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临床试验/NCT06662981
NCT06662981已完成不适用

The Effect of Preoperative Information and Education in the Clinical Outcome of Total Hip Arthroplasty

National and Kapodistrian University of Athens4 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2022年10月31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
100
试验地点
4
主要终点
Hip pain and functionality

研究概览

简要总结

Preoperative patient information and education is an essential aspect of modern surgical care, particularly for patients undergoing total hip arthroplasty (THA). This prospective, randomized trial aims to assess the effects of structured preoperative education and information on clinical outcomes in patients undergoing THA.

详细描述

A total of 100 patients will be randomized into two groups: the intervention group (n = 50) receiving standardized preoperative information and education, and the control group (n = 50) receiving standard preoperative care without a formal educational component. Postoperative outcomes, including pain, functionality, mobility, length of hospital stay (LOS), health-related quality of life, anxiety and depression will be compared between the 2 groups.

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
50 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

结局指标

主要结局

Hip pain and functionality

时间窗: 30 days postoperatively

Assessed using modified Harris Hip Score (mHHS), validated in Greek, one day preoperatively and one month postoperatively

Length of Hospital Stay

时间窗: 30 days postoperatively

Duration of hospitalization, measured in days

Anxiety and Depression

时间窗: 30 days postoperatively

Assessed using the Hospital Anxiety and Depression Scale (HADS), validated in Greek, one day preoperatively, one day before discharge from hospital, and one month postoperatively

Health-related quality of life

时间窗: 30 days postoperatively

Assessed using EQ-5D-5L index and EQ-5D-5L visual analog scale (VAS), validated in Greek one day preoperatively, one day before discharge from hospital, and one month postoperatively

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

SARA ELENI AMPRACHIM

RN, MSc, MSc, PhD (c), General Hospital of Attica "KAT", Athens, Greece

National and Kapodistrian University of Athens

研究点 (4)

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