Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT02740465 · ClinicalTrials.gov registry record · NA

Anxiety and COPD Evaluation

A NA study of Chronic Obstructive Pulmonary Disease, sponsored by NYU Langone Health.

Completed
Registry status
NA
Development phase
200
Enrollment target
1
Study location

NCT02740465: Completed NA study of Chronic Obstructive Pulmonary Disease, sponsored by NYU Langone Health.

NCT02740465 is a NA study of Chronic Obstructive Pulmonary Disease that has completed, run by NYU Langone Health. The registered enrollment target is 200 participants, below the 1,752-participant average among 86 other Chronic Obstructive Pulmonary Disease trials with a reported enrollment target (89% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02740465, a NA study of Chronic Obstructive Pulmonary Disease, has completed, sponsored by NYU Langone Health.

COMPLETED
Registry status
NA
Development phase
200 participants
Enrollment target
1
Study location

Study Summary

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

Primary Outcome

The Montreal Cognitive Assessment (MoCA) was developed as a brief screening instrument to detect mild cognitive impairment. It is a paper-and-pencil tool that requires approximately 10 minutes to administer, and is scored out of 30 points. The MoCA assesses multiple cognitive domains including attention, concentration, executive functions, memory, language, visuospatial skills, abstraction, calculation and orientation. It is widely used around the world and is translated to 36 languages and dial

Interventions

  • BEHAVIORAL Hospital Anxiety and Depression Scale (HADS)
  • BEHAVIORAL Anxiety Inventory for Respiratory Disease (AIR)

Study Locations (1)

New York

  • New York University School of Medicine - New York

Trial Details

FieldValue
Enrollment Target 200 participants
Start Date 2016-01
Est. Completion 2019-03-01
Phase NA
NYU Langone Health

1,164 total trials

What the finished NCT02740465 record still lists

NCT02740465 is an interventional study that assigns participants to a tested intervention. The registered 200 participants enrollment target is mid-sized for trials with a published cap, below the 1,752-participant average among 86 other Chronic Obstructive Pulmonary Disease trials with a reported enrollment target (89% lower).

The record links to 1 condition, with Chronic Obstructive Pulmonary Disease appearing as the primary indexed condition, and to 2 interventions - of which Hospital Anxiety and Depression Scale (HADS) is the first listed.

NCT02740465 reports a single indexed study location in New York.

Frequently Asked Questions

What is clinical trial NCT02740465 about?

NCT02740465 is a clinical study titled "Anxiety and COPD Evaluation". 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 dete...

What is the current status of trial NCT02740465?

This trial is currently completed. It is a NA study. The enrollment target is 200 participants. The study started on 2016-01. Estimated completion is 2019-03-01.

What conditions does trial NCT02740465 study?

This clinical trial studies the following conditions: Chronic Obstructive Pulmonary Disease.

What interventions are being tested in trial NCT02740465?

The interventions under investigation include: Hospital Anxiety and Depression Scale (HADS) (BEHAVIORAL), Anxiety Inventory for Respiratory Disease (AIR) (BEHAVIORAL).

Who is sponsoring clinical trial NCT02740465?

This trial is sponsored by NYU Langone Health, which has 1,164 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02740465 being conducted?

This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Chronic Obstructive Pulmonary Disease

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT02740465's enrollment target sits among peer trials

200 38th of 86 higher than 48 of 86 other Chronic Obstructive Pulmonary Disease trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Chronic Obstructive Pulmonary Disease trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00107289 · 200 participants · Phase 2

    Iodine I 131 Metaiodobenzylguanidine in Treating Patients With Recurrent, Progressive, or Refractory Neuroblastoma or Malignant Pheochromocytoma or Paraganglioma

  • NCT00109174 · 200 participants · NA

    MRS Measurement of Glutamate and GABA Metabolism in Brain

  • NCT00177268 · 200 participants

    Blood, Urine, and Tissue Collection for Cutaneous Lymphoma, Eczema, and Atopic Dermatitis Research

  • NCT00493688 · 200 participants

    A Study to Determine Whether Perioperative Energy Dynamics Correlates With Postoperative Outcomes

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT02740465, the US trial registry maintained by the National Library of Medicine. NCT02740465 (mid enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.