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Smoking Cessation in Rural Hospitals

NCT01063972 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 606

Last updated 2019-04-08

Study results available
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Summary

Our long-term goal is to improve smoking cessation treatment for rural smokers. The objective is to assess the effectiveness of a centralized disease management program for hospitalized smokers that coordinates care across treatment settings and links smokers to existing resources. Our central hypothesis is that Centralized Disease Management (CDM) will increase the use of smoking cessation treatments and lead to greater long term smoking cessation than Counseling alone. Demonstrating the effectiveness of a disease management program and identifying the critical components of such a program will provide a basis for improving the utilization of existing smoking cessation resources while enhancing the treatment of rural hospitalized smokers.

Conditions

  • Smoking Cessation

Interventions

BEHAVIORAL

Centralized disease management (CDM)

Centralized Disease Management (CDM) arm will receive smoking cessation counseling with coordination of pharmacotherapy with their insurance coverage and their health care provider

BEHAVIORAL

Counseling (C)

Counseling (C) arm will receive counseling without the care coordination services.

Sponsors & Collaborators

  • National Cancer Institute (NCI)

    collaborator NIH

  • Edward Ellerbeck, MD, MPH

    lead OTHER

Principal Investigators

  • Edward Ellerbeck, MD, MPH · University of Kansas Medical Center

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2010-03-31
Primary Completion
2015-02-28
Completion
2015-02-28

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01063972 on ClinicalTrials.gov