Trial Outcomes & Findings for Treating Tobacco Dependence in Inpatient Psychiatry - 1 (NCT NCT00136812)

NCT ID: NCT00136812

Last Updated: 2024-04-11

Results Overview

Recruitment status

COMPLETED

Study phase

NA

Target enrollment

224 participants

Primary outcome timeframe

3 mo, 6 mo, 12 mo, and 18 mo post-baseline

Results posted on

2024-04-11

Participant Flow

Adult smokers (N=224) were recruited between July 2006 and December 2008 from the adult inpatient psychiatry unit at the Langley Porter Psychiatric Institute (LPPI) located on the University of California, San Francisco (UCSF) medical school campus.

Participant milestones

Participant milestones
Measure
Control
Usual care provided NRT during hospitalization with brief cessation advice.
Brief Treatment
The intervention included a Transtheoretical Model-tailored computerized program and print workbook; brief on-unit counseling session; and nicotine replacement therapy (NRT) during hospitalization with access to 10 weeks of NRT post-hospitalization.
Overall Study
STARTED
111
113
Overall Study
COMPLETED
111
113
Overall Study
NOT COMPLETED
0
0

Reasons for withdrawal

Withdrawal data not reported

Baseline Characteristics

Treating Tobacco Dependence in Inpatient Psychiatry - 1

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Control
n=111 Participants
Usual care provided NRT during hospitalization with brief cessation advice.
Brief Treatment
n=113 Participants
The intervention included a Transtheoretical Model-tailored computerized program and print workbook; brief on-unit counseling session; and nicotine replacement therapy (NRT) during hospitalization with access to 10 weeks of NRT post-hospitalization.
Total
n=224 Participants
Total of all reporting groups
Age, Continuous
39.9 years
STANDARD_DEVIATION 14.1 • n=5 Participants
39.9 years
STANDARD_DEVIATION 13.5 • n=7 Participants
39.9 years
STANDARD_DEVIATION 14 • n=5 Participants
Sex/Gender, Customized
Female
71 participants
n=5 Participants
63 participants
n=7 Participants
134 participants
n=5 Participants
Sex/Gender, Customized
Male
36 participants
n=5 Participants
48 participants
n=7 Participants
84 participants
n=5 Participants
Sex/Gender, Customized
Other
4 participants
n=5 Participants
2 participants
n=7 Participants
6 participants
n=5 Participants

PRIMARY outcome

Timeframe: 3 mo, 6 mo, 12 mo, and 18 mo post-baseline

Outcome measures

Outcome measures
Measure
Control
n=111 Participants
Usual care provided NRT during hospitalization with brief cessation advice.
Brief Treatment
n=113 Participants
The intervention included a Transtheoretical Model-tailored computerized program and print workbook; brief on-unit counseling session; and nicotine replacement therapy (NRT) during hospitalization with access to 10 weeks of NRT post-hospitalization.
7 Day Point Prevalence of Cigarette Abstinence
3 month
3 Participants
14 Participants
7 Day Point Prevalence of Cigarette Abstinence
6 month
6 Participants
14 Participants
7 Day Point Prevalence of Cigarette Abstinence
12 month
10 Participants
18 Participants
7 Day Point Prevalence of Cigarette Abstinence
18 month
7 Participants
18 Participants

Adverse Events

1: Enhanced Standard Care Control

Serious events: 0 serious events
Other events: 0 other events
Deaths: 2 deaths

2: Intervention

Serious events: 0 serious events
Other events: 0 other events
Deaths: 2 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Adverse event data not reported

Additional Information

Judith Prochaska, PhD, MPH; Associate Professor

Stanord University

Phone: 650-724-3608

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place