容量型呼吸训练器在老年结直肠肿瘤患者围术期的应用效果评价

注册号:

Registration number:

ChiCTR2500111497 

最近更新日期:

Date of Last Refreshed on:

2025-10-31 16:52:28 

注册时间:

Date of Registration:

2025-10-31 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

容量型呼吸训练器在老年结直肠肿瘤患者围术期的应用效果评价

Public title:

The application of volume-based respiratory training device in the perioperative period of elderly colorectal tumor patients

注册题目简写:

English Acronym:

研究课题的正式科学名称:

容量型呼吸训练器在老年结直肠肿瘤患者围术期的应用效果评价

Scientific title:

The application of volume-based respiratory training device in the perioperative period of elderly colorectal tumor patients

研究课题代号(代码):

Study subject ID:

在二级注册机构或其它机构的注册号:

The registration number of the Partner Registry or other register:

申请注册联系人:

廖曦 

研究负责人:

廖曦 

Applicant:

Liao Xi 

Study leader:

Liao Xi 

申请注册联系人电话:

Applicant telephone:

+86 28 8542 2480

研究负责人电话:

Study leader's
telephone:

+86 28 8542 2480

申请注册联系人传真 :

Applicant Fax:

研究负责人传真:

Study leader's fax:

申请注册联系人电子邮件:

Applicant E-mail:

2379133447@qq.com

研究负责人电子邮件:

Study leader's E-mail:

2379133447@qq.com

申请单位网址(自愿提供):

Applicant website(voluntary supply):

研究负责人网址(自愿提供):

Study leader's website(voluntary supply):

申请注册联系人通讯地址:

四川省成都市国学巷37号

研究负责人通讯地址:

四川省成都市国学巷37号

Applicant address:

#37 Guoxue Lane, Wuhou District, Chengdu City, Sichuan Province

Study leader's address:

#37 Guoxue Lane, Wuhou District, Chengdu City, Sichuan Province

申请注册联系人邮政编码:

Applicant postcode:

研究负责人邮政编码:

Study leader's postcode:

申请人所在单位:

四川大学华西医院

Applicant's institution:

West China Hospital ,Sichuan University

研究负责人所在单位:

四川大学华西医院

Affiliation of the Leader:

West China Hospital of Sichuan University

是否获伦理委员会批准:

Approved by ethic committee:

Yes

伦理委员会批件文号:

Approved No. of ethic committee:

2025年审(1534)号

伦理委员会批件附件:

Approved file of Ethical Committee:

查看附件View

批准本研究的伦理委员会名称:

四川大学华西医院生物医学伦理审查委员会

Name of the ethic committee:

Ethics Committee on Biomedical Research West China Hospital of Sichuan University

伦理委员会批准日期:

Date of approved by ethic committee:

2025-09-09 00:00:00

伦理委员会联系人:

李娜

Contact Name of the ethic committee:

Li Na

伦理委员会联系地址:

四川省成都市国学巷37号

Contact Address of the ethic committee:

#37 Guoxue Lane, Wuhou District, Chengdu City, Sichuan Province

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 28 85422654

伦理委员会联系人邮箱:

Contact email of the ethic committee:

188974152@qq.com

研究实施负责(组长)单位:

四川大学华西医院

Primary sponsor:

West China Hospital of Sichuan University

研究实施负责(组长)单位地址:

四川省成都市国学巷37号

Primary sponsor's address:

#37 Guoxue Lane, Wuhou District, Chengdu City, Sichuan Province

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

四川省

市(区县):

Country:

China

Province:

Sichuan

City:

单位(医院):

四川大学华西医院

具体地址:

四川省成都市国学巷37号

Institution
hospital:

West China Hospital of Sichuan University

Address:

#37 Guoxue Lane, Wuhou District, Chengdu City, Sichuan Province

经费或物资来源:

四川省科技厅

Source(s) of funding:

Sichuan Provincial Department of Science and Technology

研究疾病:

结直肠肿瘤;肺部感染  

Target disease:

Colorectal tumor;Pulmonary infection

研究疾病代码:

Target disease code:

研究类型:

干预性研究

Study type:

Interventional study

研究所处阶段:

其它 

Study phase:

N/A

研究设计:

随机平行对照 

Study design:

Parallel 

研究目的:

主要目的:研究老年结直肠肿瘤患者在围手术期使用容量型呼吸训练器,对于提升肺功能与降低术后肺部并发症的效果评价; 次要目的:研究老年结直肠肿瘤患者在围手术期使用容量型呼吸训练器,对术后生活质量、活动能力、其他术后并发症的发生率和住院时间等方面的影响。  

Objectives of Study:

Main purpose: The effect evaluation of using volume-based respiratory trainer in perioperative period of elderly colorectal tumor patients on improving pulmonary function and postoperative pulmonary complications; Secondary purpose: The effect of using a volume-based respiratory trainer in the perioperative period of elderly patients with colorectal tumors on postoperative of life, activity ability, the incidence of other postoperative complications, and hospital stay.

药物成份或治疗方案详述:

 

Description for medicine or protocol of treatment in detail:

 

纳入标准:

Inclusion criteria

排除标准:

1.吸气肌疲劳、呼吸肌功能重度受损、生命体征不稳定、谵妄、意识模糊、严重营养 不良(如低蛋白血症,血清白蛋白<25g/L)、恶病质、气胸、肺大泡、肺水肿、近期心 梗或不稳定心绞痛、中重度肝功能不全、近期面部-口腔-颅底手术或外伤、术后活动性出血、高度怀疑或确诊存在吻合口瘘与疝气的患者、化疗灌注术后患者(尤其腹腔热灌 注化疗 HIPEC)、阑尾肿瘤需要灌注的患者、活动性腹腔内感染/脓肿、中-大量的胸腔 积液与腹腔积液、腹水、腹腔粘连或肠梗阻、正在使用特定抗血管生成靶向药物的患者 (如贝伐珠单抗),以及长期激素的术后患者。

Exclusion criteria:

1.Patients with inspiratory muscle fatigue, severe impairment of respiratory muscle function, unstable vital signs, delirium, confusion, severe malnutritionsuch as hypoproteinemia, serum albumin (<25g/L), cachexia, pneumothorax, pulmonary bullae, pulmonaryema, recent myocardial infarction or unstable angina, moderate-severe hepatic insufficiency, recent facial-oral-cranial base surgery trauma, postoperative active bleeding, highly suspected or confirmed anastomotic leakage and hernia, patients after chemotherapy perfusion (especially HIPEC), patients with appendice tumors requiring perfusion, active intra-abdominal infection/abscess, moderate-large amount of pleural effusion and ascites, ascites, intra-abdom adhesions or intestinal obstruction, patients using specific anti-angiogenic targeted drugs (such as bevacizumab), and patients after long-term hormone use .

研究实施时间:

Study execute time:

From 2025-11-01 00:00:00 To 2026-11-01 00:00:00  

征募观察对象时间:

Recruiting time:

From 2025-11-01 00:00:00 To 2026-11-01 00:00:00

干预措施:

Interventions:

组别:

试验组

样本量:

50

Group:

Experimental group

Sample size:

干预措施:

容量型呼吸训练器

干预措施代码:

Intervention:

Volume-based respiratory training device

Intervention code:

组别:

对照组

样本量:

50

Group:

Control group

Sample size:

干预措施:

常规呼吸训练

干预措施代码:

Intervention:

Routine respiratory training

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

四川省 

市(区县):

 

Country:

China

Province:

Sichuan

City:

单位(医院):

四川大学华西医院 

单位级别:

三级甲等 

Institution
hospital:

West China Hospital of Sichuan University

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

生活质量

指标类型:

次要指标

Outcome:

Quality of life

Type:

Secondary indicator

测量时间点:

术前 1 天、术后 1 天、出院当天与术后 2 周。

测量方法:

使用FACT-G 问卷(大肠癌特异性量表)、EORTC-QLQ-CR38(大肠癌生活质量特异性量表)、癌症疲乏表(CFS)评估

Measure time point of outcome:

Preoperative 1 day; postoperative 1 day; day of discharge and 2 weeks after surgery.

Measure method:

Use of the FACT-G questionnaire (colorectal cancer-specific scale), EORTC-QLQ-CR38 (coloreal cancer-specific quality of life scale), and the cancer fatigue scale (CFS) to assess.

