery intervention to use through the remainder of pregnancy plus a physiologic guided imagery intervention during the third stage of labor. These interventions were scripted and prerecorded on CDs.

    Behavioral: Guided imagery

Interventions

  • BehavioralGuided imagery

    A relaxation focused guided imagery intervention was used through the remainder of pregnancy plus a physiologic guided imagery intervention was used during the third stage of labor.

06

What researchers measure

Primary outcomes

  1. Blood Loss

Secondary outcomes

  1. Length of third stage of labor

07

Study locations

1 site
  • Vanderbilt University Medical Center
    Nashville, Tennessee 37240, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 22, 2009, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00826735
Lead sponsor
Vanderbilt University
Collaborators
Sigma Theta Tau International, Iota chapter, Sigma Theta Tau International, Delta Psi chapter, American College of Nurse-Midwive - ACNM Foundation
First posted
Jan 22, 2009
Start date
Jan 2007
Primary completion
Dec 2007
Completion
Dec 2007
Last update
Jan 22, 2009

Study contacts

Mavis N Schorn, PhD
principal investigator · Vanderbilt University School of Nursing

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2009. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion