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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: |
ChiCTR2400082393 |
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最近更新日期: Date of Last Refreshed on: |
2024-03-28 08:23:12 |
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注册时间: Date of Registration: |
2024-03-28 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: |
丹栀逍遥散加减联合绘画心理治疗对非酒精性脂肪肝治疗的临床效果研究 |
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Public title: |
Clinical study on the treatment effects of modified Danzhi Xiaoyao Powder combined with art therapy on non-alcoholic fatty liver disease (NAFLD) |
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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: |
丹栀逍遥散加减联合绘画心理治疗对非酒精性脂肪肝治疗的临床效果研究 |
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Scientific title: |
Clinical study on the treatment effects of modified Danzhi Xiaoyao Powder combined with art therapy on non-alcoholic fatty liver disease (NAFLD) |
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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: |
刘振毅 |
研究负责人: |
林少陈 |
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Applicant: |
Liu zhenyi |
Study leader: |
Lin Shaochen |
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申请注册联系人电话: Applicant telephone: |
+86 182 1358 2125 |
研究负责人电话:
Study leader's |
+86 178 6521 6918 |
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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: |
liuzhenyi55@qq.com |
研究负责人电子邮件: Study leader's E-mail: |
3201809377@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: |
云南师范大学 |
研究负责人通讯地址: |
云南省昆明市盘龙区穿金路733号 |
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Applicant address: |
Yunnan Normal University, Yuhua District 1 |
Study leader's address: |
733 Wangjin Road, Panlong District, Kunming, Yunnan |
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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: |
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申请人所在单位: |
云南师范大学 |
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Applicant's institution: |
Yunnan Normal University |
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研究负责人所在单位: |
云南省精神病医院 |
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Affiliation of the Leader: |
Yunnan Provincial Psychiatric Hospital |
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是否获伦理委员会批准: |
是 |
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Approved by ethic committee: |
Yes |
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伦理委员会批件文号: Approved No. of ethic committee: |
YNJS-20240301-0011 |
伦理委员会批件附件: Approved file of Ethical Committee: |
查看附件View |
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批准本研究的伦理委员会名称: |
云南省精神病医院医学伦理委员会 |
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Name of the ethic committee: |
Medical Ethics Committee of Yunnan Psychiatric Hospital |
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伦理委员会批准日期: Date of approved by ethic committee: |
2024-03-01 00:00:00 | ||
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伦理委员会联系人: |
鲍天昊 |
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Contact Name of the ethic committee: |
Bao Tianhao |
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伦理委员会联系地址: |
云南省精神病院昆明市盘龙区穿金路733号 |
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Contact Address of the ethic committee: |
733 Wangjin Road, Panlong District, Kunming, Yunnan |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 137 0065 7352 |
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: |
云南省精神病医院 |
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Primary sponsor: |
Yunnan Provincial Psychiatric Hospital |
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研究实施负责(组长)单位地址: |
云南省精神病院昆明市盘龙区穿金路733号 |
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Primary sponsor's address: |
733 Wangjin Road, Panlong District, Kunming, Yunnan |
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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: |
Self-financed |
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研究疾病: |
非酒精性脂肪肝 |
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Target disease: |
non-alcoholic fatty liver disease |
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研究疾病代码: |
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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: |
I期临床试验 | ||||||||||||||||||||||
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Study phase: |
1 |
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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: |
采用丹栀逍遥散加减联合绘画疗法对非酒精性脂肪肝的临床治疗其目的是减轻病症最终达到治愈的目的以及对疾病所产生的伴随性心理疾病进行及时识别与治疗 |
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Objectives of Study: |
