- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07747077
The Effect of the Brain-Based Learning Model
July 30, 2026 updated by: Rukiye Burucu, Necmettin Erbakan University
The Effect of the Brain-Based Learning Model on Nursing Students' Knowledge and Skills in Diabetic Foot Examination: A Randomized Controlled Trial
Modern nursing education necessitates that students are prepared for clinical practice at a level of professional competency.
This preparation requires the integration of high-level cognitive and psychomotor skills.
However, current traditional teaching paradigms remain insufficient in ensuring long-term knowledge retention and the development of advanced cognitive and psychomotor skills, such as transforming complex clinical tasks into habitual behaviors.
Consequently, alternative pedagogical methods are being proposed, one of which is "Brain-Based Learning" (BBL).
The objective of this research is to determine the impact of the brain-based learning model on nursing students' knowledge levels regarding diabetic foot care and their practical skills in performing diabetic foot examinations.
It is anticipated that this study will provide a significant contribution to the existing literature.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
62
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
-
-
-
Konya, Turkey (Türkiye), 42370
- Necmettin Erbakan Univercity
-
-
Meram
-
Konya, Meram, Turkey (Türkiye), 42090
- Necmettin Erbakan University Seydişehir Kamil Akkanat Health Scıence Faculty
-
-
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
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Being enrolled in the Diabetic Nursing course.
- Volunteering to participate in the research
Exclusion Criteria:
- Repeating the "Diabetic Nursing" course for the second or third time.
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: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: İntervention Group
The lesson will be delivered in accordance with the Brain-Based Learning (BBL) model
|
The diabetic foot examination course will be delivered using the Brain-Based Learning (BBL) method
|
|
No Intervention: Control Group
The lesson will be delivered using a standard teaching approach
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Student' diabetic foot knowledge level
Time Frame: Day 1, pre-training
|
A Diabetic Foot Knowledge Assessment Scale will be used
|
Day 1, pre-training
|
|
Students' foot examination practices
Time Frame: Day 1, post-training
|
Students will be asked to perform foot examinations on one another, and the practice will be evaluated.
|
Day 1, post-training
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Student' diabetic foot knowledge level
Time Frame: After the practice session
|
Assessing students' knowledge regarding diabetic foot
|
After the practice session
|
|
Students' foot examination practices
Time Frame: 4 weeks after
|
Assessing students' foot examination practices
|
4 weeks after
|
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 (Actual)
April 1, 2026
Primary Completion (Actual)
May 1, 2026
Study Completion (Actual)
May 30, 2026
Study Registration Dates
First Submitted
March 22, 2026
First Submitted That Met QC Criteria
July 30, 2026
First Posted (Actual)
August 5, 2026
Study Record Updates
Last Update Posted (Actual)
August 5, 2026
Last Update Submitted That Met QC Criteria
July 30, 2026
Last Verified
July 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 28301.R1
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
The data sets used and/or analyzed during the current study are available from the corresponding author on reasonable request, provided that data sharing is deemed appropriate after the publication of the research
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.