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Clinical Trials/NCT03017092
NCT03017092
Completed
Not Applicable

Tobacco Pilot Study for Low Income Smokers

University of Wisconsin, Madison1 site in 1 country20 target enrollmentJanuary 18, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Tobacco Use Disorder
Sponsor
University of Wisconsin, Madison
Enrollment
20
Locations
1
Primary Endpoint
Ease of use of tablet-guided tobacco intervention assessed by interview and summarized across study participants
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

Pilot study to test feasibility of delivering a motivational smoking cessation intervention to low income smokers via a computer tablet.

Detailed Description

Twenty Salvation Army clients will be recruited to pilot test a motivational smoking cessation counseling intervention that is delivered via a tablet computer. Study participants will be given brief instructions on how to use the tablet. They will then complete a brief survey on the tablet. This will be followed by the researcher using the tablet to provide the motivational intervention. Finally, study participants will be interviewed to establish this perceptions of the intervention.

Registry
clinicaltrials.gov
Start Date
January 18, 2017
End Date
January 27, 2017
Last Updated
6 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • current smoker (≥ 10 cigarettes/week for the past six months who are not currently trying to quit)
  • age ≥ 18 years
  • English speaking/writing

Exclusion Criteria

  • not receiving services for the Salvation Army

Outcomes

Primary Outcomes

Ease of use of tablet-guided tobacco intervention assessed by interview and summarized across study participants

Time Frame: Immediately after exposure to intervention

At the end of the intervention, each study participant will be interviewed regarding how easy the tablet computer was to use. This qualitative information will by summarized across all study participants.

Study Sites (1)

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