跳至主要内容
临床试验/NCT03359798
NCT03359798撤回不适用

The Effect of a Counseling Intervention on Post-cesarean Section Narcotic Use: a Randomized Controlled Trial

Brigham and Women's Hospital0 个研究点开始时间: 2017年12月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
撤回
主要终点
quantity of narcotics used in-hospital

研究概览

简要总结

This study is a randomized controlled trial to investigate the effect of a simple counseling intervention on post-operative narcotic requirements, with the hypothesis that women receiving this intervention will use fewer narcotics for pain management following cesarean section.

详细描述

All women undergoing scheduled cesarean section at Brigham and Women's Hospital who meet eligibility for the study will be approached in the pre-operative area on the Labor and Delivery floor prior to her scheduled cesarean section. For eligible patients interested in participation, consent will be obtained, and the participant will be randomized to receive either an intervention script containing counseling about post-op narcotic use, or the control script containing information regarding post-partum depression. This script will then be read to the participant in the pre-operative area prior to her scheduled cesarean section.

Two types of data will then be collected: inpatient data, and outpatient data. Regarding inpatient data, study investigators will collect information from the electronic medical record about the quantity of narcotics used in the hospital, pain scores while in the hospital, and demographic information. In terms of outpatient data, study investigators will contact participants at 2 weeks and 6 weeks post-partum with questions from the Edinburgh post-partum depression scale score and the WHOQOL-BREF scale score, along with questions regarding their narcotic use at home. Specifically, participants will be asked during the informed consent process whether they agree to 1) receive an email with a brief online survey at 2 weeks post-partum, and 2) receive a follow-up phone call within the week after the email survey was sent if survey responses are not received, 3) receive a second email with a brief online survey at 6 weeks post-partum, 4) receive a follow-up phone call within the week after the second email survey was sent if survey responses are not received. Surveys will be emailed to participants using the Partner's REDCap service that is located behind the Partner's firewall. Investigators will also mine information about each participant's narcotic use from the MassPAT prescription monitoring database.

The endpoint of the study will be enrollment of our desired sample size.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者
是

入选标准

  • •Delivery by scheduled cesarean section at Brigham and Women's Hospital

排除标准

  • •Answer "yes" to the question: "Has any provider talked to you this pregnancy about medications for pain control after your c-section?"
  • •History of opiate abuse
  • •Use of chronic opiates, benzodiazepines or gabapentin
  • •History of chronic pain
  • •Cesarean hysterectomy
  • •Vertical skin incision
  • •Myomectomy at the time of cesarean section
  • •Non English-speaking
  • •Patient of the investigator performing the recruitment

研究组 & 干预措施

Narcotic counseling script

Experimental

Study participants will be read a script regarding post-cesarean section narcotic use.

干预措施: Narcotic counseling script (Behavioral)

Post-partum depression counseling script

Sham Comparator

Study participants will be read a script of the same length, and much of the same wording as the experimental script. However, this script's content is focused on post-partum depression.

干预措施: Post-partum depression counseling script (Behavioral)

结局指标

主要结局

quantity of narcotics used in-hospital

时间窗: 4 days

次要结局

  • quantity acetaminophen used in-hospital(4 days)
  • quantity ibuprofen used in-hospital(4 days)
  • quantity ketorolac used in-hospital(4 days)
  • pain scale in-hospital(1 day, 4 days)
  • narcotic prescription filled after discharge(2 weeks)
  • quantity of narcotics taken after discharge(2 weeks)
  • Edinburgh post-partum depression score(2 weeks and 6 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Julian N Robinson

Chief of Obstetrics, Associate Professor of Obstetrics and Gynecology

Brigham and Women's Hospital

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