ChiCTR2400092275 版本V1.0 版本创建时间2024/11/13 16:22:52 中国临床试验注册中心

审核状态:

Project audit state:

通过审核

Successful

注册号:

Registration number:

ChiCTR2400092275 

最近更新日期:

Date of Last Refreshed on:

2024-11-13 16:22:43 

注册时间:

Date of Registration:

2024-11-13 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

基于小脑连接组学探索未服药青少年强迫症的神经机制研究

Public title:

A Study on the Neuromechanisms of drug-free Adolescent Obsessive-Compulsive Disorder Based on Cerebellar Connectomics

注册题目简写:

English Acronym:

研究课题的正式科学名称:

基于小脑连接组学探索未服药青少年强迫症的神经机制研究

Scientific title:

A Study on the Neuromechanisms of drug-free Adolescent Obsessive-Compulsive Disorder Based on Cerebellar Connectomics

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:

李坤 

研究负责人:

李坤 

Applicant:

Kun Li 

Study leader:

Kun Li 

申请注册联系人电话:

Applicant telephone:

+86 195 5370 0077

研究负责人电话:

Study leader's
telephone:

+86 195 5370 0077

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:

likunyjs@163.com

研究负责人电子邮件:

Study leader's E-mail:

likunyjs@163.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:

山东省济宁市任城区济戴路1号

研究负责人通讯地址:

山东省济宁市任城区济戴路1号

Applicant address:

1 Jidai Road, Rencheng District, Jining City, Shandong Province

Study leader's address:

1 Jidai Road, Rencheng District, Jining City, Shandong 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:

山东省戴庄医院

Applicant's institution:

Shandong Daizhuang Hospital

研究负责人所在单位:

山东省戴庄医院

Affiliation of the Leader:

Shandong Daizhuang Hospital

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:

2024科研第56号-202410KS-1

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:

山东省戴庄医院伦理委员会

Name of the ethic committee:

Ethics Committee of Shandong Daizhuang Hospital

伦理委员会批准日期:

Date of approved by ethic committee:

2024-10-23 00:00:00

伦理委员会联系人:

崔健

Contact Name of the ethic committee:

Jian Cui

伦理委员会联系地址:

山东省济宁市任城区济戴路1号

Contact Address of the ethic committee:

1 Jidai Road, Rencheng District, Jining City, Shandong Province

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 136 5537 9322

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:

山东省戴庄医院

Primary sponsor:

Shandong Daizhuang Hospital

研究实施负责(组长)单位地址:

山东省济宁市任城区济戴路1号

Primary sponsor's address:

1 Jidai Road, Rencheng District, Jining City, Shandong 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):

山东

市(区县):

济宁

Country:

china

Province:

shandong

City:

jining

单位(医院):

山东省戴庄医院

具体地址:

山东省济宁市任城区济戴路1号

Institution
hospital:

Shandong Daizhuang Hospital

Address:

1 Jidai Road, Rencheng District, Jining City, Shandong Province

经费或物资来源:

山东省卫生健康委员会

Source(s) of funding:

Health Commission of Shandong Province

研究疾病:

青少年强迫症  

Target disease:

Adolescent Obsessive-Compulsive Disorder

研究疾病代码:

Target disease code:

研究类型:

观察性研究

Study type:

Observational study

研究所处阶段:

探索性研究/预试验 

Study phase:

0

研究设计:

病例对照研究 

Study design:

Case-Control study 

研究目的:

(1)揭示青少年OCD的小脑连接学特征:我们的主要目标是确定青少年OCD患者小脑的功能和结构连接特征,并与健康对照组进行对比。这将为我们提供宝贵的信息,帮助我们理解OCD的神经基础。 (2) 确定小脑连接组学与强迫症状的关系:我们希望揭示小脑连接模式与OCD的临床表现之间的关系,从而更好地理解这种关系背后的生物学机制。 (3)为OCD的诊断和治疗提供新视角:多模态数据整合分析,获得多维度特征关联信息, 寻找可以用于诊断的“多维度生物标记谱型”,并在以后工作中验证“多维度生物标记诊断谱型”的信度与效度并优化。通过深入了解OCD中的小脑连接,我们希望为临床实践提供新的策略,从而改进疾病的诊断和治疗。  

