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Chronic Obstructive Pulmonary DiseaseNCT00863616

High Frequency Chest Wall Oscillation in Chronic Obstructive Pulmonary Disease (COPD)

A study testing HFCWO - SmartVest in people with Chronic Obstructive Pulmonary Disease, run by East and North Hertfordshire NHS Trust at 1 site in United Kingdom.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Patients with Chronic obstructive pulmonary disease (COPD) tend to have cough, excess mucus production and breathlessness as cardinal features. The excess mucus production often leads to frequent infections, exacerbations and poor quality of life. Read more about this study

Who is it for?
Ages 40 to 85 years
Conditions the study is for
Chronic Obstructive Pulmonary Disease
What is being tested?
HFCWO - SmartVest
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
32 participants
Where
1 siteUnited Kingdom
Study dates
Aug 2006to Oct 2007
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 40 to 85 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • COPD; patients defined by a history of cough, breathlessness and/ mucus/sputum production with lung function showing FEV1/FVC <70% and FEV1<80% predicted and < 20% reversibility from baseline on administration of nebulised b2-agonist (Salbutamol 5mg)
  • Age 40-85 years
  • Mucus hypersecretion ( > 25 ml/72 h collection)

Who cannot join

  • Chest wall deformity (i.e., kyphoscoliosis, Rib fractures)
  • Severe osteoporosis
  • Haemoptysis within the last 3 months
  • Thoracic or abdominal surgery within 3 months
  • Respiratory failure on non-invasive ventilator therapy
  • Tracheostomy or neck deformities
Show all 11Show fewer
  • Neuro-muscular dysfunction or disability (i.e., Paralysis due to cerebrovascular disease) which may make it impossible to use the device safely
  • Congestive heart failure (decompensated)
  • Any other mucolytic therapy
  • Significant hiatus hernia or gastro-esophageal reflux disease
  • Recent myocardial infarction or unstable angina

Trial locations and contacts

1 site in 1 country.

United Kingdom1 site
  • East & North Herts NHS Trust

    Stevenage, Herts, SG1 4AB

Other trials in United Kingdom

About this study

Official title: Self-Administered High Frequency Chest Wall Oscillation Technique for Mucus Clearance in COPD: An Exploratory Pilot Project Using the SMARTVEST Device

Patients with Chronic obstructive pulmonary disease (COPD) tend to have cough, excess mucus production and breathlessness as cardinal features. The excess mucus production often leads to frequent infections, exacerbations and poor quality of life. Mucociliary clearance may have an impact on improving symptoms, exercise tolerance, quality of life and reduce exacerbations.

High frequency chest wall oscillation(HFCWO) devices use percussion to the chest wall delivered from a pump through a close fitting inflatable vest. This technique has been shown to enhance mucus clearance in patients with cystic fibrosis and Bronchiectasis. This pilot study was designed to explore the feasibility, tolerance and effectiveness of the HFCWO in patients with advanced COPD.

Read the detailed description

1.1 Background

Chronic obstructive pulmonary disease (COPD) is a major health problem across the world and its medical, societal and economic impacts continue to grow. COPD is characterized by chronic obstruction of expiratory flow affecting peripheral airways, associated with chronic bronchitis (mucus hypersecretion with goblet cell and submucosal gland hyperplasia) and emphysema (destruction of airway parenchyma), together with fibrosis and tissue damage, and inflammation of the small airways1. The beneficial effects of smoking cessation in slowing the decline in lung function and the progression of disease have been clearly established. Whether other factors such as mucus hypersecretion, respiratory infections and airway hyper-reactivity contribute to disease progression independent of cigarette smoking is still being debated2.

Patients with COPD are often distressed by mucus hypersecretion which is one of the hallmarks of the disease but little is known about the impact of current therapies on mucus hypersecretion due to the logistical challenges of objectively quantifying mucus in clinical studies 3. Mucus hypersecretion occurs as a direct result of airway inflammation. Neutrophils that die by necrosis disgorge proteases and reactive oxygen species into the lumen. It is concluded that neutrophil death via necrosis leads to the high concentrations of free neutrophil elastase and reactive oxygen species in the sputum of patients with airway neutrophilia and mucus hypersecretion. Inflammatory cells (neutrophils), molecules (neutrophil elastase and reactive oxygen species), signaling pathways (EGFR), and cellular processes (neutrophil necrosis) contribute to mucus hypersecretion in COPD4.

