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审核状态: Project audit state: |
通过审核 Successful |
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注册号: Registration number: |
ChiCTR2100047946 |
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最近更新日期: Date of Last Refreshed on: |
2021-06-28 03:53:20 |
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注册时间: Date of Registration: |
2021-06-28 00:00:00 |
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注册号状态: |
预注册 |
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Registration Status: |
Prospective registration |
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注册题目: |
请于伦理委员会批准后才开始征募参试者,并与我们联系上传伦理批件。 水疗与经颅直流电刺激结合对儿童脑瘫的疗效观察 |
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Public title: |
Combined effect of hydrotherapy and Transcranial Direct-Current Stimulation on children with cerebral palsy. |
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注册题目简写: |
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English Acronym: |
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研究课题的正式科学名称: |
水疗与经颅直流电刺激结合对儿童脑瘫的疗效观察 |
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Scientific title: |
Combined effect of hydrotherapy and Transcranial Direct-Current Stimulation on children with cerebral palsy. |
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研究课题代号(代码): Study subject ID: |
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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: |
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申请注册联系人: |
陈晓亮 |
研究负责人: |
陈晓亮 |
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Applicant: |
Xiao-Liang Chen |
Study leader: |
Xiao-Liang Chen |
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申请注册联系人电话: Applicant telephone: |
13919088491 |
研究负责人电话: Study leader's telephone: |
13919088491 |
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申请注册联系人传真 : Applicant Fax: |
研究负责人传真: Study leader's fax: |
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申请注册联系人电子邮件: Applicant E-mail: |
2010662788@qq.com |
研究负责人电子邮件: Study leader's E-mail: |
2010662788@qq.com |
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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): |
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申请注册联系人通讯地址: |
黑龙江省齐齐哈尔市龙沙区中华西路37号 |
研究负责人通讯地址: |
黑龙江省齐齐哈尔市龙沙区中华西路37号 |
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Applicant address: |
No.37, Zhonghua West Road, Longsha District, Qiqihar City, Heilongjiang Province |
Study leader's address: |
No.37, Zhonghua West Road, Longsha District, Qiqihar City, Heilongjiang Province |
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申请注册联系人邮政编码: Applicant postcode: |
161041 |
研究负责人邮政编码: Study leader's postcode: |
161041 |
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申请人所在单位: |
齐齐哈尔医学院附属第二医院 |
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Applicant's institution: |
the Second Affiliated Hospital of Qiqihar Medical University |
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研究负责人所在单位: |
齐齐哈尔医学院附属第二医院 |
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Affiliation of the Leader: |
the Second Affiliated Hospital of Qiqihar Medical University |
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是否获伦理委员会批准: |
否/No |
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Approved by ethic committee: |
No |
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伦理委员会批件文号: Approved No. of ethic committee: |
伦理委员会批件附件: Approved file of Ethical Committee: |
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批准本研究的伦理委员会名称: |
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Name of the ethic committee: |
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伦理委员会批准日期: Date of approved by ethic committee: |
2013-08-26 00:00:00 |
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伦理委员会联系人: |
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Contact Name of the ethic committee: |
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伦理委员会联系地址: |
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Contact Address of the ethic committee: |
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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: |
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研究实施负责(组长)单位: |
齐齐哈尔医学院附属第二医院 |
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Primary sponsor: |
the Second Affiliated Hospital of Qiqihar Medical University |
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研究实施负责(组长)单位地址: |
黑龙江省齐齐哈尔市龙沙区中华西路37号 |
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Primary sponsor's address: |
No.37, Zhonghua West Road, Longsha District, Qiqihar City, Heilongjiang Province |
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试验主办单位(项目批准或申办者): Secondary sponsor: |
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经费或物资来源: |
自费 |
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Source(s) of funding: |
none |
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Target disease: |
cerebral palsy |
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Target disease code: |
