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CompletedNCT01893697Updated May 28, 2015

The Influence of Posture on Airway Diameter, Resistance and Airflow Distribution in Healthy Subjects

An observational study in Healthy Participants, sponsored by University Hospital, Antwerp. Completed at 1 site in Belgium. Open to participants aged 18 Years to 40 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2015-05-28.

Sponsored by University Hospital, Antwerp · Observational

Study type
Observational
Model
Case-crossover
Time perspective
Prospective
Enrollment
5
Ages
18 Years to 40 Years
Sex
All
01

Study summary

FRI could give the opportunity to investigate the possible effect of a lateral posture on airway diameter and airflow distributions. This physiological study in healthy subjects may help to identify the role of positioning as an aid in airway clearance techniques for patients with respiratory diseases.

Read the detailed description

Many respiratory diseases require a physiotherapeutic treatment that focusses on clearance of excessive mucus from the airways.

The underlying physiological hypothesis why those mucus clearance techniques are effective is based on the development of an optimal expiratory airflow velocity that applies shearing forces on the mucus at the inner surface of the airway. These shearing forces eventually lead to displacement of mucus to the central airways were it could be evacuated.To accomplish optimal velocity with the same expiratory airflow, it is necessary to decrease the airway diameter and hence increase in the airflow velocity. In other words, the airway diameter and resistance are important factors to take into account in mucus clearance techniques.

In many mucus clearance techniques, postural position is used to facilitate this clearance. Clinical trials in patients with chronic obstructive pulmonary disease (COPD) and cystic fibrosis where they combined clearance techniques with different postural positions showed to be effective.

The influence of posture has been evaluated in the lateral decubitus position and resulted in a greater clearance of mucus in the depended lung. The authors suggested that this may be due to a better deflation of the depended lung that is favored by 3 forces: gravity, mediastinum weight and pressure of abdominal viscera on the infra lateral lung. Deflation of this lung leads not only to a decrease in lung volume, but also results in a decrease in airway diameter. Nevertheless, it is not known to what extend this decrease in diameter occurs in a lateral position. Furthermore, an optimal expiratory flow must be retained in the underlying lung at lower lung volumes. These regional changes in the underlying lung cannot be measured by for example classic lung function tests since these test are not sensitive enough. Indeed, Washko et. al. found no significant changes of overall residual volume (RV), total lung capacity (TLC) and vital capacity (VC) between the different positions in healthy subject.

However, Functional respiratory imaging (FRI) is able to assess the regional changes in healthy subjects. This 3D imaging technique in combination with computational fluid dynamics (CFD) is accurate in calculating regional changes such as airway diameter, volume and resistance. In addition, repetitive FRI measures are able to assess lobar expansion, which is an indirect measure of airflow distribution in a specific part of the lung.

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Conditions studied

  • Healthy Participants
03

In context

Lead sponsor

University Hospital, Antwerp is the lead sponsor of 242 studies on the registry; 69 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 40 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Healthy subjects

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Men or female patients age > 18
  2. No respiratory disease in the days prior to the enrollment
  3. Able to perform a lung function tests
  4. Motivated to participate.
  5. Written informed consent from the subject prior to the participation

Exclusion criteria

Exclusion Criteria:

  1. Serious co-morbidity which would interfere with the examinations
  2. One or multiple CT scans of the chest during the last year.
  3. Deformities or complications preventing patients to maintain side lying position during the scanning procedure
05

Study design

Observational model
Case-crossover
Time perspective
Prospective
Enrollment
5 participants (actual)
Patient registry
No

Groups and cohorts

  • Healthy Participants

    HRCT scan in a specific postural position

    Other: HRCT scan in a specific postural position

Interventions

  • OtherHRCT scan in a specific postural position

    HRCT Scan taken in supine and lateral position

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What researchers measure

Primary outcomes

  1. Functional Respiratory Imaging

    A low dose 3D spiral high resolution computed tomography (HRCT) scan will be taken on 2 volumes TLC and functional residual capacity (FRC) in both supine and lateral decubitus position. Image post processing is performed to look at local changes in airway or lobar volume \[liter\] and airway resistance \[kiloPascal.seconds/liter\] distribution in the lung

    Time frame: 1 study visit (1 day)

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Study locations

1 site
  • UZA
    Antwerp, Edegem 2650, Belgium
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References and documents

Publications

  • Ides KM, De Backer WA, Lanclus M, Leemans G, Dierckx W, Lauwers E, Vissers D, Steckel J, De Backer JW. The effect of posture on airflow distribution, airway geometry and air velocity in healthy subjects. BMC Pulm Med. 2022 Dec 15;22(1):477. doi: 10.1186/s12890-022-02276-5. PubMed 36522658 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 28, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT01893697
Responsible party
Wilfried De Backer (Prof. Dr. W De Backer, University Hospital, Antwerp) — Principal investigator
First posted
Jul 9, 2013
Start date
Apr 2013
Primary completion
Sep 2014
Completion
Sep 2014
Last update
May 28, 2015

Study contacts

Wilfried De Backer, MD PhD
principal investigator · University Hospital, Antwerp

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in May 2015. You cannot join it, but the record below documents what was studied.

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