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Trial · NCT01833026

COPD Assessment and Management Bundle Versus Usual Care

NCT01833026, Not applicable, Completed, University of Illinois Chicago; results first posted 2019-12-24

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. COPD Assessment and Management Bundle Versus Usual Care. Trials, record NCT01833026. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01833026

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
COPD Assessment and Management Bundle Versus Usual Care
NCT number
NCT01833026
Status
Completed
Phases
Not applicable
Enrollment
56 participants, actual
Lead sponsor
University of Illinois Chicago
Conditions
Chronic Obstructive Pulmonary Disease
Interventions
Spirometry test, Levalbuterol
First posted
2013-04-16
Last updated
2019-12-24
Results first posted
2019-12-24

Source ClinicalTrials.gov

Registered outcomes1

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryNumber of Participants With Accurate Classification of Irreversible Airflow Obstructionspirometry was performed at the first visit for intervention group and at 1 year from recruitment for the usual care group, one time assessment for both groups
accuracy of diagnosis was the outcome measure. The results of the spirometry test (done in the beginning for the intervention group and ant the end of 1 year for the usual care groups) were reviewed in conjunction with the initial physician diagnosis of COPD and/or asthma to confirm whether the diagnosis was accurate, not accurate, or indeterminate. Accuracy of diagnosis of COPD was determined by spirometry results if the FEV1/FVC ratio was \<0.7.

Outcomes1

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYNumber of Participants With Accurate Classification of Irreversible Airflow Obstructionspirometry was performed at the first visit for intervention group and at 1 year from recruitment for the usual care group, one time assessment for both groupsParticipantsCOUNT_OF_PARTICIPANTS

Results by group2

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Number of Participants With Accurate Classification of Irreversible Airflow ObstructionCOPD Assessment and Management Recommendations10Participants
Number of Participants With Accurate Classification of Irreversible Airflow ObstructionUsual Care5Participants

Participant flow6

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDUsual Care22
Overall StudySTARTEDIntervention34
Overall StudyCOMPLETEDUsual Care22
Overall StudyCOMPLETEDIntervention34
Overall StudyNOT COMPLETEDUsual Care0
Overall StudyNOT COMPLETEDIntervention0

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityCOPD Assessment and Management Recommendations
Total, all-cause mortalityUsual Care
Total, other adverse eventsCOPD Assessment and Management Recommendations034
Total, other adverse eventsUsual Care022
Total, serious adverse eventsCOPD Assessment and Management Recommendations034
Total, serious adverse eventsUsual Care022

Papers26

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
1792447BACKGROUNDPubMed
7815660BACKGROUNDPubMed
7956395BACKGROUNDPubMed
10673466BACKGROUNDPubMed
10770147BACKGROUNDPubMed
10847262BACKGROUNDPubMed
10999980BACKGROUNDPubMed
12198919BACKGROUNDPubMed
12220364BACKGROUNDPubMed
15078751BACKGROUNDPubMed

1 to 10 of 26

See all 26 papers

Grants1

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

ProjectTitlePrincipal investigatorsOrganizationFunderFiscal years
K23HL094461Enhancing Control of Pulmonary Disease Through Spirometry: Project COPDJOO, MIN JUNIVERSITY OF ILLINOIS AT CHICAGONATIONAL HEART, LUNG, AND BLOOD INSTITUTE2009 to 2013

Trial comparisons2

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

ComparisonSource
COPD Assessment and Management Recommendations vs Usual Care: Number of Participants With Accurate Classification of Irreversible Airflow ObstructionTrial comparisons
COPD Assessment and Management Recommendations vs Usual Care: serious adverse eventsTrial comparisons

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT01833026

GET https://conductscience.org/api/trials/v1/NCT01833026/papers?page=2