Asthma Clinical Trial
Official title:
Indirect Cost of Illness Study of Moderate and Severe Asthma in Quebec
| NCT number | NCT02153346 |
| Other study ID # | 200347 |
| Secondary ID | |
| Status | Completed |
| Phase | N/A |
| First received | |
| Last updated | |
| Start date | June 22, 2014 |
| Est. completion date | April 22, 2016 |
| Verified date | June 2018 |
| Source | GlaxoSmithKline |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
Rationale Asthma is a chronic inflammatory disorder of the airways affecting persons of all
ages and is recognized as one of the most common chronic diseases. Canada has one of the
highest asthma prevalence rates in the world (8.5%, aged 12 and over) and it is a major cause
of hospitalization. The cost of asthma varies dramatically across disease severity, and it is
expected that these costs are greater when the condition is sub-optimally managed and
controlled. Although a number of publications have been reported on the economic burden of
asthma, there is a lack of information on the cost of asthma based on disease severity and
level of disease control in Canada. The proposed study aims to i) estimate the annual
indirect cost of asthma and ii) the impact of asthma on absenteeism, presenteeism and work
productivity in Canada. This information is essential to further quantify the burden of
asthma on patients and the healthcare system in the Canadian setting.
Overall Objectives The overall objective of this study is to describe the impact of asthma on
patients with moderate to severe asthma and to estimate the indirect costs of asthma care in
asthmatic patients followed in tertiary clinics specialized in the field of asthma in Quebec,
Canada.
Study Design
A prospective cohort study will be conducted to measure the indirect economical burden of
asthma on patients. Patients will be selected and recruited from the BD-Asthma registry and
followed prospectively for 1 year. Recruited patients will be asked to complete
questionnaires at regular intervals for 1 year to measure indirect cost of disease, using the
Valuation of lost productivity (VOLP) questionnaire.
Data Collected For each patient, the following data will be collected
- Patient demographics
- Age
- Sex
- Income
- Level of education
- Smoking
- Disease management and Treatment utilization in the year prior to recruitment
- Physician visits and follow up
- Hospitalizations (number and total days)
- Emergency room visits
- Disease characteristics
- Asthma history
- Year of first diagnosis of asthma severity
- Asthma Control Questionnaire score
- Lung function measures
Data Analysis Methods For each participant, the percentage of time missed from work over a
year will be calculated. We will use the human capital approach to calculate the costs of
asthma due to lost productivity, incorporating both absenteeism and presenteeism in the
calculation of the productivity loss. We will calculate the number of work days in which the
person was unable to attend the workplace, and the number of days and percentage of time lost
during the days the person's work was affected by their asthma. The fraction of time lost
from work in the past year will be multiplied by the average income in Quebec. Finally, this
value will be multiplied by the coefficient generated by the VOLP, which reflects the
relative value of the productivity loss. In addition, we will calculate the VOLP multiplier
for each participant which, combined with the percentage of time missed from work, will
create a measure of productivity loss adjusted for the relative importance and
replace-ability of the participant's profession.
Sample Size and Power
One hundred subjects will be randomly selected from the BD-Asthma registry.
Limitations
The study population may not be representative of the general asthma population, as moderate
to severe asthma will be over represented in these tertiary centers.
| Status | Completed |
| Enrollment | 101 |
| Est. completion date | April 22, 2016 |
| Est. primary completion date | April 1, 2016 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years and older |
| Eligibility |
Inclusion Criteria: - Part of the BD-Asthma registry - Age 18 years and older - Patients who signed consent for research with the BD-Asthma registry and signed consent to participate in the indirect cost study. - Must be alive at the time of recruitment Exclusion Criteria: • Patients with a diagnosis of COPD recorded in BD-Asthma at the time of enrolment. |
| Country | Name | City | State |
|---|---|---|---|
| Canada | GSK Investigational Site | Montreal | Quebec |
| Lead Sponsor | Collaborator |
|---|---|
| GlaxoSmithKline |
Canada,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Indirect Cost of Asthma Per Participant Per 3 Months at Baseline (BL) and 12-month Follow-up (FUP) | Participants completed questionnaires within 2 weeks post-recruitment, 4, 8 and 12 months to measure indirect cost of disease, specifically related to productivity. The following questionnaires were used: WPAI helps to determine presenteeism, absenteeism, and total cost calculation (TCC) possible (number of days during the year of study), while VOLP is used to assess the impact of health conditions on lost productivity in monetary units (United states dollars). The following parameters were calculated: Cost of absenteeism due to asthma (CAA), cost of presenteeism due to asthma (CPA), cost of absenteeism due to asthma in whom TCC was possible (CAA TCC), cost of presenteeism due to asthma in whom TCC was possible (CPA TCC), and total indirect cost due to asthma (TICA). | BL and at 12-month FUP | |
