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Smoking Treatment of Prisoners

Smoking Treatment of Prisoners: Project STOP

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00110630
Acronym
STOP
Enrollment
250
Registered
2005-05-11
Start date
2005-06-30
Completion date
2007-09-30
Last updated
2017-01-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tobacco Use Cessation, Tobacco Use Disorder

Keywords

nicotine dependence

Brief summary

The purpose of this study is to determine the efficacy of a 10-week smoking cessation therapy combined with NicoDerm CQ for smoking cessation among female prisoners.

Detailed description

This is a randomized controlled trial utilizing a wait-list control group to examine 10-week group therapy and nicotine replacement compared to wait-list for smoking cessation among female prisoners.

Interventions

BEHAVIORAL10-week smoking cessation group therapy combined with NicoDerm CQ

Sponsors

GlaxoSmithKline
CollaboratorINDUSTRY
National Institute on Drug Abuse (NIDA)
Lead SponsorNIH

Study design

Allocation
RANDOMIZED
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 100 Years
Healthy volunteers
Yes

Inclusion criteria

* 1\) current smoker and (2) seeking group treatment to quit smoking.

Exclusion criteria

* (1) non-english speaking, (2) housed in segregation, (3) presence of active, severe mental illness as defined by active psychosis, manic episode, or imminently suicidal/homicidal, (4) mental retardation such that they cannot provide informed consent, and (5) due to be released or transferred to another facility within the next year.

Design outcomes

Primary

MeasureTime frame
smoking cessation

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026