- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05232617
The Effects of Online Rheumatological Rehabilitation Education in Intern Physiotherapy Students
January 26, 2022 updated by: Nilay Arman, Istanbul University
The Effects of Online Rheumatological Rehabilitation Education on Readiness, Clinical Decision Making and Perceived Self-efficacy in Intern Physiotherapy Students
The aim of the study is to investigate the effect of online rheumatological rehabilitation training on readiness, clinical decision making and perceived self-efficacy in intern physiotherapy students.
In the study, online rheumatological rehabilitation training is planned.
Online rheumatological rehabilitation training will be video-based via the Edpuzzle application and interactively via the zoom application.
Online trainings are planned for 15-person intern physiotherapy student groups 4 days a week, 2 hours a day, for 4 weeks on a case-based basis.
In the study, readiness, clinical decision making and perceived self-efficacy levels will be evaluated in intern physiotherapy students before and after online rheumatological rehabilitation training.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
60
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
-
-
Buyukcekmece
-
Istanbul, Buyukcekmece, Turkey, 34500
- İstanbul University-Cerrahpaşa
-
-
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
18 years to 25 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Intern physiotherapy students taking the Rheumatology Internship course at Istanbul University Cerrahpaşa Faculty of Health Sciences, Physiotherapy and Rehabilitation will be included in the study.
In the 2020-2021 academic year, 60 intern physiotherapy students who took the Rheumatology Internship course will be included.
Consent will be obtained from all participants with a voluntary information form on google forms.
Description
Inclusion Criteria:
- To be taking Rheumatological Rehabilitation internship course
Exclusion Criteria:
- To have taken the Rheumatological Rehabilitation Internship course before, but failed to complete it successfully
- Lack of internet access
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
- Observational Models: Case-Only
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Rheumatological rehabilitation training
|
Online rheumatological rehabilitation training is planned.
Online rheumatological rehabilitation training will be video-based via the Edpuzzle application and interactively via the zoom application.
Online trainings are planned for 15-person intern physiotherapy student groups 4 days a week, 2 hours a day, for 4 weeks on a case-based basis.
With the Edpuzzle application, videos will be prepared for 10 different rheumatological diseases.
In each video, a case with rheumatic disease will be introduced, evaluations made from a physiotherapy perspective and their results will be included.
Before the lesson, students will watch the video defined for them every day from the application called Edpuzzle, answer the questions and plan a disease-specific assessment and treatment program according to the directions in the video.
Then, the assessment and treatment programs prepared by a group of 15 people through the zoom platform will be discussed during the lesson.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Readiness Scale for Mobile Learning
Time Frame: Change from baseline to 4 weeks
|
Mobile Learning Readiness Scale will be used to determine students' readiness for mobile learning.
Scale, Lin et al. and Gokcearslan et al. adapted to Turkish and its validity and reliability were made.
While there are 19 items in the original version of the scale, there are 17 items in the Turkish version.
Scale items; "self-efficacy (items 1-2-3-4-5-6), optimism (items 7-8-9-10-11-12-13), and self-learning (items 14-15-16-17)" are grouped.
The variance rate of the scale was 76.9% and the internal consistency coefficient (Cronbach alpha) was 0.95.
The reliability coefficient of the scale is 0.959.
The items in the scale are 7-point Likert type; degree of agreement is scored between (1) "I strongly disagree" and (7) "I strongly agree".
The lowest 17 points and the highest 119 points can be obtained from the scale.
The data are evaluated over the total score.
|
Change from baseline to 4 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Melbourne Decision-Making Scale I-II
Time Frame: Change from baseline to 4 weeks
|
Students' clinical decision making skills Mann et al. "Melbourne Decision-Making Scale (MKVÖ) I-II" was developed to determine the self-esteem and decision-making styles of university students in decision-making.
It consists of six items and a single sub-factor, and three items are scored straight and three items are scored in the opposite direction.
"Correct" answer given to scoring items is made as 2 points, "Sometimes True" answer is 1 point, "Not True" answer is given 0 points.
The maximum score that can be obtained from the scale is 12. High scores indicate high self-esteem in decision making.
II.
Part (MCDS II): It consists of 22 items and measures decision-making styles.
High scores indicate the use of the relevant decision-making style.
It has four sub-factors.
They are Mindful Decision Making Style (6 items), Avoidant Decision Making Style (6 items), Procrastinating Decision Making Style (5 items) and Panic Decision Making Style (5 items).
This scale is answered like MKVÖ I.
|
Change from baseline to 4 weeks
|
|
General Self-Efficacy Scale
Time Frame: Change from baseline to 4 weeks
|
Students' self-efficacy levels will be evaluated with the General Self-Efficacy Scale.
This scale is a measurement tool for self-assessment.
The Turkish validity and reliability study of the scale was conducted by Yıldırm et al. made by.
In the scale, there are five reversed items and two positive statements.
The score of each question varies between 1-5.
An increase in the total score indicates an increase in self-efficacy belief.
|
Change from baseline to 4 weeks
|
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)
October 6, 2020
Primary Completion (Actual)
June 18, 2021
Study Completion (Actual)
November 18, 2021
Study Registration Dates
First Submitted
June 17, 2021
First Submitted That Met QC Criteria
January 26, 2022
First Posted (Actual)
February 10, 2022
Study Record Updates
Last Update Posted (Actual)
February 10, 2022
Last Update Submitted That Met QC Criteria
January 26, 2022
Last Verified
January 1, 2022
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 09/12/2020-161414
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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