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Engaging Patients in Tobacco Cessation Resources in Dental Settings

NCT03656874 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 56

Last updated 2022-06-28

Study results available
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Summary

The overarching goal of this project is to reduce smoking-associated morbidity and mortality by increasing the number of patients who are referred for tobacco cessation counseling. Using a stratified, group-randomized, controlled, 2-arm trial conducted in two settings, the investigators will compare smoking-related clinical decision support (CDS) to usual care.

Conditions

  • Smoking

Interventions

OTHER

Clinical Decision Support

The clinical decision support will provide clinical practice guideline-supported, evidence-based, and personalized scripts that are tailored based on patients' self-reported smoking attributes to deliver interventions consistent with the standard of care

Sponsors & Collaborators

  • National Institute of Dental and Craniofacial Research (NIDCR)

    collaborator NIH

  • University of Sydney

    collaborator OTHER

  • University of Pittsburgh

    collaborator OTHER

  • Indiana University

    collaborator OTHER

  • HealthPartners Institute

    lead OTHER

Principal Investigators

  • D. Brad Rindal, DDS · HealthPartners Institute

  • Heiko Spallek, DMD,PhD,MSBA · University of Sydney

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-03-29
Primary Completion
2020-12-30
Completion
2021-06-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03656874 on ClinicalTrials.gov