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NCT00670514 Clinical Trial

Smoking Cessation in a Dentistry Setting

Smoking Clinical Trial

Official title:
A Comparing Study of the Smoking Cessation Program NIX Individual and the Self-Help Program Fimpa Dig Fri

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00670514
Other study ID # Smoking cessation project
Secondary ID
Status Completed
Phase N/A
First received April 16, 2008
Last updated April 30, 2008
Start date April 2003

Study information
Verified date April 2008
Source Uppsala University
Contact n/a
Is FDA regulated No
Health authority Sweden: Regional Ethical Review Board
Study type Interventional

Clinical Trial Summary

Aim: to assess relative effectiveness of a high and a low intensity intervention for smoking cessation support in a dental clinic setting.

Method: 300 smokers were randomly assigned to support with either low (LTI) or high treatment intensity (HTI).

Main outcome measures were self-reported point-prevalence and continuous abstinence (≥183 days).

Recruitment information / eligibility
Status Completed
Enrollment 300
Est. completion date
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 20 Years and older
Eligibility Inclusion Criteria:

- Adult daily smokers in the county of Västmanland

Exclusion Criteria:

- Reading difficulties

- Not fluent in the Swedish language

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind

Related Conditions & MeSH terms

Intervention

Behavioral:
• Nix Individual
Eight 40-minutes sessions at the local dental clinic during 4 months. Written material and counseling by a dental hygienist with special training in smoking cessation, according to a fixed program. A traditional smoking cessation program with a mixture of behavior therapy, coaching and pharmacological advises. Two questionnaires.
• Fimpa dig fri
One 30-minute counseling session at the local dental clinic, focusing on explaining the content of a traditional self-help program ("Fimpa dig fri"). The leaflet contains an 8-week program with instructions and tasks to perform. Two questionnaires.

Locations
Country Name City State
Sweden Centre for clinical research, Central Hospital Västerås

Sponsors (2)
Lead Sponsor Collaborator
Uppsala University Västmanland County Council, Sweden

Country where clinical trial is conducted

Sweden, 

Outcome
Type Measure Description Time frame Safety issue
Primary Point prevalence abstinence
Secondary Continuous abstinence
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