DPBRN Hygienists Internet Quality Improvement in Tobacco Cessation (HiQuit) (HiQuit)

January 24, 2013 updated by: Dental Practice-Based Research Network

Hygienists Internet Tobacco Cessation Study (HiQuit)

Our overall goal is to advance science related to using the Internet in health services delivery, and specifically smoking cessation by targeting dental hygienists. Our proposed intervention is the first Internet-delivered intervention to target the dental microsystem for smoking cessation-providing access to hygienists and patients.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

This study is designed to allow dental hygienists and dentists to provide additional tobacco cessation counseling with little additional marginal effort. This would be done using an Internet-based referral to external resources. This system, termed "ReferASmoker", will allow hygienists and dentists to refer patients to a patient education, self-management website, "Decide2Quit" and accompanying Quitline, while the patient is still in the dental office. We anticipate that hygienists will be the primary drivers of this intervention. Our intervention has several innovations designed to support the dental practice in their tobacco cessation activities and maximize patient cessation rates. We will randomize 80 community-based primary dental practices into a clinical trial.

Aim 1. To test hypothesis 1(H1)that the number of patients REFERRED to the self-management resource website will be larger in the intervention practices compared to control practices.

Aim 2. To test hypothesis 2 (H2) that the proportion of patients referred who GO to the patient self-management website will be larger in intervention practices compared to control practices

Aim 3. To test hypothesis 3 (H3) that the proportion of smokers who are referred who QUIT at six months will be larger among intervention compared to control because of the additional connectivity of the intervention.

Study Type

Interventional

Enrollment (Actual)

80

Phase

  • Early Phase 1

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Alabama
      • Birmingham, Alabama, United States, 35294
        • University of Alabama at Birmingham
    • Minnesota
      • Minneapolis, Minnesota, United States
        • Health Partners Research Foundation

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

19 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Community-based practices with internet access available in the office seeing an average of five or more smokers in a week.

Exclusion Criteria:

  • Exclude practices that have ongoing computer-based smoking cessation programs for patients.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Triple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Electronic Referrals
Dental practices randomized to the experimental group will have options on how to refer patients to the tobacco cessation website.
Dental practices in this arm will be able to have option of making electronic patient referrals to the Decide2Quit website.
No Intervention: Routine Referral
Dental practices in this arm will refer patients to the Decide2Quit website by using an information prescription.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Number of smokers referred to tobacco cessation website
Time Frame: 12 months
We will asses the number of patient referrals that the dental hygienists make to the tobacco cessation website.
12 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Proportion of smokers who go to the tobacco cessation website
Time Frame: 12 months
We will assess the proportion of smokers who were referred to the tobacco cessation website to the number of patients who registered on the website.
12 months
Point prevalence smoking cessation
Time Frame: 6 months
Tobacco cessation behaviors will be assessed by follow-up email and/or telephone interviews at six months from website enrollment.
6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Chair: Gregg H. GIlbert, DDS, MBA, Dental Practice-Based Research Network (DPBRN)
  • Principal Investigator: Midge N. Ray, RN, MSN, CCS, University of Alabama School of Health Professons at Birmingham

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

April 1, 2010

Primary Completion (Actual)

June 1, 2011

Study Completion (Actual)

June 1, 2011

Study Registration Dates

First Submitted

April 20, 2010

First Submitted That Met QC Criteria

April 20, 2010

First Posted (Estimate)

April 22, 2010

Study Record Updates

Last Update Posted (Estimate)

January 25, 2013

Last Update Submitted That Met QC Criteria

January 24, 2013

Last Verified

January 1, 2013

More Information

Terms related to this study

Other Study ID Numbers

  • 122286
  • U01DE016747 (U.S. NIH Grant/Contract)

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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