Pulmonary Disease, Chronic Obstructive Clinical Trial
This observational study will examine the care-seeking behaviors of Veterans with chronic obstructive pulmonary disease (COPD) to see whether patients' perceived need for care or lack of access to care leads to delays in getting care for COPD exacerbations. Participants complete a baseline in-person visit and receive calls every two weeks for one year to monitor for COPD exacerbations. Detailed information about each exacerbation and time to care are obtained. A sample of participants and their caregivers participate in in-depth interviews. Approximately half the participants will also use a remote inhaler monitor to record their albuterol inhaler use to see if this approach can identify early exacerbations. Results from this study will be used to develop an intervention that will assist Veterans in the early identification, evaluation, and treatment of exacerbations, and will be integrated with the VA primary care team.
Prompt treatment of chronic obstructive pulmonary disease (COPD) exacerbations with oral
steroids and/or antibiotics, ideally within 3 days of onset of symptoms, can decrease the
severity and duration of exacerbations and may reduce the risk of COPD hospitalizations. This
observational study will examine Veterans' care-seeking behaviors and will focus on patients'
perceived need for care and perceived access to care and whether these factors delay seeking
care for COPD exacerbations, increasing the risk for hospitalizations. This study will also
evaluate one approach of identifying early exacerbations through the use of a remote inhaler
monitoring system.
This observational cohort study enrolled 412 Veterans with COPD at high-risk for
exacerbations. As of March 2019, 246 participants have completed the 1 year follow-up; 133
are in follow-up. The Specific Aims are: 1) Examine the barriers to seeking care for COPD
exacerbations or worsening breathing; 2) Test the use of a real-time remote inhaler monitor
to identify early exacerbations.
All participants attended one in-person baseline visit to complete spirometry and baseline
questionnaires. Participants are contacted every 2 weeks for 1 year using an interactive
voice response system that screens for COPD exacerbations with 4 yes/no questions.
Participants with a positive screen are called back by research staff to obtain additional
detailed information on the exacerbation and how it was treated. Data analysis will examine
whether access to care and baseline factors are associated with a delay in treatment.
The participants enrolled at two sites: 252 participants at VA Puget Sound in Seattle, WA and
160 participants at the VA Eastern Colorado in Denver, CO. For Aim 1, 60 participants who
reported a COPD exacerbation (either hospitalized, seen in the emergency department, treated
as outpatients, or did not seek treatment) participated in in-depth semi-structured
interviews by a trained research staff to understand how they responded to their worsening
symptoms and decided whether to seek care. 24 caregivers for these Veterans were interviewed
about their perspective on the exacerbation event.
In Aim 2, 145 participants from Aim 1 used an inhaler monitor with their albuterol inhaler
during the 12-month follow-up period, which transmits real-time data about their daily
inhaler use. Data analysis will measure whether a change in albuterol use can predict patient
reported COPD exacerbations to determine the appropriate cut-offs that can be used in a
future intervention trial.
These aims will provide detailed information on how best to intervene to ensure prompt
identification and treatment of COPD exacerbations. New health care delivery approaches will
assist Veterans in early identification of exacerbations and provide early access to care
that can be integrated into the VA primary care, emergency medicine and pulmonary specialty
care settings.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT05043428 -
The Roles of Peers and Functional Tasks in Enhancing Exercise Training for Adults With COPD
|
N/A | |
Completed |
NCT00528996 -
An Efficacy and Safety Study to Compare Three Doses of BEA 2180 BR to Tiotropium and Placebo in the Respimat Inhaler.
|
Phase 2 | |
Completed |
NCT03740373 -
A Study to Assess the Pulmonary Distribution of Budesonide, Glycopyrronium and Formoterol Fumarate
|
Phase 1 | |
Completed |
NCT05393245 -
Safety of Tiotropium + Olodaterol in Chronic Obstructive Pulmonary Disease (COPD) Patients in Taiwan: a Non-interventional Study Based on the Taiwan National Health Insurance (NHI) Data
|
||
Completed |
NCT05402020 -
Effectiveness of Tiotropium + Olodaterol Versus Inhaled Corticosteroids (ICS) + Long-acting β2-agonists (LABA) Among COPD Patients in Taiwan
|
||
Completed |
NCT04011735 -
Re-usable Respimat® Soft MistTM Inhaler Study
|
||
Enrolling by invitation |
NCT03075709 -
The Development, Implementation and Evaluation of Clinical Pathways for Chronic Obstructive Pulmonary Disease (COPD) in Saskatchewan
|
||
Completed |
NCT03764163 -
Image and Model Based Analysis of Lung Disease
|
Early Phase 1 | |
Completed |
NCT00515268 -
Endotoxin Challenge Study For Healthy Men and Women
|
Phase 1 | |
Completed |
NCT04085302 -
TARA Working Prototype Engagement Evaluation: Feasibility Study
|
N/A | |
Completed |
NCT03691324 -
Training of Inhalation Technique in Hospitalized Chronic Obstructive Pulmonary Disease (COPD) Patients - a Pilot Study
|
N/A | |
Completed |
NCT02236611 -
A 12-week Study to Evaluate the Efficacy and Safety of Umeclidinium 62.5 Microgram (mcg) Compared With Glycopyrronium 44 mcg in Subjects With Chronic Obstructive Pulmonary Disease (COPD)
|
Phase 4 | |
Completed |
NCT00153075 -
Flow Rate Effect Respimat Inhaler Versus a Metered Dose Inhaler Using Berodual in Patients With Chronic Obstructive Pulmonary Disease (COPD)
|
Phase 4 | |
Completed |
NCT01017952 -
A Study to Evaluate Annual Rate of Exacerbations and Safety of 3 Dosage Strengths of Fluticasone Furoate (FF)/GW642444 Inhalation Powder in Subjects With Chronic Obstructive Pulmonary Disease (COPD)
|
Phase 3 | |
Completed |
NCT01009463 -
A Study to Evaluate the Efficacy and Safety of Fluticasone Furoate (FF)/GW642444 Inhalation Powder in Subjects With Chronic Obstructive Pulmonary Disease (COPD)
|
Phase 3 | |
Completed |
NCT04882124 -
Study of Effect of CSJ117 on Symptoms, Pharmacodynamics and Safety in Patients With COPD
|
Phase 2 | |
Completed |
NCT02853123 -
Effect of Tiotropium + Olodaterol on Breathlessness in COPD Patients
|
Phase 4 | |
Completed |
NCT02619357 -
Method Validation Study to Explore the Sensitivity of SenseWear Armband Gecko for Measuring Physical Activity in Subjects With Chronic Obstructive Pulmonary Disease (COPD) & Asthma
|
Phase 1 | |
Recruiting |
NCT05858463 -
High Intensity Interval Training and Muscle Adaptations During PR
|
N/A | |
Not yet recruiting |
NCT05032898 -
Acute Exacerbation of Chronic Obstructive Pulmonary Disease Inpatient Registry Study Stage II
|