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【ChiCTR2100053637】Effect of a patient education video and prehabilitation on the quality of preoperative person-centred coordinated care experience: a randomized controlled trial

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基本信息

登记号

ChiCTR2100053637

试验状态

正在进行

药物名称

药物类型

规范名称

首次公示信息日的期

2021-11-26

临床申请受理号

靶点

适应症

quality of preoperative person-centred coordinated care experience

试验通俗题目

Effect of a patient education video and prehabilitation on the quality of preoperative person-centred coordinated care experience: a randomized controlled trial

试验专业题目

Effect of a patient education video and prehabilitation on the quality of preoperative person-centred coordinated care experience: a randomized controlled trial

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临床试验信息

试验目的

The primary objective of this randomized controlled trial (RCT) is to evaluate the effect of prehabilitation (patient education video and multimodal prehabilitation) on the preoperative patient-centred coordinated care experience. The secondary objective is to assess the effect of prehabilitation on preoperative anxiety and depression levels, quality of recovery and days alive and at home within 30 days after surgery (DAH30).

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试验类型

随机平行对照

试验分期

其它

随机化

The study design is a single-centre, single-blinded, two-group, parallel, superiority RCT. Patients will be randomized to receive either preoperative patient education comprising of a video and prehabilitation program with standard care (intervention) or standard care (control). Block randomization with 1:1 ration.

盲法

Not stated

试验项目经费来源

department funding

试验范围

目标入组人数

实际入组人数

第一例入组时间

2023-10-26

试验终止时间

2024-12-31

是否属于一致性

入选标准

1. Adults (> 18y old) undergoing major to ultra-major elective surgery cardiac (CABG+/-valve/valve only surgery; 2. Adults (>= 50 years) undergoing major colorectal, hepatobiliary-pancreatic or urology surgery; 3. Primary language is either English or Cantonese; 4. Prefrail to moderately frail patients with a Clinical Frailty Scale (CFS) of 4-6 at the time of accepting surgery at the outpatient surgical/nurse clinic; 5. Patients with estimated >= 4 weeks of surgical waiting list time.；

排除标准

Contraindications for prehabilitation, such as those with cognitive deficits who are unable to comply with study procedures, physical limitations that would preclude prehabilitation and inability to regularly attend prehabilitation sessions, such as those who are severely frail (CSF 7-9).；

研究者信息

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试验机构

Department of Anesthesia and Intensive Care, The Chinese University of Hong Kong

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