Ignite Creation Date:
2024-05-06 @ 2:03 AM
Last Modification Date:
2024-10-26 @ 11:13 AM
Study NCT ID:
NCT01952236
Status:
COMPLETED
Last Update Posted:
2019-02-12
First Post:
2013-07-25
Brief Title:
Web and Mobile Smoking Cessation
Sponsor:
Oregon Research Institute
Organization:
Oregon Research Institute
Study Overview
Official Title:
Web and Mobile Smoking Cessation Interventions
Status:
COMPLETED
Status Verified Date:
2019-02
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
MobileQuit
Brief Summary:
This study seeks to develop and then perform a controlled efficacy Randomized Controlled Trial assessing tobacco abstinence of a best-practices Web-based PC-delivered smoking cessation intervention QuitOnline compared to a Mobile Smartphone-delivered intervention MobileQuit Study participants are randomized to one of two conditions a Web Only intervention and the WebMobile intervention The hypothesis is that the WebMobile approach will yield greater efficacy than the Web Only condition
Detailed Description:
The primary aims of this project are to
1 Use an iterative formative development process to create two separate Web-based smoking cessation programs WebMobile Web Only
2 Compare the efficacy of the two smoking cessation programs in terms of tobacco abstinence The investigators hypothesize that the WebMobile condition will be significantly more efficacious in terms of tobacco abstinence than the Web Only condition
3 Evaluate program usageparticipant engagement treatment acceptability and consumer satisfaction The investigators hypothesize that both conditions will be acceptable and that the WebMobile condition will have significantly greater usage and higher consumer satisfaction than the Web Only condition
The secondary aims of this proposal are to
1 Evaluate the differences between conditions on ancillary tobacco outcomes The investigators hypothesize that the participants assigned to the WebMobile condition who continue to smoke will nonetheless report a greater decline in the smoking rate and more quit attempts
2 Evaluate predictors and condition moderators of tobacco abstinence The investigators will conduct exploratory analyses of the association of treatment outcomes to participant characteristics eg baseline smoking rate nicotine dependence level partners tobacco use prior quitting attempts prior use of pharmacological adjuncts and other demographic factors
3 Evaluate putative mechanisms of change The investigators will test whether change in the putative mechanisms of change ie self-efficacy program use use of pharmacological adjuncts mediate the association between the intervention condition and 3-month sustained abstinence from the 3 month to 6 month assessments
1 Use an iterative formative development process to create two separate Web-based smoking cessation programs WebMobile Web Only
2 Compare the efficacy of the two smoking cessation programs in terms of tobacco abstinence The investigators hypothesize that the WebMobile condition will be significantly more efficacious in terms of tobacco abstinence than the Web Only condition
3 Evaluate program usageparticipant engagement treatment acceptability and consumer satisfaction The investigators hypothesize that both conditions will be acceptable and that the WebMobile condition will have significantly greater usage and higher consumer satisfaction than the Web Only condition
The secondary aims of this proposal are to
1 Evaluate the differences between conditions on ancillary tobacco outcomes The investigators hypothesize that the participants assigned to the WebMobile condition who continue to smoke will nonetheless report a greater decline in the smoking rate and more quit attempts
2 Evaluate predictors and condition moderators of tobacco abstinence The investigators will conduct exploratory analyses of the association of treatment outcomes to participant characteristics eg baseline smoking rate nicotine dependence level partners tobacco use prior quitting attempts prior use of pharmacological adjuncts and other demographic factors
3 Evaluate putative mechanisms of change The investigators will test whether change in the putative mechanisms of change ie self-efficacy program use use of pharmacological adjuncts mediate the association between the intervention condition and 3-month sustained abstinence from the 3 month to 6 month assessments
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None