Pager-Assisted Smoking Cessation Treatment

University of California San Francisco (UCSF)

Status: Completed

Conditions: Smoking Cessation

Treatments: Device: alphanumeric pager; Behavioral: smoking cessation counseling; Drug: Nicotine patch

Study type: Interventional

Funder types: Other

Identifiers

NCT01207310

11RT0009

Details and patient eligibility

About

The proposed study tests the efficacy of using pager-assisted messages combined with nicotine patches in facilitating smoking cessation and relapse prevention in a 2-arm randomized clinical trial. The hypothesis is that the proportion of biochemically-verified quitters at 3 and 12 months in the study arm randomized to receive therapeutic messages on alphanumeric pagers for 3 months along with individual smoking cessation counseling and nicotine patches will be greater that the proportion of biochemically-verified quitters who receive only individual smoking cessation counseling and nicotine patches.

Full description

A total of 224 current smokers were enrolled in a randomized controlled smoking cessation trial. Participants were community-living adult smokers of ≥10 cigarettes per day during the pre-enrollment week who were interested in quitting and recruited from the local area by means of print, media, and online advertisements. To be eligible, they needed to be smoking 10 or more cigarettes per day, aged 18 or older, motivated to quit smoking, prepared to set a quit date, willing to use nicotine patches, and able to come to therapy sessions and be followed by telephone. Participants in the pager treatment were provided with alpha-numeric pagers free of charge for three months. Using specially-designed communication software, text messages were sent to participants aimed at facilitating motivation to quit, cessation strategies, and coping skills to maintain abstinence. Participants in both treatment groups were seen for two 60-minute sessions of standard smoking cessation counseling, and received three follow-up phone calls and two months of nicotine patches.

Enrollment: 224 patients

Sex: All

Ages: 18 to 80 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• smoking 10 or more cigarettes per day
• aged 18 or older
• motivated to quit smoking and prepared to set a quit date
• willing to use nicotine patches
• ability to come to therapy sessions and be followed by telephone

Exclusion criteria

• individuals who are psychotic
• severely depressed
• organically brain impaired
• actively abusing alcohol or other substances, and/or who have been drug dependent during the past six months
• terminally ill
• unable to be contacted by phone,currently using nicotine replacement or smoking cessation medications
• those with contraindications to nicotine patches, female smokers who are pregnant or breastfeeding

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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224 participants in 2 patient groups

Pager Arm

Experimental group

Description:

Participants in the Pager Arm will be provided with alphanumeric pagers and will receive therapeutic messages on these pagers for 3 months in addition to individual smoking cessation counseling and nicotine patches.

Treatment:

Drug: Nicotine patch

Behavioral: smoking cessation counseling

Device: alphanumeric pager

Control Arm

Active Comparator group

Description:

Participants in the Control Arm will receive individual smoking cessation counseling and nicotine patches.

Treatment:

Drug: Nicotine patch

Behavioral: smoking cessation counseling