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Lung; DiseaseCF_DyspneaNCT01799642

Evaluating Sensations of Breathlessness in Patients With Cystic Fibrosis

An observational study of Lung; Disease and Cystic Fibrosis, run by University of British Columbia at 1 site in Canada.

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

Shortness of breath (dyspnea) during exercise is a major source of distress and is a commonly reported symptom in patients with cystic fibrosis (CF). Due to the investigators' poor understanding of how dyspnea develops, there are no treatments that consistently reduce dyspnea in this population. Read more about this study

Who is it for?
Ages 19 to 50 yearsHealthy volunteers can take part
Conditions the study is for
Lung; Disease, Cystic Fibrosis, Healthy
How many people
50 participants
Where
1 siteCanada
Study dates
Jun 2013to Dec 2014
Phase
Observational
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 19 to 50 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Study population: The CF patients will be recruited from the St. Paul's Hospital Adult CF Clinic. Healthy control participants will be recruited from the Vancouver area.

Who may be able to join

  • CF patients (confirmed based on abnormal sweat chloride testing and/or CF Transmembrane Conductance Regulator (CFTR) genotyping)
  • Between the ages of 19 to 50 (inclusive)
  • Stable clinical status (CF: no changes in therapy in the past 4 weeks)
  • Forced Expiratory Volume in 1 second (FEV1.0) >40% predicted
  • Body mass index greater than 18 or less than 30
  • Currently non-smoking or a past smoking history of less than 20 pack-years
  • Able to read and understand English

Who cannot join

  • A disease other than CF that could contribute to dyspnea or exercise limitation
  • Having either of the chronic infections Mycobacterium abscessus or Burkholderia cepacia complex
  • Contraindications to clinical exercise testing
  • Use of supplemental oxygen or desaturation less than 85% with exercise
  • Diagnosis of pneumothorax in the past 4 weeks

Trial locations and contacts

1 site in 1 country.

Canada1 site
  • UBC James Hogg Research Centre, St. Paul's Hospital

    Vancouver, British Columbia, V6Z1Y6

Other trials in Canada

About this study

Official title: Qualitative Descriptors of Dyspnea During Exercise in Cystic Fibrosis

Shortness of breath (dyspnea) during exercise is a major source of distress and is a commonly reported symptom in patients with cystic fibrosis (CF). Due to the investigators' poor understanding of how dyspnea develops, there are no treatments that consistently reduce dyspnea in this population. The investigators aim to acquire a more comprehensive understanding of the physiological mechanisms of exertional dyspnea in CF patients. This study will likely identify an important physiological mechanism of dyspnea in CF and may contribute to the development and use of effective treatments to reduce dyspnea in this population.

The central hypothesis is that the impaired tidal volume (VT) response during exercise in CF, in the setting of increased ventilatory demand will give rise to different qualitative descriptions of exertional dyspnea compared with healthy age and sex-matched controls. Specifically, CF patients will select "increased work and effort" as their dominant descriptor of dyspnea up to the VT inflection/plateau. Beyond this point, CF patient's dominant descriptor will become "unsatisfied inspiration." In contrast, healthy control participants will report "increased work and effort" throughout all phases of exercise and will not report "unsatisfied inspiration", even after the VT inflection/plateau.

Read the detailed description

The purpose of this study is to determine if sensations of breathlessness (dyspnea) are qualitatively and quantitatively different in patients with cystic fibrosis (CF) compared to age and sex-matched healthy controls during exercise, and to determine if these differences can be explained by differences in the ventilatory response to exercise.

Understanding the progression of dyspnea during exercise will enable the investigators to better understand the pathophysiological mechanisms of this debilitating symptom in patients with CF. A more comprehensive understanding of the mechanisms underlying exertional dyspnea may ultimately lead to new therapeutic interventions (pharmacologic and non pharmacologic) that would positively impact exercise limitations in CF. A healthy control group will enable investigators to better identify the "normal" physiological and perceptual responses to exercise so that direct comparisons to patients with CF may be drawn.

Experimental Overview: Participants with CF and healthy control participants will report to the exercise laboratory for one visit. Informed consent, medical history screening, evaluation of chronic activity-related dyspnea and anthropometric measurements will firstly be obtained. Subjects will then be familiarized with the cycle ergometer, breathing apparatus and symptom scales. This will be followed by simple spirometry testing. After which participants will rest prior to a symptom limited incremental cycle exercise test. Detailed physiological and sensory measurements will be obtained during the familiarization and exercise test sessions. Data from the exercise test will address our hypotheses.

