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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05475353
Other study ID # 2/2021.K-20
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 20, 2022
Est. completion date September 13, 2022

Study information

Verified date July 2022
Source Istanbul Kültür University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study aims to determine the effects of asynchronous and synchronous exercises, which are added to ergonomics awareness education, on musculoskeletal disorders, physical activity and quality of life.


Recruitment information / eligibility

Status Completed
Enrollment 12
Est. completion date September 13, 2022
Est. primary completion date July 20, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: - Aged between 18-45 - Working at home at least 5 hours a day - Not having one or more diagnosed musculoskeletal disorders Exclusion Criteria: - Limited access to technology or not being able to actively use the technology - Had musculoskeletal trauma or surgery - Pregnancy

Study Design


Intervention

Behavioral:
Asyncronized Exercise
This group will be informed about ergonomics and protective exercises for the musculoskeletal system with an online seminar.
Procedure:
Syncronized Exercise
This group will be informed about ergonomics and protective exercises for the musculoskeletal system with an online seminar. Then, participants will complete the 6 weeks of exercise training at an online video conference program two times a week under the physiotherapist's supervise.

Locations

Country Name City State
Turkey Istanbul Kültür Üniversitesi Istanbul

Sponsors (1)

Lead Sponsor Collaborator
Istanbul Kültür University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Physical activty status International Physical. Activity Questionnaire-short form Baseline
Primary Physical activty status International Physical. Activity Questionnaire-short form 6 weeks
Primary Quality of life status Short Form 36 Baseline
Primary Quality of life status Short Form 36 6 weeks
Primary Musculoskeletal Discomfort level Cornell Musculoskeletal Discomfort Questionnaires: Higher scores indicate higher musculoskeletal discomfort. Baseline
Primary Musculoskeletal Discomfort level Cornell Musculoskeletal Discomfort Questionnaires: Higher scores indicate higher musculoskeletal discomfort. 6 weeks
Primary Ergonomic risk level Rapid Upper Limb Assesment: Higher scores indicate higher risk. Baseline
Primary Ergonomic risk level Rapid Upper Limb Assesment: Higher scores indicate higher risk. 6 weeks
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