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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04687085
Other study ID # 2019P003456
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 21, 2020
Est. completion date November 30, 2021

Study information

Verified date March 2022
Source Brigham and Women's Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Given the high prevalence of neuraxial analgesia use during labor and the anxiety associated with these procedures, a method to decrease this anxiety could benefit millions of laboring women each year. Mindfulness practice has been used by many groups to decrease anxiety during pregnancy with optimistic results. However, there has been no major study evaluating the role of mindfulness interventions on anxiety associated with neuraxial placement. The purpose of our study is to address this gap in knowledge.


Description:

The primary objective of this study is to evaluate the effects of a brief mindful meditation intervention on anxiety and satisfaction regarding epidural catheter placement for laboring parturients.The investigators hypothesize that a brief mindful meditation intervention, consisting of a 10 minute auditory instructional practice, implemented before epidural catheter placement will: 1. Decrease anxiety 2. Increase satisfaction compared to a neutral 10 minute auditory recording control, in participants undergoing labor epidural catheter placement. The secondary objective of this study is to evaluate whether anesthesia providers experience a difference in satisfaction with labor epidural catheter placement in participants who listen to a brief mindful meditation intervention prior to epidural catheter placement. The investigators hypothesize that anesthesia providers placing labor epidural catheters in patients who listen to a brief mindful meditation intervention prior to labor epidural catheter placement will: 1. Experience an increase in satisfaction with labor epidural catheter placement.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date November 30, 2021
Est. primary completion date November 30, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: - Patients are eligible for enrollment if they are greater than 18 years of age, admitted for vaginal delivery, anticipating epidural analgesia, and report a numerical pain scale rating of 3 or less at the time of enrollment. Exclusion Criteria: - Do not speak English or admitted for cesarean delivery will be excluded from the study

Study Design


Related Conditions & MeSH terms


Intervention

Other:
10 minute mindful meditation recording
10 minute mindful meditation recording

Locations

Country Name City State
United States Brigham and Women's Hospital Boston Massachusetts

Sponsors (1)

Lead Sponsor Collaborator
Brigham and Women's Hospital

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Anxiety level after epidural catheter placement Level of anxiety on a numerical rating scale Measure 1 time, 10 minutes after epidural catheter placement
Primary Pain level after epidural catheter placement Level of pain on a numerical rating scale Measure 1 time, 10 minutes after epidural catheter placement
Secondary Provider satisfaction level after epidural catheter placement Anesthesia provider placing the epidural catheter satisfaction with placement conditions on a numerical rating scale Measure 1 time, 10 minutes after epidural catheter placement
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