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Sevice-learning in Physiotherapy and Heart Transplantation and Acute Coronary Syndrome

2021年4月16日 更新者:Elena Marques-Sule、University of Valencia

The Effects of Sevice-learning in Physiotherapy Students: Exercise Program for Patients With Heart Transplantation and Acute Coronary Syndrome

A service-learning programme in physiotherapy students will be performed. 30 physiotherapy students will be randomly assigned to an intervention group (n=16) or to a control group (n=16). Intervention group will perform a service-learning program with real patients with heart transplantation, and will have to perform a physical therapy program adapted to a real patient. Two meetings will be performed in order to establish groups, explain the project and search information based on evidence in scientific databases. In addition, three meetings with patients will be stated in order to establish the adapted program based on the real patient's needs and characteristics. The control group will have to perform a physiotherapy program without meeting real patients.

研究概览

地位

完全的

条件

详细说明

This study aims at determining the effect of a Service-Learning program on knowledge, ethical sensitivity and acquired transversal competences. On the other hand, we aim at evaluating the service performed, the skills acquired, the participation, the degree of participatory evaluation and the level of satisfaction of the intervention group. All variables will be measured with validated scales or questionnaires.

Both groups will have to describe the specific characteristics of the program, different phases of the process, types of exercises recommended, contraindications, safety ranges with respect to the intensity of the exercise, ways of calculating the intensity and self-control. Likewise, they will have to defend the usefulness and duration of the final product through an oral presentation of the program to the patients themselves. Finally, the possible doubts that should exist will be solved.

研究类型

介入性

注册 (实际的)

32

阶段

  • 不适用

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

      • Valencia、西班牙、46010
        • University of Valencia

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 40年 (成人)

接受健康志愿者

是的

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Physiotherapy students

Exclusion Criteria:

  • Prior courses on cardiac rehabilitation

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:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:单身的

武器和干预

参与者组/臂
干预/治疗
实验性的:Service-learning group
Intervention group will perform a service-learning program with real patients with heart transplantation and coronary syndrome, and will have to perform a physical therapy program adapted to a real patient. Two meetings will be performed in order to establish groups, explain the project and search information based on evidence in scientific databases. In addition, three meetings with patients will be stated in order to establish the adapted program based on the real patient's needs and characteristics.
Intervention group will perform a service-learning program with real patients with heart transplantation, and will have to perform a physical therapy program adapted to a real patient. Two meetings will be performed in order to establish groups, explain the project and search information based on evidence in scientific databases. In addition, three meetings with patients will be stated in order to establish the adapted program based on the real patient's needs and characteristics.
无干预:Control group
Control group will perform a physical therapy program for heart transplantation and coronary syndrome, but without meeting real patients. One meeting will be performed in order to establish groups and search information based on evidence in scientific databases.

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
Ethical sensitivity
大体时间:baseline
Ethical sensitivity Questionnaire, composed of of 9 items with six possible responses (Likert scale from 1, indicating total disagreement, to 6, indicating total agreement). The minimum score is 9 and the maximum score is 54. The more score, the more ethical sensitivity. Cronbach's alpha=0.76
baseline
Ethical sensitivity
大体时间:3 months
Ethical sensitivity Questionnaire, composed of of 9 items with six possible responses (Likert scale from 1, indicating total disagreement, to 6, indicating total agreement). The minimum score is 9 and the maximum score is 54. The more score, the more ethical sensitivity. Cronbach's alpha=0.76
3 months

次要结果测量

结果测量
措施说明
大体时间
Service performed (by the students of the experimental group)
大体时间:3 months
Service-learning Questionnaire, using the part of the questionnaire about service
3 months
Skills acquired (by the students of the experimental group)
大体时间:3 months
Service-learning Questionnaire, using the part of the questionnaire about skills
3 months
Participation (of the students of the experimental group)
大体时间:3 months
Service-learning Questionnaire,using the part of the questionnaire about participation
3 months
Degree of participatory evaluation (of the students of the experimental group)
大体时间:3 months
Questionnaire of Participatory evaluation, Service-learning and university
3 months
Level of satisfaction (of the students of the experimental group)
大体时间:3 months
ad-hoc satisfaction questionnaire
3 months
Knowledge on physiotherapy in heart transplantation
大体时间:baseline
A 10-question test exam will be created ad-hoc
baseline
Knowledge on physiotherapy in heart transplantation
大体时间:3 months
A 10-question test exam will be created ad-hoc
3 months
Acquired transversal competences
大体时间:baseline
Questionnaire of Higher education, transversal skills and gender, consisted of 6 items about gender and competencies (Likert scale of 7 points: level 4 was set as neutral, scores above 4 were considered positive, and those below 4 were taken as negative scores)
baseline
Acquired transversal competences
大体时间:3 months
Questionnaire of Higher education, transversal skills and gender, consisted of 6 items about gender and competencies (Likert scale of 7 points: level 4 was set as neutral, scores above 4 were considered positive, and those below 4 were taken as negative scores)
3 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:Elena Marques-Sule, PT, PhD、University of Valencia

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)

2020年3月1日

初级完成 (实际的)

2020年6月1日

研究完成 (实际的)

2020年7月31日

研究注册日期

首次提交

2019年1月2日

首先提交符合 QC 标准的

2020年2月6日

首次发布 (实际的)

2020年2月10日

研究记录更新

最后更新发布 (实际的)

2021年4月20日

上次提交的符合 QC 标准的更新

2021年4月16日

最后验证

2021年4月1日

更多信息

与本研究相关的术语

其他研究编号

  • H1542195894247

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

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.

Service-learning program的临床试验

3
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