VR Smoking Cessation During a Dental Hygiene Visit

NCT04524533 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 440

Last updated 2025-09-03

No results posted yet for this study

Summary

The goal of this randomized controlled trial (RCT) is to test whether a smoking cessation induction intervention delivered during a dental cleaning appointment increases the utilization of evidence-based treatments (EBTs) for smoking cessation within 7 months post-dental cleaning appointment.

Approximately 400 cigarette smokers who are scheduled for a dental cleaning appointment at the Boston University Goldman School of Dental Medicine (BUGSDM) patient treatment center will be recruited and enrolled. Participants will be randomized to either the intervention or control group

Conditions

  • Smoking Cessation

Interventions

BEHAVIORAL

Experimental smoking cessation video

Participants who are randomized to the intervention group will watch an educational video that includes tips on quitting smoking during a dental cleaning. The video is approximately 10 minutes long and tailored to readiness to quit at the time of the dental visit.

BEHAVIORAL

Control video

Participants randomized to the control group will watch a 10 minute video.

OTHER

Brochure of smoking cessation EBTs

All participants will receive identical print materials on EBTs consistent with smoking cessation standard clinical care.

BEHAVIORAL

Tailored text message program

Participants randomized to the intervention group will be enrolled in a 4-week tailored text message program which includes assessment questions in addition to text messages geared towards motivating and facilitating EBT utilization for individuals ready to quit smoking and individuals who are not ready to quit smoking.

OTHER

Assessment text messages

Participants randomized to the control group will be enrolled in a different 4-week text message program that includes only assessment questions.

Sponsors & Collaborators

  • National Institute of Dental and Craniofacial Research (NIDCR)

    collaborator NIH
  • Boston University

    lead OTHER

Principal Investigators

  • Belinda Borrelli, PhD · Henry M Goldman School of Dental Medicine

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-01-04
Primary Completion
2025-03-19
Completion
2025-09-30

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 NCT04524533 on ClinicalTrials.gov