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Computer-Assisted Instruction: Arterial Blood Gases (CAI)

2016年3月14日 更新者:Phongthara Vichitvejpaisal"、Mahidol University

Development and Assessment of On-line Computer-Assisted Instruction: Arterial Blood Gases

This research work develops a diagnostic and feedback-providing system for self-learning by volunteers who are asked to log in to a website to study the required subjects in three weeks.

The system establishes students' learning weaknesses and offered guidelines for their improvement until all such weaknesses are corrected.

Assessment is based on students' relative growth scores, and their record profiles.

研究概览

地位

未知

条件

详细说明

Website development: The www.nmac.in.th website contains the learning courseware database. The program is interactive, with personal files for each student along with other details like code, password, name, surname, date-month-year, test scores, and log-in periods and time.

Students can, on their own, plan their learning for each subject; they are free to record and copy the articles on the website. There is no log-in limit from any place with internet connection around the clock.

Learning courseware: We developed a set of learning courseware of the specified topics as activities and diagnostic tests for arterial blood gases (ABGs).

The activities covered topics under the table of specification, whereas the diagnostic tests probed the weaknesses of students' understanding of activities so as to assess their learning skills in analytical thinking of patients' problems under assorted circumstances to be faced in clinical practice.

Each set of courseware contained three levels: beginner, intermediate, and advanced.

Students are required to pass each in an orderly way, at least once with a minimum score of 80% before advancing to the next level.

Once they have passed certain courseware, they are free to review all learning courseware as often as they wanted to.

Learning sources: Interactive with students, the program identifies learning weaknesses while avoiding giving them direct answers immediately after each test.

What it does is instead to link the student to begin a search for the well-prepared content, which contains details of the subject.

Construction of test forms: Pre-test and post-test forms are designed to be parallel under the table of specification, thus preventing the carry-over effect by testing them three weeks afterward and alternating the questions or changing them.

The tests underwent verification for content validity and had their index of item objective congruence (IOC) determined by four clinical experts.

Deciding whether the tests and behavioral objectives aligned, they set the IOCs at 0.79 for pre-tests and 0.73 for post-tests.

  • Two sets of pre-tests and post-tests of 10 questions each, with each question containing four sub-items requiring short answers
  • 15 activities and 10 diagnostic tests of the multiple-choice (4) questions

System testing: We introduced the elements, namely the learning courseware, tests, and sources of learning, to the developed system before testing it under the research and development approach, the logical approach, and empirical approach.

Different sample sizes were used, and logical comments were analyzed to test the system efficiency under three stages:

First-stage system development and assessment:

  • The sample group was 4 sixth year medical students who underwent system testing during a three-week period
  • Objectives:
  • To test system operating units and system log-ins
  • To test the objectivity of the tools
  • Findings:
  • The system operating units were flexible to students' interactive behavior, instruction responsiveness, and network connection. Access to the system through the website provided ready access to the information, was user-friendly, and was stable.
  • The tools were objective, covered complete details, and were clear, with elements of the subject content in proper order.
  • Improvement:
  • Making the system interactive with the network; focusing on conciseness; adding channels for answering questionnaires through the website; adding the record on downloading articles from the website; notifying students of their performance on the tests, question by question; and enabling the website to accommodate no less than 100 concurrent users.
  • Adjustment of fonts to match general personal-computer sets and updating the wording of the questions to be more relevant with the circumstances of patients.

Second-stage system development and assessment:

  • The sample group was 32 nurse anesthetist students and 21 first year residents in anesthesiology who underwent system testing during a three-week period.
  • Objectives
  • To test criterion-referenced tool quality
  • To determine learning achievement
  • Findings:
  • The pre-test and post-test registered 0.48 and 0.50 in item difficulty (p) values; 0.72 and 0.73 in sensitivity indices (s); 0.85 and 0.88 in content validity; concurrent validity through calculation of Pearson Product moment against a standard test of 0.82; and 0.91 reliability for the internal consistency by the Kuder-Richardson method 20.
  • The diagnostic tests registered 0.87, 0.91, 0.87 and 0.93, 0.93, 0.86 in item difficulty (p) values; 0.17, 0.11, 0.20 and 0.15, 0.08, 0.21 in sensitivity indices; 0.89, 0.80, 0.95 in content validity; and 0.85, 0.66, 0.95 and 0.91, 0.77, 0.88 reliability for the internal consistency.
  • Learning achievement:
  • The post-test scores with a full mark of 40, were significantly higher than pre-test scores: 4.52 ± 3.04 against 23.90 ± 7.69 among the nurse student group and 7.60 ± 5.69 and 26.96 ± 7.47 among the resident group.
  • Improvement: We chose quality test questions and introduced 'distracters' most often picked by respondents in each pre-test and post-test in developing the tests for our target group.

Third-stage development and assessment: Consisting in a trial application on the target preclinical 3rd year medical students and nurses in critical care unit throughout the country who volunteer to join the study. They are asked to log in to a website to study the required subjects in three weeks. Students' profiles are periodically updated.

研究类型

介入性

注册 (预期的)

1000

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

  • 孩子
  • 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:

  • 3rd year medical students
  • Nurses in Critical care unit

Exclusion Criteria:

  • non-volunteer

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

  • 分配:非随机化
  • 介入模型:并行分配
  • 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:3th year medical students
pretest and post-test scores are calculated for relative growth scores
其他名称:
  • relative growth scores
实验性的:nurses in critical care units
pretest and post-test scores are calculated for relative growth scores
其他名称:
  • relative growth scores

研究衡量的是什么?

主要结果指标

结果测量
大体时间
Number of Participants with Learning Achievement as a Measure of Relative Growth Scores.
大体时间:1 year
1 year

次要结果测量

结果测量
大体时间
Scores on the Web Record Profiles.
大体时间:1 year
1 year

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。

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

2011年6月1日

初级完成 (实际的)

2015年10月1日

研究完成 (预期的)

2016年4月1日

研究注册日期

首次提交

2012年4月19日

首先提交符合 QC 标准的

2012年6月25日

首次发布 (估计)

2012年6月26日

研究记录更新

最后更新发布 (估计)

2016年3月16日

上次提交的符合 QC 标准的更新

2016年3月14日

最后验证

2016年3月1日

更多信息

与本研究相关的术语

其他研究编号

  • 029/2554(EC1)

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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