Home Telemonitoring of Resting Spontaneous Breathing in Severe Asthma: a Pilot Study (AsthmaDom)
Primary Purpose
Asthma
Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
anharmonic morphological analysis of the respiratory signals (AMARS)
Sponsored by
About this trial
This is an interventional health services research trial for Asthma focused on measuring Asthma, Exacerbations, Telemonitoring, Biomarkers
Eligibility Criteria
Inclusion Criteria:
- male or female aged more than 18 yrs
- written informed consent
- diagnosis of asthma according to Global Initiative For Asthma (GINA) criteria
- history of at least one moderate to severe exacerbation in the previous 12 months
Exclusion Criteria:
- smoker or former smoker (> 10 packs-year)
- concomitant asthma exacerbation (at V1)
- prisoners
- protected adults
- no affiliation to the French Social Security System
Sites / Locations
- Grenoble University Hospital
- Bordeaux University Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
AMARS
Arm Description
Evaluation the resting ventilatory flow by applying a new technique called anharmonic morphological analysis of the respiratory signals (AMARS).
Outcomes
Primary Outcome Measures
Sensibility parameters resting breath parameter to predict asthma exacerbation
Specificity of resting breath parameters to predict asthma exacerbation
Positive predictive value of resting breath parameters to predict asthma exacerbation
Negative predictive value of resting breath parameters to predict asthma exacerbation
Secondary Outcome Measures
FEV1
Volume that has been exhaled at the end of the first second of forced expiration
FEV1
Volume that has been exhaled at the end of the first second of forced expiration
FEV1
Volume that has been exhaled at the end of the first second of forced expiration
Asthma exacerbation severity
The number of asthma exacerbations between Day 1 and month 12 will be quoted and defined according to the protocol (abnormal asthma symptoms increase requiring change in asthma medication). Each exacerbation will be quoted according to its severity as mild (requiring increased in inhaled beta2 agonists use for 7 days as assessed by item6 of the Asthma Control Questionnaire (ACQ)), moderate (requiring short course of oral steroid and/or antibiotics) or severe (i.e., requiring hospitalization).
Asthma exacerbation severity
The number of asthma exacerbations between Day 1 and month 12 will be quoted and defined according to the protocol (abnormal asthma symptoms increase requiring change in asthma medication). Each exacerbation will be quoted according to its severity as mild (requiring increased in inhaled beta2 agonists use for 7 days as assessed by item6 of the Asthma Control Questionnaire (ACQ)), moderate (requiring short course of oral steroid and/or antibiotics) or severe (i.e., requiring hospitalization).
Asthma quality of life questionnaires
Asthma quality of life questionnaires
Asthma quality of life questionnaires
Asthma Control Test questionnaires
Asthma Control Test questionnaires
Asthma Control Test questionnaires
Forced Vital Capacity (FVC)
Forced vital capacity: the determination of the vital capacity from a maximally forced expiratory effort
FVC
Forced vital capacity: the determination of the vital capacity from a maximally forced expiratory effort
FVC
Forced vital capacity: the determination of the vital capacity from a maximally forced expiratory effort
FEV1/FVC ratio
FEV1/FVC ratio
FEV1/FVC ratio
Forced Expiratory Flow (FEF25-75%)
Forced expiratory flow related to some portion of the FVC curve; modifiers refer to amount of FVC already exhaled
FEF25-75%
Forced expiratory flow related to some portion of the FVC curve; modifiers refer to amount of FVC already exhaled
FEF25-75%
Forced expiratory flow related to some portion of the FVC curve; modifiers refer to amount of FVC already exhaled
PEF
Peak expiratory flow: The highest forced expiratory flow measured with a peak flow meter
PEF
Peak expiratory flow: The highest forced expiratory flow measured with a peak flow meter
PEF
Peak expiratory flow: The highest forced expiratory flow measured with a peak flow meter
Full Information
NCT ID
NCT02990247
First Posted
December 2, 2016
Last Updated
December 11, 2018
Sponsor
University Hospital, Bordeaux
1. Study Identification
Unique Protocol Identification Number
NCT02990247
Brief Title
Home Telemonitoring of Resting Spontaneous Breathing in Severe Asthma: a Pilot Study
Acronym
AsthmaDom
Official Title
Home Telemonitoring of Resting Spontaneous Breathing in Severe Asthma: a Pilot Study
Study Type
Interventional
2. Study Status
Record Verification Date
December 2018
Overall Recruitment Status
Completed
Study Start Date
November 14, 2016 (Actual)
Primary Completion Date
November 6, 2018 (Actual)
Study Completion Date
November 6, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Bordeaux
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Asthma exacerbations account for a significant morbidity and disproportionate health care costs. However, there is no currently available biomarker or lung function parameter that can accurately predict the risk of future exacerbations. The current work aims at evaluating the resting ventilatory flow by applying a new technique called anharmonic morphological analysis of the respiratory signals (AMARS). We hypothesize that monitoring AMARS is potentially able to detect an increased risk of asthma exacerbations.
