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The Correlation Between Prelabor Analgesic Plan and Actual Labor Analgesia With Satisfaction, Postpartum Depression, and Breast Feeding Success

2017年11月16日 更新者:sharonorbach、Rabin Medical Center

In this study the investigators would like to evaluate how prelabor analgesic plan and actual labor analgesia effects the labor satisfaction, breastfeeding success, and whether or not it reduces postpartum depression.

Although postpartum depression has been researched and reviewed, there is little information on how satisfaction during labor affects postpartum outcomes. The relationship between epidural analgesia is also complex, and there has yet to be found a valid correlation between the two parameters.

In addition although an attempt has been made to evaluate relationship between breastfeeding and epidural analgesia, results are unclear and further research is needed.

研究概览

地位

完全的

详细说明

This is a prospective, single center study, which will be conducted at the Rabin Medical Center (Beilinson Campus), Petach Tikva, Israel, a tertiary university hospital.

All women undergoing vaginal delivery on the first day postpartum will be enrolled after filling out an informed consent.

They will be given out a labor satisfaction questionnaire detailing initial desire for epidural analgesia, final desire for epidural analgesia, adequacy of pain relief during labor and satisfaction with labor. (see appendix 1).

The investigators will evaluate breastfeeding success according to the latch scoring system in the first day postpartum which is routinely administered by nurses/ lactation consultants in the maternity ward.

According to their initial desire verses final analgesic choice they will be divided into four groups:

  1. Women who initially didn't want and didn't receive one.
  2. Initially didn't want and did receive one.
  3. Initially wanted an epidural and didn't received one
  4. Initially wanted an epidural and did receive one.

On the third day postoperatively the parturients will be called and assessed for mood and signs of postpartum depression using Edinborough Postnatal Depression scale validated into Hebrew (10) , and the investigators will assess whether or not they are breastfeeding.

At 6 weeks the investigators will follow-up to assess breastfeeding duration ,and postpartum depression using the Edinborough Postnatal Depression scale.

The investigators' comparison will include average pain scores, breast feeding success, and postpartum depression assessment.

研究类型

观察性的

注册 (实际的)

1954

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

      • Petach tikvah、以色列
        • Beilinson Hospital

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 至 55年 (成人)

接受健康志愿者

是的

有资格学习的性别

女性

取样方法

非概率样本

研究人群

Women above 18 undergoing vaginal delivery in Beilinson Hospital

描述

Inclusion Criteria:

  • Women above 18 undergoing vaginal delivery in Beilinson Hospital
  • following obtaining written informed consents
  • ability to comply with the study requirements will be included in the investigators' study

Exclusion Criteria:

  • Women undergoing cesareans sections.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

队列和干预

团体/队列
干预/治疗
Initially didn't want an epidural and didn't receive one.
Initially didn't want an epidural and did receive one.
Initially wanted an epidural and didn't received one

Parturients will be asked to fill out a labor satisfaction questionnaire detailing initial desire for epidural analgesia, final desire for epidural analgesia, adequacy of pain relief during labor and satisfaction with laborOn the third day postoperatively the parturients will be called and assessed for mood and signs of postpartum depression using Edinborough Postnatal Depression scale validated into Hebrew (10) , and we will assess whether or not they are breastfeeding.

At 6 weeks we will follow-up to assess breastfeeding duration ,and postpartum depression using the Edinborough Postnatal Depression scale.

Our comparison will include average pain scores, breast feeding success, and postpartum depression assessment.

Initially wanted an epidural and did receive one.

Parturients will be asked to fill out a labor satisfaction questionnaire detailing initial desire for epidural analgesia, final desire for epidural analgesia, adequacy of pain relief during labor and satisfaction with laborOn the third day postoperatively the parturients will be called and assessed for mood and signs of postpartum depression using Edinborough Postnatal Depression scale validated into Hebrew (10) , and we will assess whether or not they are breastfeeding.

At 6 weeks we will follow-up to assess breastfeeding duration ,and postpartum depression using the Edinborough Postnatal Depression scale.

Our comparison will include average pain scores, breast feeding success, and postpartum depression assessment.

研究衡量的是什么?

主要结果指标

结果测量
大体时间
Assessment of postpartum depression using Edinborough Postnatal Depression scale
大体时间:One year
One year

次要结果测量

结果测量
大体时间
Assessment of breast feeding duration in women undergoing vaginal deliveries
大体时间:one year
one year
Increases in labor satisfaction defined as a vas (visual analog scale) satisfaction over 7 in women undergoing vaginal deliveries
大体时间:one year
one year

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

一般刊物

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2015年6月1日

初级完成 (实际的)

2016年8月1日

研究完成 (实际的)

2016年9月1日

研究注册日期

首次提交

2015年6月17日

首先提交符合 QC 标准的

2015年7月10日

首次发布 (估计)

2015年7月13日

研究记录更新

最后更新发布 (实际的)

2017年11月17日

上次提交的符合 QC 标准的更新

2017年11月16日

最后验证

2017年11月1日

更多信息

与本研究相关的术语

其他研究编号

  • 0666-14-RMC

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