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Academic PerformancePBARNCT04336813

Phone-based Audience Response System as an Adjunct in Orthodontic Teaching of Undergraduate Dental Students

A study testing Audience Response system in people with Academic Performance, run by Prince Sattam Bin Abdulaziz University at 2 sites in Saudi Arabia.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Methodology :A cross-over randomised controlled trial comparing two teaching methods Duration :Start date 6th December 2017 to 29st May 2018 Objective : To evaluate the effectiveness phone-based audience response system (PB-ARS) on knowledge retention and performance in teaching orthodontics for dental undergraduate… Read more about this study

Who is it for?
Any age, men onlyHealthy volunteers can take part
Conditions the study is for
Academic Performance
What is being tested?
Audience Response system
Could I receive a placebo?
No, everyone receives an active treatment
How many people
34 participants
Where
2 sitesSaudi Arabia
Study dates
6 Dec 2017to 29 May 2018
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • Men only
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Who may be able to join

  • fourth-year undergraduate dental student

Who cannot join

  • Other undergraduate dental students from levels other than the 4th

Trial locations and contacts

2 sites in 1 country.

Saudi Arabia2 sites
  • Prince Sattam Bin Abdulaziz University

    Al Kharjah

  • Prince Sattam University

    Riyadh

Other trials in Saudi Arabia

About this study

Official title: Phone-based Audience Response System as an Adjunct in Orthodontic Teaching of Undergraduate Dental Students: a Cross-over Randomised Controlled Trial

Methodology :A cross-over randomised controlled trial comparing two teaching methods Duration :Start date 6th December 2017 to 29st May 2018 Objective : To evaluate the effectiveness phone-based audience response system (PB-ARS) on knowledge retention and performance in teaching orthodontics for dental undergraduate students in a Saudi Dental School Number:The cohort of the trial includes 34 fourth-year dental students that represents whole fourth-year undergraduate class Main Inclusion criteria : whole fourth-year undergraduate class in a Saudi Dental college.

Statistical Analysis : The normal distribution will be tested. The Mann-Whitney U test will used to compare the median score for each answer that would be given by students in the questionnaires. Scores will be analyzed and compared to assess knowledge retention using cross-over analysis with Mann-Whitney U test

Read the detailed description

Design:

The trial was designed as a cross-over clustered randomized control trial (each group was a cluster), so that each group acted as their own control for their knowledge's retention and perception.

Setting and consent: College of Dentistry, Prince Sattam Bin Abdulaziz University/Alkharj/ Saudi Arabia. Written consents were obtained from students before commencing the trail.

Participants : The cohort of the trial included the whole fourth-year undergraduate class (34 undergraduate dental students) in order to eliminate selection bias. Participants in this study had no prior orthodontic teaching, hence, no bias associated with increased knowledge in any orthodontic field was anticipated.

Randomization: Students were allocated to one of two even groups (G1 or G2) using computer generated randomization. each group (G1 and G2) consisted of 17 male students with a mean age of (23.27 years ± 0.86).

Intervention :

Lectures : Simultaneously, G1 and G2 attended two lectures (L1\&L2): L1 was titled "Management of Class III malocclusion", L2 was titled "Management of open bite and cross-bite". Both lectures were presented at the main campus of Prince Sattam Bin Abdulaziz College of Dentistry and they were conducted in an identical manner in all aspects including:

  • Presentation in PowerPoint (Microsoft Corp, Redmond, WA)
  • Both lectures were delivered by the same registered specialist orthodontist (FA),
  • Learning outcomes of the delivered lectures (T1 and T2) were based on teaching outcomes specified by the National Commission for Academic Accreditation and Assessment in Saudi Arabia, and
  • Both lectures delivered over the same period of time. Prior to lectures, students were instructed to register with the audience response system (ARS) and download its application (Poll Everywhere, San Francisco, California, USA, https://www.polleverywhere.com). Additional smart phones were available to students who do not have smart phones at the time of the lecture. Students were unaware of their allocation until the beginning of the first lecture.

In the lecture hall, G1 was separated from G2, and both groups completed an assessment of written multiple-choice questions (MCQs) scored out of 20, before the lecture. During L1, phone based (ARS) questions (PB-ARS) secretly displayed on the smart phones of the students in G1, and they were allowed to read the question and answer it, while those in parallel arm of the trial (G2) were blinded to those questions and answers. At the end of L1, both groups completed the same written MCQs assessment . A similar protocol was undertaken during L2 a week later, except that the groups were crossed-over, hence, the group which has had ARS integrated lecture in the previous week, has received in a non-ARS integrated lecture, and vice versa.

