- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06330285
Comparison of E-Learning and Face-to-Face Learning in Cardiopulmonary Exercise Test Training
Comparison of E-Learning and Face-to-Face Learning in Cardiopulmonary Exercise Test Training: Randomized Controlled Study
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
CPET is the most objective and valuable test for the cardiopulmonary rehabilitation (CPR) program to be planned for back-up for patients with cardiopulmonary diseases.
CPET is performed in a small number of centers in Turkey, in Physical Medicine and Rehabilitation (PTR) Units. Depending on the equipment available during specialty training, not all specialty students can access this training.
CPET is the first test performed for planning cardiopulmonary rehabilitation (CPR). According to the results, an appropriate CPR plan is made for the patient.
CPET indications, contraindications, application of the test, evaluation of the test with patient samples, and appropriate interventions for complications that may develop during the test are important.
It is important that all specialist students have access to this training. The aim of this study is; To evaluate the impact of e-learning with PGME and to reach all specialist students in the future, if necessary, based on the results.
The focus of this study is to examine the changes in doctors' success levels, motivations, distance education attitudes, cognitive flexibility and anxiety levels, especially in the pre- and post-training periods, and to compare these changes with face-to-face training.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: HAVVA TALAY ÇALIŞ, Prof
- Phone Number: 05326874541
- Email: htalaycalis@yahoo.com
Study Contact Backup
- Name: Hasan Kara, MD
- Phone Number: 00905552592665
- Email: hasankara@erciyes.edu.tr
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Those who gave consent,
- Graduates of the Faculty of Medicine and currently receiving specialist training,
- Those who can do what the training requires during the training period (participating in live classes, answering scales, etc.)
Exclusion Criteria:
- Those who cannot attend the training program regularly
- In addition, those who cannot attend more than 4 classes with or without an excuse will be excluded from the study.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Group 1
e-learning
|
CPET (Cardiopulmonary exercise test) e-learning application The content, planning and design of 4 lessons are as follows:
Other Names:
|
|
Active Comparator: Group 2
face to face learning
|
CPET (Cardiopulmonary exercise test) face to face education. The content, planning and design of 4 lessons are as follows: Contents:
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Open-Ended Achievement Test
Time Frame: at baseline, After the training is completed (at the 4. week)
|
Open-Ended Achievement Test: It is used to measure doctors' knowledge and skill levels on CPET.
It will be prepared by the trainers for each lesson.
|
at baseline, After the training is completed (at the 4. week)
|
|
Adult Motivation Scale
Time Frame: at baseline, After the training is completed (at the 4. week)
|
Used to evaluate doctors' motivation towards the training process.
The purpose of the scale is to determine the motivation levels and orientations of adults.
It consists of two factors and 21 items in total.
In the analyzes conducted for the reliability of the scale, the Cronbach Alpha reliability coefficient was found to be 0.94.
This value shows that the scale has high internal consistency.
|
at baseline, After the training is completed (at the 4. week)
|
|
Distance Education Attitude Scale in Lifelong Learning
Time Frame: at baseline, After the training is completed (at the 4. week)
|
It is used to measure doctors' attitudes towards distance education.
"Distance Education Attitude Scale in Lifelong Learning" is designed to evaluate attitudes towards distance education.
|
at baseline, After the training is completed (at the 4. week)
|
|
Cognitive Flexibility Scale
Time Frame: at baseline, After the training is completed (at the 4. week)
|
Used to evaluate doctors' ability to solve problems, adapt and respond to different situations.
The Cognitive Flexibility Scale (CFS) is used to measure how individuals adapt their behavior to new and unexpected situations occurring in their environment.
CFS was developed by Dennis and Vander Wall and adapted into Turkish.
CFs is a self-report type assessment tool with a total of 20 items, consisting of 'alternatives' and 'control' subscales.
Cronbach's alpha value of the Alternatives subscale at the first and last measurement was .91.
Cronbach's alpha values of the control subscale are .86 in the first measurement and .84 in the last measurement.
|
at baseline, After the training is completed (at the 4. week)
|
|
State and Trait Anxiety Scale
Time Frame: at baseline, After the training is completed (at the 4. week)
|
It is used to measure the momentary and continuous anxiety states of doctors during the training process.
This scale is used to evaluate individuals' momentary and persistent anxiety states.
State Anxiety and Trait Anxiety.
There are 20 items in the state anxiety scale.
There are 20 more items in the trait anxiety scale.
There are 40 items in the scale in total.
Kuder-Richardson reliability of the inventory was .83 to .87 for the Trait Anxiety Subscale; For the State Anxiety Subscale, it was found to be between .94 and .96.
Item reliability correlations were .34 to .72 for the Trait Anxiety Subscale; For the State Anxiety Subscale, the range between .42 and .85
indicates that the Turkish translated items are reliable.
The test-retest reliability rates of the inventory are .71
to .86 for the Trait Anxiety Subscale; For the State Anxiety Subscale, it is between .26 and .68 and is considered sufficient.
|
at baseline, After the training is completed (at the 4. week)
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Study Director: HAVVA TALAY ÇALIŞ, Health Sciences University, Kayseri Medical Faculty
Study record dates
Study Major Dates
Study Start (Estimated)
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
Other Study ID Numbers
- e learning pgme/cpet
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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