基于循证医学的老年全膝关节置换术后患者康复锻炼方案的构建

注册号:

Registration number:

ChiCTR2600122792 

最近更新日期:

Date of Last Refreshed on:

2026-04-17 16:24:34 

注册时间:

Date of Registration:

2026-04-17 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

基于循证医学的老年全膝关节置换术后患者康复锻炼方案的构建

Public title:

Construction of an Evidence-Based Postoperative Rehabilitation Exercise Intervention Program for Elderly Knee Osteoarthritis Patients Following Total Knee Arthroplasty (TKA)

注册题目简写:

English Acronym:

研究课题的正式科学名称:

基于循证医学的老年全膝关节置换术后患者康复锻炼方案的构建

Scientific title:

Construction of an Evidence-Based Postoperative Rehabilitation Exercise Intervention Program for Elderly Knee Osteoarthritis Patients Following Total Knee Arthroplasty (TKA)

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:

阚亚楠 

研究负责人:

阚亚楠 

Applicant:

Kan Yanan 

Study leader:

Kan Yanan 

申请注册联系人电话:

Applicant telephone:

+86 19560480870

研究负责人电话:

Study leader's
telephone:

+86 19560480870

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:

277387925@qq.com

研究负责人电子邮件:

Study leader's E-mail:

277387925@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:

中国浙江省杭州市上城区邮电路54号

研究负责人通讯地址:

中国浙江省杭州市上城区邮电路54号

Applicant address:

54 Youdian Road, Shangcheng District, Hangzhou, Zhejiang, China

Study leader's address:

54 Youdian Road, Shangcheng District, Hangzhou, Zhejiang, China

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:

浙江省中医院

Applicant's institution:

The First Affiliated Hospital of Zhejiang Chinese Medical University

研究负责人所在单位:

浙江省中医院

Affiliation of the Leader:

Zhejiang Provincial Hospital of TCM

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:

2026-KLS-051-01

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:

浙江中医药大学附属第一医院(浙江省中医院)伦理委员会

Name of the ethic committee:

EC/IRB of the First Affiliated Hospital of Zhejiang Chinese Medical University

伦理委员会批准日期:

Date of approved by ethic committee:

2026-01-19 00:00:00

伦理委员会联系人:

夏冰

Contact Name of the ethic committee:

Xia Bing

伦理委员会联系地址:

中国浙江省杭州市上城区邮电路54号

Contact Address of the ethic committee:

54 Youdian Road, Shangcheng District, Hangzhou, Zhejiang, China

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 571 86620373

伦理委员会联系人邮箱:

Contact email of the ethic committee:

allan.xia.1989@163.com

研究实施负责(组长)单位:

浙江省中医院

Primary sponsor:

Zhejiang Provincial Hospital of TCM

研究实施负责(组长)单位地址:

中国浙江省杭州市上城区邮电路54号

Primary sponsor's address:

54 Youdian Road, Shangcheng District, Hangzhou, Zhejiang, China

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

浙江

市(区县):

Country:

China

Province:

Zhejiang

City:

单位(医院):

浙江省中医院

具体地址:

中国浙江省杭州市上城区邮电路54号

Institution
hospital:

Zhejiang Provincial Hospital of TCM

Address:

54#Youdian Road,Hangzhou,Zhejiang

经费或物资来源:

自筹

Source(s) of funding:

Self-funded

研究疾病:

膝骨关节炎  

Target disease:

Knee osteoarthritis

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:

探索性研究/预试验 

Study phase:

0

研究设计:

随机平行对照 

Study design:

Parallel 

研究目的:

主要目标:为老年全膝关节置换术患者构建循证术后康复锻炼方案,并评估其可行性和初步疗效。 次要目标:优化老年全膝关节置换术患者的术后功能恢复、独立生活能力及生活质量。  

Objectives of Study:

Primary Objective To construct an evidence-based postoperative rehabilitation exercise program for elderly KOA patients following TKA (via evidence synthesis, qualitative interviews, and Delphi expert consultation) and evaluate its feasibility, safety, and preliminary effectiveness through a pilot study. Secondary Objective To improve postoperative functional recovery, independence in activities of daily living, and health-related quality of life in elderly TKA patients via the structured rehabilitation program.

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. 严重认知障碍导致沟通或决策障碍; 2. 需再次入院治疗的重大术后并发症; 3. 严重合并症显著限制运动耐受力(如终末期心脏病或未控制高血压)。 4. 严重听力障碍、疲劳或其他妨碍参与的健康状况; 5. 同时参与其他康复试验或接受冲突性干预措施。

Exclusion criteria:

1. Severe cognitive impairment leads to communication or decision-making disorders; 2. Major postoperative complications requiring readmission; 3. Severe comorbidities significantly limit exercise tolerance (such as end-stage heart disease or uncontrolled hypertension). 4. Severe hearing impairment, fatigue or other health conditions that hinder participation; 5. At the same time, participate in other rehabilitation trials or receive conflicting intervention measures.

研究实施时间:

Study execute time:

From 2026-01-19 00:00:00 To 2026-12-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2026-05-01 00:00:00 To 2026-07-31 00:00:00

干预措施:

Interventions:

组别:

干预组

样本量:

5

Group:

Intervention Group

Sample size:

干预措施:

结构化循证康复方案:住院期间接受术前教育、渐进性阻力训练及早期活动;出院后3个月通过微信进行数字化随访与监测。

干预措施代码:

Intervention:

Structured evidence-based rehabilitation program: preoperative education, progressive resistance training, and early mobilization during hospitalization; digital follow-up and monitoring via WeChat for 3 months after discharge.

Intervention code:

组别:

对照组

样本量:

5

Group:

Control Group

Sample size:

干预措施:

常规术后康复:住院期间接受常规锻炼及口头指导;出院后仅维持常规锻炼及简单肌力训练的口头指导,无结构化随访或数字化支持。

干预措施代码:

Intervention:

Routine postoperative rehabilitation: regular exercises and verbal instructions during hospitalization; maintenance of routine exercises and simple strength training with verbal guidance only after discharge, without structured follow-up or digital support.

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

浙江 

市(区县):

 

Country:

China

Province:

Zhejiang

City:

单位(医院):

浙江省中医院 

单位级别:

三级甲等 

Institution
hospital:

Zhejiang Provincial Hospital of TCM

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

改良膝关节功能恢复评分(MKFRS)的变化

指标类型:

主要指标

Outcome:

Change in Modified Knee Function Recovery Score (MKFRS)

Type:

Primary indicator

测量时间点:

出院后3个月

测量方法:

改良膝关节功能恢复评分量表(MKFRS)

Measure time point of outcome:

3 months after discharge

Measure method:

Modified Knee Function Recovery Score (MKFRS) Scale

指标中文名:

健康相关生活质量

指标类型:

次要指标

Outcome:

Health-Related Quality of Life

Type:

Secondary indicator

测量时间点:

基线、出院后3个月

测量方法:

SF-36量表

Measure time point of outcome:

Baseline, 3 months after discharge

Measure method:

SF-36 Health Survey

指标中文名:

功能独立性

指标类型:

次要指标

Outcome:

Functional Independence

Type:

Secondary indicator

测量时间点:

基线、出院时、出院后3个月

测量方法:

巴氏指数

Measure time point of outcome:

Baseline, at discharge, 3 months after discharge

Measure method:

Barthel Index

指标中文名:

康复锻炼自我效能与依从性

指标类型:

次要指标

Outcome:

Self-efficacy and Adherence to Rehabilitation Exercises

Type:

Secondary indicator

测量时间点:

基线、出院后1个月、出院后3个月

测量方法:

康复锻炼自我效能与依从性量表

Measure time point of outcome:

Baseline, 1 month after discharge, 3 months after discharge

Measure method:

Rehabilitation Exercise Self-efficacy and Adherence Scale

指标中文名:

不良事件发生率及严重程度

指标类型:

副作用指标

Outcome:

Incidence and Severity of Adverse Events

Type:

Adverse events

测量时间点:

整个研究期间

测量方法:

不良事件报告表

Measure time point of outcome:

Throughout the study period

Measure method:

Adverse Event Report Form

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 NA 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):

随机分组将采用生物统计团队生成的计算机随机数列进行。通过使用序列编号的不透明密封信封确保分配隐蔽。

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

Random grouping will be conducted using a computer random sequence generated by the biostatistics team. Ensure the concealment of distribution by using sequence-numbered opaque sealed envelopes.

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:

鉴于康复干预的特性,受试者与干预提供者无法实施盲法;但结局评估者将对分组情况保持盲态

Blinding:

Given the characteristics of rehabilitation intervention, blinding cannot be implemented between the subjects and the intervention providers. However, the outcome evaluators will remain blind to the grouping situation

是否共享原始数据:

IPD sharing

否No

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):

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

None

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:

病历记录表

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

Case Record Form, CRF

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2026-04-17 16:24:22