Skip to main content
Clinical Trials/NCT04460417
NCT04460417CompletedNot Applicable

Health Behavior and Feedback Among Chicago Area Communities

University of Chicago2 sites in 1 country204 target enrollmentStarted: October 1, 2017Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
204
Locations
2
Primary Endpoint
Smoking reduction

Study Overview

Brief Summary

The study examined smokers from the initial COMPASS survey who live in one of three local Census tracks with large concentrations of minority populations and smoking rates, including Washington Park (98.8% African American, 60.5% smoker), Gage Park (76.7% Hispanic, 26.7% smoker), and Bridgeport (34.5% Asian, 27.0% Hispanic, 29.3% smoker), randomizing them to receipt of treatment as usual care advice (via a pamphlet form the National Cancer Institute) versus theoretically-driven and empirically-supported smoking cessation advice session delivered in-person at the UCM.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Currently reside in either the Washington Park, Gage Park, or Bridgeport communities based on current physical address at the time of initial contact for study participation
  • Identify as a current smoker (verified by self-report and exhaled carbon monoxide)
  • Willing and able to sign an informed consent
  • Stable residence and contact information throughout the follow-up period

Exclusion Criteria

  • Not a current smoker
  • Does not live within the pre-determined neighborhood locations
  • Unable to sign informed consent

Arms & Interventions

Treatment as Usual

Active Comparator

Participants will receive the National Cancer Institute (NCI) pamphlet "Clearing the Air" and access to related online resources, which includes brief advice to quit smoking and medication information.

Intervention: TAU (Behavioral)

Outcomes

Primary Outcomes

Smoking reduction

Time Frame: Past-week CPD at 1- and 6-month follow-up

Change in average cigarettes per day (CPD)

Quit attempts

Time Frame: Any reported (and serious) quit attempts since last session at 1- and 6-month follow-up

Change in number of any and serious (12+hr) quit attempts

Motivation to change smoking

Time Frame: Increases in stage of change at 1- and 6-month follow-ups

Increase in motivation to change smoking behavior via smoking contemplation ladder (Biener-Abrams Contemplation Ladder) scores. Scores are on a 10-point scale from 0-10, with higher scores indicating higher motivation to quit smoking.

Nicotine Replacement Therapy (NRT) use

Time Frame: Any reported NRT use since last session at 1- and 6- month follow-up

Change in frequency of NRT use

Nicotine Replacement Therapy (NRT) knowledge

Time Frame: More accurate knowledge about NRT at 1- and 6-month follow-ups

Increase in accurate knowledge about NRT assessed by two items rated from a 1 (strongly disagree) to 7 (strongly agree) scale measuring agreement to the NRT myths, "NRT causes cancer" and "NRT is only used by weak people".

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

Loading locations...

Similar Trials