Mucus hypersecretion leads to increased work of breathing, reduced exercise tolerance, deteriorating lung function and increases dyspnoea and cough. Often the mucus hypersecretion also interferes with nocturnal sleep and has a further negative impact on health related quality of life. Combined mucus hypersecretion, reduced clearance, and impairment of the lung defence mechanisms explain why COPD patients even with stable condition, carry potential respiratory pathogens in significant concentration, paving the way for infection and acute exacerbations of COPD5;6. In the natural history of COPD chronic mucus hypersecretion is thought to be linked to the accelerated decline of forced expiratory volume in one second (FEV1)5 7 .

Although mucoactive drugs (which improve the ease of mucus clearance) may be effective in mucus hypersecretion, the uncertainty surrounding their effectiveness, due primarily to the relative lack of evidence from randomised controlled trials and an uncertainty from epidemiological studies linking mucus hypersecretion with mortality8-11, have led to their poor diffusion and adoption in international guidelines 7. However, in combination with newer therapeutic strategies currently in research and development phase targeting airway inflammation and thus reducing mucus hypersecretion, there is a renewed interest in re-evaluating mucus clearance strategies in improving HRQL, exacerbations and morbidity associated with COPD 12;13.

Airway clearance forms a vital part the management of patients with CF14, Bronchiectasis and neuro-muscular diseases15 and has a positive impact on lung function, infection rate and mortality16;17. Individually tailored chest physiotherapy18 with forced expiratory manoeuvres is often considered the gold standard in airway clearance19, although self-administered techniques may be equally effective20 and preferred by patients17;21. Self-administered airway clearance techniques using devices which create a turbulent airflow thus encourage shearing of mucus from bronchial wall, have shown promise in improving HRQL and function in COPD patients22.

High frequency chest wall oscillation (HFCWO)23 is known to reduce respiratory rate but improve ventilation in patients with COPD24 and CF25. Experimental results suggest that shearing at the air-mucus interface could be a significant factor in the enhanced tracheal mucus clearance during HFCWO26. Unlike in CF patients who often have greater support from family members and show high levels of motivation and thus compliance in adhering to self-administered airway clearance techniques, COPD patients have low motivation and poor compliance. Thus self-administered techniques for mucosal clearance may be less effective in clinical settings away from dedicated research programs. Thus the HCFWO may offer a more passive modality of airway clearance with consequently higher compliance, if found to be equally effective and well-tolerated in this group of patients. If HFCWO is shown to improve HRQL, symptoms and exercise tolerance then it may have a significant role in reducing exacerbations and hospital admissions as well as allowing effective management in the community setting. The cost benefit of such improvements will need to be explored in larger studies in the future.

Being tested
HFCWO - SmartVest
Keywords
COPD, Mucus hypersecretion, HRQL, ESWT, HFCWO
Medical subject headings
Pulmonary Disease, Chronic Obstructive

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • HFCWO - SmartVestDevice

    Also called SmartVest

    SmartVest with vest administered for 20min at 11-13Hz

Study groups in NCT00863616
Study groupRoleWhat they receive
HFCWOExperimentalHFCWO twice a day delivered by SmartVest device at 13Hz FOR 20min x2. Duration 4 weeks in each phase with a 2week washout.
Receives: Device: HFCWO - SmartVest
Placebo/ControlNo interventionSelf-administered breathing exercises

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Health related quality of life (St George's Respiratory Questionnaire)

    Measured: 3 months

Secondary outcomes (1)
  1. Exercise tolerance (Endurance Shuttle Walk Time achieved)

    Measured: 3 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted18 Mar 2009 (estimated)
  2. Study startAug 2006
  3. Primary completionOct 2007
  4. Study completionOct 2007

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Crossover
Masking
None (open label)
Enrolment
32 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00863616
Sponsor's protocol ID
06/Q0303/57
Status last verified
Mar 2009
First submitted
17 Mar 2009
Last updated
18 Mar 2009
Results posted
No
Data monitoring committee
Yes

Publications

  • Chakravorty I, Chahal K, Austin G. A pilot study of the impact of high-frequency chest wall oscillation in chronic obstructive pulmonary disease patients with mucus hypersecretion. Int J Chron Obstruct Pulmon Dis. 2011;6:693-9. doi: 10.2147/COPD.S22896. Epub 2011 Dec 14.

    PubMed 22259246

Questions about this trial

What is this clinical trial studying?

A study testing HFCWO - SmartVest in people with Chronic Obstructive Pulmonary Disease, run by East and North Hertfordshire NHS Trust at 1 site in United Kingdom.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 11 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 18 Mar 2009. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United Kingdom. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Health related quality of life (St George's Respiratory Questionnaire) (time frame: 3 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT00863616, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Mar 2009.

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