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Clinical Trials/NCT00656500
NCT00656500CompletedNot Applicable

Increasing QUITPLAN Helpline Utilization in Surgical Patients

Mayo Clinic1 site in 1 country300 target enrollmentStarted: July 1, 2007Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
300
Locations
1
Primary Endpoint
Completion of one quitline counseling session

Study Overview

Brief Summary

Elective surgery represents a teachable moment to deliver tobacco interventions. The overall goal of this proposal is to increase the utilization of the QUITPLANSM Helpline by surgical patients who smoke. Two specific aims will be pursued using a multidisciplinary research team. In the first aim, we will develop a practice-based intervention to promote QUITPLANSM Helpline utilization by surgical patients (Specific Aim 1A) using a combination of key informant interviews (approximately 30 subjects), and focus groups (approximately 25 subjects) then develop methods to educate providers in its implementation (Specific Aim 1B) and test their effectiveness in approximately 20 providers. In the second aim, we will perform a randomized clinical trial of this intervention in 300 patients scheduled for elective surgery, with the primary outcome being utilization of the QUITPLANSM Helpline (Specific Aim 2). Subjects will be randomized to receive either the intervention developed in Specific Aim 1, or a brief control intervention.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Single Group
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Patients ≥ 18 yrs. scheduled for elective surgery at Mayo Clinic Rochester.
  • •Current smoking before the scheduling of surgery, defined as > 100 cigarettes lifetime consumption and self-reports of smoking either every day or some days. Patients who are in the midst of a quit attempt initiated since learning about surgery are eligible.

Exclusion Criteria

  • •Patient is not available for telephone follow-up

Arms & Interventions

1

Active Comparator

Brief assistance with smoking abstinence

Intervention: Standard brief advice (Behavioral)

2

Experimental

Brief intervention to promote quitline utilization

Intervention: Quitline intervention (Behavioral)

Outcomes

Primary Outcomes

Completion of one quitline counseling session

Time Frame: Three months postoepratively

Secondary Outcomes

  • Smoking behavior at six months postoperatively(six months postoperatively)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

David Warner

MD

Mayo Clinic

Study Sites (1)

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