|
注册号: Registration number: |
ChiCTR2200066361 |
|
最近更新日期: Date of Last Refreshed on: |
2023-06-13 22:16:38 |
|
注册时间: Date of Registration: |
2022-12-02 00:00:00 |
|
注册号状态: |
预注册 |
|
Registration Status: |
Prospective registration |
|
注册题目: |
接纳承诺疗法对经颅磁治疗后老年脑卒中幸存者的效果研究 |
|
Public title: |
Effect of acceptance commitment therapy on elderly stroke survivors after transcranial magneticstimulation |
|
注册题目简写: |
|
|
English Acronym: |
|
|
研究课题的正式科学名称: |
接纳承诺疗法对经颅磁治疗后老年脑卒中幸存者的效果研究 |
|
Scientific title: |
Effect of acceptance commitment therapy on elderly stroke survivors after transcranial magnetic stimulation |
|
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: |
周巧 |
研究负责人: |
周巧 |
|
Applicant: |
Zhou Qiao |
Study leader: |
Zhou Qiao |
|
申请注册联系人电话: Applicant telephone: |
+86 139 7482 8729 |
研究负责人电话:
Study leader's |
+86 139 7482 8729 |
|
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: |
408644182@qq.com |
研究负责人电子邮件: Study leader's E-mail: |
408644182@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: |
湖南省长沙市天心区劳动西路176号 |
研究负责人通讯地址: |
湖南省长沙市天心区劳动西路176号 |
|
Applicant address: |
176, Laodong West Road, Tianxin District, Changsha, Hunan |
Study leader's address: |
176, Laodong West Road, Tianxin District, Changsha, Hunan |
|
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: |
长沙市第三医院 |
||
|
Applicant's institution: |
The Third hospital of Changsha |
||
|
研究负责人所在单位: |
长沙市第三医院 |
||
|
Affiliation of the Leader: |
The Third hospital of Changsha |
||
|
是否获伦理委员会批准: |
是 |
||
|
Approved by ethic committee: |
Yes |
||
|
伦理委员会批件文号: Approved No. of ethic committee: |
KY-EC(会审)-2022-007 |
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: |
长沙市第三医院伦理委员会 |
||
|
Name of the ethic committee: |
Ethics Committee of Changsha Third Hospital |
||
|
伦理委员会批准日期: Date of approved by ethic committee: |
2022-09-05 00:00:00 | ||
|
伦理委员会联系人: |
叶超 |
||
|
Contact Name of the ethic committee: |
Ye Chao |
||
|
伦理委员会联系地址: |
湖南省长沙市天心区劳动西路176号 |
||
|
Contact Address of the ethic committee: |
176, Laodong West Road, Tianxin District, Changsha, Hunan |
||
|
伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 751 85171341 |
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: |
长沙市第三医院 |
||||||||||||||||||||||
|
Primary sponsor: |
The Third hospital of Changsha |
||||||||||||||||||||||
|
研究实施负责(组长)单位地址: |
湖南省长沙市天心区劳动西路176号 |
||||||||||||||||||||||
|
Primary sponsor's address: |
176, Laodong West Road, Tianxin District, Changsha, Hunan |
||||||||||||||||||||||
|
试验主办单位(项目批准或申办者): Secondary sponsor: |
|
||||||||||||||||||||||
|
经费或物资来源: |
无 |
||||||||||||||||||||||
|
Source(s) of funding: |
No |
||||||||||||||||||||||
|
研究疾病: |
老年脑卒中幸存者 |
||||||||||||||||||||||
|
Target disease: |
Elderly stroke survivors |
||||||||||||||||||||||
|
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: |
探讨接纳承诺疗法对颅磁治疗后老年脑卒中幸存者卒中后抑郁、心理灵活性、心理痛苦和生活质量的影响。 |
||||||||||||||||||||||
|
Objectives of Study: |
To explore the effect of acceptance commitment therapy on post-stroke depression, psychological flexibility, psychological pain and quality of life of elderly stroke survivors after craniomagnetic therapy. |
||||||||||||||||||||||
|
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.佩戴心脏起搏器或者体内有金属植入物,耳蜗植入者和颅内有金属物者; 2.颅内压增高者,有癫痫病史或者有癫痫家族史者,近期脑电图提示癫痫波者; 3.近6个月有脑外伤或头部手术史者; 4.急性传染性疾病患者; 5.最近1月内电抽搐治疗者; 6.近期服用三环类抗抑郁药物或降低痫性发作阙值药物(如卡马西平、丙戊酸钠)的患者; 7.合并其他脑器质性疾病,伴有呼吸、心血管、消化、内分泌及血液系统疾病等严重躯体疾病; 8.确诊精神分裂症,伴有强烈自伤、自杀意愿,或者出现冲动性伤人、毁物行为的患者; 9.有酒精或者其他精神活性物质滥用或者依赖史。 |
||||||||||||||||||||||
|
Exclusion criteria: |
1. Wearing a pacemaker or having metal implants in the body, cochlear implants, and intracranial metal objects; 2. People with increased Intracranial pressure, epilepsy history or family history of epilepsy, and recent Electroencephalography indicates epileptic waves; 3. Those with a history of brain injury or head surgery in the past 6 months; 4. Patients with acute infectious diseases; 5. Those who have received electroconvulsive therapy within the past month; 6. Patients who have recently taken tricyclic antidepressants or drugs to reduce the threshold of epileptic seizures (such as Carbamazepine and sodium valproate); 7. Merge with other organic brain diseases, accompanied by serious physical diseases such as respiratory, cardiovascular, digestive, endocrine, and hematological diseases; 8. Patients diagnosed with schizophrenia, accompanied by strong self harm, suicidal intention, or impulsive injury or destruction behavior; 9. Have a history of alcohol or other psychoactive Substance abuse abuse or dependence. |
||||||||||||||||||||||
|
研究实施时间: Study execute time: |
从 From 2022-12-09 00:00:00至 To 2023-02-02 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2022-12-09 00:00:00 至 To 2023-01-02 00:00:00 |
|
干预措施: Interventions: |
|
|
研究实施地点: Countries of recruitment and research settings: |
|
||||||||||||||||||||||||||||
|
测量指标: Outcomes: |
|
|
采集人体标本:
Collecting sample(s)
|
|
|
征募研究对象情况: Recruiting status: |
尚未开始 Not yet recruiting |
年龄范围: Participant age: |
|
||||||
|
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): |
本研究采用随机分组方法将符合纳入标准的66例患者随机分为TMS组、ACT +TMS组、每组33例。具体如下:对自愿参加研究的患者,以入院时间先后顺序编号;利用SPSS 26.0软件生成66个随机数,并按从小到大顺序排列;取随机数字前1~33位所对应的编号为TMS组,第34~66位所对应的编号为ACT+TMS组。 |
||||||||
|
Randomization Procedure (please state who generates the random number sequence and by what method): |
In this study, 66 patients who met the inclusion criteria were randomly divided into TMS group, act +tms group, with 33 patients in each group. The details are as follows: the patients who volunteered to participate in the study were numbered in the order of admission time; Using SPSS 26.0 software& |
||||||||
|
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: |
无 |
|
Blinding: |
None |
|
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): |
通过文章发表分享数据 |
|
The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Share data through article publishing |
|
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: |
无 |
|
Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
None |
|
数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |