Clinical Effect of Shu-Jin-Hui-Xuan Manipulation Treatment on Knee Osteoarthritis Based on Proprioception

注册号:

Registration number:

ITMCTR2000003170

最近更新日期:

Date of Last Refreshed on:

2020-04-01

注册时间:

Date of Registration:

2020-04-01

注册号状态:

Registration Status:

预注册

Prospective registration

注册题目:

基于本体感觉研究舒筋回旋手法对膝骨关节炎的临床疗效

Public title:

Clinical Effect of Shu-Jin-Hui-Xuan Manipulation Treatment on Knee Osteoarthritis Based on Proprioception

注册题目简写:

English Acronym:

研究课题的正式科学名称:

基于本体感觉研究舒筋回旋手法对膝骨关节炎的临床疗效

Scientific title:

Clinical Effect of Shu-Jin-Hui-Xuan Manipulation Treatment on Knee Osteoarthritis Based on Proprioception

研究课题的正式科学名称简写:

Scientific title acronym:

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:

ChiCTR2000031442 ; ChiMCTR2000003170

申请注册联系人:

陈锦

研究负责人:

刘文刚

Applicant:

Chen Jin

Study leader:

Liu Wengang

申请注册联系人电话:

Applicant telephone:

+86 15521116950

研究负责人电话:

Study leader's telephone:

+86 13924037789

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:

819680872@qq.com

研究负责人电子邮件:

Study leader's E-mail:

914194079@qq.com

申请单位网址(自愿提供):

Study leader's 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:

广州市恒福路60号

研究负责人通讯地址:

广州市恒福路60号

Applicant address:

60 Hengfu Road, Guangzhou, Guangdong, China

Study leader's address:

60 Hengfu Road, Guangzhou, Guangdong, China

申请注册联系人邮政编码:

Applicant postcode:

510095

研究负责人邮政编码:

Study leader's postcode:

510095

申请人所在单位:

广东省第二中医院

Applicant's institution:

Guangdong Second Traditional Chinese Medicine Hospital

是否获伦理委员会批准:

Approved by ethic committee:

伦理委员会批件文号:

Approved No. of ethic committee:

粤二中医(2019)伦审第15号

伦理委员会批件附件:

Approved file of Ethical Committee:

View

批准本研究的伦理委员会名称:

广东省第二中医院伦理委员会

Name of the ethic committee:

Ethics Committee of Guangdong Second Traditional Chinese Medicine Hospital

伦理委员会批准日期:

Date of approved by ethic committee:

2019/4/10 0:00:00

伦理委员会联系人:

夏进

Contact Name of the ethic committee:

Xia Jin

伦理委员会联系地址:

广州市恒福路60号

Contact Address of the ethic committee:

60 Hengfu Road, Guangzhou, Guangdong, China

伦理委员会联系人电话:

Contact phone of the ethic committee:

伦理委员会联系人邮箱:

Contact email of the ethic committee:

研究实施负责(组长)单位:

广东省第二中医院

Primary sponsor:

Guangdong Second Traditional Chinese Medicine Hospital

研究实施负责(组长)单位地址:

广州市恒福路60号

Primary sponsor's address:

60 Hengfu Road, Guangzhou, Guangdong, 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):

广东

市(区县):

广州

Country:

China

Province:

Guangdong

City:

Guangzhou

单位(医院):

广东省第二中医院

具体地址:

恒福路60号

Institution
hospital:

Guangdong Second Traditional Chinese Medicine Hospital

Address:

60 Hengfu Road

经费或物资来源:

广东省中医药局科研项目

Source(s) of funding:

Scientific Research Project of Guangdong Province Traditional Chinese Medicine Bureau

研究疾病:

膝骨关节炎

研究疾病代码:

Target disease:

Knee Osteoarthritis

Target disease code:

研究类型:

Study type:

干预性研究

Interventional study

研究设计:

Study design:

随机平行对照

randomized controlled trial(parallel group design)

研究所处阶段:

Study phase:

探索性研究/预试验

Pilot clinical trial

研究目的:

基于本体感觉评估舒筋回旋手法对膝骨关节炎(Knee Osteoarthritis,KOA)的临床疗效,并探讨其潜在的生物力学机制,旨在延缓 KOA 病情发展及提高患者生活质量,丰富“骨筋肉并重(肌骨同治)”学术理论,为KOA的临床治疗及科研探索提供依据。

Objectives of Study:

To evaluate the clinical effect of Shu Jin Hui Xuan Manipulation Knee Osteoarthritis(KOA)based on proprioception, and explore its potential biomechanical mechanism.