Study Participants: The study will include 40 participants in total. Of the 40 participants, 20 will be patients with CF and 20 will be healthy age and sex-matched controls.

Exercise Protocol: A symptom-limited incremental exercise test will be performed using an electronically braked cycle ergometer according to recommended guidelines. The test will consist of steady-state rest for 10 minutes, a 1 minute warm-up at 0 watts, and 20 watt stepwise increases in work rate every 2 minutes until symptom-limitation.

Measurements Familiarization Session: Participants and control participants will exercise on the cycle ergometer at a very low work rate (0W and 20W) for 2 minutes at each intensity in order to become familiarized with the cycle ergometer, breathing apparatus and symptom scales (see details below).

Pulmonary Function: Spirometry and maximum respiratory pressures, will be performed according to standard recommendations. A commercially available cardiopulmonary testing system (Vmax 229d with Autobox 6,200 DL; SensorMedics, Yorba Linda, CA) will be used, and all measurements will be expressed as percent of predicted normal values.

Dyspnea Evaluation: Dyspnea intensity (defined as "the sensation of laboured or difficult breathing") and perceived leg discomfort will be evaluated at rest, every minute during exercise, and at peak exercise using the modified 10-point Borg scale on all testing visits. Participants will be asked to describe their dyspnea during exercise prior to the intensity ratings and at end-exercise using the following 3 descriptors: (1) "my breathing requires more work and effort" (work and effort); (2) "I cannot get enough air in" (unsatisfied inspiration); (3) "I cannot get enough air out" (unsatisfied expiration). None to all 3 of the descriptors can be chosen at any one time. Upon exercise cessation, participants will be asked to verbalize their main reason(s) for stopping exercise (i.e., breathing discomfort, leg discomfort, combination of breathing and legs, or some other reason) and to select qualitative descriptors of breathlessness using an established questionnaire.

Cardio-respiratory Responses to Exercise: Standard cardio-respiratory measures will be recorded on a breath-by-breath basis and averaged over 30-second epochs, including minute ventilation (V'E), oxygen consumption (VO2), carbon dioxide production (CO2), partial pressure of end-tidal CO2, VT, and breathing frequency (Vmax 229d with Autobox 6,200 DL; SensorMedics, Yorba Linda, CA). Operating volumes (i.e., end-expiratory and end-inspiratory lung volumes) will be derived from dynamic inspiratory capacity (IC) manoeuvres as previously described. An indirect measure of neural respiratory drive will be obtained non-invasively using bi-polar surface electromyography (EMG) electrodes placed over the right parasternal intercostals and sternocleidomastoid as previously described. For safety purposes, electrocardiography will be monitored using a 12-lead electrocardiogram (ECG), blood pressure will be measured using a manual sphygmomanometer, and arterial oxygen saturation will be monitored using pulse oximetry. All exercise tests will be administered by experienced exercise physiologists. Tests involving patients with CF and healthy controls will be supervised by a physician. Exercise tests will be terminated based on established criteria as per American College of Sports Medicine guidelines.

Muscle oxygenation and hemodynamics: Muscle oxygenation will be noninvasively monitored using near infrared spectroscopy in all participants. A four-channel continuous-wave near-infrared spectroscope (Oxymon M III, Artinis Medical Systems, BV, The Netherlands) will be used to determine oxyhemoglobin, deoxyhemoglobin, and total hemoglobin by measuring light attenuation at 760 and 864 nm wavelengths, and analyzed using algorithms based on the modified Beer-Lambert law. This data will be used for descriptive exploratory purposes to examine the relationship between muscle oxygenation of the leg (vastus lateralis) and respiratory muscles (sternocleidomastoid, parasternal, and intercostals), and sensory responses to exercise in CF patients.

Computed Tomography Phenotyping: Existing chest computed tomography (CT) scans, obtained through routine clinical practice, will be used for descriptive exploratory purposes to examine the relationship between the extent of bronchiectasis vs. mucus plugging vs. air trapping (based on CF-specific CT scoring) on the physiological and sensory responses to exercise in patients with CF.

Inflection Point of the VT and V'E Relationship: VT data will be averaged over 30-second epochs and will be plotted against V'E at rest and throughout all exercise intensities for each individual participant. The point at which VT deviates from linearity and begins to plateau will be defined as the inflection point of the VT and V'E relationship. Two different observers will determine the inflection point for each participant during the incremental exercise test by examining individual Hey plots.

