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NCT01709591 Clinical Trial

Effect of Prenatal Education on Perceptions of Epidural Acceptance

Labor Pain Clinical Trial

Official title:
Effect of Targeted Prenatal Education on Perceptions of Epidural on Acceptance of Epidural Analgesia: a Randomized Controlled Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01709591
Other study ID # 10-081
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 2011
Est. completion date August 2018

Study information
Verified date August 2020
Source Santa Clara Valley Health & Hospital System
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of the study is to determine if targeted prenatal educational program on womens' perceptions of epidural increases the acceptance of intrapartum epidural analgesia relative to the control group.

Description:

Racial/ethnic disparities exist in the proportion of patients receiving epidural analgesia. The purpose of our study is to determine if culturally-sensitive educational program targeting womens' perceptions of epidural increases the acceptance of intrapartum epidural use.

Recruitment information / eligibility
Status Completed
Enrollment 111
Est. completion date August 2018
Est. primary completion date August 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

1. Women with viable intrauterine gestation seeking prenatal care

2. Candidates for Intrapartum epidural analgesia

Exclusion Criteria:

1. Intrapartum epidural analgesia is contraindicated

2. Trial of labor is contraindicated.

3. Patients planning an elective cesarean

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• Prenatal education

Locations
Country Name City State
United States Santa Clara Valley Health and Hospital System San Jose California

Sponsors (1)
Lead Sponsor Collaborator
Santa Clara Valley Health & Hospital System

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary pre and post intervention PEQ survey results to elucidate the changes in perceptions of epiduralepidural based on the PEQ survey All subjects will be asked to fill out the Perceptions on Epidural Questionnaire (PEQ) to elucidate their desire to receive intrapartum pain control & their attitude towards epidural to patients. Each survey will take approximately five to ten minutes to complete. The survey will be distributed in English and Spanish. One year time period
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