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NCT04510077 Clinical Trial

SmartQuit Program for Smoking Cessation

Cigarette Smoking-Related Carcinoma Clinical Trial

Official title:
Study of SmartQuit, a Smartphone-Based Smoking Cessation Program

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04510077
Other study ID # RG1001139
Secondary ID NCI-2020-0565882
Status Completed
Phase N/A
First received
Last updated
Start date October 22, 2014
Est. completion date August 11, 2015

Study information
Verified date August 2020
Source Fred Hutchinson Cancer Research Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This trial investigates how well a smartphone-based smoking cessation program called SmartQuit works to help patients stop smoking. SmartQuit is an smartphone application-based smoking cessation program that includes a defined program consisting of interactive evidence-based exercises for dealing more effectively with urges to smoke, a place to track desired behaviors, personalized plans for quitting, and a certificate of completion once the recommended program components are completed. SmartQuit may help patients quit smoking, lower healthcare costs and reduce premature tobacco-related deaths.

Description:

OUTLINE:

Patients use the SmartQuit program to learn and practice skill modules as often as they wish over 6 months.

Recruitment information / eligibility
Status Completed
Enrollment 99
Est. completion date August 11, 2015
Est. primary completion date May 31, 2015
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Smokes at least five cigarettes daily for at least past 12 months

- Wants to quit in the next 30 days

- Interested in learning skills to quit smoking

- Resides in United States (US)

- Has at least daily access to their own smartphone

- Knows how to login and download a smartphone application from their smartphone

- Willing and able to read in English

- Not participating in other smoking cessation interventions (including our other intervention studies)

- Must be an employee of a company who is participating in recruitment

- Willing to complete one follow-up survey

- Provide email, phone, and mailing address

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• SmartQuit Smoking and Tobacco Cessation Program
Use SmartQuit program
Other:
• Survey Administration
Ancillary studies

Locations
Country Name City State
United States Fred Hutch/University of Washington Cancer Consortium Seattle Washington

Sponsors (2)
Lead Sponsor Collaborator
Fred Hutchinson Cancer Research Center Life Sciences Discovery Fund

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Number of participants with 7-day cigarette smoking cessation at 2 months. No smoking at all in the past 7 or more days (7-day point prevalence quit rate). At 2 month follow-up
Secondary 24-hour point prevalence quit rate At 2 month follow-up
Secondary Change in number of cigarettes smoked per day At 2 month follow-up
Secondary Number of intentional 24-hour quit attempts At 2 month follow-up
Secondary Change in readiness to quit Differences in a participant's readiness to quit will be assessed by comparing their responses to the baseline survey readiness to quit questions with their responses to the 2 month follow-up survey At 2 month follow-up
Secondary Nicotine dependence level Participants will share their nicotine dependence level via survey at their 2 month follow-up At 2 month follow-up
Secondary Number of times logged into the application Will be assessed via 2 month follow-up survey At 2 month follow-up
Secondary Time spent on the application Will be assessed via 2 month follow-up survey At 2 month follow-up
Secondary Participant satisfaction with the application Will be assessed via 2 month follow-up survey At 2 month follow-up
Secondary Participant opinion of the usefulness of the application for quitting smoking Will be assessed via 2 month follow-up survey At 2 month follow-up
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