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Completed No phase listed Observational

Observational Study Of An Electronic Questionnaire In Patients With Chronic Obstructive Pulmonary Disease (COPD)

ClinicalTrials.gov ID: NCT00259909

Public ClinicalTrials.gov record NCT00259909. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 26, 2026, 7:57 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Prospective Observational Study for the Psychometric Validation of a Patient-reported Questionnaire in Acute Exacerbations of Chronic Obstructive Pulmonary Disease (AECOPD)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The aim of the study is to develop a new patient-reported outcome (PRO) questionnaire measuring the impact of an acute exacerbation on daily lives of patients with chronic obstructive pulmonary disease (COPD). This questionnaire will aim to detect an acute exacerbation and resolution of exacerbation from the patient's perspective. At a later stage of development, this questionnaire will be able to measure the effect of anti bacterials in the treatment of acute exacerbations of COPD (AECOPD). This study will evaluate the factor structure, validity, reliability, and responsiveness of the GSK questionnaire in subjects who experience acute exacerbations of their COPD.

Study identification

NCT ID
NCT00259909
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
259 participants

Conditions and interventions

Eligibility (public fields only)

Age range
40 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 2, 2005 (Actual)
Primary completion
Nov 7, 2006 (Actual)
Completion
Nov 7, 2006 (Actual)
Last update posted
Oct 12, 2017

2005 – 2006

United States locations

U.S. sites
79
U.S. states
26
U.S. cities
72
Facility City State ZIP Site status
GSK Investigational Site Birmingham Alabama 35209 —
GSK Investigational Site Birmingham Alabama 35233 —
GSK Investigational Site Birmingham Alabama 35294 —
GSK Investigational Site Hueytown Alabama 35023 —
GSK Investigational Site Jasper Alabama 35501 —
GSK Investigational Site Rancho Mirage California 92270 —
GSK Investigational Site Riverside California 92506 —
GSK Investigational Site San Diego California 92120 —
GSK Investigational Site Denver Colorado 80206 —
GSK Investigational Site Fort Collins Colorado 80528 —
GSK Investigational Site Wheat Ridge Colorado 80033 —
GSK Investigational Site Hartford Connecticut 06105 —
GSK Investigational Site Hartford Connecticut 06106 —
GSK Investigational Site Melbourne Florida 32901 —
GSK Investigational Site Pensacola Florida 32503 —
GSK Investigational Site Pensacola Florida 32504 —
GSK Investigational Site Sarasota Florida 34239 —
GSK Investigational Site Tampa Florida 33613 —
GSK Investigational Site Atlanta Georgia 30342 —
GSK Investigational Site Austell Georgia 30106 —
GSK Investigational Site Decatur Georgia 30033 —
GSK Investigational Site Chicago Illinois 60612 —
GSK Investigational Site Hines Illinois 60141-5099 —
GSK Investigational Site North Chicago Illinois 60064 —
GSK Investigational Site Peoria Illinois 62526 —
GSK Investigational Site Springfield Illinois 62702 —
GSK Investigational Site Newburgh Indiana 47630 —
GSK Investigational Site South Bend Indiana 46601 —
GSK Investigational Site Dubuque Iowa 52001 —
GSK Investigational Site Waterloo Iowa 50702 —
GSK Investigational Site Baton Rouge Louisiana 70806 —
GSK Investigational Site Covington Louisiana 70433 —
GSK Investigational Site Lafayette Louisiana 70503 —
GSK Investigational Site Sunset Louisiana 70584 —
GSK Investigational Site Auburn Maine 04210 —
GSK Investigational Site Towson Maryland 21286 —
GSK Investigational Site Detroit Michigan 48202 —
GSK Investigational Site DeWitt Michigan 48820 —
GSK Investigational Site Plainwell Michigan 49080 —
GSK Investigational Site Richland Michigan 49083 —
GSK Investigational Site Saint Joseph Michigan 49085 —
GSK Investigational Site Picayune Mississippi 39466 —
GSK Investigational Site Columbia Missouri 65211 —
GSK Investigational Site Kansas City Missouri 64108 —
GSK Investigational Site Kirkwood Missouri 63122 —
GSK Investigational Site Saint Charles Missouri 63301 —
GSK Investigational Site Omaha Nebraska 68131 —
GSK Investigational Site East Brunswick New Jersey 08816 —
GSK Investigational Site Summit New Jersey 07091 —
GSK Investigational Site Buffalo New York 14215-1199 —
GSK Investigational Site Great Neck New York 11023 —
GSK Investigational Site Kingston New York 12401 —
GSK Investigational Site Mineola New York 11501 —
GSK Investigational Site New York New York 10016 —
GSK Investigational Site New York New York 10021 —
GSK Investigational Site New York New York 10032 —
GSK Investigational Site Elizabeth City North Carolina 27909 —
GSK Investigational Site Winston-Salem North Carolina 27103 —
GSK Investigational Site Cincinnati Ohio 45224 —
GSK Investigational Site Columbus Ohio 43212 —
GSK Investigational Site Allentown Pennsylvania 18102 —
GSK Investigational Site Allentown Pennsylvania 19140 —
GSK Investigational Site Audubon Pennsylvania 19403 —
GSK Investigational Site King of Prussia Pennsylvania 19406 —
GSK Investigational Site Philadelphia Pennsylvania 19140 —
GSK Investigational Site Pittsburgh Pennsylvania 15243 —
GSK Investigational Site Plymouth Meeting Pennsylvania 19462 —
GSK Investigational Site East Providence Rhode Island 02914 —
GSK Investigational Site Charleston South Carolina 29406-7108 —
GSK Investigational Site Greer South Carolina 29651 —
GSK Investigational Site Spartanburg South Carolina 29303 —
GSK Investigational Site Summerville South Carolina 29485 —
GSK Investigational Site Clarksville Tennessee 37043 —
GSK Investigational Site Morristown Tennessee 37813 —
GSK Investigational Site Corsicana Texas 75110 —
GSK Investigational Site Houston Texas 77030 —
GSK Investigational Site San Antonio Texas 78229 —
GSK Investigational Site Lynchburg Virginia 24501 —
GSK Investigational Site Richmond Virginia 23225 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 44 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00259909, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 12, 2017 · Synced Oct 26, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00259909 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →