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Clinical Trials/NCT01166464
NCT01166464
Completed
Not Applicable

Examining a Text Message Intervention for Smoking Cessation

The Miriam Hospital1 site in 1 country84 target enrollmentJuly 2009
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ConditionsTobacco Use DisorderNicotine Dependence

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Tobacco Use Disorder
Sponsor
The Miriam Hospital
Enrollment
84
Locations
1
Primary Endpoint
Smoking abstinence
Status
Completed
Last Updated
12 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

The primary goal of this study is to use qualitative interviews and focus groups to aid us in adapting a face-to-face smoking cessation intervention for delivery through text messaging. After design is completed, the intervention will be pilot tested with a sample of young adults (ages 18-35) who smoke. Final assessments will be conducted at 7 weeks (end of treatment) and both 3 and 6 month follow up.

Registry
clinicaltrials.gov
Start Date
July 2009
End Date
October 2012
Last Updated
12 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Beth Bock, Ph.D.

Staff Psychologist

The Miriam Hospital

Eligibility Criteria

Inclusion Criteria

  • •Age 18 to 35
  • •Current daily smoker
  • •Has a cell phone with text messaging capability
  • •Uses text messaging at least once monthly
  • •Interested in quitting smoking
  • •Willing to set a quit date within the next 30 days
  • •Has access to a physician

Exclusion Criteria

  • •Does not read and speak English with adequate comprehension
  • •Is currently participating in a smoking cessation program
  • •Concurrent drug/alcohol abuse
  • •Mental health issues that would interfere with study compliance

Outcomes

Primary Outcomes

Smoking abstinence

Time Frame: Six months post-treatment

7-day point prevalence abstinence will be measured at 6 months post-treatment.

Secondary Outcomes

  • Usability and Acceptability of the intervention(7 weeks (end of treatment))

Study Sites (1)

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