Anxiety and COPD Evaluation
Status: | Completed |
---|---|
Conditions: | Chronic Obstructive Pulmonary Disease, Pulmonary |
Therapuetic Areas: | Pulmonary / Respiratory Diseases |
Healthy: | No |
Age Range: | 40 - Any |
Updated: | 3/24/2019 |
Start Date: | January 2016 |
End Date: | March 1, 2019 |
Anxiety and COPD Evaluation (ACE)
This prospective, multicenter, cohort study is designed to validate Anxiety Inventory
Respiratory Disease questionnaire in patients with Chronic Obstructive Pulmonary Disease
(COPD).
The primary purpose of this study is to assess the validity of the Anxiety Inventory
Respiratory (AIR) scale in detecting anxiety in relation to the DSM-V criteria in patients
with COPD.
- To evaluate associations between COPD symptom scores assessed by the CAT questionnaire
and MMRC dyspnea scale and measures of depression and anxiety
- To evaluate associations between physiologic measures of lung function (spirometry) and
exercise tolerance (6 minute walk) and measures of depression and anxiety
- To evaluate associations between exacerbations of COPD and the prevalence of anxiety and
depression in a cohort of COPD patients
Respiratory Disease questionnaire in patients with Chronic Obstructive Pulmonary Disease
(COPD).
The primary purpose of this study is to assess the validity of the Anxiety Inventory
Respiratory (AIR) scale in detecting anxiety in relation to the DSM-V criteria in patients
with COPD.
- To evaluate associations between COPD symptom scores assessed by the CAT questionnaire
and MMRC dyspnea scale and measures of depression and anxiety
- To evaluate associations between physiologic measures of lung function (spirometry) and
exercise tolerance (6 minute walk) and measures of depression and anxiety
- To evaluate associations between exacerbations of COPD and the prevalence of anxiety and
depression in a cohort of COPD patients
The goal of the Anxiety and COPD Evaluation (ACE) study is to validate the AIR scale by
employing the Mini International Neuropsychiatric Interview to identify anxiety in 200
patients recruited at participating centers from the American Lung Association (ALA) Airways
Research Network.
Confidential, not
employing the Mini International Neuropsychiatric Interview to identify anxiety in 200
patients recruited at participating centers from the American Lung Association (ALA) Airways
Research Network.
Confidential, not
Inclusion Criteria:
- Post-bronchodilation FEV1 < 80% of the predictive normal value and FEV1 (forced
expiratory volume in one second) / Forced vital capacity(FVC) ratio < 0.7
- Clinically stable COPD as defined by stable maintenance of COPD medications and
absence of an exacerbation of symptoms requiring treatment with an antibiotic or
corticosteroids
Exclusion Criteria:
- Exacerbation of respiratory symptoms in the past six weeks that resulted in the need
for treatment or hospitalization
- Unstable coronary heart disease such as recent myocardial infarction (within 3
months), untreated arrhythmia, or unstable angina
- Major psychiatric disorders (except for depression and anxiety disorders) such as
schizophrenia, schizoaffective, or other disorders that in the opinion of the study
physician that would affect study participation
- Montreal Cognitive Assessment (MoCA) < 18
- Disease or condition expected to cause death within six months or inability to perform
study procedures, as judged by study physician
We found this trial at
1
site
550 1st Ave
New York, New York 10016
New York, New York 10016
(212) 263-7300
Principal Investigator: Joan Reibman, MD
New York University School of Medicine NYU School of Medicine has a proud history that...
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