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Advancing the Patient Experience in Chronic Obstructive Pulmonary Disease (APEX COPD)

Advancing the Patient Experience in Chronic Obstructive Pulmonary Disease (APEX COPD)

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04285047
Acronym
APEX COPD
Enrollment
4500
Registered
2020-02-26
Start date
2019-03-23
Completion date
2022-12-31
Last updated
2020-02-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Obstructive Pulmonary Disease (13645005)

Keywords

Chronic Obstructive Pulmonary Disease, Chronic Obstructive Lung Disease, Chronic Obstructive Airway Disease, Registry, Electronic Health Record, Electronic Medical Record, Patient Reported Information and Outcomes, Treatment, Therapy

Brief summary

APEX COPD is registry to provide a mechanism to standardize, store and utilize data to enable greater power to answer key research questions, and to improve patient outcomes in COPD primary care.

Detailed description

In the process of creating of a high-quality longitudinal dataset combining COPD templates and patient reported information and outcome (PRIO) to evaluate outcomes the APEX COPD registry supports changes and improvements in medical practice and deliver high quality research through the following mechanisms: * Templates integrated into the primary care clinical systems to support standardization of care and data over time. * Informing doctors at the point of consultation about the status of their patients through data-driven feedback. * Pre-filled electronic data templates from existing EHR data and questionnaires to reduce administrative burden for Primary Care Clinicians (PCC). * Engaging primary care clinicians in ongoing quality improvement initiatives directly at the point of care. * Research publications regarding treatment effectiveness and associated risk in mild to moderate COPD, reason for therapy switch/escalation and hidden undiagnosed and untreated COPD patients in primary care. * A strong network of primary care clinicians caring for patients with COPD in the US to drive the initiative and ensure impact on clinical practice through educational events, academic organizations and research outputs. The APEX COPD steering committee (SC) comprise of collective clinical expertise, scientific knowledge and experience in EHR, databases and research, forming an essential element of the APEX COPD registry. The SC plays an essential role in the development and governance of the APEX COPD registry, representing the sites participating, and providing the expertise necessary to implement and drive the initiative. Within this committee a smaller management group guides the operational aspects of the registry. The research database uses the Observational Medical Outcomes Partnership (OMOP) v5 Common Data Model (CDM) and the OMOP terminology will be updated at least bi-annually. Standardized OMOP Concept IDs will utilize SNOMED, RxNorm and may be adjusted to improve data compatibility with other OPC COPD databases.

Interventions

OTHERAdvancing Patient Experience (APEX) in COPD

Involves both EMR and PRIO data

Sponsors

Boehringer Ingelheim
CollaboratorINDUSTRY
DARTNet Institute
CollaboratorOTHER_GOV
American Academy of Family Physicians National Research Network (AAFP NRN)
CollaboratorUNKNOWN
Respiratory Effectiveness Group
CollaboratorOTHER
Optimum Patient Care
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
35 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Diagnostic code for COPD or COPD monitoring review code prior to or at consultation * Aged ≥35 years at COPD diagnosis

Exclusion criteria

* Patients receiving hospice care * Patients being actively treated for a cancer diagnosis (not skin)

Design outcomes

Primary

MeasureTime frameDescription
Describe and characterize the COPD primary care patient population's natural history31 December 2018 to 31 December 2022Baseline data from electronic health record (EHR) and patient reported information and outcomes (PRIO). The EHR data will be updated every three months.
Evaluate the comparative clinical, safety and cost effectiveness of current COPD treatments by class of therapy for COPD overall and in specific patient groups/phenotypes, to understand the predictors of response to available COPD treatment options31 December 2018 to 31 December 2022Patient reported information and outcomes (PRIO) will be collected annually and before very visit to their doctor

Secondary

MeasureTime frame
Improve quality of care, and primary care patient outcomes31 December 2018 to 31 December 2022
Understand the clinical phenotypes31 December 2018 to 31 December 2022
Understand the current burden and minimize side effects31 December 2018 to 31 December 2022
Support the development of effective and efficient diagnostic routines31 December 2018 to 31 December 2022
comparing clinician-diagnosed COPD at baseline against established31 December 2018 to 31 December 2022
Describe disease management pattern31 December 2018 to 31 December 2022
Describe risk factors31 December 2018 to 31 December 2022
Assess the occurrence of exacerbations and other conditions31 December 2018 to 31 December 2022
Assess biomarker data and estimate their predictive value for disease diagnosis31 December 2018 to 31 December 2022
identify patients who may be eligible for participation in future research studies31 December 2018 to 31 December 2022
Describe factors associated with treatment choice at baseline31 December 2018 to 31 December 2022
Assess impact of inhaler technique31 December 2018 to 31 December 2022

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026