| Primary | Indirect Cost of Asthma by Level of Asthma Control Per Participant Per 3 Months at BL and 12-month FUP | Costs of asthma are greater when the asthma is sub-optimally managed and controlled and varies depending on the par. asthma control. Asthma control was assessed using the Asthma Control Questionnaire (ACQ) and par. were asked to recall their experiences during the previous week and respond to the 6 specified questions on a 7-point Likert scale (0=well-controlled; 6=maximum impairment [poorly controlled]; a score of =0.75 indicates well controlled symptoms. The following parameters were presented: Cost of absenteeism due to asthma (CAA), cost of presenteeism due to asthma (CPA), cost of absenteeism due to asthma in whom TCC was possible (CAA TCC), cost of presenteeism due to asthma in whom TCC was possible (CPA TCC), and total indirect cost due to asthma (TICA). Only 59 par. were active workers. When stratified by asthma control and severity each stratum had a sample less than 59. Although results are presented. data may not be reliable due to the low number of par. in each stratum. | BL and 12-month FUP | |
| Primary | Indirect Cost of Asthma by Level of Asthma Severity Per Participant Per 3 Months at BL and 12-month FUP | Costs of asthma may vary depending on the participant's asthma severity. Asthma severity was based on the standard definitions for severity and ACQ scores: Mild (<0.75), Moderate (>0.75) and Severe (any ACQ score). The following parameters were presented: Cost of absenteeism due to asthma (CAA), cost of presenteeism due to asthma (CPA), cost of absenteeism due to asthma in whom TCC was possible (CAA TCC), cost of presenteeism due to asthma in whom TCC was possible (CPA TCC), and total indirect cost due to asthma (TICA). | BL and 12-month FUP | |
| Secondary | Work Productivity Loss as Assessed in Hours Using Work Productivity and Activity Impairment (WPAI) During the Specified Time Points | WPAI is a self-administered instrument to determine the degree to which asthma affected work productivity while at work and affected activities outside of work in the last 7 days and yields 4 types of scores: Absenteeism (work time missed/missed due to other reasons); Presenteeism (actual time worked); Work Productivity Loss (affected productivity while working); and Activity Impairment (affected regular activities). The following parameters were presented: Hours (Hrs) missed due to asthma (HMA), Hrs missed due to other reasons (HMO), and Hrs actually worked (HAW); all in the last 7 days. | At BL, 4-Month, 8-Month and 12-Month FUP |
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Terminated |
NCT04410523 -
Study of Efficacy and Safety of CSJ117 in Patients With Severe Uncontrolled Asthma
|
Phase 2 | |
| Completed |
NCT04624425 -
Additional Effects of Segmental Breathing In Asthma
|
N/A | |
| Active, not recruiting |
NCT03927820 -
A Pharmacist-Led Intervention to Increase Inhaler Access and Reduce Hospital Readmissions (PILLAR)
|
N/A | |
| Completed |
NCT04617015 -
Defining and Treating Depression-related Asthma
|
Early Phase 1 | |
| Recruiting |
NCT03694158 -
Investigating Dupilumab's Effect in Asthma by Genotype
|
Phase 4 | |
| Terminated |
NCT04946318 -
Study of Safety of CSJ117 in Participants With Moderate to Severe Uncontrolled Asthma
|
Phase 2 | |
| Completed |
NCT04450108 -
Vivatmo Pro™ for Fractional Exhaled Nitric Oxide (FeNO) Monitoring in U.S. Asthmatic Patients
|
N/A | |
| Completed |
NCT03086460 -
A Dose Ranging Study With CHF 1531 in Subjects With Asthma (FLASH)
|
Phase 2 | |
| Completed |
NCT01160224 -
Oral GW766944 (Oral CCR3 Antagonist)
|
Phase 2 | |
| Completed |
NCT03186209 -
Efficacy and Safety Study of Benralizumab in Patients With Uncontrolled Asthma on Medium to High Dose Inhaled Corticosteroid Plus LABA (MIRACLE)
|
Phase 3 | |
| Completed |
NCT02502734 -
Effect of Inhaled Fluticasone Furoate on Short-term Growth in Paediatric Subjects With Asthma
|
Phase 3 | |
| Completed |
NCT01715844 -
L-Citrulline Supplementation Pilot Study for Overweight Late Onset Asthmatics
|
Phase 1 | |
| Terminated |
NCT04993443 -
First-In-Human Study to Evaluate the Safety, Tolerability, Immunogenicity, and Pharmacokinetics of LQ036
|
Phase 1 | |
| Completed |
NCT02787863 -
Clinical and Immunological Efficiency of Bacterial Vaccines at Adult Patients With Bronchopulmonary Pathology
|
Phase 4 | |
| Recruiting |
NCT06033833 -
Long-term Safety and Efficacy Evaluation of Subcutaneous Amlitelimab in Adult Participants With Moderate-to-severe Asthma Who Completed Treatment Period of Previous Amlitelimab Asthma Clinical Study
|
Phase 2 | |
| Completed |
NCT03257995 -
Pharmacodynamics, Safety, Tolerability, and Pharmacokinetics of Two Orally Inhaled Indacaterol Salts in Adult Subjects With Asthma.
|
Phase 2 | |
| Completed |
NCT02212483 -
Clinical Effectiveness and Economical Impact of Medical Indoor Environment Counselors Visiting Homes of Asthma Patients
|
N/A | |
| Recruiting |
NCT04872309 -
MUlti-nuclear MR Imaging Investigation of Respiratory Disease-associated CHanges in Lung Physiology
|
||
| Withdrawn |
NCT01468805 -
Childhood Asthma Reduction Study
|
N/A | |
| Recruiting |
NCT05145894 -
Differentiation of Asthma/COPD Exacerbation and Stable State Using Automated Lung Sound Analysis With LungPass Device
|