- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04670159
Online Physical Activity and Ergonomics Training in Physiotherapy Students Receiving Distance Education
The Effectiveness of Online Physical Activity and Ergonomics Training in Physiotherapy Students Receiving Distance Education
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Avcılar
-
Istanbul, Avcılar, Turkey, 34320
- Istanbul University Cerrahpasa
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Volunteering to participate in the study
- Being receiving distance education due to the Covid pandemic
- Being in the age range of 18-25
Exclusion Criteria:
- Congenital or subsequent disability affecting the musculoskeletal system
- Presence of cognitive impairment
- Having a diagnosed psychiatric disorder
- Having a neurological or cardiovascular disease
- Exercising regularly
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: Online Education Group
|
Online ergonomics, exercise and physical activity training will be provided 3 times a week for 6 weeks.
The trainings it is planned to be made with a video-based online platform called Edpuzzle.
With the online classroom created, the student education will be provided.
A total of 18 training videos will be prepared, each video is 6-10 minutes.
After the training there will be an individual motivational interview with the students in the this group with the zoom application.
With motivational interview solutions by revealing the willingness, obstacles and indecision of the student to transfer the learned information to his daily life will be recommended.
|
|
Experimental: Brochure Group
|
An e-brochure will be prepared for students in this group to provide information on ergonomics, physical activity and exercise.
and the e-brochure will be sent to the students via e-mail after the initial evaluation.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in ergonomic risks in the distance education process
Time Frame: Baseline, change from baseline ergonomics risks levels at 6 weeks
|
The ergonomic risk levels of the participants in the distance education process will be determined by Rapid Office Strain Assessment (ROSA) .The Rapid Office Strain Assessment (ROSA) was designed to quickly quantify risks associated with computer work and to establish an action level for change based on reports of worker discomfort.
Ergonomic risk assessment will be done after online training and brochure information for all participants.
|
Baseline, change from baseline ergonomics risks levels at 6 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Measuring the prevalence of musculoskeletal disorder By Cornell questionniare Questionnaire
Time Frame: Baseline, 6 weeks
|
The Cornell Musculoskeletal Discomfort Questionnaire is an outcome measure used widely when examining musculoskeletal disorders in various occupational groups and students alike.The Cornell Musculoskeletal Discomfort Questionnaire was taken from the instruments provided by Human Factors and Ergonomics Laboratory at Cornell University. The changes in the musculoskeletal disorders of the participants will be evaluated before and after the online training and brochure information. |
Baseline, 6 weeks
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
- 10832
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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