LONG TERM FOLLOW UP OF CLUBFOOT

马蹄内翻足的长期随访

• 批准号: 7604844
• 负责人: JOSE ANTONIO MORCUENDE
• 金额: $ 0.01万
• 依托单位: UNIVERSITY OF IOWA
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-03-01 至 2007-09-16
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7604844
• 关键词: Age; Appearance; Clinic; Computer Retrieval of Information on Scientific Projects Database; Congenital Abnormality; Congenital clubfoot; Control Groups; Deformity; Effectiveness; Funding; Grant; Hour; Institution; Measures; Methods; Numbers; Occupations; Operative Surgical Procedures; Ophthalmology; Pain; Patients; Physical activity; Population Control; Purpose; Questionnaires; Reference Standards; Relapse; Research; Research Personnel; Resources; Source; Stress; United States National Institutes of Health; Weight; day; follow-up; foot; functional outcomes

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. The purpose of this study is to evaluate the effectiveness of the Ponseti method for the correction of clubfoot in patients who were treated before 1971. This group of patients represents the first group of clubfoot patients to be treated with the Ponseti method and so this study will represent the longest follow-up to date. This study will evaluate the initial treatment variables (including number of casts required for correction, surgeries, and relapses), the radiographic appearance of the foot and the present day functional outcome (as measured by pain, mobility, and deformity). Information concerning the stresses placed on the foot will include BMI, weight, occupation, hours spent standing each day, and level of physical activity through the years. This study will also utilize an age-matched control group without congenital abnormalities of the feet as a standard reference with which to compare the patients that were treated for clubfoot. This control population will be obtained from the Ophthalmology clinic and will undergo a physical exam to rule out any congenital abnormality and will fill out a functional foot questionnaire. No x-rays will be obtained from the control group.

该副本是利用众多研究子项目之一 由NIH/NCRR资助的中心赠款提供的资源。子弹和 调查员（PI）可能已经从其他NIH来源获得了主要资金， 因此可以在其他清晰的条目中代表。列出的机构是 对于中心，这不一定是调查员的机构。 这项研究的目的是评估Ponseti方法在1971年接受治疗的患者中校正俱乐部的有效性。这组患者代表了使用Ponseti方法进行治疗的第一组俱乐部患者，因此这项研究将代表迄今为止最长的随访。 这项研究将评估初始治疗变量（包括校正所需的铸件数量，手术和复发所需的铸件），脚的X线摄影外观和当今的功能结果（如疼痛，迁移率和畸形衡量）。 有关脚上压力的信息将包括BMI，体重，职业，每天花费的时间以及多年来的体育锻炼水平。 这项研究还将利用一个年龄匹配的对照组，而没有脚步的先天性异常，作为标准参考，以比较接受俱乐部俱乐部的患者。 该控制人群将从眼科诊所获得，并将进行体格检查以排除任何先天性异常，并填写功能性的足部问卷。 不会从对照组获得X射线。