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NCT03714191 Clinical Trial

Optimizing the Tobacco Cessation Clinical Decision Support Tool.

Tobacco Use Cessation Clinical Trial

Official title:
Using Rapid Cycle Randomized Controlled Trials to Study a Tobacco Cessation Best Practice Advisory.

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03714191
Other study ID # QI-Tobacco Cessation
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 3, 2018
Est. completion date February 29, 2020

Study information
Verified date July 2021
Source NYU Langone Health
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The existing tobacco cessation best practice advisory (BPA) fires for providers (physicians, residents, fellows, midwives, nurse practitioners, physician assistants) during outpatient encounters when a patient is identified as a current tobacco user in the Social History section of their chart. The BPA was designed to help facilitate tobacco cessation interventions; it is part of the The Centers for Medicare & Medicaid Services (CMS) Quality Payment Program (QPP). The purpose of the project is to optimize this BPA utilization and improve patient outcomes by comparing multiple versions of the tobacco cessation BPA.

Recruitment information / eligibility
Status Completed
Enrollment 54417
Est. completion date February 29, 2020
Est. primary completion date May 24, 2019
Accepts healthy volunteers No
Gender All
Age group 12 Years and older
Eligibility Inclusion Criteria: - All providers of patients at NYU Langone Health (including NYU Winthrop) who are identified as currents smokers, as documented in the social history of their patient chart, and are eligible to receive the best practice advisory for tobacco cessation. Exclusion Criteria: - non smokers

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Patient Outcomes
The intervention includes different versions of the BPA design and message.
• Billing documentation
The intervention includes different versions of the BPA design and message.
• Regulatory
The intervention includes different versions of the BPA design and message.

Locations
Country Name City State
United States New York University School of Medicine New York New York

Sponsors (1)
Lead Sponsor Collaborator
NYU Langone Health

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Alert acceptance rate 1 year
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