指标中文名:

肺部并发症

指标类型:

主要指标

Outcome:

Pulmonary complications

Type:

Primary indicator

测量时间点:

住院期间观察和术后 2 周

测量方法:

采用Clavien-Dindo 分级或术后肺部并发症标准化定义

Measure time point of outcome:

Observation during hospitalization and 2 weeks postoperatively

Measure method:

Adopted the Clavien-Dindo grade or the standardized definition of postoperative pulmonary complications.

指标中文名:

改良Borg呼吸困难量表

指标类型:

主要指标

Outcome:

Modified Borg Dyspnea scale

Type:

Primary indicator

测量时间点:

术前 1 天、术后 1 天、出院当天与术后 2 周。

测量方法:

使用改良Borg呼吸困难量表评估

Measure time point of outcome:

Preoperative 1 day; postoperative 1 day; day of discharge and 2 weeks after surgery.

Measure method:

Use the modified Borg Dyspnea scale to assess.

指标中文名:

6 分钟步行距离

指标类型:

次要指标

Outcome:

6 minute walk test,6MWT

Type:

Secondary indicator

测量时间点:

术前 1 天、术后 1 天、出院当天与术后 2 周。

测量方法:

是让患者采用徒步的运动方式,测试其在6分钟内,在平坦硬地上,以能承受的最快速度行走的最远距离。

Measure time point of outcome:

Preoperative 1 day; postoperative 1 day; day of discharge and 2 weeks after surgery.

Measure method:

It tests how far a patient can walk in six minutes at the fastest speed they can manage on a flat hard surface.

指标中文名:

咳嗽效能评分

指标类型:

主要指标

Outcome:

Cough efficacy score

Type:

Primary indicator

测量时间点:

术前 1 天、术后 1 天、出院当天与术后 2 周。

测量方法:

根据患者咳嗽的声音、力量、咳嗽频率等表现进行评分,分为1-4分。

Measure time point of outcome:

Preoperative 1 day; postoperative 1 day; day of discharge and 2 weeks after surgery.

Measure method:

Scoring based on the sound, strength, frequency of coughing.Scored 1-4 points.

指标中文名:

低氧血氧并发症

指标类型:

次要指标

Outcome:

Hypoxemia complication

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

住院天数

指标类型:

次要指标

Outcome:

Number of days hospitalized

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

术后30天再入院率

指标类型:

次要指标

Outcome:

30-day readmission rate after surgery

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

血液指标

指标类型:

次要指标

Outcome:

Blood indicators

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

采集人体标本:

Collecting sample(s)
from participants:

标本中文名:

组织:

Sample Name:

NA

Tissue:

人体标本去向

其它  

说明

Fate of sample:

0thers  

Note:

征募研究对象情况:

Recruiting status:

尚未开始

Not yet recruiting

年龄范围:

Participant age:

最小 Min age 60 years
最大 Max age 80 years

性别:

男女均可

Gender:

Both

随机方法(请说明由何人用什么方法产生随机序列):

由研究者采用计算机随机分组法

Randomization Procedure (please state who generates the random number sequence and by what method):

Computerized random grouping method by the researcher

是否公开试验完成后的统计结果:

Calculated Results after the Study Completed public access:

不公开/Private

盲法:

对研究参与者、数据分析者设盲

Blinding:

Blinding for study participants and data analysts

是否共享原始数据:

IPD sharing

是Yes

共享原始数据的方式(说明:请填入公开原始数据日期和方式,如采用网络平台,需填该网络平台名称和网址):

研究结束后6个月,经研究者同意后可邮箱获取;

The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url):

Six months after the study ends, it can be obtained by email with the researcher's consent;

数据采集和管理(说明:数据采集和管理由两部分组成,一为病例记录表(Case Record Form, CRF),二为电子采集和管理系统(Electronic Data Capture, EDC),如ResMan即为一种基于互联网的EDC:

本研究的数据采集和管理由两部分组成,一为使用自制的病例记录表采集数据,二为使用电子管理系统管理患者数据。

Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture:

The data collection and management in this study consist of two parts: one is to collect data using self-made case record forms, and the other is to manage patient data using an electronic management system.

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2025-10-31 16:51:51