Objectives of Study:

(1) Unveiling the Cerebellar Connectomics Features of Adolescent obsessive-compulsive disorder (OCD): Our primary objective is to identify the functional and structural connectivity features of the cerebellum in adolescent OCD patients and compare them with those of a healthy control group. This will provide us with valuable information to help us understand the neural basis of OCD. (2) Determining the Relationship between Cerebellar Connectomics and Compulsive Symptoms: We aim to reveal the relationship between cerebellar connectivity patterns and the clinical manifestations of OCD, thereby gaining a better understanding of the biological mechanisms underlying this relationship. (3) Providing a New Perspective for the Diagnosis and Treatment of OCD: Through the integration of multimodal data analysis, we will obtain multi-dimensional feature association information, search for a "multi-dimensional biomarker profile" that can be used for diagnosis, and in future work, validate the reliability and validity of the "multi-dimensional biomarker diagnostic profile" and optimize it. By gaining a deeper understanding of cerebellar connections in OCD, we hope to offer new strategies for clinical practice, thereby improving the diagnosis and treatment of the disease.

药物成份或治疗方案详述:

 

Description for medicine or protocol of treatment in detail:

 

纳入标准:

未服药青少年强迫症组 (1)通过定式临床访谈SCID-V符合DSM-V中关于OCD的诊断标准; (2)年龄10-18岁; (3)患者自愿参加研究,征得家属同意,并签署知情同意书; (4)理解书面语言,能进行问卷调查; (5)儿童强迫症量表(Children's Yale-Brown Obsessive-Compulsive Scale, CY-BOCS)评分≥16 分; (6)汉族,右利手; (7)入组前至少8周以上时间未服用强迫症药物。 健康对照组: (1)年龄10-18岁; (2)自愿参加研究,征得家属同意,并签署知情同意书; (3)理解书面语言,能进行问卷调查; (4)汉族,右利手。

Inclusion criteria

Drug-Free Adolescent Obsessive-Compulsive Disorder Group: (1) Meet the DSM-5 diagnostic criteria for OCD through structured clinical interview (SCID-V); (2) Age between 10 to 18 years old; (3) Patients voluntarily participate in the study, have obtained family consent, and have signed an informed consent form; (4) Understand written language and are able to complete questionnaires; (5) Score of ≥16 on the Children's Yale-Brown Obsessive-Compulsive Scale (CY-BOCS); (6) Han ethnicity, right-handed; (7) Have not taken any medication for OCD for at least 8 weeks prior to enrollment. Healthy Control Group: (1) Age between 10 to 18 years old; (2) Voluntarily participate in the study, have obtained family consent, and have signed an informed consent form; (3) Understand written language and are able to complete questionnaires; (4) Han ethnicity, right-handed.

排除标准:

未服药青少年强迫症组: (1)有物质依赖病史;有可以达 SCID 轴 I 诊断标准的精神疾病或病史;有脑外伤、癫痫或其他脑器质性疾病; (2)实验室检查显示有肝肾功能损害或其他严重躯体疾病及代谢障碍; (3)有 MRI禁忌症者; (4)孕妇或哺乳期患者; (5)既往有癫痫家族史或发作史。 健康对照组: (1)有物质依赖病史;有可以达 SCID 轴 I 、II的任何精神疾病或病史;有脑外伤、癫痫或其他脑器质性疾病; (2)曾有意识丧失史; (3)两系及三代精神病家族史阳性者; (4)曾服用过抗精神病药、抗抑郁药;MRI检查前一个月使用过苯二氮卓类或其他影响中枢神经系统的药物;6个月内接受过连续药物治疗; (5)测试不合作或不能有效完成者; (6)实验室检查显示有肝肾功能损害或其他严重躯体疾病及代谢障碍; (7)有 MRI禁忌症者; (8)孕妇或哺乳期; (9)色盲。

Exclusion criteria:

