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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: |
ChiCTR2600116997 |
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最近更新日期: Date of Last Refreshed on: |
2026-01-19 08:36:44 |
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注册时间: Date of Registration: |
2026-01-19 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: |
基于健康信念模型的ICU重症产妇母乳喂养健康教育方案的构建及效果评价 |
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Public title: |
Construction and effect evaluation of breastfeeding health education program for intensive care unit (ICU) critically ill puerpera based on health belief model |
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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: |
基于健康信念模型的ICU重症产妇母乳喂养健康教育方案的构建及效果评价 |
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Scientific title: |
Construction and effect evaluation of breastfeeding health education program for intensive care unit (ICU) critically ill puerpera based on health belief model |
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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: |
杨玲 |
研究负责人: |
杨玲 |
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Applicant: |
Yang Ling |
Study leader: |
Yang Ling |
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申请注册联系人电话: Applicant telephone: |
+86 185 8073 9789 |
研究负责人电话: Study leader's telephone: |
+86 185 8073 9789 |
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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: |
489739215@qq.com |
研究负责人电子邮件: Study leader's E-mail: |
489739215@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: |
中国重庆市两江新区龙山路120号 |
研究负责人通讯地址: |
中国重庆市两江新区龙山路120号 |
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Applicant address: |
No. 120, Longshan Road, Liangjiang New Area, Chongqing City, China |
Study leader's address: |
No. 120, Longshan Road, Liangjiang New Area, Chongqing City, China |
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申请注册联系人邮政编码: Applicant postcode: |
401147 |
研究负责人邮政编码: Study leader's postcode: |
400000 |
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申请人所在单位: |
重庆医科大学附属妇女儿童医院(重庆市妇幼保健院) |
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Applicant's institution: |
Women and Children’s Hospital of Chongqing Medical University(Chongqing Health Center for Women and Children) |
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研究负责人所在单位: |
重庆医科大学附属妇女儿童医院(重庆市妇幼保健院) |
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Affiliation of the Leader: |
Women and Children’s Hospital of Chongqing Medical University(Chongqing Health Center for Women and Children) |
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是否获伦理委员会批准: |
是/Yes |
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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: |
(2025)伦理(科)127号 |
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: |
重庆市妇幼保健院医学伦理委员会 |
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Name of the ethic committee: |
Medical Ethics Committee of Chongqing Health Center for Women and Children |
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伦理委员会批准日期: Date of approved by ethic committee: |
2025-12-12 00:00:00 |
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伦理委员会联系人: |
刘禄斌 |
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Contact Name of the ethic committee: |
Liu Lubin |
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伦理委员会联系地址: |
中国重庆市两江新区龙山路120号 |
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Contact Address of the ethic committee: |
No. 120, Longshan Road, Liangjiang New Area, Chongqing City, China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 186 2308 8100 |
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: |
重庆医科大学附属妇女儿童医院(重庆市妇幼保健院) |
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Primary sponsor: |
Women and Children’s Hospital of Chongqing Medical University(Chongqing Health Center for Women and Children) |
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研究实施负责(组长)单位地址: |
中国重庆市两江新区龙山路120号 |
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Primary sponsor's address: |
No. 120, Longshan Road, Liangjiang New Area, 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: |
自筹 |
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Source(s) of funding: |
Self-financed |
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Target disease: |
Postpartum health problems related to breastfeeding in critically ill parturients in the ICU |
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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: |
其它 | ||||||||||||||||||||||
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Study phase: |
N/A |
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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: |
1.基于 HBM 理论六大核心维度(感知易感性、感知严重性、感知益处、感知障碍、自我效能、社会支持),系统探究影响 ICU 产妇母乳喂养行为的关键因素; 2.结合质性研究结果、循证证据及专家共识,构建科学、可行、个性化的 ICU 产妇母乳喂养健康教育方案; 3.通过类随机对照试验验证该干预方案对产后泌乳启动时间、纯母乳喂养率、母乳喂养自我效能及心理状态(焦虑、抑郁)的改善效果,为临床优化危重孕产妇母乳喂养护理策略提供理论依据与实践指导。 |
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Objectives of Study: |
1.To systematically explore the key factors influencing breastfeeding behaviors of parturients in ICU based on the six core dimensions of the Health Belief Model (HBM): perceived susceptibility, perceived severity, perceived benefits, perceived barriers, self-efficacy, and social support. 2.To construct a scientific, feasible, and individualized health education program for breastfeeding of parturients in ICU by integrating qualitative research results, evidence-based evidence, and expert consensus. 3.To verify the improvement effect of the intervention program on the initiation time of postpartum lactation, exclusive breastfeeding rate, breastfeeding self-efficacy, and psychological status (anxiety and depression) through a quasi-randomized controlled trial, so as to provide theoretical basis and practical guidance for optimizing clinical breastfeeding nursing strategies for critically ill pregnant and lying-in women. |
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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: 年龄18-50周岁 ; 2: 入住ICU的产妇; 3: 病情相对稳定; 4: 精神状态及认知良好; 5: 有母乳喂养意愿并知情同意接受试验的产妇。 |
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Inclusion criteria |
1: Aged 18-50 years old; 2: Parturients admitted to ICU; 3: Relatively stable condition; 4: Good mental state and cognition; 5: Willing to breastfeed and informed consent to participate in the trial. |
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排除标准: |
1: 罹患精神疾病或沟通交流障碍; 2: 母乳喂养禁忌证。 |
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Exclusion criteria: |
1: Suffering from mental illness or communication disorders; 2: Contraindications to breastfeeding. |
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研究实施时间: Study execute time: |
从 From 2026-01-20 00:00:00至 To 2026-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从From 2026-01-20 00:00:00 至 To 2026-12-31 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: |
女性 |
Gender: |
Female |
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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): |
由研究团队的统计人员采用随机数字法生成随机序列,将符合入组标准的 ICU 产妇按 1:1 比例随机分配至干预组与对照组。 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
The statistician of the research team generates a random sequence using the random number method, and randomly assigns eligible ICU parturients to the intervention group and the control group at a 1:1 ratio. |
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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: |
单盲(对受试者隐藏分组),对评估者不隐藏分组 |
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Blinding: |
Single-blind (group allocation is concealed from participants), while group allocation is not concealed from assessors. |
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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 |
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: |
采用 “病例记录表(Case Record Form, CRF)+ 电子数据采集系统(Electronic Data Capture, EDC)” 结合的方式:1. 由经过培训的研究人员填写纸质 CRF,记录患者基线信息、干预过程及结局指标;2. 同步将 CRF 数据录入 EDC 系统(采用医院科研专用 EDC 平台),定期进行数据核查与备份,确保数据完整性与准确性。 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
A combination of "Case Record Form (CRF) + Electronic Data Capture (EDC)" is adopted: 1. Trained researchers fill in paper CRFs to record patients' baseline information, intervention process and outcome indicators; 2. CRF data is simultaneously entered into the EDC system (using the hospital's research-specific EDC platform), and data verification and backup are performed regularly to ensure data integrity and accuracy. |
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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 |