药物成份或治疗方案详述:

Description for medicine or protocol of treatment in detail:

纳入标准:

(1)符合中西医诊断标准; (2)BMI<35且年龄40-80岁的单侧膝骨关节炎患者; (3)Kellgren-Lawrence影像学分级属0-II级患者; (4)自愿试验,有良好的依从性者。

Inclusion criteria

1. Meet the diagnostic criteria of traditional Chinese and Western medicine for knee osteoarthritis; 2. Patients with unilateral knee osteoarthritis with BMI < 35 and ages 40-80 years; 3. K-L imaging classification belongs to grade 0-II; 4. Voluntary test with good compliance.

排除标准:

(1)代谢性、感染性、先天性、外伤性膝关节疾病患者; (2)合并髋关节、踝关节或脊柱相关疾病的患者; (3)合并有重要脏器功能障碍或精神、智力障碍而难以配合的患者; (4)妊娠或哺乳期患者; (5)皮肤破损、溃烂、局部感染等不适应进行推拿操作的患者; (6)正在参加其他临床试验的患者; (7)由于其他原因引起的本体感觉异常的患者。

Exclusion criteria:

1. Patients with metabolic, infectious, congenital and traumatic knee diseases; 2. Patients with hip, ankle or spine related diseases; 3. Patients with significant organ dysfunction or mental or intellectual disability who are having difficulty cooperating; 4. Pregnant or lactating patients; 5. Patients with broken skin, ulceration, local infection and other maladjustment to massage operation; 6. Patients who are participating in other clinical trials; 7. Patients with proprioception due to other causes.

研究实施时间:

Study execute time:

From 2020-05-01

To      2021-12-31

征募观察对象时间:

Recruiting time:

From 2020-05-01

To      2020-10-31

干预措施:

Interventions:

组别:

试验组

样本量:

32

Group:

experimental group

Sample size:

干预措施:

舒筋回旋手法

干预措施代码:

1

Intervention:

Shu Jin Hui Xuan Manipulation

Intervention code:

组别:

对照组

样本量:

32

Group:

control group

Sample size:

干预措施:

关节松动术

干预措施代码:

2

Intervention:

Joint Mobilization Technique

Intervention code:

样本总量 Total sample size : 64

研究实施地点:

Countries of recruitment
and research settings:

国家:

中国

省(直辖市):

广东

市(区县):

广州

Country:

China

Province:

Guangdong

City:

Guangzhou

单位(医院):

广东省第二中医院

单位级别:

三甲

Institution/hospital:

Guangdong Second Traditional Chinese Medicine Hospital

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

稳定指数

指标类型:

主要指标

Outcome:

stability index

Type:

Primary indicator

测量时间点:

测量方法:

Prokin动静态平衡仪

Measure time point of outcome:

Measure method:

指标中文名:

完成时间

指标类型:

主要指标

Outcome:

execution test time

Type:

Primary indicator

测量时间点:

测量方法:

Prokin动静态平衡仪

Measure time point of outcome:

Measure method:

指标中文名:

平均轨迹误差

指标类型:

主要指标

Outcome:

average track error (ATE)

Type:

Primary indicator

测量时间点:

测量方法:

Prokin动静态平衡仪

Measure time point of outcome:

Measure method:

指标中文名:

躯干总标准差

指标类型:

次要指标

Outcome:

total trunk standard deviation

Type:

Secondary indicator

测量时间点:

测量方法:

Prokin动静态平衡仪

Measure time point of outcome:

Measure method:

指标中文名:

平均力量差

指标类型:

次要指标

Outcome:

average force difference

Type:

Secondary indicator

测量时间点:

测量方法:

Prokin动静态平衡仪

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:

N/A

Tissue:

人体标本去向

其它

说明

Fate of sample 

Others

Note:

征募研究对象情况:

尚未开始

Not yet recruiting

年龄范围:

最小
Min age years
最大
Max age years

Recruiting status:

Participant age:

性别:

Gender:

男女均可

Both

随机方法(请说明由何人用什么方法产生随机序列):

运用SPSS 25.0软件产生随机入组表、随机分组表,将所有患者进行随机分为观察组32例,对照组32例。

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

SPSS 25.0 software is used to generate random entry table and random group table.

盲法:

未说明

Blinding:

Not stated

是否共享原始数据:

IPD sharing:

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):

ResMan平台, http://www.medresman.org.cn.

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

ResMan platform, http://www.medresman.org.cn.

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:

ResMan平台

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

ResMan platform

数据管理委员会:

Data Managemen Committee:

Yes

研究计划书或研究结果报告发表信息
(杂志名称、期、卷、页,时间;或网址):

Publication information of the protocol/research results report
(name of the journal, volume, issue, pages, time; or website):

ITMCTR BJ-ICP:07032215-5 Tip: IE8 is recommended Use the system with widescreen display resolution above