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Social Perception of Microtia

2026年7月20日 更新者:University Medical Center Groningen

The Social Perception of Microtia and Auricular Reconstruction in Children.

Rationale: Microtia is a congenital craniofacial condition characterized by the underdevelopment of the external ear. Children with microtia become aware of their deformity at a young age, and this awareness intensifies in school, where they often face social comparison. This can impact both their mental well-being and social standing. In this process, not only their self-image but also others' perceptions play important roles. Given the significant time children spend with peers, it is crucial to investigate how children of similar ages perceive microtia and whether this perception changes after auricular reconstruction.

Objective: To examine the social perception of children regarding peers with microtia and auricular reconstruction.

Study design: The study is of cross-sectional nature. Study population: The study population consists of primary and secondary school children aged 6 to 18 years old.

Intervention: All children will be shown one of the following photos: a child with a normal ear, a child with preoperative microtia, or a child with a postoperative reconstructed ear. Subsequently, all children will evaluate the photo they have seen using 7 questions based on a visual analogue scale (VAS) ranging from a score of 0 to 10.

Study endpoints: The study includes several endpoints. It will examine children's perception of peers with a normal ear, microtia, or a reconstructed ear in terms of the following social attributes: athleticism, confidence, friendliness, health, intelligence, popularity and willingness to interact. Additionally, it will explore whether there is a difference in the perception of primary school children and secondary school children regarding the above-mentioned social attributes.

研究概览

研究类型

观察性的

注册 (实际的)

1271

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Provincie Groningen
      • Groningen、Provincie Groningen、荷兰、9713 GZ
        • University Medical Center Groningen

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

  • 孩子

接受健康志愿者

是的

取样方法

非概率样本

研究人群

Children aged 6-17 years attending primary or secondary schools were eligible for participation

描述

Inclusion Criteria:

  • Attending primary or secondary school

Exclusion Criteria:

-

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

队列和干预

团体/队列
Children aged 6-17 years were eligible for participation.
Attending primary or secondary school

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
Difference in social perception scores
大体时间:The entire assessment can be completed directly after enrollment and takes a maximum of 5 minutes.
The primary outcome was the difference in social perception scores between the three image groups. Responses will be recorded using a visual analogue scale (VAS) ranging from 0 to 100, with higher scores indicating a more favorable perception of the attribute.
The entire assessment can be completed directly after enrollment and takes a maximum of 5 minutes.

次要结果测量

结果测量
措施说明
大体时间
Differences in social perception scores between primary and secondary school
大体时间:The entire assessment can be completed directly after enrollment and takes a maximum of 5 minutes.
Secondary analyses examined differences in social perception scores between primary and secondary school students. Responses will be recorded using a visual analogue scale (VAS) ranging from 0 to 100, with higher scores indicating a more favorable perception of the attribute.
The entire assessment can be completed directly after enrollment and takes a maximum of 5 minutes.

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。

调查人员

  • 首席研究员:Myrthe KS Hol, Prof. dr.、University Medical Center Groningen

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 (实际的)

2026年3月4日

初级完成 (实际的)

2026年6月22日

研究完成 (实际的)

2026年6月22日

研究注册日期

首次提交

2026年7月13日

首先提交符合 QC 标准的

2026年7月20日

首次发布 (实际的)

2026年7月23日

研究记录更新

最后更新发布 (实际的)

2026年7月23日

上次提交的符合 QC 标准的更新

2026年7月20日

最后验证

2025年6月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

未定

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

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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