- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06397495
Comparison of Learning Models in Physical Therapy Education
March 25, 2026 updated by: Ziya Yildiz, Isparta University of Applied Sciences
Comparison of Flipped and Team-Based Learning Models in Cervical Region Manual Therapy Teaching: A Mixed Method Study
With the pandemic affecting the world, education systems have been subjected to mandatory changes without sufficient thought on teaching content, delivery and pedagogy.
In this process, physiotherapy courses involving psychomotor skills such as manual therapy became difficult to teach and evaluate.
Although the pandemic is over, it is suggested that technological approaches should be used in learning systems and incorporated into physiotherapy education.
These technology-supported education models are called blended education models.
The use of the flipped training model, a variant of blended training models, can improve practical skill performance.
In this study, it was aimed to determine the effect of two different models on the quality of teaching and learning in cervical region manual therapy teaching.
Suleyman Demirel University Physiotherapy and Rehabilitation senior students (n=100) will be randomly divided into two groups.
The control group (n=49) will be given monologue education with in-class team-based traditional education model.
The practical part of the course will be taught in the classroom and applied with patient-clinician role model technique.
Homework will be assigned for students to read scientific articles and analyze case examples.
The entire six-week teaching program will take place in the classroom.
The experimental group (n=51) will be applied the flipped model.
The theoretical and practical knowledge of the course will be provided at home with the EdPuzzle education platform.
They will be encouraged to read articles and analyze cases at home.
The classroom environment will be used to ask questions related to the theoretical part of the course and to practice the practical application as a patient/clinician role model.
The seven-week teaching program is planned in the classroom and home environment.
In the evaluation of the research, explanatory sequential design method from mixed research methods will be applied.
Pre-test/post-test/knowledge retention test, instructional materials motivation questionnaire and skill level/performance evaluation form will be used to evaluate the quantitative data.
A lesson observation form will be used to evaluate whether the trainer provided the same competence to both groups.
Semi-structured case study will be used to evaluate the reverse-face model to the experimental group with qualitative data.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
66
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
-
-
Isparta
-
Isparta, Isparta, Turkey (Türkiye), 32000
- Süleyman Demirel Univesity
-
-
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
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Not to have participated in a vocational course program on manual therapy of the cervical region,
- Sufficient internet access,
- Acceptance of distance education if included in the experimental group,
- Having and actively using a cell phone or computer with a smart operating system,
- Volunteering to participate in the study
Exclusion Criteria:
- The student wants to quit the study and does not fill in the data collection forms
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: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Flipped Groups
|
Cervical region manual therapy training will be given with flipped learning models.
|
|
No Intervention: Traditional Learning Groups
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Academic motivation survey data
Time Frame: 1 year
|
Academic motivation survey data will be the first data to be obtained between the groups.
|
1 year
|
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)
October 9, 2023
Primary Completion (Actual)
November 27, 2023
Study Completion (Actual)
May 24, 2024
Study Registration Dates
First Submitted
April 25, 2024
First Submitted That Met QC Criteria
April 29, 2024
First Posted (Actual)
May 3, 2024
Study Record Updates
Last Update Posted (Actual)
March 31, 2026
Last Update Submitted That Met QC Criteria
March 25, 2026
Last Verified
March 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SülDemirelUni_YildizZ_001
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
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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