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Comparison · NCT03207776-a810ee10

Intervention vs Control: Quality, Comfort, and Care (QCC) Defined Readmission Rate

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Intervention vs Control: Quality, Comfort, and Care (QCC) Defined Readmission Rate. Trial comparisons, record NCT03207776-a810ee10. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03207776-a810ee10

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.1220.1090.135wilson
Risk in group 20.1290.1170.143wilson
Risk difference, group 1 minus group 2-0.00794-0.02660.0108newcombe hybrid score
Risk ratio, group 1 over group 20.9390.8091.09log
Odds ratio, group 1 over group 20.930.7841.1log
Number needed to treat, for one fewer participant with the outcome on Intervention than on Control126from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: control.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Intervention
A group of 4 Usual Care components that are applied consistently and completely amongst all patients who present with COPD acute exacerbation symptoms, plus access to navigator services (COPD Clinical Pathway).~COPD Clinical Pathway: A group of 4 Usual Care components that are applied consistently and completely amongst all patients who present with COPD acute exacerbation symptoms, plus access to navigator services.
2862,353OG001
Group 2Control
Treatment of patients in the usual manner based on their diagnosis and resources available at that site (Usual Care).~Usual Care: Treatment of patients in the usual manner based on their diagnosis and resources available at that site.
3212,479OG000

Outcome

Type
SECONDARY
Title
Quality, Comfort, and Care (QCC) Defined Readmission Rate
Description
Readmission to the same facility
Time frame
30 days
Population

Source ClinicalTrials.gov

Trial

Title
An Evaluation of Post Discharge Utilization Among Patients With an Acute Exacerbation of COPD
NCT number
NCT03207776
Phases
NA
Conditions
Chronic Obstructive Pulmonary Disease
Interventions
Usual Care, COPD Clinical Pathway
Lead sponsor
Wake Forest University Health Sciences
Results first posted
2019-10-14

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
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

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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