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Study on the Association Between the Introduction of Complementary Feeding and Infant Gut Microbiome Composition

2026年9月25日 更新者:University Children's Hospital, Zurich

FamilyFeedBiome Pilot Project: Observational Study on the Association Between the Introduction of Complementary Feeding and the Composition of the Gut Microbiome in Infants

The goal of this observational study is to assess the feasibility of investigating the association between the introduction of complementary feeding and gut microbiome composition in infants. The main question it aims to answer is:

Can we reach the feasibility targets for questionnaire completeness and data quality, the proportion of stool samples suitable for analysis, protocol adherence, and recruitment rate?

Parents will complete questionnaires about their infant's health and nutrition and collect stool samples from their infant at three timepoints around the introduction of complementary feeding.

研究概览

地位

尚未招聘

条件

详细说明

Patient and Public Involvement and Engagement (PPIE) is embedded throughout the planning, conduct and dissemination of this observational study.

研究类型

观察性的

注册 (估计的)

20

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

2个月 至 7个月 (孩子)

接受健康志愿者

是的

有资格学习的性别

全部

取样方法

非概率样本

研究人群

Infants recruited from a pediatric practice and a University Children's Hospital.

描述

Inclusion Criteria:

  • Healthy infants
  • Formula or breastfed
  • Born at term (≥ 37 weeks gestation)
  • Parents/caregivers willing and able to collect stool samples and complete questionnaires
  • Written informed consent signed by parent or caregiver
  • Parent/caregiver at least 18 years of age

Exclusion Criteria:

  • Preterm infants (< 37 weeks gestation)
  • Infants with congenital or chronic conditions affecting digestion or the immune system
  • Use of antibiotics within the last 4 weeks before start of complementary feeding
  • Food allergies or intolerances that would significantly restrict complementary feeding
  • Parents/caregivers have insufficient proficiency in German to understand study materials and provide informed consent

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 观测模型:COHORT
  • 时间观点:PROSPECTIVE

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Feasibility of complete questionnaire data collection
大体时间:At study completion, approximately 5 months

Percentage of questionnaires completed by recruited families (feasibility target: ≥ 80 %).

At study completion, approximately 5 months
Feasibility of high-quality questionnaire data collection
大体时间:At study completion, approximately 5 months

Percentage of families for whom no contradictory or inconsistent information is identified across the three questionnaires (feasibility target: ≥ 80 %).

At study completion, approximately 5 months
Feasibility of adherence to questionnaire timepoints
大体时间:At study completion, approximately 5 months

Percentage of answered questionnaires that comply with the predefined data collection timepoints between start of complementary feeding (CF) and T1, T2 and T3: T1 - CF: 0 - 8 days, CF - T2: 6 - 8 days, CF - T3: 13 - 15 days (feasibility target: ≥ 80 %).

At study completion, approximately 5 months
Feasibility of adherence to stool sample collection timepoints
大体时间:At study completion, approximately 5 months

Percentage of collected stool samples that comply with the predefined data collection timepoints between start of complementary feeding (CF) and T1, T2 and T3: T1 - CF: 0 - 8 days, CF - T2: 6 - 8 days, CF - T3: 13 - 15 days (feasibility target: ≥ 80 %).

At study completion, approximately 5 months
Feasibility of collecting analyzable stool samples
大体时间:At study completion, approximately 5 months

Percentage of collected stool samples for which 16S rRNA analysis was successfully completed (feasibility target: ≥ 90 %).

At study completion, approximately 5 months
Feasibility of study participant recruitment
大体时间:At study completion, approximately 5 months

Recruitment rate will be described as number of recruited study participants per month. Reasons of withdrawal will be reported.

At study completion, approximately 5 months

次要结果测量

结果测量
措施说明
大体时间
Feasibility of PPIE activities assessed by the project leader using the Public and Patient Engagement Evaluation Tool (PPEET) project questionnaire and by the PPIE participants using a modified Patient Engagement in Research Scale (PEIRS) tool.
大体时间:At study completion, approximately 5 months

The level of involvement achieved will be assessed by the project leader and PPIE participants using single-choice questions in the questionnaires. PPIE activities will be considered feasible if all PPIE activities can be conducted at the predefined level of involvement. Challenges and barriers encountered during the implementation of PPIE activities and their impact on the feasibility of PPIE activities will be assessed descriptively by the project leader and PPIE participants in the questionnaires.

At study completion, approximately 5 months

其他结果措施

结果测量
措施说明
大体时间
Preliminary data on the association between complementary feeding and gut microbiome composition
大体时间:7 days before introduction of complementary feeding, 7 days after introduction of complementary feeding, 14 days after introduction of complementary feeding

Participant's health and dietary characteristics, as well as gut microbiome composition will be summarized at each timepoint using descriptive statistics. Where appropriate, plots will be used to visualize changes over time and patterns in gut microbiome composition. Gut microbiome composition will be described based on the relative abundance of the most common bacteria, microbial diversity within individual samples (α-diversity), and differences in overall microbial community composition between timepoints (β-diversity). Any statistical analyses investigating associations between the introduction of complementary feeding and gut microbiome composition will be considered explanatory and reported using confidence internals. These analyses will not include p-values or support confirmatory conclusions.

7 days before introduction of complementary feeding, 7 days after introduction of complementary feeding, 14 days after introduction of complementary feeding

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

赞助

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年9月1日

初级完成 (估计的)

2027年1月1日

研究完成 (估计的)

2027年2月1日

研究注册日期

首次提交

2026年9月9日

首先提交符合 QC 标准的

2026年9月25日

首次发布 (实际的)

2026年10月1日

研究记录更新

最后更新发布 (实际的)

2026年10月1日

上次提交的符合 QC 标准的更新

2026年9月25日

最后验证

2026年9月1日

更多信息

与本研究相关的术语

其他研究编号

  • 2026-01319
  • 2026__SG_293 (其他赠款/资助编号:Graduate Campus Universität Zürich)

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

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