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CompletedNCT01084512SCIUpdated Mar 10, 2010

Chest Wall Kinematics and Respiratory Muscle Action During Supine Breathing in Individuals With and Without Spinal Cord Injury

An observational study in Spinal Cord Injury, sponsored by National Taiwan University Hospital. Completed at 1 site in Taiwan. Open to male participants aged 20 Years to 60 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2010-03-10.

Sponsored by National Taiwan University Hospital · Observational

Study type
Observational
Model
Case-control
Time perspective
Cross-sectional
Enrollment
50
Ages
20 Years to 60 Years
Sex
Male
01

Study summary

Objective: To investigate the movement strategy of breathing based on three-compartment model measured by optoelectronic plethysmography (OEP) and electromyography (EMG ) among individuals with and without spinal cord injury in supine posture during deep inspiration.

Design: cross sectional repeated-measure with age matched control group. Setting: Motion Analysis Laboratory Participants: Seven tetraplegic and five paraplegic subjects and twelve age matched healthy controls were recruited.

Intervention: Not applicable.

Read the detailed description

Main Outcome Measures: The volume changes of chest wall and respiratory electromyographic ( EMG ) muscle activity were measured simultaneously by OEP and surface EMG. The variables included volume changes (ΔV ), ratio of volume changes (ΔVr ), peak velocity of volume changes ( PV ), the percentage of peak velocity occurs ( PPV ) in three compartments (upper thorax, UT; lower thorax, LT; and abdominal compartment, AB), and Root Mean Square EMG ( RMS EMG ) of sternocleidomastoid and diaphragm (combined with intercostalmuscles).

Results: Ttetraplegic individuals had smallerΔVUT andΔVLT than those of control subjects(P\< .006 and .006, respectively). Furthermore, the ΔVr of AB was greater than those of UT and LT( P\< .006, .006, respectively), PVAB was smaller than PVLT ( P\< .006), PPVUT was greater than PPVLT and PPVAB ( P\< .008, .008, respectively ). The paraplegic subjects had smallerΔVLT than that of control subjects ( P\< .006 ). ΔVr of UT was greater than that of LT, and both PVUT and PVAB were greater than PVLT ( P\< .006 and .006, respectively). However, the paraplegic subjects preferred to all three compartments to achieve the maximal inspiration, like control group. In control group, onlyΔVAB was comparable with other compartments. ΔVr of UT was greater than LT, and PVUT was greater than PVLT and PVAB ( P\<.006 and .006, respectively). For the RMS EMG, it demonstrated that average RMS EMG of two muscles in both tetraplegic and paraplegic group were greater than that in control group (P\< .017 and .017, respectively).

Conclusion: The results applied the three-compartment model of chest wall to investigate the breathing pattern by OEP in individuals with and without SCI during inspiration of vital capacity breathing in supine posture. There were some interesting findings that (1) the tetraplegic subjects used AB contributed most volume changes, they can expand the AB more easily, and the UT took the responsibility to performed the final adjust during the inspiration; (2) the paraplegic subjects used UT contributed the most volume changes, they expanded the both UT and AB more easily, and all three compartment moved together during the inspiration; (3) the control subjects used UT to increase the most volume changes, they can expand UT more than the others, and all three compartments moved together during the inspiration phase, (4) the results of RMS EMG showed that the central neural drive in both tetraplegic and paraplegic subjects were greater than control group.

02

Conditions studied

  • Spinal Cord Injury

Keywords

  • kinematic analysis,
  • three-compartment model,
  • chest wall motion,
  • spinal cord injury.
03

In context

Spinal Cord Injuries

1,948 studies on the registry are indexed under Spinal Cord Injuries; 505 are open to participants now.

This study's planned enrollment of 50 is below the median of 60 across 323 observational studies indexed under Spinal Cord Injuries.

Browse Spinal Cord Injuries studies →

Lead sponsor

National Taiwan University Hospital is the lead sponsor of 2,563 studies on the registry; 569 are open to participants now.

Of its 11 completed or terminated interventional studies of FDA-regulated products, 2 (18%) have results posted.

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

04

Who can participate

Ages eligible
20 Years to 60 Years
Sexes eligible
Male
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

community sample

Inclusion criteria

  • (1) motor complete loss below level of injury with American Spinal Injury Association Classification (ASIA) class A or B19;
  • (2) post-injury duration at least 0.5 year;
  • (3) male subject due to high incidence rate in Taiwan20and the necessity of total exposure of the chest wall during the data collection.

Exclusion criteria

Exclusion Criteria:

  • (1) with any traumatic history of the chest wall,
  • (2) with any respiratory disease and musculoskeletal problem that interfered with the experimental protocol;
  • (3) having infections during the data collection period.
05

Study design

Observational model
Case-control
Time perspective
Cross-sectional
Enrollment
50 participants (estimated)

Groups and cohorts

  • Healthy group

    control subjects

  • Paraplegic group

    Paraplegic subjects

  • Tetraplegic group

    tetraplegic subjects

06

What researchers measure

Primary outcomes

  1. Chest wall motion

    Time frame: 6 months after spinal cord injury

Secondary outcomes

  1. ultrasonography

    Time frame: 6 months after spinal cord injury

07

Study locations

1 site
  • School and graduate institute of physical therapy
    Taipei, 100, Taiwan
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 10, 2010, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01084512
Lead sponsor
National Taiwan University Hospital
Collaborators
National Science Council, Taiwan
First posted
Mar 10, 2010
Start date
Jul 2005
Primary completion
Jul 2008
Completion
Jul 2008
Last update
Mar 10, 2010

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Feb 2010. You cannot join it, but the record below documents what was studied.

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