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Standardized Home Exercise Prescription Education

2017年11月17日 更新者:University of Florida

Standardized Home Exercise Prescription: Education of Family Medicine Residents

This project will encompass an evaluation of the educational value of having evidence based home exercise protocols available for family medicine residents in regard to the prescription of home exercise treatment for common musculoskeletal conditions. Investigators will be evaluating resident knowledge on home exercise prescription as well as their level of comfort in educating their patients before and after a series of didactic sessions and implementation of exercise protocols.

研究概览

详细说明

This study aims to fill the gap in this area of the literature pertaining to home exercise prescription. The justification of this study's scientific merit comes from the lack of literature and the need for research in this area. There have been multiple studies that have shown different exercise modality treatments for common musculoskeletal (MSK) complaints significantly improve both disability and overall quality of life. Despite the evidence of the short and long term effectiveness of exercise based therapies, there is a general lack of confidence of residents in prescribing and teaching patients rehab exercises.Additionally, many of the patients seen in the University of Florida (UF) Family medicine residency program cannot afford or do not have time to attend physical therapist led rehab sessions. This makes physician led education and the ability of prescribing exercise based treatments for musculoskeletal (MSK) complaints a very important component of patient care.

研究类型

介入性

阶段

  • 不适用

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

20年 至 90年 (成人、年长者)

接受健康志愿者

是的

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Resident of the Family Medicine Department at the University of Florida.

Exclusion Criteria:

  • None

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

  • 主要用途:其他
  • 分配:不适用
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Musculoskeletal (MSK) Exercise Prescription
  • Phase I: Residents will be surveyed as to their knowledge and confidence in both diagnosing specific musculoskeletal (MSK) issues and prescribing the correct home rehabilitation regimen.
  • In between phase 1 and phase 2 there will be a series of didactic lectures to educate resident on home exercise prescription and get them familiarized with the handouts.
  • Phase II: Residents will be surveyed again in May 2017 with the same multiple choice questions and Likert style confidence scales from phase 1

The survey will consist of multiple choice and short essay questions, focused on the most common musculoskeletal (MSK) injuries seen in the primary care setting.

In between phase 1 and phase 2 there will be a series of didactic lectures to educate resident on home exercise prescription and get them familiarized with the handouts.
In between phase 1 and phase 2, residents will use home exercise hand-outs readily available and educate their patients in regards to those.

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
Improvement in knowledge about Musculoskeletal (MSK) Exercises
大体时间:at 6 months
Knowledge scores should be at least overall 80% regarding MSK rehabilitation exercises.
at 6 months
Confidence in educating patients about Musculoskeletal (MSK) Exercises
大体时间:at 6 months
Improvement of at least 20% in Medical Residents' confidence regarding education of Musculoskeletal (MSK) to patients
at 6 months

次要结果测量

结果测量
措施说明
大体时间
Confidence in prescribing Musculoskeletal (MSK) Exercises to patients
大体时间:at 6 months
Improvement of at least 20% in Medical Residents' confidence regarding prescription of Musculoskeletal (MSK) exercises
at 6 months
Improvement in prescribing Musculoskeletal (MSK) Exercises to patients
大体时间:at 6 months
Prescription scores should be at least overall 80% regarding MSK rehabilitation exercises
at 6 months

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:Charlie Michaudet, MD、University of Florida

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)

2017年3月15日

初级完成 (预期的)

2017年9月30日

研究完成 (预期的)

2017年12月31日

研究注册日期

首次提交

2017年2月17日

首先提交符合 QC 标准的

2017年2月21日

首次发布 (实际的)

2017年2月27日

研究记录更新

最后更新发布 (实际的)

2017年11月21日

上次提交的符合 QC 标准的更新

2017年11月17日

最后验证

2017年11月1日

更多信息

与本研究相关的术语

其他研究编号

  • IRB201602626

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

IPD 计划说明

No individual participant data (IPD) will be shared.

药物和器械信息、研究文件

研究美国 FDA 监管的药品

研究美国 FDA 监管的设备产品

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