- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04253821
Relationship Between Head Posture Muscles, Pulmonary Capacity and Functional Capacity: a Myotonometric Assessment
October 17, 2023 updated by: Cagtay Maden, Çağtay Maden
Relationship Between the Tonus, Stiffness, and Elasticity of Head Posture Muscles and Pulmonary Capacity and Functional Capacity: a Myotonometric Assessment
Forward head posture (FHP) is known to have a large influence on respiratory function by weakening the respiratory muscles.
This cross-sectional study is designed to examine the relationship between the tonus, stiffness, and elasticity of head posture muscles and pulmonary capacity.
Sixteen FHP individuals and seventeen NFHP individuals were evaluated.
The muscle tonus, stiffness and elasticity of upper trapezius (UT), semispinalis capistis (SSC), pectoral muscles (PM) and sternocleidomastoideus muscles (SCM) were measured by using MyotonPro® device.
Functional capacity was measured with six-minute walk test.
Pulmonary function tests was evaluated with spirometer.
The neck disability index (NDT) was applied.
The forward head posture was determined by measurements of craniovertebral angle (CVA).
Physical activity levels of participants were evaluated by Physical Activity Index (FIT).
Study Overview
Status
Completed
Study Type
Interventional
Enrollment (Actual)
33
Phase
- Not Applicable
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
-
-
Şahinbey
-
Gaziantep, Şahinbey, Turkey
- Hasan Kalyoncu Universty
-
-
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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- the participants do not have any known pulmonary, systemic and muscular system disease and, any neurological symptoms and neck pain that affects daily living activities.
Exclusion Criteria:
- have headache and dizziness
- steroid use or muscle relaxants
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
- Primary Purpose: Other
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: Forward head posture
|
The muscle tonus, stiffness and elasticity of upper trapezius (UT), semispinalis capistis (SSC), pectoral muscles (PM) and sternocleidomastoideus muscles (SCM) were measured by using MyotonPro® device.
Functional capacity was measured with six-minute walk test.
Pulmonary function tests was evaluated with spirometer.
The neck disability index (NDT) was applied.
The forward head posture was determined by measurements of craniovertebral angle (CVA).
Physical activity levels of participants were evaluated by Physical Activity Index (FIT).
|
Active Comparator: Non-Forward head posture
|
The muscle tonus, stiffness and elasticity of upper trapezius (UT), semispinalis capistis (SSC), pectoral muscles (PM) and sternocleidomastoideus muscles (SCM) were measured by using MyotonPro® device.
Functional capacity was measured with six-minute walk test.
Pulmonary function tests was evaluated with spirometer.
The neck disability index (NDT) was applied.
The forward head posture was determined by measurements of craniovertebral angle (CVA).
Physical activity levels of participants were evaluated by Physical Activity Index (FIT).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
muscle tonus, stiffness and elasticity
Time Frame: 1 day
|
The measurements of muscle tone, stiffness and elasticity were made by using MyotonPro® device.
Participants were seated on the chair and hands were placed on the knee, UT, SSC and SCM muscles were measured in this position.
The pectoralis major muscle was measured in the supine position.
|
1 day
|
six-minute walk test.
Time Frame: 1 day
|
Functional capacity was measured with six-minute walk test.
|
1 day
|
Vital Capacity
Time Frame: 1 day
|
Pulmonary function tests was evaluated with spirometer.It is the volume of air in the lungs that varies between full inspiration and maximum expiration.
|
1 day
|
Forced Vital Capacity (FVC)
Time Frame: 1 day
|
Pulmonary function tests was evaluated with spirometer.It is the volume of air that comes out with rapid and powerful exhalation following deep inspiratory.
Healthy people can normally extract 80% of their lung volume in 6 seconds or less.
|
1 day
|
Forced Expiratory Volume in 1 Second (FEV1)
Time Frame: 1 day
|
Pulmonary function tests was evaluated with spirometer.It is the volume of air released in the first second from the beginning of the difficult vital capacity maneuver.
In general, it gives information about the restriction in major airlines.
FEV1 / FVC ratio decrease shows obstruction, FEV1 shows the severity of obstruction.
|
1 day
|
Peak Expiratory Flow (PEF)
Time Frame: 1 day
|
Pulmonary function tests was evaluated with spirometer.It is measured by the maximum exhalation maneuver following the maximum inspiration.
It gives information about obstruction in large airways.
|
1 day
|
The neck disability index
Time Frame: 1 day
|
The neck disability index was applied.
the total score is 50.
As the test score rises, disability increases.0-4
score no disability, 5-14 mild disability, 15-24 moderate degree, 25-34 severe disability, 35 and above completely disabled
|
1 day
|
Physical Activity Index
Time Frame: 1 day
|
The FIT index was used to classify the individuals' physical activity levels.
This research instrument used to classify and assign a score from 1 to 100 to a person's physical fitness level based on their frequency, intensity, and time engaged in physical fitness activities.
The physical activity score was obtained by multiplying the frequency, intensity and time of the activity.
According to the FIT score, the physical activity level is interpreted as 0-20 sedentary, 21-40 weak, 41-60 normal, 61-80 good and 81-100 very good.
|
1 day
|
Forward head posture assessment
Time Frame: 1 day
|
Forward head posture was assessed by a goniometric method which is accepted as a reliable method.
Participants were assessed in a relaxed sitting position.
To measure the craniovertebral angle (CVA) of FHP, the center of the goniometer is placed at the level of the orifice of the external ear with the fixed arm pointing vertically towards the ceiling and the moving arm against the subject's 7th neck bonee.
|
1 day
|
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)
January 1, 2020
Primary Completion (Actual)
March 1, 2020
Study Completion (Actual)
March 10, 2020
Study Registration Dates
First Submitted
January 27, 2020
First Submitted That Met QC Criteria
February 1, 2020
First Posted (Actual)
February 5, 2020
Study Record Updates
Last Update Posted (Actual)
October 18, 2023
Last Update Submitted That Met QC Criteria
October 17, 2023
Last Verified
October 1, 2023
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2019/24
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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