Drug-Free Adolescent Obsessive-Compulsive Disorder Group: (1) History of substance dependence; history of mental disorders that meet the SCID Axis I diagnostic criteria; history of brain trauma, epilepsy, or other organic brain diseases; (2) Laboratory tests indicate liver or kidney dysfunction or other severe physical diseases and metabolic disorders; (3) Contraindications for MRI; (4) Pregnant or breastfeeding patients; (5) Family history or personal history of epilepsy. Healthy Control Group: (1) History of substance dependence; history of any mental disorders that meet the SCID Axis I or II diagnostic criteria; history of brain trauma, epilepsy, or other organic brain diseases; (2) History of loss of consciousness; (3) Positive family history of mental illness in two generations and three degrees; (4) History of taking antipsychotic or antidepressant medications; use of benzodiazepines or other central nervous system affecting drugs within one month before MRI; continuous medication treatment within the past 6 months; (5) Uncooperative in testing or unable to effectively complete tests; (6) Laboratory tests indicate liver or kidney dysfunction or other severe physical diseases and metabolic disorders; (7) Contraindications for MRI; (8) Pregnant or breastfeeding; (9) Color blindness.

研究实施时间:

Study execute time:

From 2024-01-01 00:00:00 To 2025-12-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2024-12-01 00:00:00 To 2025-10-31 00:00:00

干预措施:

Interventions:

组别:

未服药青少年强迫症组

样本量:

70

Group:

Drug-Free Adolescent Obsessive-Compulsive Disorder Group

Sample size:

干预措施:

干预措施代码:

Intervention:

None

Intervention code:

组别:

健康对照组

样本量:

70

Group:

Healthy Control Group

Sample size:

干预措施:

干预措施代码:

Intervention:

None

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

山东 

市(区县):

济宁 

Country:

China

Province:

Shandong

City:

Jining

单位(医院):

山东省戴庄医院 

单位级别:

三甲 

Institution
hospital:

Shandong Daizhuang Hospital

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

儿童版耶鲁-布朗强迫症状量表评分

指标类型:

主要指标

Outcome:

Children's Yale-Brown Obsessive-Compulsive Scale

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

父母及教师评定量表评分

指标类型:

次要指标

Outcome:

Swanson, Nolan, and Pelham, Version IV

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

耶鲁综合抽动严重程度评估报告

指标类型:

次要指标

Outcome:

Yale Global Tic Severity Scale

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

强迫症家庭顺应行为量表调查员评定版评分

指标类型:

次要指标

Outcome:

Family Accommodation Scale – Interviewer Rated

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

强迫量表儿童版评分

指标类型:

次要指标

Outcome:

Obsessive-Compulsive Inventory - Child Version

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

儿童抑郁量表评分

指标类型:

次要指标

Outcome:

Children's Depression Inventory

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

Spence儿童焦虑量表评分

指标类型:

次要指标

Outcome:

Spence Children's Anxiety Scale

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

青少年睡眠问题评估问卷评分

指标类型:

次要指标

Outcome:

The Adolescent Sleep Disturbance Questionnaire

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

瑞文推理测试

指标类型:

次要指标

Outcome:

Raven’s Progressive Matrices

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

青少年生活事件量表评分

指标类型:

次要指标

Outcome:

Adolescent Self-Rating Life Events Check List

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

艾森克个性问卷评分

指标类型:

次要指标

Outcome:

Eysenck Personality Questionnaire

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

认知量表评分

指标类型:

次要指标

Outcome:

Cognitive Scale

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

功能磁共振

指标类型:

主要指标

Outcome:

functional magnetic resonance imaging

Type:

Primary 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:

None

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 10 years
最大 Max age 18 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):

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

None

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

盲法:

Blinding:

试验完成后的统计结果(上传文件):

Calculated Results after
the Study Completed(upload file):

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):

试验完成后有需要可联系likunyjs@163.com索取

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

to send e-mail to likunyjs@163.com to ask for the data

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:

采用CRF表录入受试者研究资料,所有研究资料均由课题负责单位统一保存

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

CRF will be used to record all the data, all the material will be kepted by the primary sponsor.

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2024-11-13 16:22:43