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Completed Phase 4 Interventional Results available

Validation of a New Shortness of Breath With Daily Activities Questionnaire in Patients With Chronic Obstructive Pulmonary Disease

ClinicalTrials.gov ID: NCT00984659

Public ClinicalTrials.gov record NCT00984659. 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 25, 2026, 11:48 PM EDT

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

Brief summary

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

The purpose of this study is to evaluate a new questionnaire to capture the patient experience of COPD. The information collected will be used to validate the Shortness of Breath with Daily Activities Questionnaire.

Study identification

NCT ID
NCT00984659
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
366 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
Oct 29, 2009 (Type not available)
Primary completion
Jul 1, 2010 (Actual)
Completion
Jul 1, 2010 (Actual)
Last update posted
Aug 29, 2018

2009 – 2010

United States locations

U.S. sites
39
U.S. states
20
U.S. cities
38
Facility City State ZIP Site status
GSK Investigational Site Jasper Alabama 35501 —
GSK Investigational Site Mobile Alabama 36608 —
GSK Investigational Site Los Angeles California 90095-1690 —
GSK Investigational Site Riverside California 92506 —
GSK Investigational Site Wheat Ridge Colorado 80033 —
GSK Investigational Site Stamford Connecticut 06902 —
GSK Investigational Site Tamarac Florida 33321 —
GSK Investigational Site Decatur Georgia 30033 —
GSK Investigational Site Lawrenceville Georgia 30046 —
GSK Investigational Site Evansville Indiana 47710 —
GSK Investigational Site Evansville Indiana 47714 —
GSK Investigational Site South Bend Indiana 46617 —
GSK Investigational Site Madisonville Kentucky 42431 —
GSK Investigational Site New Orleans Louisiana 70115 —
GSK Investigational Site Sunset Louisiana 70584 —
GSK Investigational Site St Louis Missouri 63141 —
GSK Investigational Site Summit New Jersey 07091 —
GSK Investigational Site Charlotte North Carolina 28207 —
GSK Investigational Site Elizabeth City North Carolina 27909 —
GSK Investigational Site Canton Ohio 44718 —
GSK Investigational Site Cincinnati Ohio 45231 —
GSK Investigational Site Lake Oswego Oregon 97035 —
GSK Investigational Site Portland Oregon 97213 —
GSK Investigational Site Erie Pennsylvania 16508 —
GSK Investigational Site Philadelphia Pennsylvania 19140 —
GSK Investigational Site Charleston South Carolina 29406-7108 —
GSK Investigational Site Chester South Carolina 29706 —
GSK Investigational Site Clinton South Carolina 29325 —
GSK Investigational Site Easley South Carolina 29640 —
GSK Investigational Site Gaffney South Carolina 29340 —
GSK Investigational Site Greenwood South Carolina 29646 —
GSK Investigational Site Seneca South Carolina 29678 —
GSK Investigational Site Spartanburg South Carolina 29303 —
GSK Investigational Site Johnson City Tennessee 37601 —
GSK Investigational Site Houston Texas 77054 —
GSK Investigational Site New Braunfels Texas 78130 —
GSK Investigational Site Abingdon Virginia 24210 —
GSK Investigational Site Richmond Virginia 23229 —
GSK Investigational Site Spokane Washington 99204 —

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00984659, 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 Aug 29, 2018 · Synced Oct 25, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00984659 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →