Dissemination of Tobacco Tactics for Hospitalized Smokers



Status:Completed
Conditions:Smoking Cessation
Therapuetic Areas:Pulmonary / Respiratory Diseases
Healthy:No
Age Range:18 - Any
Updated:11/30/2013
Start Date:July 2011
End Date:September 2014
Contact:Andrea H Waltje, RN, MS
Email:waltjea@umich.edu
Phone:734.647.0103

Use our guide to learn which trials are right for you!

Dissemination of Tobacco Tactics Versus 1-800-QUIT-NOW for Hospitalized Smokers


Nurse-administered smoking cessation interventions have been shown to be efficacious, but
are seldom implemented due to lack of training and time. This project aims to disseminate
and test the nurse-administered Tobacco Tactics intervention in 6 hospitals.


Background: Dr. Duffy has developed, tested, and refined the efficacious, nurse-administered
Tobacco Tactics intervention and has packaged it into a Toolkit for dissemination in two
Veterans Affairs (VA) hospitals. However, rigorous testing of dissemination outside of the
VA is needed.

Objectives: Using 6 community hospitals in the Trinity Health System, the objectives of this
study are to:

1. Determine provider and patient receptivity, barriers, and facilitators to implementing
the nurse-administered, inpatient Tobacco Tactics intervention versus usual care using
face-to-face feedback and surveys.

2. Compare the effectiveness of the nurse-administered, inpatient Tobacco Tactics
intervention versus usual care across hospitals, units, and patient characteristics
using biochemically confirmed 7-day point-prevalence abstinence at 6-month cessation as
the primary outcome.

3. Determine the cost-effectiveness of the nurse-administered, inpatient Tobacco Tactics
intervention versus usual care including the cost per quitter, cost per life-year
saved, and cost per quality-adjusted life-year saved.

Methods: This effectiveness study will be a cluster randomized control trial in 6 Michigan
community hospitals of which 3 will get the nurse-administered Tobacco Tactics intervention
and the other 3 will provide their usual care in accordance to how the hospital responds to
current Joint Commission on Accreditation of Healthcare Organization's (JC) standards. A
research nurse will disseminate the intervention in the 3 out of 6 sites to Master Trainers
who will teach staff nurses on all shifts on all units, until all staff nurses are trained.
The interventions will become the standard of care within the intervention sites. Research
nurses will also conduct rolling evaluation to identify barriers and facilitators to
dissemination and implement measures to ensure sustainability of the intervention. It is
expected that 7,868 inpatient smokers per year will be eligible to participate in the study
of which the investigators expect to recruit 2,350 to have sufficient power to analyze the
objectives. Descriptive statistics (means and frequency distributions) will be used to
summarize the nurses' survey results, participation rates, smokers' receipt of specific
cessation services, and satisfaction with services. Logistic regressions and t-tests will
be used to determine differences between intervention groups on satisfaction and quit rates,
respectively, with adjustment for the clustering of patients within units and hospitals.
Regression analyses will test the moderation of the effects of the interventions by patient
characteristics such as confidence in ability to quit, nicotine addiction, alcohol intake,
depression, demographics and a smoking related diagnosis such as heart disease.
Cost-effectiveness will be assessed by constructing 3 ratios including the cost per quitter,
cost per life-year saved, and the cost per quality-adjusted life-year saved.

Inclusion Criteria:

1. are at least 18 years of age;

2. have smoked within one month prior to hospitalization;

3. have a projected hospital stay of at least 24 hours; and

4. are willing to complete the interview surveys.

Exclusion Criteria:

1. are too ill to participate;

2. are terminal;

3. are involved in a concurrent trial that includes intervention on smoking; and

4. are non-English speaking (the intervention is currently only in English);

5. have significant cognitive impairment; and

6. have significant communication barriers.
We found this trial at
6
sites
Muskegon, Michigan 49444
?
mi
from
Muskegon, MI
Click here to add this to my saved trials
Ann Arbor, Michigan 48197
?
mi
from
Ann Arbor, MI
Click here to add this to my saved trials
Grand Rapids, Michigan 49503
?
mi
from
Grand Rapids, MI
Click here to add this to my saved trials
Livonia, Michigan 48154
?
mi
from
Livonia, MI
Click here to add this to my saved trials
Muskegon, Michigan 49442
?
mi
from
Muskegon, MI
Click here to add this to my saved trials
Pontiac, Michigan 48341
?
mi
from
Pontiac, MI
Click here to add this to my saved trials