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临床试验/NCT01582984
NCT01582984已完成不适用

Patient Understanding and Satisfaction in Informed Consent for Total Knee Arthroplasty

jasvinder singh2 个研究点 分布在 1 个国家目标入组 176 人开始时间: 2008年2月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
176
试验地点
2
主要终点
Knowledge of efficacy and complications

研究概览

简要总结

A structured consent process, in combination with one or a number of the aforementioned modalities (nursing education, handout, video, etc), may reasonably be expected to improve surgical informed consent. The investigators hypothesized that overall patient knowledge/retention would be influenced by the type of consent process and that more intensive training and review would result in better patient retention and recall. The investigators further hypothesized that the knowledge retention would decline following the consent process and surgery, but in a stratified manner based on the nature of preoperative teaching.

详细描述

please see details above

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
None

入排标准

年龄范围
18 Years 至 110 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • recommended total knee arthroplasty

排除标准

  • Unwilling to participate
  • Unable to complete questionnaire in English

结局指标

主要结局

Knowledge of efficacy and complications

时间窗: 6-week postoperative

answers to questionnaire assessing knowledge

次要结局

  • Patient satisfaction(day of surgery and postoperative 6-weeks)
  • Knowledge regarding peri- and post-operative results(day of surgery and postoperative 6-weeks)
  • knowledge regarding procedural questions with regard to the surgery and implants(Day of surgery and 6-week postoperative)
  • knowledge regarding risks of surgery(day of surgery and postoperative 6-weeks)

研究者

申办方类型
Fed
责任方
Sponsor Investigator
主要研究者

jasvinder singh

worker without compensation

Minneapolis Veterans Affairs Medical Center

研究点 (2)

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