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研究类型: |
干预性研究 |
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Study type: |
Interventional study |
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研究所处阶段: |
探索性研究/预试验 | ||||||||||||||||||||||
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Study phase: |
0 |
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研究设计: |
随机平行对照 |
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Study design: |
Parallel |
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研究目的: |
评估经颅直流电刺激和水疗联合应用对儿童脑瘫的疗效。 |
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Objectives of Study: |
To estimate the efficacy of a combined application of tDCS and hydrotherapy in patients with CP, compared to treatment as usual. |
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药物成份或治疗方案详述: |
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Description for medicine or protocol of treatment in detail: |
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纳入标准: |
(1) 4-14 岁脑瘫患者, (2) 根据中华医学会康复专科组诊断标准诊断为脑瘫患者, (3) 自愿参加并签署知情同意书。 |
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Inclusion criteria |
(1) cerebral palsy patients between 4 and 14 years old, (2) cerebral palsy was diagnosed according to the diagnostic criteria of CP found in the Subspecialty Group of Rehabilitation of Chinese Medical Association, (3) voluntary participation and informed consent signed. |
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排除标准: |
(1)影响评价结果的视觉、听觉、精神障碍; (2) 药物治疗无法控制的癫痫患儿; (3) 开放性伤口或活动性感染等皮肤问题; (4) 项目开始前6个月内接受过肉毒杆菌毒素注射或手术; (5) 参加另一项临床试验; (6)意识不清,行为异常或无法控制,在治疗过程中易发生医疗事故d的患者。 |
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Exclusion criteria: |
(1) visual, auditory, and mental disorders affecting the results assessment; (2) children with epilepsy who are uncontrolled with medication; (3) skin problems such as open wounds or active infection; (4) receiving botulinum toxin injections or surgery no earlier than 6 months before project start; (5) participation in another clinical trial; (6) unconscious, behaving strangely or uncontrollably, and are prone to medical accidents during treatment. |
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研究实施时间: Study execute time: |
从 From 2021-08-01 00:00:00至 To 2023-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从From 2021-08-01 00:00:00 至 To 2023-06-01 00:00:00 |
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干预措施: Interventions: |
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研究实施地点: Countries of recruitment and research settings: |
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测量指标: Outcomes: |
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采集人体标本:
Collecting sample(s)
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征募研究对象情况: Recruiting status: |
尚未开始 Not yet recruiting |
年龄范围: Participant age: |
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性别: |
男女均可 |
Gender: |
Both |
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随机方法(请说明由何人用什么方法产生随机序列): |
随机序列将通过随机数字表法和密封的不透明信封进行分配。 该过程将由不参与招募过程或研究开发的研究团队成员完成。 本研究将使用一系列编号的、密封的、不透明的信封。 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
The randomization sequence will be distributed by numerically sequenced and sealed opaque envelopes. This process will be completed out by a member of the research team who is not involved in the recruitment process or development of the study. A series of numbered, sealed, opaque envelopes will be used |
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是否公开试验完成后的统计结果: Calculated Results after the Study Completed public access: |
公开/Public |
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盲法: |
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Blinding: |
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试验完成后的统计结果(上传文件): |
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Calculated Results after
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是否共享原始数据: IPD sharing |
Yes |
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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): |
不适用 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
not applicable |
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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: |
我们将在治疗开始时和治疗10周后通过问卷对CP儿童进行评估。 记录所有研究参与者的结局指标和基本特征,例如年龄、性别、体重、身长、CP类型和结果。 数据将被收集并输入到计算机中的患者病历中,所有与患者相关的文件将被安全存储。 只有与研究相关的研究人员才能访问试验数据集。 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
We will evaluate the CP children with subjective tests and objective questionnaires at the beginning of the treatment and after 10 weeks of therapy. Descriptive measures a.nd characteristics, such as age, gender, body weight, length, type of CP and the outcomes were recorded for all study participants. The data will be collected and entered into the patient’s medical record in a computer, and all patient related documents will be securely stored. Only the study-related investigators will be allowed to access to the trial dataset. |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
暂未确定/Not yet |