- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04467827
Connection of Body Posture From the Level and Form of Physical Activity in a Group of Young People
December 5, 2022 updated by: Medical University of Silesia
Assessment of Body Posture Connection From the Level and Form of Physical Activity in a Group of Young People
The assumption of the research is to assess the change in body posture depending on the given level of physical activity in young people.
The aim of the study is to assess body posture in young healthy people depending on their level of physical activity.
The research will allow the analysis of the correlation between the level of energy expenditure and the occurrence of changes in body posture.
The obtained results will allow the development of diagnostic and therapeutic programs for the prevention of overload changes in the spine in young people.
Study Overview
Detailed Description
The study will be conducted in a group of 200 people aged 19-25.
Posture assessment will concern the measurement of curvatures in the sagittal plane of the spine using a gravitational Rippstein plurimeter and performing a three-dimensional analysis of the spine using the DIERS 3D device.
In addition, a modified Matthias test will be performed using the DIERS 3D device, where kyphosis and lordosis parameters in the sagittal plane of the spine at isometric tension of the spinal muscles will be assessed.
The spinal motion in the sagittal and frontal planes will also be measured using a digital inclinometer.
In the second stage of the study, the participants will participate in the activity in the form of endurance training "Nordic Walking" (NW) for a period of 8 weeks 3 times a week.
The recording of energy expenditure during a normal day of activity will be done using an Actigraph GT3X accelerometer.
After a period of 8 weeks, all measurements will be repeated.
Study Type
Observational
Enrollment (Anticipated)
200
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Jacek Durmała, PhD MD
- Phone Number: +48 32 252 43 70
- Email: jdurmala@sum.edu.pl
Study Contact Backup
- Name: Bartosz Wnuk, PhD PT
- Phone Number: +48 32 252 43 70
- Email: bwnuk@sum.edu.pl
Study Locations
-
-
Katowice Ochojec
-
Katowice,, Katowice Ochojec, Poland, 40-635
- Recruiting
- The Department of Rehabilitation, Faculty of Health Sciences in Katowice, Medical University of Silesia, Katowice,
-
Contact:
- Jacek Durmała, M.D.
- Email: jdurmala@sum.edu.pl
-
Sub-Investigator:
- Bartosz Wnuk, Ph.D.
-
-
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
19 years to 25 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Students of Medical University of Silesia in Katowice, Poland
Description
Inclusion Criteria:
- age from 19 to 25 years old
- good health enabling the exercise of various forms of physical effort -cardiologically stable persons, without significant respiratory, nervous and musculoskeletal disorders / no other diseases
- written consent of the examined person
Exclusion Criteria:
- age below 19 and above 25,
- health condition preventing the exercise of various forms of physical effort (cardiologically unstable persons with significant respiratory, nervous and musculoskeletal disorders / other diseases that prevent physical activity,
- lack of written consent of the examined person,
- lack of cooperation of the examined person during the test
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: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Group A1 male
back shape neutral - a vertical line applied to the back of the body meets at the level of the thoracic segment and buttocks
|
Posture assessment in young healthy people depending on their level of physical activity
|
Group A2 female
back shape neutral - a vertical line applied to the back of the body meets at the level of the thoracic segment and buttocks
|
Posture assessment in young healthy people depending on their level of physical activity
|
Group B1 male
round back shape - a vertical line applied to the back of the body contacts only at the level of the thoracic segment
|
Posture assessment in young healthy people depending on their level of physical activity
|
Group B2 female
round back shape - a vertical line applied to the back of the body contacts only at the level of the thoracic segment
|
Posture assessment in young healthy people depending on their level of physical activity
|
Group C1 male
round back shape - a vertical line applied to the back of the body only touches the level of the buttock section
|
Posture assessment in young healthy people depending on their level of physical activity
|
Group C2 female
round back shape - a vertical line applied to the back of the body only touches the level of the buttock section
|
Posture assessment in young healthy people depending on their level of physical activity
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Body posture parameters assessed:
Time Frame: 9 weeks
|
|
9 weeks
|
Physical activity parameters assessed:
Time Frame: 9 weeks
|
accelerometer ActiGraph GT3X - assessment of MET energy expenditure and the number of steps performed during one day
|
9 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)
May 16, 2022
Primary Completion (Anticipated)
January 27, 2023
Study Completion (Anticipated)
February 24, 2023
Study Registration Dates
First Submitted
July 1, 2020
First Submitted That Met QC Criteria
July 10, 2020
First Posted (Actual)
July 13, 2020
Study Record Updates
Last Update Posted (Estimate)
December 6, 2022
Last Update Submitted That Met QC Criteria
December 5, 2022
Last Verified
May 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- BW- 2020- SUM
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
product manufactured in and exported from the U.S.
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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