Detailed Description
Asthma exacerbations represent an acute or sub-acute worsening in symptoms and lung function from the patient's usual status. Early detection of exacerbations is a major public health issue. In clinic, management of asthma involves asthma control questionnaires and pulmonary function tests (Forced Expiratory Volume (FEV1), Fractional exhaled nitric oxide or FeNO). At home, the peak expiratory flow rate (PEFR) measured by the peak flow meter is an aid to monitor asthma but its ability to predict asthma exacerbations remains controversial. Anharmonic morphological analysis of the respiratory signals (AMARS) is a new morpho-mathematic biomarker that produces objective and accurate measures of the shape of the ventilatory flow. The current study aims at monitoring the resting spontaneous breathing at home in asthmatics. Changes in AMARS may be a predictor of early symptoms of asthma exacerbations. We will recruit 120 asthmatic patients. Patients will be given a portable device for telemonitoring. Resting spontaneous breathing will be measured during 2-3 min in the morning and in the evening, twice a week at least for 12 months. Three visits will be scheduled in Clinical Investigation Center before (V1), after 6-month (V2) and 12-month (V3) telemonitoring period.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Asthma
Keywords
Asthma, Exacerbations, Telemonitoring, Biomarkers
7. Study Design
Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
120 (Actual)
8. Arms, Groups, and Interventions
Arm Title
AMARS
Arm Type
Experimental
Arm Description
Evaluation the resting ventilatory flow by applying a new technique called anharmonic morphological analysis of the respiratory signals (AMARS).
Intervention Type
Device
Intervention Name(s)
anharmonic morphological analysis of the respiratory signals (AMARS)
Primary Outcome Measure Information:
Title
Sensibility parameters resting breath parameter to predict asthma exacerbation
Time Frame
12 months
Title
Specificity of resting breath parameters to predict asthma exacerbation
Time Frame
12 months
Title
Positive predictive value of resting breath parameters to predict asthma exacerbation
Time Frame
12 months
Title
Negative predictive value of resting breath parameters to predict asthma exacerbation
Time Frame
12 months
Secondary Outcome Measure Information:
Title
FEV1
Description
Volume that has been exhaled at the end of the first second of forced expiration
Time Frame
Day 1
Title
FEV1
Description
Volume that has been exhaled at the end of the first second of forced expiration
Time Frame
6 months
Title
FEV1
Description
Volume that has been exhaled at the end of the first second of forced expiration
Time Frame
12 months
Title
Asthma exacerbation severity
Description
The number of asthma exacerbations between Day 1 and month 12 will be quoted and defined according to the protocol (abnormal asthma symptoms increase requiring change in asthma medication). Each exacerbation will be quoted according to its severity as mild (requiring increased in inhaled beta2 agonists use for 7 days as assessed by item6 of the Asthma Control Questionnaire (ACQ)), moderate (requiring short course of oral steroid and/or antibiotics) or severe (i.e., requiring hospitalization).
Time Frame
Day 1
Title
Asthma exacerbation severity
Description
The number of asthma exacerbations between Day 1 and month 12 will be quoted and defined according to the protocol (abnormal asthma symptoms increase requiring change in asthma medication). Each exacerbation will be quoted according to its severity as mild (requiring increased in inhaled beta2 agonists use for 7 days as assessed by item6 of the Asthma Control Questionnaire (ACQ)), moderate (requiring short course of oral steroid and/or antibiotics) or severe (i.e., requiring hospitalization).
Time Frame
12 months
Title
Asthma quality of life questionnaires
Time Frame
Day 1
Title
Asthma quality of life questionnaires
Time Frame
6 months
Title
Asthma quality of life questionnaires
Time Frame
12 months
Title
Asthma Control Test questionnaires
Time Frame
day 1
Title
Asthma Control Test questionnaires
Time Frame
6 months
Title
Asthma Control Test questionnaires
Time Frame
12 months
Title
Forced Vital Capacity (FVC)
Description
Forced vital capacity: the determination of the vital capacity from a maximally forced expiratory effort
Time Frame
day 1
Title
FVC
Description
Forced vital capacity: the determination of the vital capacity from a maximally forced expiratory effort
Time Frame
6 months
Title
FVC
Description
Forced vital capacity: the determination of the vital capacity from a maximally forced expiratory effort
Time Frame
12 months
Title
FEV1/FVC ratio
Time Frame
Day 1
Title
FEV1/FVC ratio
Time Frame
6 months
Title
FEV1/FVC ratio
Time Frame
12 months
Title
Forced Expiratory Flow (FEF25-75%)
Description
Forced expiratory flow related to some portion of the FVC curve; modifiers refer to amount of FVC already exhaled
Time Frame
Day 1
Title
FEF25-75%
Description
Forced expiratory flow related to some portion of the FVC curve; modifiers refer to amount of FVC already exhaled
Time Frame
6 months
Title
FEF25-75%
Description
Forced expiratory flow related to some portion of the FVC curve; modifiers refer to amount of FVC already exhaled
Time Frame
12 months
Title
PEF
Description
Peak expiratory flow: The highest forced expiratory flow measured with a peak flow meter
Time Frame
Day 1
Title
PEF
Description
Peak expiratory flow: The highest forced expiratory flow measured with a peak flow meter
Time Frame
6 months
Title
PEF
Description
Peak expiratory flow: The highest forced expiratory flow measured with a peak flow meter
Time Frame
12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
male or female aged more than 18 yrs
written informed consent
diagnosis of asthma according to Global Initiative For Asthma (GINA) criteria
history of at least one moderate to severe exacerbation in the previous 12 months
Exclusion Criteria:
smoker or former smoker (> 10 packs-year)
concomitant asthma exacerbation (at V1)
prisoners
protected adults
no affiliation to the French Social Security System
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Patrick Berger, MD, PhD
Organizational Affiliation
University Hospital, Bordeaux
Official's Role
Principal Investigator
Facility Information:
Facility Name
Grenoble University Hospital
City
Grenoble
ZIP/Postal Code
38043
Country
France
Facility Name
Bordeaux University Hospital
City
Pessac
ZIP/Postal Code
33600
Country
France
12. IPD Sharing Statement
Plan to Share IPD
No
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Home Telemonitoring of Resting Spontaneous Breathing in Severe Asthma: a Pilot Study
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