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Evaluating a Telemedicine Smoking Cessation Program in Rural Primary Care Practices

Telemedicine for Smoking Cessation in Rural Primary Care

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00843505
Enrollment
566
Registered
2009-02-13
Start date
2009-06-30
Completion date
2012-04-30
Last updated
2012-10-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Smoking

Keywords

Smoking Cessation, Motivational Interviewing, Quitline, Telemedicine, Stop Smoking Medication

Brief summary

People who smoke cigarettes and live in rural areas may not have access to a wide variety of resources to help them stop smoking. This study will evaluate two smoking cessation programs-an Internet-based telemedicine program and a telephone-based quitline program-among rural residents.

Detailed description

People who live in rural areas are more likely to smoke cigarettes than people who live in urban and suburban areas. However, many smoking cessation resources and programs may not be available to residents of rural areas. Toll-free tobacco telephone quitlines are proven to help people stop smoking and are available to almost everyone living in the United States, but only 1% to 5% of smokers actually use them. Another option for helping people stop smoking may involve having doctors provide smoking cessation programs in their offices or clinics; however, most doctors' offices do not have the resources to provide this type of service. Telemedicine provides medical information over the phone or through the Internet by using various technologies, including Webcams or video conferencing equipment. It has been used successfully to provide psychiatric care and addictions counseling, but there have been no studies that have examined the effectiveness of a telemedicine smoking cessation program. The purpose of this study is to compare the effectiveness of a telemedicine smoking cessation program that takes place in a doctor's office versus the effectiveness of a traditional telephone quitline smoking cessation program among rural smokers. The study will be conducted at 25 rural doctors' offices in Kansas. Participants will be randomly assigned to participate in a telephone quitline program or a telemedicine program. Participants in the telephone quitline program will receive four sessions of telephone quitline counseling from smoking cessation counselors over an 8-week period. Participants in the telemedicine program will receive four sessions of telemedicine counseling from smoking cessation counselors over an 8-week period, which will be delivered through two-way Webcams at computers in the doctors' offices. All participants will receive educational handouts and individually tailored quit plans, including information on smoking cessation medications. At baseline and Months 3, 6, and 12, all participants will take part in telephone interviews with study researchers to assess smoking habits. At baseline and Month 12, participants will mail a saliva sample to researchers for the purposes of determining the level of nicotine in the body.

Interventions

BEHAVIORALTelephone Quitline Smoking Cessation Program

Participants will receive four sessions of smoking cessation counseling delivered by telephone in their homes over an 8-week period.

BEHAVIORALTelemedicine Smoking Cessation Program

Participants will receive four sessions of telemedicine smoking cessation counseling over an 8-week period. The telemedicine sessions will be delivered by two-way Webcams mounted on desktop computers in the doctors' offices.

Sponsors

National Heart, Lung, and Blood Institute (NHLBI)
CollaboratorNIH
Kimber Richter, PhD, MPH, MA
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Smokes cigarettes every day * Smokes five or more cigarettes per day * Has smoked cigarettes for at least 1 year before study entry * Has a home address and phone number * Willing to participate in phone assessments * Willing to be assigned to either of the two study programs

Exclusion criteria

* Pregnant or breastfeeding * Another household member is enrolled in the study * Moving out of the area of residence in the 14 months after study entry * Primary care provider is not participating in the study * Use of other forms of tobacco products (e.g., cigars, spit, snuff) in addition to cigarettes * Use of a smoking cessation medication

Design outcomes

Primary

MeasureTime frame
7-day point prevalence abstinenceMeasured at Months 3, 6, and 12

Secondary

MeasureTime frame
Prolonged abstinenceMeasured at Months 3, 6, and 12

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 20, 2026