Assessing Body Posture and Postural Balance Among Young Adults With Bronchial Asthma

April 28, 2023 updated by: Centro Universitário Augusto Motta

Evaluation of Body Posture and Postural Balance Among Young Adults With Bronchial Asthma in the United Arab Emirates - A Correlational Cross Sectional Study

The purpose of the study is to assess the relationship between body posture and dynamic balance in adults with childhood-onset asthma and compare them to a non-asthmatic control group matched for gender, age, weight, and height.

Study Overview

Detailed Description

Participants will sign a consent form and provide personal information such as gender, age, weight, and height for calculating BMI, pulmonary function test, and respiratory muscle strength test, as well as their asthmatic/clinical history. After collecting demographic information and obtaining consent from participants, they will be asked to remove their T-shirts and stand in the usual relaxed standing position facing the opposite side of the machine's window. When the machine is properly positioned, it will take photographs. which will then be converted into three-dimensional images on the computer for further analysis. When the participant is fully dressed and ready, the second test will be performed using the Biodex balance machine. The parameters and testing mode to begin the dynamic balance test will be entered into the machine, and the procedure will begin. The participants will be thanked for their participation and contribution to our study

Study Type

Observational

Enrollment (Actual)

124

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

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 50 years (Adult)

Accepts Healthy Volunteers

Yes

Sampling Method

Probability Sample

Study Population

bronchial asthma -18 years above health group ( non bronchial asthma )

Description

Inclusion Criteria:

  • For the healthy subjects referred by a consultant pulmonologist/physician
  • age- and gender-matched volunteers were recruited from the community

Exclusion Criteria:

  • Other health issues, such as cardiorespiratory issues, neurological deficits
  • musculoskeletal problems and peripheral vascular diseases& pregnancy may affect test performance

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-Control
  • Time Perspectives: Cross-Sectional

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
bronchial asthma

Inclusion criteria:

Participants over the age of 18 who have had mild to moderate bronchial asthma since childhood and have been referred by a pulmonologist or physician

Exclusion criteria:

Participants with other health issues such as cardiorespiratory issues, neurological deficits or diseases such as nerve compressions, any chronic diseases or suffering from respiratory tract infections, participants with a history of previous serious injuries to the musculoskeletal system, which may result in body posture disturbances Any disease that impairs one's sense of balance

3D/4D spine and posture analysis "DIERS FORMETRIC 4D" for postural analysis assessment

,The Biodex Balance System SD- for balance assessment

non-asthmatic control group:

Inclusion and Exclusion criteria for non-asthmatic control group:

Inclusion criteria:

For the healthy subjects referred by a consultant pulmonologist/physician, age- and gender-matched volunteers were recruited from the community

Exclusion criteria:

Other health issues, such as cardiorespiratory issues, neurological deficits, musculoskeletal problems, and peripheral vascular diseases& pregnancy may affect test performance.

3D/4D spine and posture analysis "DIERS FORMETRIC 4D" for postural analysis assessment

,The Biodex Balance System SD- for balance assessment

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
body posture assessment using DIERS FORMETRIC 4D,
Time Frame: baseline
From a single image, the instrument will generate 40 named spine shape parameters, like( lateral deviation (mm), trunk imbalance (mm), shoulder tilt (mm) )
baseline
postural balance assessment by biodex balance system machine
Time Frame: baseline
Double Leg Eyes Open (DLEO) Degree (angle), Double Leg Eyes Closed (DLEC) Degree (angle), Single Leg Eyes Open (SLEO) Degree (angle), single Leg Eyes closed (SLEC) Degree (angle), Overall Balance/stability Index (OBI/OSI )Degree (angle), ANT/POST Balance Index (APBI )Degree (angle), MED/LAT Balance Index (MLBI)Degree (angle),
baseline

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Chair: Arthur De Sa Ferreira, phd, Augusto Motta University Centre

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)

February 1, 2022

Primary Completion (Actual)

April 22, 2023

Study Completion (Actual)

April 22, 2023

Study Registration Dates

First Submitted

April 15, 2022

First Submitted That Met QC Criteria

May 10, 2022

First Posted (Actual)

May 13, 2022

Study Record Updates

Last Update Posted (Actual)

May 3, 2023

Last Update Submitted That Met QC Criteria

April 28, 2023

Last Verified

October 1, 2022

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Sharing Time Frame

very month

IPD Sharing Access Criteria

through mail

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP
  • ICF
  • ANALYTIC_CODE
  • CSR

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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