Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE3
600 participants
INTERVENTIONAL
2006-03-31
2010-04-30
Brief Summary
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Detailed Description
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Our specific aims are as follows:
1. Compare the population-based recruitment yields and costs of three proactive outreach approaches: 1) outreach calls only to those teen smokers who are seen, advised, and referred to us by their clinician; 2) outreach calls to a random sample of teens shown as being smokers in the EMR; and 3) outreach calls to a sample of all teens
2. Assess efficacy/effectiveness in a randomized trial with 600 teen smokers to evaluate the hypothesis that proactive telephone-based counseling integrated with an interactive website will increase 6- and 12-month abstinence rates (30-day point prevalence) relative to a control condition receiving mailed cessation materials alone
3. Assess the hypothesis that the telephone and web-based intervention will improve longer-term maintenance of abstinence at an 12-month follow-up point compared to the control condition
4. Describe use patterns for key intervention process measures (e.g., calls completed, use of website) and determine if intervention affects outcome through theoretical mediators (e.g., pros/cons, stage, efficacy)
5. Determine the total costs of the telephone and web-based program from the perspective of the HMO and replication costs in other settings, and report costs as incremental costs per member per month, per program participant, and per quit.
Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Telephone counseling + interactive website
Teen has access to interactive website and receives tailored telephone counseling
Telephone counseling + interactive website = more abstinence
Control with interactive website
Teen only has access to interactive website.
Behavioral: interactive website
Interventions
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Telephone counseling + interactive website = more abstinence
Behavioral: interactive website
Eligibility Criteria
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Inclusion Criteria
* both males and females
* smoking cigarettes at least four days a month
* some interest in quitting (will take all teen regardless of stage of readiness
* no evidence of treatment for depression, alcohol, or drugs in last year
* must consent
* have physician's approval for outreach to their panel
* have (or able to get) Internet access and phone access
* willingness to participate in study and follow-up procedures.
Exclusion Criteria
* \>18 years old
* treated within 1 year for depression, alcohol, or drugs
* No internet access or phone access
15 Years
18 Years
ALL
No
Sponsors
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National Cancer Institute (NCI)
NIH
Kaiser Permanente
OTHER
Responsible Party
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Principal Investigators
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Jack F Hollis, Ph.D.
Role: PRINCIPAL_INVESTIGATOR
Kaiser Permanente
Locations
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Oregon Research Institute
Eugene, Oregon, United States
Kaiser Permanente Center for Health Research
Portland, Oregon, United States
Free & Clear, Inc.
Seattle, Washington, United States
Countries
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References
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