- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00820495
Effectiveness of a Web-Assisted Quitline for Smokeless Tobacco Users
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Many Americans engage in the habitual use of smokeless tobacco (ST), and many wish to quit but lack resources. There is a need for innovative, validated, and easily delivered low-cost interventions to facilitate ST cessation in this under-served population of tobacco users. In our current ChewFree study, we have developed a user-friendly, interactive Web-based intervention, and in a randomized trial we have shown this website to be more efficacious than a rigorous control condition that offered Web-based basic textual information on ST cessation. We now seek to extend this proven approach by marrying it with a quitline telephone counseling service that has been used with noteworthy success for smoking abstinence but has not yet been evaluated with ST users. Our 2 x 2 design and large sample size allow us to test both main effects - Web program, phone counseling - as well as explore planned comparisons to examine the value-added contribution of the Web-based intervention to phone counseling, and vice-versa.
This project takes advantage of the opportunity to conduct a study of two tobacco cessation interventions that are growing in use. The use of tobacco help lines is now almost ubiquitous, with more than 30 state and national services now being offered. The use of the Internet for health information and behavior change (including tobacco cessation) has been growing in popularity as well. The proposed project would be an extension of both lines of research, evaluating the relative efficacy of our Internet-based program, telephone counseling, and the combination of both.
We will use a multifaceted promotional plan to recruit more than 2,000 ST users. The recruitment plan builds on the collaborative marketing efforts of a state tobacco control organization and organized promotion through media mailings, on-line advertising, and direct mailing. Follow-up assessment data will be collected electronically via the Internet supplemented by telephone follow-up. Additional data will be derived from phone counselor notes and measures of website usage.
Study Type
Enrollment (Actual)
Phase
- Phase 2
Contacts and Locations
Study Locations
-
-
California
-
San Diego, California, United States, 92111
- University of California, San Diego
-
-
Oregon
-
Eugene, Oregon, United States, 97403
- Oregon Research Institute
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- current users of smokeless tobacco products (snuff or chewing tobacco)
- use of smokeless tobacco products for at least 1 year
- use of at least one tin or pouch per week
- interest in quitting all tobacco
- U.S. resident 18 years of age or older
- ability to read English
- willingness to share a phone number, e-mail, and mailing address
- use of personal Internet e-mail account at least once per week
- informed consent
Exclusion criteria:
- none
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Web + Phone
Highly interactive tailored Web-based smokeless tobacco cessation program plus phone counseling
|
Web + Phone
Other Names:
|
|
Experimental: Web Only
Highly interactive tailored Web-based smokeless tobacco cessation program
|
Web Only
Other Names:
|
|
Experimental: Phone Only
Phone counseling intervention for smokeless tobacco cessation
|
Phone Only
Other Names:
|
|
Experimental: Control
Usual care (initial call plus self-help materials)
|
Usual Care
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Prolonged abstinence from all tobacco
Time Frame: 3 months and 6 months
|
3 months and 6 months
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
7-day point prevalence for smokeless tobacco use
Time Frame: 3 months and 6 months
|
3 months and 6 months
|
|
7-day point prevalence for all tobacco use
Time Frame: 3 months and 6 months
|
3 months and 6 months
|
Collaborators and Investigators
Sponsor
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- R01CA084225 (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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