The purpose of the clinical treatment of non-alcoholic fatty liver disease (NAFLD) using the adjusted Danzhi Xiaoyao Powder combined with art therapy is to alleviate symptoms with the ultimate goal of curing the disease, as well as to promptly identify and treat the accompanying psychological disorders caused by the illnes |
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药物成份或治疗方案详述: |
治疗方式1:丹栀逍遥散加减:按照标准剂量,每日两次,连续治疗6个月。焦栀子 10 g,牡丹皮 15 g,当归 15 g,柴胡 10 g,白芍 15 g,白术 15 g,茯苓 20 g,茵陈 25 g,赤芍 10 g, 泽泻 15 g,山楂 15 g,旱莲草 10 g,炒枳壳 10 g,苍术 10 g,丹参 15 g,生甘草 8 g,水煎顿服,早晚各 1 次,1 剂 /d,用药期间忌油腻、辛辣、生冷食物,切勿饮酒。持续6个月。 治疗方式2:绘画治疗每月两次,每次两小时,由专业心理治疗师指导,持续6个月。 |
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Description for medicine or protocol of treatment in detail: |
Treatment 1: Dan gardenia free and easy san plus reduction: according to the standard dosage, twice a day, continuous treatment for 6 months.Jiao gardenia 10 g, mudanpi 15 g, angelica sinensis 15 g, chaihu 10 g, white peony 15 g, atractylodes macrocephala 15 g, poria 20 g, chennai 25 g, red peony 10 g, zedoary 15 g, hawthorn 15 g, dry lotus herb 10 g, fried hedgerow shells 10 g, cangzhu 10 g, salvia miltiorrhiza 15 g, raw glycyrrhiza glabra 8 g, decocted with water and taken in the morning and evening 1 time each time, 1 dose /d, avoid oily and spicy food during the period of using the medicine,cold food, do not drink alcohol.Continue for 6 months. Treatment 2: Painting therapy twice a month, two hours each time, under the guidance of a professional psychotherapist, for 6 months. |
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纳入标准: |
(1)年龄在25-30岁之间的年轻男女患者,其目的确保没有其他机体功能的衰变导致的肝功能问题。 (2)经B超或CT诊断为非酒精性脂肪肝。 (3)未接受过其他脂肪肝特定治疗。 (4)满足上述1.2.3的基础上在心理健康量表上同时满足对生活质量评分低以及HAMA量表上体现出高度焦虑才可纳入样本群体 |
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Inclusion criteria |
1) Young male and female patients aged between 25 and 30 years, with the purpose to ensure that there are no liver function issues caused by the decline of other bodily functions. (2) Diagnosed with non-alcoholic fatty liver disease (NAFLD) via ultrasound or CT scan. (3) Have not received any other specific treatments for fatty liver disease. (4) On the basis of satisfying conditions 1, 2, and 3, only those who also have a low quality of life score on a mental health scale and exhibit high anxiety (on the HAMA (Hamilton Anxiety Rating Scale) can be included in the sample group |
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排除标准: |
(1)有严重心脏、肝脏、肾脏或其他系统性疾病的患者。 (2)孕妇或哺乳期妇女。 (3)对研究药物或材料过敏的患者。 (4)满足非酒精性脂肪肝的诊断标准但是没有同时满足生活质量得分上得分低或HAMA得分上未满足焦虑诊断标准 |
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Exclusion criteria: |
(1) Patients with severe cardiac, hepatic, renal, or other systemic diseases. (2) Pregnant or breastfeeding women. (3) Patients allergic to the study medication or materials. (4) Those who meet the diagnostic criteria for non-alcoholic fatty liver disease but do not have a low score in quality of life or do not meet the anxiety diagnostic criteria on the HAMA scale. |
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研究实施时间: Study execute time: |
从 From 2024-03-28 00:00:00至 To 2024-07-29 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2024-03-29 00:00:00 至 To 2024-03-31 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): |
采用分层抽样的随机方法,随机序列由R语言程序产生并且进行编码,在选符合标准的大样本1000人进行并分组,分成10组,每组100人,再从每组100人中分为10组,每组抽取10人,最后总共抽取抽取100人,100人在按干预方法分成对照组50人,实验组50人进行干预实验。 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
Using a stratified random sampling method, random sequences are generated and coded by the R programming language. Among the large sample of 1,000 individuals who meet the inclusion criteria, patients are divided into 10 groups, each consisting of 100 individuals. Then, from each group of 100 individuals, further divide into 10 subgroups, from which 10 individuals are drawn, resulting in a total of 100 selected participants. These 100 individuals are then divided according to the intervention method into a control group of 50 individuals and an experimental group of 50 individuals to conduct the intervention experiment. |
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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: |
无 |
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Blinding: |
None |
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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 |
否No |
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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): |
ResMan, http://www.medresman.org.cn/uc/projectsh/projectlistauthor.aspx |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
ResMan, http://www.medresman.org.cn/uc/projectsh/projectlistauthor.aspx |
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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: |
电子采集和管理系统 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Electronic Data Capture, EDC |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |