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临床试验/NCT03301610
NCT03301610已完成不适用

The Impact of Mobile Education Delivery on Postoperative Pain Outcomes

Mayo Clinic2 个研究点 分布在 1 个国家目标入组 133 人开始时间: 2017年10月23日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
Mayo Clinic
入组人数
133
试验地点
2
主要终点
Difference in self-reported pain scores

研究概览

简要总结

The purpose of this study is to explore the clinical impact of pain management education using a mobile web-based education delivery system compared to standard education delivery. This study seeks to understand the difference between two different education delivery methodologies and the effect on the postoperative pain experience, including participation in treatment plan, knowledge, pain outcomes, and opioid requirements in patients undergoing major hip (THA) and knee (TKA) arthroplasty. It is hypothesized that a real-time, interactive, mobile education system will demonstrate improved pain associated outcomes and higher patient participation when compared to the current standard education delivery method.

研究设计

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

入排标准

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

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Mobile Education Delivery

Experimental

The participants in the study arm will receive comprehensive pain management education delivered using mobile iPads at the point of care. The mobile based education modules will be inclusive of the use of the pain rating scale and assessment of pain; communication with healthcare providers; daily expectations for pain and pain management; pharmacologic and non-pharmacologic treatment options; medication side effects and safety; and discharge instructions including safe handling of opioids, disposal, tapering, and when to call the provider. It will also include an interactive pain and discomfort menu, knowledge based questions, and medication tracking log.

干预措施: Mobile Education Delivery (Other)

Standard verbal and written education

Placebo Comparator

The control group will receive the current standard of care which consists of verbal instruction and pain management educational pamphlets. At a minimum, the patients will receive two educational pamphlets titled Your Pain and Discomfort Management Menu and Communicating About Your Pain. Verbal instruction is nurse dependent. At a minimum the nurse will provide the two pamphlets to the patient and follow-up with the patient to address any questions.

干预措施: Standard Verbal and Written Education (Other)

结局指标

主要结局

Difference in self-reported pain scores

时间窗: Post-intervention, at the time of discharge from the hospital (between 1 and 5 days post-surgery)

Scores are measured using a 10 point (Lickert) pain rating scale. The scale ranges from 0 to 10 with the lower score indicating less pain and the higher score indicating greater pain.

次要结局

  • Difference in self-reported participation in pain management(Post-intervention, at the time of discharge from the hospital (between 1 and 5 days post-surgery))
  • Difference in post-operative opioid requirements(Post-intervention, at the time of discharge from the hospital (between 1 and 5 days post-surgery))
  • Difference in usefulness of education(Post-intervention, at the time of discharge from the hospital (between 1 and 5 days post-surgery))
  • Change in pain management knowledge(Pre-intervention (between 1 and 5 days before surgical procedure) and post-intervention, at the time of discharge from the hospital (between 1 and 5 days post-surgery))
  • Difference in use of non-pharmacologic pain modalities(Post-intervention, at the time of discharge from the hospital (between 1 and 5 days post-surgery))

研究者

发起方
Mayo Clinic
申办方类型
Other
责任方
Principal Investigator
主要研究者

Amber M. Stitz

Clinical Nurse Specialist

Mayo Clinic

研究点 (2)

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