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注册号: Registration number: |
ChiCTR2600123527 |
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最近更新日期: Date of Last Refreshed on: |
2026-04-27 16:56:20 |
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注册时间: Date of Registration: |
2026-04-27 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: |
慢性移植物抗宿主病(cGVHD)患者症状负担、健康相关生活质量及诊疗现状的多中心、纵向真实世界研究 |
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Public title: |
A multicenter, longitudinal real-world study on symptom burden, health-related quality of life, and diagnosis and treatment status in patients with chronic graft-versus-host disease (cGVHD) |
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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: |
慢性移植物抗宿主病(cGVHD)患者症状负担、健康相关生活质量及诊疗现状的多中心、纵向真实世界研究 |
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Scientific title: |
A multicenter, longitudinal real-world study on symptom burden, health-related quality of life, and diagnosis and treatment status in patients with chronic graft-versus-host disease (cGVHD) |
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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: |
王筱淇 |
研究负责人: |
张曦 |
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Applicant: |
Xiaoqi Wang |
Study leader: |
Zhang Xi |
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申请注册联系人电话: Applicant telephone: |
+86 18223239605 |
研究负责人电话:
Study leader's |
+86 23 68763198 |
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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: |
xiaoqiwang27@sina.com |
研究负责人电子邮件: Study leader's E-mail: |
zhangxxi@sina.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: |
中国重庆市沙坪坝区新桥正街183号 |
研究负责人通讯地址: |
中国重庆市沙坪坝区新桥正街183号 |
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Applicant address: |
No. 183, Xinqiao Main Street, Shapingba District, Chongqing City, China |
Study leader's address: |
No. 183, Xinqiao Main Street, Shapingba District, Chongqing City, China |
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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: |
陆军军医大学新桥医院血液病医学中心 |
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Applicant's institution: |
Medical Center of Hematology, Xinqiao Hospital of Army Medical University |
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研究负责人所在单位: |
中国人民解放军陆军军医大学第二附属医院 |
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Affiliation of the Leader: |
The Second Affiliated Hospital of the Army Medical University |
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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: |
2026-研第091-01 |
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: |
中国人民解放军陆军军医大学第二附属医院医学伦理委员会 |
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Name of the ethic committee: |
Medical Ethics Committee of Second Affiliated Hospital of Army Medical University PLA |
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伦理委员会批准日期: Date of approved by ethic committee: |
2026-03-15 00:00:00 | ||
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伦理委员会联系人: |
胡岚岚 |
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Contact Name of the ethic committee: |
Hu Lanlan |
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伦理委员会联系地址: |
中国重庆市沙坪坝区新桥正街183号 |
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Contact Address of the ethic committee: |
No. 183, Xinqiao Main Street, Shapingba District, Chongqing City, China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 23 68755422 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
35341579@qq.com |
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研究实施负责(组长)单位: |
中国人民解放军陆军军医大学第二附属医院 |
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Primary sponsor: |
The Second Affiliated Hospital of the Army Medical University |
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研究实施负责(组长)单位地址: |
中国重庆市沙坪坝区新桥正街183号 |
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Primary sponsor's address: |
No. 183, Xinqiao Main Street, Shapingba District, Chongqing City, China |
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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: |
国家、军队或地方政府机构提供的批准项目的补助金 |
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Source(s) of funding: |
Grants for approved projects provided by national, military, or local government bodies. |
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研究疾病: |
慢性移植物抗宿主病 |
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Target disease: |
Chronic graft-versus-host 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: |
观察性研究 |
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Study type: |
Observational study |
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研究所处阶段: |
其它 | ||||||||||||||||||||||
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Study phase: |
N/A |
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研究设计: |
横断面 |
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Study design: |
Cross-sectional |
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研究目的: |
1.主要目的:描绘症状与生活质量的纵向变化,描述中国cGVHD患者从基线到6个月随访期间,症状负担(LSS)和多维度健康相关生活质量(SF-36, FACT-BMT, EQ-5D-5L)的变化轨迹,分析其变化与人口学特征、基线疾病严重程度(NIH评分)及治疗调整的关系。 2.次要目的: (1)分析诊疗路径的动态演变与效果:追踪cGVHD患者的治疗模式演变(治疗升级、转换或降级)、治疗转换的具体原因、不良反应发生情况,并评估基线至6个月期间治疗反应率(基于NIH评分和PRO变化)及其影响因素。 (2)评估PRO工具的动态性能:验证Lee症状量表(LSS)、健康调查简表(SF-36)、癌症治疗功能评估-骨髓移植量表(FACT-BMT)和欧洲五维健康量表(EQ-5D-5L)在中国cGVHD患者中的重测信度、反应度及最小临床重要差异。 (3)产出动态管理指导性文件:基于纵向研究发现,撰写并发布《中国慢性GVHD患者纵向管理与生活质量演变蓝皮书》,为临床动态评估、治疗决策调整及患者长期随访管理提供循证依据。 |
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Objectives of Study: |
1. Main objective: to describe the longitudinal changes of symptoms and quality of life, describe the change trajectory of symptom burden (LSS) and multidimensional health-related quality of life (SF-36, FACT-BMT, eq-5d-5l) in Chinese patients with cGVHD from baseline to 6-month follow-up, and analyze the relationship between the changes and demographic characteristics, baseline disease severity (NIH score) and treatment adjustment. 2. Secondary purpose: (1) Objective: to analyze the dynamic evolution and effect of diagnosis and treatment path: to track the evolution of treatment mode (treatment upgrade, conversion or degradation), the specific causes of treatment conversion, and the occurrence of adverse reactions in patients with cGVHD, and to evaluate the treatment response rate (based on NIH score and pro changes) and its influencing factors from baseline to 6 months. (2) To evaluate the dynamic performance of Pro Tools: to verify the test-retest reliability, responsiveness and minimal clinically significant differences of Lee symptom scale (LSS), short form of Health Survey (SF-36), FACT-BMT and eq-5d-5l in Chinese patients with cGVHD. (3) Output dynamic management guidance document: Based on the longitudinal research findings, the blue book on longitudinal management and quality of life evolution of Chinese patients with chronic GVHD was written and released to provide evidence-based basis for clinical dynamic assessment, treatment decision-making adjustment and long-term follow-up management of patients. |
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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: |
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Inclusion criteria |
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排除标准: |
1.移植相关信息记录欠缺或无法获取外院移植病例资料; 2.移植前后有精神疾病史、经历严重生活事件或失眠史; 3.预计无法完成6个月随访(如居住地过远、计划迁居、依从性差)。 |
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Exclusion criteria: |
1. Incomplete records of transplantation-related information or inability to obtain the allo-HSCT medical records from the external hospital where the procedure was performed; 2. History of psychiatric disorders, experience of major life events, or history of insomnia either before or after transplantation; 3. Anticipated inability to complete the 6-month follow-up (e.g., due to excessive geographical distance, planned relocation, or poor compliance). |
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研究实施时间: Study execute time: |
从 From 2026-04-30 00:00:00至 To 2027-12-01 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2026-04-30 00:00:00 至 To 2027-10-31 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): |
无 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
None |
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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: |
不公开/Private |
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盲法: |
无 |
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Blinding: |
None |
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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): |
无 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
None |
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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: |
使用统一的问卷采集系统来收集和存储问卷数据,确保数据的准确性和完整性。所有数据将通过在线平台实时上传,以便中央监控和分析。 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Use a unified questionnaire collection system to collect and store questionnaire data, ensuring the accuracy and completeness of the data. All data will be uploaded in real-time through an online platform for central monitoring and analysis. |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |