|
审核状态: Project audit state: |
通过审核 Successful |
|
注册号: Registration number: |
ChiCTR2500102758 |
|
最近更新日期: Date of Last Refreshed on: |
2025-05-20 08:28:52 |
|
注册时间: Date of Registration: |
2025-05-20 00:00:00 |
|
注册号状态: |
预注册 |
|
Registration Status: |
Prospective registration |
|
注册题目: |
基于连续性护理的笑疗法对白内障手术患者干眼症干预效果的研究 |
|
Public title: |
To study the intervention effect of smile therapy based on continuous nursing on dry eye syndrome in patients undergoing cataract surgery |
|
注册题目简写: |
|
|
English Acronym: |
|
|
研究课题的正式科学名称: |
基于连续性护理的笑疗法对白内障手术患者干眼症干预效果的研究 |
|
Scientific title: |
To study the intervention effect of smile therapy based on continuous nursing on dry eye syndrome in patients undergoing cataract surgery |
|
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: |
谭月红 |
研究负责人: |
谭月红 |
|
Applicant: |
Tan Yuehong |
Study leader: |
Tan Yuehong |
|
申请注册联系人电话: Applicant telephone: |
+86 150 0015 5579 |
研究负责人电话: Study leader's telephone: |
+86 150 0015 5579 |
|
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: |
363510021@qq.com |
研究负责人电子邮件: Study leader's E-mail: |
363510021@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: |
上海市长宁区虹桥路1440号 |
研究负责人通讯地址: |
上海市长宁区虹桥路1440号 |
|
Applicant address: |
No. 1440, Hongqiao Road, Changning District, Shanghai |
Study leader's address: |
No. 1440, Hongqiao Road, Changning District, Shanghai |
|
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: |
上海市眼病防治中心 |
||
|
Applicant's institution: |
Shanghai Eye Disease Prevention and Treatment Center |
||
|
研究负责人所在单位: |
上海市眼病防治中心 |
||
|
Affiliation of the Leader: |
Shanghai Eye Disease Prevention and Treatment Center |
||
|
是否获伦理委员会批准: |
是/Yes |
||
|
Approved by ethic committee: |
Yes |
||
|
伦理委员会批件文号: Approved No. of ethic committee: |
EC-20250307-02 |
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: |
上海市眼病防治中心伦理委员会 |
||
|
Name of the ethic committee: |
Ethics Committee of Shanghai Eye Disease Prevention and Treatment Center |
||
|
伦理委员会批准日期: Date of approved by ethic committee: |
2025-03-14 00:00:00 |
||
|
伦理委员会联系人: |
贺江南 |
||
|
Contact Name of the ethic committee: |
He Jiangnan |
||
|
伦理委员会联系地址: |
上海市长宁区虹桥路1440号 |
||
|
Contact Address of the ethic committee: |
No. 1440, Hongqiao Road, Changning District, Shanghai |
||
|
伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 139 1690 5704 |
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: |
上海市眼病防治中心 |
||||||||||||||||||||||
|
Primary sponsor: |
Shanghai Eye Disease Prevention and Treatment Center |
||||||||||||||||||||||
|
研究实施负责(组长)单位地址: |
上海市长宁区虹桥路1440号 |
||||||||||||||||||||||
|
Primary sponsor's address: |
No. 1440, Hongqiao Road, Changning District, Shanghai |
||||||||||||||||||||||
|
试验主办单位(项目批准或申办者): Secondary sponsor: |
|
||||||||||||||||||||||
|
经费或物资来源: |
自筹经费 |
||||||||||||||||||||||
|
Source(s) of funding: |
Self-funded |
||||||||||||||||||||||
|
Target disease: |
Dry eye syndrome |
||||||||||||||||||||||
|
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: |
本研究旨在评估笑疗法对白内障手术后患者干眼症状的影响,探索其在提高患者心理健康和生活质量方面的潜在益处。 |
||||||||||||||||||||||
|
Objectives of Study: |
The aim of this study is to assess the impact of laughter therapy on dry eye symptoms in patients after cataract surgery and to explore its potential benefits in improving patients' mental health and quality of life. |
||||||||||||||||||||||
|
药物成份或治疗方案详述: |
|
||||||||||||||||||||||
|
Description for medicine or protocol of treatment in detail: |
|
||||||||||||||||||||||
|
纳入标准: |
1)单眼行白内障手术,且近期无对侧眼手术计划 ; 2)手术前后能配合完成各项眼部检查; 3)患者知情同意自愿参加本次研究并签署知情同意书 ; 4)符合干眼的诊断标准。 5)基础健康状况:无严重眼部疾病,无严重系统性疾病,不影响干眼症或笑疗法干预的治疗。 |
||||||||||||||||||||||
|
Inclusion criteria |
1. Undergoing cataract surgery in one eye, with no recent plans for surgery in the other eye. 2. Able to cooperate with and complete various eye examinations before and after surgery. 3. Patients who voluntarily agree to participate in the study and sign the informed consent form. 4. Meet the diagnostic criteria for dry eye. 5. Basic health status: no severe eye diseases, no severe systemic diseases, and no conditions affecting the treatment of dry eye or the intervention of laughter therapy. |
||||||||||||||||||||||
|
排除标准: |
1)患有眼外伤、角结膜炎、葡萄膜炎、青光眼等其他影响疗效评价的眼表疾病; 2)合并睑板腺功能障碍者,包括睑缘和睑板腺开口异常、睑酯分泌异常等; 3)6个月内使用过影响泪液分泌功能药物,如抗组胺药、抗抑郁药、各种人工泪液等; 4)6个月内有玻璃体切割手术、抗青光眼手术、翼状胬肉等眼手术史; 5)排除不能使用智能手机、平板电脑或其他数字设备的受试者,确保干预能够顺利进行。 6)精神障碍或认知障碍:有明显的精神障碍(如抑郁症、焦虑症等)或认知功能障碍,无法按照研究要求完成干预内容的患者。 |
||||||||||||||||||||||
|
Exclusion criteria: |
1. Suffering from other ocular surface diseases affecting efficacy evaluation, such as ocular trauma, keratoconjunctivitis, uveitis, glaucoma, etc. 2. Combined with meibomian gland dysfunction, abnormal lid margin and meibomian gland openings, abnormal meibum secretion, etc. 3. Use of medications affecting tear secretion function within the past 6 months, such as antihistamines, antidepressants, or various artificial tears. 4. History of ocular surgeries within theygium removal. 5. Exclude participants who cannot use smartphones, tablets, or other digital devices, ensuring smooth intervention implementation. 6. Mental or cognitive disorders: patients with significant mental disorders (such as depression, anxiety) or cognitive impairment who cannot complete the intervention as required by the study. |
||||||||||||||||||||||
|
研究实施时间: Study execute time: |
从 From 2025-07-01 00:00:00至 To 2026-01-01 00:00:00 |
征募观察对象时间: Recruiting time: |
从From 2025-07-01 00:00:00 至 To 2026-01-01 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): |
使用计算机生成的随机数表进行患者随机分配,分为两组,确保每组的基线特征均匀分布。 |
||||||||
|
Randomization Procedure (please state who generates the random number sequence and by what method): |
Use a computer-generated random number table to randomly assign patients into two groups, ensuring that baseline characteristics are evenly distributed across each group. |
||||||||
|
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: |
无 |
|
Blinding: |
None |
|
试验完成后的统计结果(上传文件): |
|
|
Calculated Results after
|
|
|
是否共享原始数据: IPD sharing |
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): |
无 |
|
The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
None |
|
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: |
病例记录表 |
|
Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Case Record Form, CRF |
|
数据与安全监察委员会: Data and Safety Monitoring Committee: |
暂未确定/Not yet |