- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06924554
Motivational Training Program for Pre-service Physical Education Teachers
April 4, 2025 updated by: Carlos Mayo Rota, Universidad de Zaragoza
Study Protocol of a Non-randomized Controlled Trial on a Circumplex Model-based Motivational Training Program for Pre-service Physical Education Teachers
This study presents the protocol for a non-randomized controlled trial evaluating a motivational-based training program for pre-service Physical Education teachers.
The experimental group will participate in a 14-hour training program based on Self-Determination Theory and the circumplex model.
The program consists of theoretical and practical training to foster motivating teaching styles and minimize demotivating ones.
The control group will follow the standard curriculum of the Master's in Physical Education Teacher Education program without exposure to the specific intervention.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
Physical Education Teacher Education is crucial, as it directly influences how pre-service Physical Education teachers will teach, motivate, and engage their future students.
However, training programs that foster motivating teaching styles while minimizing demotivating ones remain scarce, particularly during initial teacher education.
This study presents the protocol for a non-randomized controlled trial evaluating a motivational-based training program for pre-service Physical Education teachers, grounded in Self-Determination Theory and the circumplex model.
The program, embedded in a Master's in Physical Education Teacher Education, consists of theoretical and practical training to foster motivating teaching styles and minimize demotivating ones.
The study will involve at least 38 pre-service teachers, divided into an experimental group (n = 19) and a control group (n = 19).
The experimental group will participate in a 14-hour training program combining theoretical and practical components.
The control group will follow the standard Physical Education Teacher Education curriculum.
A quasi-experimental pre-post design with a mixed-methods approach will be used.
Quantitative assessments will measure changes in perceived competence, motivation for teaching, and (de)motivating teaching styles, while qualitative focus groups will provide in-depth insights into participants' experiences and program applicability.
To ensure objectivity, independent researchers will conduct assessments, and external experts will moderate the focus groups.
Findings will contribute empirical evidence on the effectiveness of Self-Determination Theory-based interventions in initial teacher education, informing curriculum development and supporting the advancement of evidence-based pedagogical training in Physical Education.
Study Type
Interventional
Enrollment (Estimated)
38
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 Contact
- Name: Carlos Mayo Rota
- Phone Number: +34655375050
- Email: cmayo@unizar.es
Study Locations
-
-
Aragón
-
Huesca, Aragón, Spain, 22003
- Recruiting
- Facultad de Ciencias Humanas y de la Educación
-
Contact:
- Carlos Mayo Rota
- Phone Number: +34665375050
- Email: cmayo@unizar.es
-
-
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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Enrollment in the Master's in Physical Education Teacher Education at the University of Zaragoza.
- 100% attendance in training sessions (experimental group).
- Completion of questionnaires at three time points (pre-test, intermediate, and post-test).
- Participation in the final focus group discussion.
Exclusion Criteria:
- Failure to complete required assessments.
- Lack of attendance in mandatory sessions.
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: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental group
The experimental group will participate in a 14-hour training program combining theoretical and practical components of Self-Determination Theory and the circumplex model.
|
This study presents the protocol for a non-randomized controlled trial evaluating a motivational-based training program for pre-service Physical Education teachers, grounded in Self-Determination Theory and the circumplex model.
The program, embedded in a Master's in Physical Education Teacher Education, consists of theoretical and practical training to foster motivating teaching styles and minimize demotivating ones.
The study will involve at least 38 pre-service teachers, divided into an experimental group (n = 19) and a control group (n = 19).
The experimental group will participate in a 14-hour training program combining theoretical and practical components.
The control group will follow the standard Physical Education Teacher Education curriculum.
|
|
No Intervention: Control group
The control group will follow the standard Physical Education Teacher Education curriculum
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
(De)motivating teaching styles
Time Frame: At baseline (Week 0), 4 weeks after baseline, and 8 months after baseline.
|
Changes in (de)motivating teaching styles (Measured using SIS-PE)
|
At baseline (Week 0), 4 weeks after baseline, and 8 months after baseline.
|
|
Teaching competence
Time Frame: At baseline (Week 0), 4 weeks after baseline, and 8 months after baseline.
|
Changes in perceived teaching competence (Measured using BPNSFS).
|
At baseline (Week 0), 4 weeks after baseline, and 8 months after baseline.
|
|
Motivation to teach
Time Frame: At baseline (Week 0), 4 weeks after baseline, and 8 months after baseline.
|
Changes in motivation to teach (Measured using EME-ES).
|
At baseline (Week 0), 4 weeks after baseline, and 8 months after baseline.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Quality of the training program
Time Frame: 4 weeks after baseline, and 8 months after baseline.
|
Perceived quality of the training program (Program evaluation questionnaire and final focus group).
|
4 weeks after baseline, and 8 months after baseline.
|
|
Applicability of the training program
Time Frame: 4 weeks after baseline, and 8 months after baseline.
|
Perceived applicability of the training program (Program evaluation questionnaire and final focus group).
|
4 weeks after baseline, and 8 months after baseline.
|
|
Strengths and weaknesses of the training program
Time Frame: 8 months after baseline.
|
Qualitative insights on the impact of the training (Final focus group discussion)
|
8 months after baseline.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 (Estimated)
September 1, 2025
Primary Completion (Estimated)
June 1, 2026
Study Completion (Estimated)
September 1, 2026
Study Registration Dates
First Submitted
March 21, 2025
First Submitted That Met QC Criteria
April 4, 2025
First Posted (Actual)
April 11, 2025
Study Record Updates
Last Update Posted (Actual)
April 11, 2025
Last Update Submitted That Met QC Criteria
April 4, 2025
Last Verified
April 1, 2025
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- PROYS01_24
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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