Formative exam:

MCQs formative tests consisted of 20 questions related to the taught topics during L1 and L2 was undertaken. In order to reduce the carry over effect, the PB-ARS questions during the lectures were not similar to the MCQs sheet. The used MCQs were piloted between authors to ensure its content validity and reliability. Contents validity was tested using test matrix and expert judgment. The test reliability was estimated using inter-rater reliability, a correlation of more than 0.7 was considered acceptable.

Summative exam:

Both groups attended their final written summative exams. L1 was undertaken 11 weeks prior to final exam while L2 was undertaken 10 weeks before the exam. The final exam was in MCQs format and included questions from all subjects taught in the second semester of the year including five questions relevant to the subjects taught in L1 and L2. The exam questions were identical for all students and were delivered at the same time under controlled conditions. Students who failed to attend the final summative exam were excluded to reduce the effect of time factor as confounding factors. The final exam scores of all student to questions related to TL1 and TL2 were anonymously collated using an excel sheet by independent tutor to reduce reporting bias. The maximum achievable score for the five questions relevant to the subjects taught in L1 and L2 was 5.

Students' perception:

At the end of L1, both groups were asked to fill a questionnaire regarding their experience with the lecture and intervention group participants were asked specific questions about their experience with PA-ARS . The used questionnaire was modified version from a previously used questionnaire to assess students experience with ARS in a recent trial . Students' responses were saved in an excel sheet after each lecture (L1, L2).

Analysis of the results:

Students' scores were saved in an excel sheet after each test. A specialized statistical analysis software was used (IBM SPSS statistics 22, version 22) The statistician was blinded to the allocation group. Scores were analyzed and compared to assess knowledge retention using cross-over analysis with Mann-Whitney U test for pre and post lecture quiz and t-test for summative test.

Being tested
Audience Response system
Keywords
ARS,, Audience response system, Education

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Audience Response systemOther

    Also called Polleverywhere

    In the lecture hall, G1 was separated from G2, and both groups completed an assessment of written multiple-choice questions (MCQs) scored out of 20, before the lecture. During L1, phone based (ARS) questions (PB-ARS) secretly displayed on the smart phones of the students in G1, and they were allowed to read the question and answer it, while those in parallel arm of the trial (G2) were blinded to those questions and answers. At the end of L1, both groups completed the same written MCQs assessment

Study groups in NCT04336813
Study groupRoleWhat they receive
Group AExperimentalReceive ARS in lecture 1 and act as controller in lecture 2
Receives: Other: Audience Response system
Group bActive comparatorReceive ARS in lecture 2 and act as controller in lecture 1
Receives: Other: Audience Response system

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Formative exam

    MCQs formative tests consisted of 20 questions related to the taught topics during L1 and L2 was undertaken

    Measured: 10 minutes

Secondary outcomes (1)
  1. Perception

    At the end of L1, both groups were asked to fill a questionnaire regarding their experience with the lecture and intervention group participants were asked specific questions about their experience with PA-ARS

    Measured: 10 minutes

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted7 Apr 2020
  2. Study start6 Dec 2017
  3. Primary completion20 Mar 2018
  4. Study completion29 May 2018

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Randomised
Intervention model
Crossover
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
34 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04336813
Sponsor's protocol ID
1439-03-001
Acronym
PBAR
Status last verified
Dec 2020
First submitted
3 Apr 2020
Last updated
29 Dec 2020
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes

Publications

  • Dhaliwal HK, Allen M, Kang J, Bates C, Hodge T. The effect of using an audience response system on learning, motivation and information retention in the orthodontic teaching of undergraduate dental students: a cross-over trial. J Orthod. 2015 Jun;42(2):123-35. doi: 10.1179/1465313314Y.0000000129. Epub 2015 Apr 7.

    PubMed 25849094

Questions about this trial

What is this clinical trial studying?

A study testing Audience Response system in people with Academic Performance, run by Prince Sattam Bin Abdulaziz University at 2 sites in Saudi Arabia.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 29 Dec 2020. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in Saudi Arabia. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Formative exam (time frame: 10 minutes). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT04336813, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 29 Dec 2020.

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