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Helping Hospitalized Patients Quit Smoking

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ClinicalTrials.gov Identifier: NCT01575145
Recruitment Status : Completed
First Posted : April 11, 2012
Last Update Posted : January 11, 2016
Sponsor:
Information provided by (Responsible Party):
David Warner, Mayo Clinic

Brief Summary:

The study is being done to determine whether an in-hospital intervention using a brief intervention to facilitate quitline utilization will increase quitline utilization by hospitalized smokers, and will increase post hospital discharge smoking abstinence rates.

Study participants will be randomized to receive either a brief quitline facilitation intervention , or a control intervention of a brief stop-smoking message.

The study will also compare healthcare costs and utilization in the first six months following hospitalization between the two groups.


Condition or disease Intervention/treatment Phase
Tobacco Abuse Cigarette Behavioral: Quitline facilitation intervention Behavioral: Brief stop-smoking intervention Phase 4

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 600 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Participant)
Primary Purpose: Treatment
Official Title: Helping Hospitalized Patients Quit Smoking
Study Start Date : May 2012
Actual Primary Completion Date : November 2015
Actual Study Completion Date : November 2015

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Smoking

Arm Intervention/treatment
Experimental: Quitline facilitation intervention
brief quitline facilitation intervention given
Behavioral: Quitline facilitation intervention
brief quitline facilitation intervention

Active Comparator: Stop-smoking intervention
brief review of tips to maintain smoking abstinence, using brochure
Behavioral: Brief stop-smoking intervention
brief review of tips to help maintain smoking abstinence, using brochure




Primary Outcome Measures :
  1. 7-day point prevalence tobacco abstinence at 6 months after hospitalization [ Time Frame: 6 months after hospitalization ]

Secondary Outcome Measures :
  1. Self-efficacy [ Time Frame: Immediately after the delivery of the brief intervention (day of enrollment) ]
    Use of Smoking Self-Efficacy Questionnaire 12



Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

Current smoker, Resident of Olmsted County, Inpatient admission to St. Marys or Rochester Methodist Hospital, Able to participate fully in all study aspects, Available for follow-up

Exclusion Criteria:

Current active treatment for tobacco use initiated prior to hospitalization


Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01575145


Locations
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United States, Minnesota
Mayo Clinic in Rochester
Rochester, Minnesota, United States, 55905
Sponsors and Collaborators
Mayo Clinic
Investigators
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Principal Investigator: David Warner, MD Mayo Clinic
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
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Responsible Party: David Warner, Associate Director of Clinical and Translational Research, Mayo Clinic
ClinicalTrials.gov Identifier: NCT01575145    
Other Study ID Numbers: 12-002207
First Posted: April 11, 2012    Key Record Dates
Last Update Posted: January 11, 2016
Last Verified: January 2016
Additional relevant MeSH terms:
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Tobacco Use Disorder
Substance-Related Disorders
Chemically-Induced Disorders
Mental Disorders