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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01166464
Other study ID # R21DA027142
Secondary ID
Status Completed
Phase N/A
First received July 16, 2010
Last updated January 31, 2014
Start date July 2009
Est. completion date October 2012

Study information

Verified date January 2014
Source The Miriam Hospital
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 84
Est. completion date October 2012
Est. primary completion date April 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 35 Years
Eligibility 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

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
text messaging for smoking cessation
A 7-week program of daily text messages
Generic text messages
non-smoking related text messages will be given on the same daily schedule as matches the active intervention to establish a control for contact time.

Locations

Country Name City State
United States The Miriam Hospital Providence Rhode Island

Sponsors (2)

Lead Sponsor Collaborator
The Miriam Hospital Live Inspired, LLC

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Smoking abstinence 7-day point prevalence abstinence will be measured at 6 months post-treatment. Six months post-treatment No
Secondary Usability and Acceptability of the intervention Usability and acceptability of the intervention will be assessed at the end of treatment (week 7). 7 weeks (end of treatment) No
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