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
| 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
| 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-baselineOutcome 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
Email: [email protected]
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place