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Working Inside for Smoking Elimination (WISE)

M

Memorial Hospital of Rhode Island

Status

Unknown

Conditions

Cigarette Smoking
Tobacco Smoking

Treatments

Behavioral: Motivational Interviewing/CBT
Other: CONcise Tapes Reviewing Obstacles to healthy Living (CONTROL)

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT01122589
1R01DA024093-01A2 (U.S. NIH Grant/Contract)
WISE 09-21

Details and patient eligibility

About

The purpose of this study is to determine the extent to which an Intentional Behavioral Intervention will increase tobacco quit rates post release among incarcerated men and women.

Full description

Quitting smoking reduces the risks of developing smoking related illnesses as well as the morbidity and mortality associated with these illnesses. In 2006 approximately 44.5 million American adults smoked an overall prevalence of 20.8%. The prevalence is much higher among incarcerated populations and approximately 80% of the women in RI smoked prior to incarceration. This proposal is designed to evaluate an intervention utilizing Motivational Interviewing (MI) and Cognitive Behavioral Therapy (CBT) to provide the skills necessary to maintain smoking abstinence after release. MI utilizes specific techniques for providing feedback on an individual's risk and self efficacy. CBT provides the skills necessary to maintain abstinence after release. The investigators plan to recruit 350 men and women from the Rhode Island Department of Corrections and randomize them to two interventions: an Intentional Behavioral Intervention (IBI) with 6 sessions of in jail MI/CBT and two post release booster sessions compared to CONcise Tapes Reviewing Obstacles to healthy Living (CONTROL) group which will receive a smoking cessation pamphlet and watch a series of six weekly 30-45 minutes general wellness videos.

Enrollment

350 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age 18 and older
  • Daily smokers over the past 30 non-institutionalized days (prior to Incarceration)
  • Expected place of residence after release within 15 miles of follow-up site
  • Agree to participate in the study protocol and be available within one month post release
  • Speak English
  • Provides at least two pieces of locator information
  • Scheduled to be released within eight weeks

Exclusion criteria

  • Inability to give informed consent secondary to organic brain function, not having own legal guardianship, or active psychosis or otherwise not able to participate in the intervention or assessments (deaf, blind, or impaired communication skills that impair ability to participate in computerized assessment or counseling)
  • Housed in a segregation unit

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

350 participants in 2 patient groups

Motivation Interviewing/CBT
Experimental group
Treatment:
Behavioral: Motivational Interviewing/CBT
Control
Active Comparator group
Description:
Receive a smoking cessation pamphlet and watch a series of six weekly 30-45 minutes general wellness videos.
Treatment:
Other: CONcise Tapes Reviewing Obstacles to healthy Living (CONTROL)

Trial contacts and locations

1

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Central trial contact

Jennifer G Clarke, MD; Jennifer A Mello, MPH

Data sourced from clinicaltrials.gov

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