Satisfaction in women who have recently given birth receiving epidural analgesia after shared-decision making before the onset of labor

Not Applicable

Completed

• Conditions: Epidural analgesia during childbirth; Pregnancy and Childbirth

• Registration Number: ISRCTN14256563
• Lead Sponsor: Chi Mei Medical Center

Brief Summary

2020 Results article in https://pubmed.ncbi.nlm.nih.gov/32689958/ results (added 22/07/2020)

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2019-12-31
• Study Start: 2020-04-15
• Last Update Posted: 26 June 2023

Recruitment & Eligibility

• Status: Completed
• Sex: Female
• Target Recruitment: 200

Inclusion Criteria

Parturients after natural spontaneous delivery who have used epidural analgesia during the natural birth process

Exclusion Criteria

1. Mental disorders or emotional disorders, regardless of whether they are receiving psychiatric medication
2. Drug addiction or drug dependence (for example, those who have a history of drug use, or who have used morphine analgesics daily for more than 30 mg of oral morphine equivalent for more than six weeks)
3. Cannot read Chinese
4. In the intensive care unit after delivery

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Satisfaction measured using a novel questionnaire combining elements of Pregnancy and Maternity Care Patients’ Experiences Questionnaire (PreMaPEQ), Preterm Birth Experience and Satisfaction Scale (P-BESS), and Women’s Views of Birth Labor Satisfaction Questionnaire (WOMBLSQ) after giving birth.

Secondary Outcome Measures

Name	Time	Method
Comprehension of the consenting process measured using a novel questionnaire combining elements of Pregnancy and Maternity Care Patients’ Experiences Questionnaire (PreMaPEQ), Preterm Birth Experience and Satisfaction Scale (P-BESS), and Women’s Views of Birth Labor Satisfaction Questionnaire (WOMBLSQ) after giving birth.