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临床试验/NCT05915650
NCT05915650已完成不适用

Application of PNE in Postoperative Pain Management of Patients With Primary Total Knee Arthroplasty

Zunyi Medical College1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2020年12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
70
试验地点
1
主要终点
Visual analogue scale pain score, (VAS)

研究概览

简要总结

This study intends to carry out pain neuroscience education intervention for TKA patients to clarify the effect of this method on the degree of postoperative pain, the incidence of pain catastrophizing, kinesiophobia, and knee joint function rehabilitation in TKA patients, so as to provide a basis for clinical nursing of such patients.

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
Single (Outcomes Assessor)

入排标准

年龄范围
45 Years 至 74 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients diagnosed as KOA according to the criteria and undergoing unilateral total knee arthroplasty for the first time;
  • The subjects included in this study were men or women aged 45-74 years;
  • Clear self-cognition, can browse the text by themselves or can answer questions correctly;
  • Those who voluntarily participated in the study and signed an informed consent form after understanding the relevant information of the study;
  • Without serious physical diseases such as heart, liver or kidney;
  • No history of mental illness or drug dependence.

排除标准

  • Combined with severe trauma in other parts;
  • Accompanied by serious damage to other organs, such as heart and cerebrovascular diseases, lung and kidney diseases;
  • Patients with knee tumor and severe knee deformity who could not complete the rehabilitation;
  • With neurological diseases that limit physical activity;
  • Participating in other investigators during the same period.

结局指标

主要结局

Visual analogue scale pain score, (VAS)

时间窗: 3 months after discharge

Status of pain

次要结局

未报告次要终点

研究者

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

Yongmei Zhang

Study Director

Zunyi Medical College

研究点 (1)

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