CHIME CRF Form H1 Monitoring Confidence Dataset in Collaborative Home Infant Monitoring Evaluation

Captures caregiver's confidence in using infant monitor
Study Description
Infants were enrolled into four groups: healthy term, preterm infants <1750g w/o significant morbidity, sibling of SIDS, and babies experiencing apparent life-threatening events. Objectives were to: determine monitor efficacy in identifying episodes endangering the infant's health; determine conditions optimizing use of apnea monitors in high risk infants; correlate physiological markers with the propensity for life-threatening events; and report on maturation of heart and respiratory function in sleeping infants. Data were collected from nightly home recordings (via CHIME Monitor device) and one sleep lab polysomnography (PSG) session (via CHIME Monitor and ALICE3 devices). CRF data include sociodemographic and medical information on mother and infant at entry and from scheduled medical follow-up visits through 1-year of age, weekly phone calls, monitor knowledge and satisfaction scales, periodic assessments with the Bayley II, NCAST, subscales of the Parenting Stress Index, and hospitalizations. Infants; ethnicity and race information is from maternal data

本数据集聚焦于看护者使用婴儿监护仪的信心水平。
研究概况：
本研究共纳入四组婴儿：健康足月婴儿、出生体重<1750g且无严重并发症的早产儿、婴儿猝死综合征（SIDS）患儿的同胞兄妹，以及曾出现疑似威胁生命事件的婴儿。本研究的目标如下：
1. 明确监护仪在识别危及婴儿健康事件中的应用效能；
2. 确定优化高危婴儿呼吸暂停监护仪使用的临床条件；
3. 分析生理标志物与威胁生命事件发生倾向的相关性；
4. 报告睡眠状态下婴儿心脏与呼吸功能的成熟进程。
数据采集来源包括：夜间家庭监护记录（通过CHIME Monitor设备采集）以及1次睡眠实验室多导睡眠图（PSG）检测（通过CHIME Monitor与ALICE3设备完成）。
病例报告表（CRF）所收录的数据包括：入组时及截至1岁的定期医疗随访中收集的母婴社会人口学与临床信息、每周电话随访数据、监护仪认知与满意度量表测评结果、定期开展的贝利婴儿发展量表第二版（Bayley II）评估、NCAST测评、育儿压力指数（Parenting Stress Index）各分量表测评结果，以及住院相关记录。
婴儿的种族与民族信息来源于母亲的建档数据。