NCT01166464

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
84

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jul 2009

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 1, 2009

Completed
1 year until next milestone

First Submitted

Initial submission to the registry

July 16, 2010

Completed
5 days until next milestone

First Posted

Study publicly available on registry

July 21, 2010

Completed
1.7 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2012

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2012

Completed
Last Updated

February 3, 2014

Status Verified

January 1, 2014

Enrollment Period

2.8 years

First QC Date

July 16, 2010

Last Update Submit

January 31, 2014

Conditions

Keywords

tobaccosmokingtext messagetherapy

Outcome Measures

Primary Outcomes (1)

  • Smoking abstinence

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

    Six months post-treatment

Secondary Outcomes (1)

  • Usability and Acceptability of the intervention

    7 weeks (end of treatment)

Study Arms (2)

Text Messaging

EXPERIMENTAL

A text message-based intervention for smoking cessation

Behavioral: text messaging for smoking cessation

Control

PLACEBO COMPARATOR

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

Interventions

A 7-week program of daily text messages

Text Messaging

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.

Control

Eligibility Criteria

Age18 Years - 35 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • 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

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

The Miriam Hospital

Providence, Rhode Island, 02903, United States

Location

Related Publications (1)

  • Bock B, Heron K, Jennings E, Morrow K, Cobb V, Magee J, Fava J, Deutsch C, Foster R. A Text Message Delivered Smoking Cessation Intervention: The Initial Trial of TXT-2-Quit: Randomized Controlled Trial. JMIR Mhealth Uhealth. 2013 Jul 30;1(2):e17. doi: 10.2196/mhealth.2522.

MeSH Terms

Conditions

Tobacco Use DisorderSmoking

Condition Hierarchy (Ancestors)

Substance-Related DisordersChemically-Induced DisordersMental DisordersBehavior

Study Officials

  • Beth C Bock, PhD

    The Miriam Hospital, Brown Medical School

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Staff Psychologist

Study Record Dates

First Submitted

July 16, 2010

First Posted

July 21, 2010

Study Start

July 1, 2009

Primary Completion

April 1, 2012

Study Completion

October 1, 2012

Last Updated

February 3, 2014

Record last verified: 2014-01

Locations