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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01575119
Other study ID # 11-009150
Secondary ID
Status Completed
Phase Phase 3
First received April 5, 2012
Last updated December 16, 2014
Start date May 2012
Est. completion date January 2014

Study information

Verified date December 2014
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

Smokers have three choices when faced with surgery: keep smoking, quit for a short time around surgery or quit for good. In the first specific aim, a decision aid was designed to help facilitate the discussion of these choices between smokers and healthcare providers. This second aim will test whether this decision aid improves the decisional quality compared with standard methods used to discuss perioperative smoking.


Recruitment information / eligibility

Status Completed
Enrollment 130
Est. completion date January 2014
Est. primary completion date January 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Current cigarette smoker

- Scheduled to undergo elective surgery at Mayo Clinic Rochester

- Age 18 years or older

- Able to fully participate in all study aspects

Exclusion Criteria:

- Unavailable for telephone follow-up

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Supportive Care


Related Conditions & MeSH terms


Intervention

Behavioral:
Decision Aid
Decision Aid tool is presented by respiratory therapist, prompting a discussion with the provider (physician or physician assistant)about smoking around time of surgery
Control intervention
Standard of care information, including distributing patent education brochure, to provide information regarding perioperative smoking
Decision Aid
Decision Aid tool is presented by respiratory therapist, prompting a discussion with the provider (physician or physician assistant)about smoking around time of surgery
Control
Standard of care information, including distributing patient education brochure, to provide information regarding perioperative smoking

Locations

Country Name City State
United States Mayo Clinic in Rochester Rochester Minnesota

Sponsors (1)

Lead Sponsor Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Measures of decisional quality The Decisional Conflict Scale and the OPTION Scale will be utilized Assessed immediately after the time of the preoperative conversation in the preoperative clinic No
Secondary Measures of intent and self-efficacy Intent to quit smoking, and self-efficacy for quitting Immediately after the preoperative evaluation in the preoperative clinic No
See also
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