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临床试验/NCT03698773
NCT03698773已完成不适用

Satisfaction of Pain Relief During Labor and Delivery Following Access to New Educational Materials

University of New Mexico2 个研究点 分布在 1 个国家目标入组 106 人开始时间: 2018年10月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
106
试验地点
2
主要终点
Patient Satisfaction With Pain Control in Labor

研究概览

简要总结

This study compares patient satisfaction after labor and delivery with access to either the default educational materials available, or to a table computer set to display an educational website, thepainlesspush.com.

详细描述

This is a prospective randomized controlled study. The investigators hypothesize that parturients with access to the website will exhibit greater satisfaction with labor and delivery pain control.

Potential participants will be recruited from the University of New Mexico Hospital (UNMH) Labor & Delivery floor. Patients will be enrolled following an oral consent process. They will be randomized into either control group or intervention group. Control group participants will have their standard of care visit with an anesthesiologist and routine hospital pain-relief information. Intervention group participants will have their standard of care visit with an anesthesiologist, plus one hour in which to view the patient education website thepainlesspush.com, on an iPad provided by the Anesthesiology department for this purpose. After their delivery and transfer to the mother/baby unit, participants will complete a satisfaction survey brought to them by a study team member. Participants will complete the survey following their delivery and prior to discharge. The primary team will notify us with expected discharge in which we will retrieve the survey from them in their room and answer any last questions. Their active participation in the study will be complete at this time. After a participant completes the satisfaction survey, research team members will collect demographic information and relevant obstetric/medical history information from the electronic medical record.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • All English- or Spanish-speaking patients who are admitted to UNMH Labor and Delivery for planned progression to active labor.

排除标准

  • Age under 18 years
  • Patients unable to provide consent for medical procedures
  • Patients who do not speak either English or Spanish

结局指标

主要结局

Patient Satisfaction With Pain Control in Labor

时间窗: Following delivery and prior to discharge, up to two days

Satisfaction as measured by agreement with Likert scale questionnaire item "I was satisfied with my choice for pain control in labor" where 1 = strongly disagree, 3 = neither agree nor disagree, and 5 = strongly agree. High scores indicate high satisfaction.

次要结局

  • Epidural Analgesia Utilization Rate(On day of delivery)

研究者

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

Kathleen Reyes

Assistant Professor

University of New Mexico

研究点 (2)

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