N/A
N=56
Engaging Patients in Tobacco Cessation Resources in Dental Settings
Smoking
Bottom Line
View on ClinicalTrials.gov: NCT03656874 ↗Enrolled (actual)
56
Serious AEs
0.0%
Results posted
Jun 2022
Primary outcome: Primary: Percentage of Smokers With Delivery of Brief Interventions and/or Referral to Treatment — 7; 36 Participants
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Clinical Decision Support (Other)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- HealthPartners Institute
- Primary completion
- Dec 2020
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Percentage of Smokers With Delivery of Brief Interventions and/or Referral to Treatment |
7; 36 | — |
| SECONDARY Percentage of Smokers With Initial Actions Related to Cessation |
3; 20 | — |
| SECONDARY Percentage of Smokers With Long-term Actions Related to Cessation |
4; 18 | — |
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.
Eligibility Criteria
DENTAL STUDENTS AND DENTAL HYGIENE STUDENTS
Inclusion Criteria
- 3rd and 4th year predoctoral students or dental hygiene students enrolled at selected dental schools
PRIVATE PRACTICE DENTISTS & HYGIENISTS
Inclusion Criteria
- General practice dentists or dental hygienists practicing at selected private practice clinics
Exclusion Criteria
- Providers not able or willing to record current tobacco use status in their electronic health record
- Providers affiliated with selected dental schools who hold a current teaching or clinical position
PATIENTS
Inclusion Criteria
- Current cigarette smokers
Exclusion Criteria
- patients requesting to opt out of research
Data sourced from ClinicalTrials.gov (NCT03656874). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.