The Effects of Standing Tutorials on Problem-Based Learning (PBL) Among Undergraduate Students

August 13, 2019 updated by: Maastricht University

Problem-based learning (PBL) is an education model utilized by Maastricht University and many other universities worldwide. PBL occurs in small, collaborative tutorials, under the facilitation of a tutor. This study explores the effects of standing tutorials, compared against sitting tutorials, on PBL among undergraduate students. A quantitative approach will be taken to objectively measure students' learning, and a qualitative approach will be taken to obtain a deeper understanding of the processes of learning.

It is hypothesized that students in the standing tutorials will be able to recall more academic concepts and link the concepts better than students in the sitting tutorials (H1). Audio-recording of the tutorials will be used to measure the discussions within the tutorials. The transcriptions obtained from the recording will be studied through text analysis. It is hypothesized that students in the standing tutorials will produce more discussions, and therefore a higher word count (H2). It is also hypothesized that the students in the standing tutorials will use more word categories that are conducive to the discussion and learning process (H3).

Through the qualitative approach, the content of the transcriptions will be analysed through a thematic analysis. It is hypothesized that the students in the standing tutorials will produce more learning-oriented interactions (H4).

Two additional factors that would be measured are subsequent physical activity and academic achievement. ActivPAL accelerometers will be used to measure the students' daily activity, to find out if the students' daily activities are affected by the standing tutorials, for example, students may sit more as a result of fatigue from the standing tutorials, or conversely transfer the active behaviour from the standing tutorials to other activities outside the tutorial group.It is hypothesized that standing tutorials do not affect the students' subsequent physical activity, and therefore there will be no significant differences of daily activity between students in the sitting and standing tutorials (H5). With regards to academic achievement, it is hypothesized that the students in the standing tutorials will have higher academic achievements after the course compared to the students in the sitting tutorials (H6).

Study Overview

Study Type

Interventional

Enrollment (Actual)

96

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Limburg
      • Maastricht, Limburg, Netherlands, 6200MD
        • Maastricht University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Matriculated undergraduate students of Maastricht University
  • Students who have given their consent to participate in this study.
  • The course subject is well-established and mandatory for all students within the specific bachelor's programme. A well-established course will be chosen so that clear scoring is possible on the concept tests (explained in the Materials and Analysis sections) that will be administered to the students. The course should be mandatory for all students within the bachelor's programme so as to reduce the selection bias that may otherwise occur if we decide to select tutorial groups that only specific groups of students signed up for. An example of a well-established and mandatory course for students in the Biomedical Sciences bachelor's programme at Maastricht University would include 'Brain, behaviour and movement, 'Human genetics, reproduction and prenatal development' and so on.
  • The course coordinators and tutors who are the gatekeepers of the students would have given their permission and cooperation in planning the study into the tutorials.
  • The duration of the course would last at least 10 tutorial classes.
  • The duration of each tutorial is 2 hours.
  • The timing of the tutorial groups will have to be similar to minimize any effects arising due to tests being carried out at different times of the day.
  • The course is taught in English.

Exclusion Criteria:

  • For the standing tutorials, those who are suffering from musculoskeletal discomfort or pathologies that may prevent or influence movement
  • Non-matriculated student of Maastricht University
  • Non-matriculated student of the chosen course for the study

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: BASIC_SCIENCE
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
NO_INTERVENTION: Sit-Sit
The participants will sit during the tutorials, and sit during the concept tests given to measure their learning.
ACTIVE_COMPARATOR: Sit-Stand
The participants will sit during the tutorials. Intervention: Behavioral: Standing during Concept Test will be administered
The participants will stand with a standing desk at an ergonomically correct height during the administration of the Concept Test.
ACTIVE_COMPARATOR: Stand-Stand
The participants will stand during the tutorials, and stand during the concept tests given to measure their learning. Intervention: Behavioral: Standing during Concept Test and regular tutorial session will be administered.
The participants will stand with a standing desk at an ergonomically correct height during the administration of the Concept Test and during their regular tutorial sessions.
ACTIVE_COMPARATOR: Stand-Sit

The participants will stand during the tutorials. Intervention: Behavioral: Standing during regular tutorial session will be administered.

However, participants will sit during the concept tests given to measure their learning.

The participants will stand with a standing desk at an ergonomically correct height during their regular tutorial sessions.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Process of Learning
Time Frame: 1 hour
The discussions that are carried out during PBL will be audio-recorded and undergo text and thematic analysis
1 hour
Outcome of Learning
Time Frame: 10 minutes
Concept Tests will be administered where students list the number of concepts they can recall, and draw a concept map. Both the recalled concepts and the map will be scored independently and combined for a final score.
10 minutes
Academic Achievement
Time Frame: 2 hours
Grades of Final Exam
2 hours

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change of Subsequent Physical Activity
Time Frame: 7 days
Participants' subsequent physical activity will be measured for 10 days, using the ActivPAL accelerometer, to measure whether standing tutorials (compared against sitting tutorials) have an affect on the participants' daily life's physical activity.
7 days
Positive and Negative Affect Schedule (PANAS)
Time Frame: 5 minutes
Participants' overall feelings and emotions are compared between groups in the standing tutorials and sitting tutorials.
5 minutes

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Attendance
Time Frame: Less than 5 minutes (recorded by tutor, as required by the course, even without this intervention study)
Student attendance across the course are compared to see if attendance is affected by the intervention
Less than 5 minutes (recorded by tutor, as required by the course, even without this intervention study)
Tutor Rating
Time Frame: Less than 5 minutes
Tutor rating by the students, that the students will give at the end of the course (even without this intervention study)
Less than 5 minutes
Search, Preparing and Reporting Phase Questionnaire
Time Frame: 5 minutes
The questionnaire contains 23 statements, each with a five-point Likert scale describing to what extent the students agreed or disagreed with each statement (1 = 'completely disagree' to 5 = 'completely agree'). Nine statements refer to the theme of "search phase", six statements refer to the theme of "preparing phase", and eight statements refer to the theme of "reporting phase". The aggregate score for each theme will be summed up from the scores on the Likert scale for each statement. Higher scores indicate more effort/preparation for each theme.
5 minutes
Group Interaction Questionnaire
Time Frame: 5 minutes
This questionnaire is given to tutors to assess the quality of learning-oriented group interactions in PBL. The questionnaire contains 11 statements, each with a five-point Likert scale describing to what extent the tutors agreed or disagreed with each statement (1 = 'completely disagree' to 5 = 'completely agree'). Four statements refer to the theme of "exploratory questions", four statements refer to the theme of "cumulative reasoning", and three statements refer to the theme of "handling conflicts". The aggregate score for each theme will be summed up from the scores on the Likert scale for each statement. Higher scores indicate better discussion quality for each theme.
5 minutes

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

April 10, 2018

Primary Completion (ACTUAL)

June 29, 2018

Study Completion (ACTUAL)

June 30, 2019

Study Registration Dates

First Submitted

March 16, 2018

First Submitted That Met QC Criteria

April 3, 2018

First Posted (ACTUAL)

April 10, 2018

Study Record Updates

Last Update Posted (ACTUAL)

August 15, 2019

Last Update Submitted That Met QC Criteria

August 13, 2019

Last Verified

March 1, 2018

More Information

Terms related to this study

Other Study ID Numbers

  • 00909

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Sharing Time Frame

December 2019 - depending on the time when summary data are published or otherwise made available.

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP
  • ICF
  • ANALYTIC_CODE
  • CSR

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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