Statistical Analysis Data will be presented as means ± standard deviation (SD) unless otherwise specified. Between group comparisons (CF vs. healthy control) for descriptive characteristics, exercise responses, and Borg ratings at standardized evaluation points (20 watt increments, VT/minute ventilation (V'E) inflection, and peak) will be compared using unpaired t-tests with Bonferroni corrections where appropriate. Pearson correlation coefficients will be used to examine the association between measured variables: parasternals electromyography, breathing pattern, operational lung volumes, Borg ratings, and exercise variables. Reasons for stopping exercise and qualitative descriptors of dyspnea will be analyzed as frequency statistics and compared between control and CF participants using the Fisher's exact test at standardized 20 watt increments in work-rate, VT/V'E inflection, and peak exercise. A P-value less than 0.05 will be regarded as statistically significant. Statistical analysis of the data will be performed using Stata v11.2 (StataCorp, Texas, USA).

Sample Size and Power Calculation: Determining adequate sample size for qualitative descriptors of dyspnea in CF is difficult because limited data exists in this population. Therefore, the sample size in the present study is based on previous studies of dyspnea intensity ratings and the VT response in patients with chronic obstructive pulmonary disease during exercise. In these studies, statistically significant results were detected using a sample size of 16, under the assumptions: a SD of approximately 1.5 units, a difference of approximately 1.5 units found between the VT/V'E inflection point and peak exercise, a two-sided test, 80% power, and α = 0.05. Thus a sample size of 20 participants in the present study will likely have adequate power for the investigators' analyses.

Keywords
dyspnea, exercise, cystic fibrosis, neuromechanical dissociation
Medical subject headings
Lung Diseases, Cystic Fibrosis, Dyspnea, Motor Activity

What participants receive

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

Study groups in NCT01799642
Study groupRoleWhat they receive
Cystic Fibrosis PatientsParticipants with Cystic Fibrosis
Healthy ControlsParticipants who do not have cystic fibrosis and are otherwise healthy.

What is being measured

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

  1. To determine if dyspnea is qualitatively and quantitatively different in patients with cystic fibrosis compared with age and sex-matched healthy controls during exercise

    Included will be 20 patients with cystic fibrosis (CF) who have no other pulmonary or extra-pulmonary limitation to exercise, as well as 20 healthy age and sex-matched control participants. All participants (CF and control) will perform an incremental symptom-limited cardio-pulmonary exercise test while detailed cardio-respiratory responses, dyspnea responses, muscle oxygenation and muscle hemodynamic data are measured.

    Measured: Parameters will be measured during the 1 visit.

Secondary outcomes (1)
  1. To determine if the dyspnea responses can be explained by differences in the ventilatory response to exercise.

    Included will be 20 patients with cystic fibrosis (CF) who have no other pulmonary or extra-pulmonary limitation to exercise, as well as 20 healthy age and sex-matched control participants. All participants (CF and control) will perform an incremental symptom-limited cardio-pulmonary exercise test while detailed cardio-respiratory responses, dyspnea responses, muscle oxygenation and muscle hemodynamic data are measured. The point at which the tidal volume deviates from linearity and begins to plateau will be defined as the inflection point of the tidal volume and minute ventilation relationship. Two different observers will determine the inflection point for each participant during the incremental exercise test by examining individual Hey plots.

    Measured: Parameters will be measured during the 1 visit.

Timeline

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

  1. First posted27 Feb 2013 (estimated)
  2. Study startJun 2013
  3. Primary completionDec 2014
  4. Study completionDec 2014

Resources

More details

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

Study design
Study type
Observational
Observational model
Case-control
Enrolment
50 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01799642
Sponsor's protocol ID
H13-00262
Acronym
CF_Dyspnea
Status last verified
Nov 2015
First submitted
25 Feb 2013
Last updated
20 Nov 2015
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

An observational study of Lung; Disease and Cystic Fibrosis, run by University of British Columbia at 1 site in Canada.

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 7 inclusion and 5 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 20 Nov 2015. 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 Canada. 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?

To determine if dyspnea is qualitatively and quantitatively different in patients with cystic fibrosis compared with age and sex-matched healthy controls during exercise (time frame: Parameters will be measured during the 1 visit.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 20 Nov 2015.

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