146
Participants
Start Date
October 1, 2011
Primary Completion Date
June 1, 2014
Study Completion Date
January 1, 2015
Nicotine Replacement Patch
Study participants will receive a baseline assessment after they consent to participate and before randomization. The intervention period will last 12 weeks (approximately 1 week for the in-office intervention and 12 weeks for all components of the Quitline intervention- telephone counseling and habitrol patches). Follow-up assessments will be administered at 3, 6, 12, \& 24 weeks after the date of the in-person intervention (for Quitline Intervention group) or the provision of the physician letter (for the Usual Care Plus group).
W F Baptist Health, Winston-Salem
National Cancer Institute (NCI)
NIH
Wake Forest University Health Sciences
OTHER