- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06945367
Active Learning and EBP Competency in Undergraduate Physiotherapy
Impact of Active Learning on Beliefs, Attitudes, Perceived Skills, and Application of Evidence-Based Practice in Undergraduate Physiotherapy Students
This study aims to evaluate the effect of an active learning-based educational intervention on competencies related to evidence-based practice (EBP) in undergraduate physiotherapy students. The intervention was embedded within a four-month Research Methods course and focused on small group activities involving literature search, critical appraisal, oral presentations, and formative assessment through rubrics.
The study follows a pre-post quasi-experimental design without a control group. Primary outcomes include students' beliefs, attitudes, perceived skills, and frequency of EBP application, assessed through a custom-developed and validated questionnaire. Secondary outcomes include academic engagement, measured using the Utrecht Work Engagement Scale - Student Version (UWES-S), and student satisfaction with the educational approach, measured using the Student Outcomes Survey. Data were collected at baseline, post-intervention, and one week after course completion.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This quasi-experimental study without a control group will be conducted at the Universidad Nacional de La Matanza (UNLaM), Argentina, between March and July 2025. The study aimed to evaluate the effect of an educational intervention based on active learning strategies on evidence-based practice (EBP) competencies among physiotherapy students.
The intervention was implemented as part of a four-month Research Methods course and included weekly group-based activities such as literature retrieval, critical appraisal, oral presentations, peer feedback, and structured assessments using rubrics. The course aimed to strengthen students' beliefs, attitudes, perceived skills, and frequency of use related to EBP.
Outcomes were assessed using a custom-developed and validated questionnaire covering four domains and key competencies in EBP. Secondary outcomes included academic engagement, measured with the Utrecht Work Engagement Scale - Student Version (UWES-S), and student satisfaction, assessed through the Student Outcomes Survey. Data collection occurred at baseline, at the end of the course, and one week after completion. The study followed TREND reporting guidelines and was approved by the institutional research ethics committee at UNLaM.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Mauro F Andreu, PhD
- Phone Number: (+54) 9 11 6 878 8298
- Email: mfandreu@gmail.com
Study Locations
-
-
Buenos Aires
-
San Justo, Buenos Aires, Argentina, B1754
- Recruiting
- Universidad Nacional de la Matanza
-
Contact:
- Mauro F Andreu, PhD
- Phone Number: 1168788298
- Email: mandreu@unlam.edu.ar
-
Contact:
- Tatiana Dias de Carvalho, PhD
- Email: tdiascarvalho@unlam.edu.ar
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Undergraduate students enrolled in the Research Methods course at the Universidad Nacional de La Matanza during the March-July 2024 term.
- Provided written informed consent.
- Attended at least 80% of course sessions.
Exclusion Criteria:
- Students who withdrew from the course before completion of the follow-up period.
- Incomplete or missing baseline or final evaluation data.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Active Learning Group
Participants in this arm are fourth-year undergraduate physiotherapy students enrolled in a Research Methods course.
They will receive a four-month educational intervention based on active learning strategies, including weekly group-based activities such as literature search, critical appraisal, structured presentations, peer feedback, and formative assessment using rubrics.
The aim was to improve beliefs, attitudes, perceived skills, and frequency of use of evidence-based practice.
|
A four-month educational intervention based on active learning strategies, delivered as part of a Research Methods course for fourth-year undergraduate students in physiotherapy.
The intervention included weekly group activities focused on literature retrieval, critical appraisal, oral presentations, peer feedback, and structured formative assessments using rubrics.
The aim was to improve beliefs, attitudes, perceived skills, and frequency of use of evidence-based practice.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Beliefs about Evidence-Based Practice
Time Frame: Baseline and immediately after the 4-month intervention
|
Assessed as part of a custom-developed and validated questionnaire covering four domains and EBP-related competencies.
Items were rated on a 5-point Likert scale.
|
Baseline and immediately after the 4-month intervention
|
|
Attitudes toward Evidence-Based Practice
Time Frame: Baseline and immediately after the 4-month intervention.
|
Assessed as part of a custom-developed and validated questionnaire covering four domains and seven EBP-related competencies.
Items were rated on a 5-point Likert scale
|
Baseline and immediately after the 4-month intervention.
|
|
Perceived Evidence-Based Practice Skills
Time Frame: Baseline and immediately after the 4-month intervention.
|
Assessed as part of a custom-developed and validated questionnaire covering four domains and EBP-related competencies.
Items were rated on a 5-point Likert scale.
|
Baseline and immediately after the 4-month intervention.
|
|
Frequency of Evidence-Based Practice Application
Time Frame: Baseline and immediately after the 4-month intervention.
|
Assessed as part of a custom-developed and validated questionnaire covering four domains and seven EBP-related competencies.
Items were rated on a 5-point Likert scale
|
Baseline and immediately after the 4-month intervention.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Academic Engagement
Time Frame: Baseline and immediately after the 4-month intervention.
|
Measured using the Utrecht Work Engagement Scale - Student Version (UWES-S), a validated 9-item instrument assessing three dimensions: vigor, dedication, and absorption.
Each item is rated on a 7-point Likert scale ranging from 0 ("never") to 6 ("always")
|
Baseline and immediately after the 4-month intervention.
|
|
Student Satisfaction with Teaching and Assessment
Time Frame: One week after the completion of the 4-month intervention.
|
Measured using the Student Outcomes Survey (Fieger, 2012), which includes 20 closed-ended items rated on a 5-point Likert scale.
The scale is organized into three domains: satisfaction with teaching (items 1-6), assessment methods (items 7-11), and learning experience (items 12-19).
Item 20 assesses overall satisfaction.
|
One week after the completion of the 4-month intervention.
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- UNLaM-AL
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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