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Examining a Text Message Intervention for Smoking Cessation

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01166464
First Posted: July 21, 2010
Last Update Posted: February 3, 2014
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Collaborator:
Live Inspired, LLC
Information provided by (Responsible Party):
Beth Bock, Ph.D., The Miriam Hospital
  Purpose
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.

Condition Intervention
Tobacco Use Disorder Nicotine Dependence Behavioral: text messaging for smoking cessation Behavioral: Generic text messages

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Examining a Text Message Intervention for Smoking Cessation

Resource links provided by NLM:


Further study details as provided by Beth Bock, Ph.D., The Miriam Hospital:

Primary Outcome Measures:
  • Smoking abstinence [ Time Frame: Six months post-treatment ]
    7-day point prevalence abstinence will be measured at 6 months post-treatment.


Secondary Outcome Measures:
  • Usability and Acceptability of the intervention [ Time Frame: 7 weeks (end of treatment) ]
    Usability and acceptability of the intervention will be assessed at the end of treatment (week 7).


Enrollment: 84
Study Start Date: July 2009
Study Completion Date: October 2012
Primary Completion Date: April 2012 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Text Messaging
A text message-based intervention for smoking cessation
Behavioral: text messaging for smoking cessation
A 7-week program of daily text messages
Placebo Comparator: Control
Individuals in this group will receive generic (non-smoking related) text messages on the same schedule as the intervention arm. This provides a control for staff/program contact time and participant burden.
Behavioral: 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.

  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   18 Years to 35 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
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
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01166464


Locations
United States, Rhode Island
The Miriam Hospital
Providence, Rhode Island, United States, 02903
Sponsors and Collaborators
The Miriam Hospital
Live Inspired, LLC
Investigators
Principal Investigator: Beth C Bock, PhD The Miriam Hospital, Brown Medical School
  More Information

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: Beth Bock, Ph.D., Staff Psychologist, The Miriam Hospital
ClinicalTrials.gov Identifier: NCT01166464     History of Changes
Other Study ID Numbers: R21DA027142 ( U.S. NIH Grant/Contract )
First Submitted: July 16, 2010
First Posted: July 21, 2010
Last Update Posted: February 3, 2014
Last Verified: January 2014

Keywords provided by Beth Bock, Ph.D., The Miriam Hospital:
tobacco
smoking
text message
therapy

Additional relevant MeSH terms:
Tobacco Use Disorder
Substance-Related Disorders
Chemically-Induced Disorders
Mental Disorders