OCAST Cessation Study

Tobacco Use Cessation Clinical Trial

— OCAST  

Official title:

Matching Brief Smoking Interventions to Stage of Change

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01921439
• Other study ID #: 3262
• Status: Completed
• Phase: N/A
• First received: August 8, 2013
• Last updated: April 7, 2017
• Start date: July 2013
• Est. completion date: December 2016

Study information

• Verified date: April 2017
• Source: University of Oklahoma
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The long-term goal is to improve the quality of life of children and their parents who smoke tobacco by facilitating parental smoking cessation in a way that is easy to administer yet effective. We aim to accomplish this goal by administering an interactive computer-based program that will facilitate motivation and readiness to engage in smoking cessation by providing personalized feedback about the financial and health effects of the parent's smoking. We will compare the changes in motivation and readiness to quit smoking after the parent has taken the computer-based program and compare them to the changes in motivation and readiness to quit in parents who receive only information about the Oklahoma Tobacco Helpline. We will also measure salivary cotinine levels in both parents and children, to objectively measure changes in smoking habits and secondhand smoke exposure. Our hypothesis is that our computer-based program will cause a greater increase in motivation and confidence to quit smoking in the group that receives the customized feedback than the group that receives only information about the Tobacco Helpline. We also predict that both parent and child cotinine levels will show a greater decrease in the group randomized to receive personalized feedback.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 152
• Est. completion date: December 2016
• Est. primary completion date: December 2016
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• Parent or primary caregiver of a child patient at the OU Children's Physicians General Pediatrics clinics

• Current cigarette user

• Able to read study forms and verbally communicate with the study staff in English

Exclusion Criteria:

• Nonsmokers

• Unable to read or speak English well enough to complete the survey and study tasks

Related Conditions & MeSH terms

• Cigarette Smoking Behavior
• Second Hand Tobacco Smoke
• Tobacco Smoking Behavior
• Tobacco Use Cessation

Intervention

Behavioral:
• Personalized Feedback
Personalized feedback reflecting the participant's current level of nicotine addiction, money spent on cigarettes, time spent smoking, and health effects of smoking.

Locations

Country	Name	City	State
United States	Oklahoma Tobacco Research Center	Oklahoma City	Oklahoma

Sponsors (2)

Lead Sponsor	Collaborator
University of Oklahoma	Oklahoma Center for the Advancement of Science and Technology

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Self-Reported Readiness and Motivation to Quit Smoking	We will assess changes in self-reported readiness and motivation to quit smoking.	Baseline, 1-month, 6-months, 12-months
Primary	Parent and Child Salivary Cotinine	We will assess change in parent and child salivary cotinine throughout the course of the study.	Baseline, 1-month, 6-months, and 12-months
Primary	Change in self-reported cigarette use	We will assess changes in self-reported cigarette use throughout the study.	baseline, 1-month, 6-months, and 12-months