Skip to content

Contingency Management and Pharmacotherapy for Smoking Cessation

Contingency Management and Pharmacotherapy for Smoking Cessation

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00683280
Acronym
Donaghue
Enrollment
59
Registered
2008-05-23
Start date
2008-05-31
Completion date
2010-08-31
Last updated
2018-01-16

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

Conditions

Cigarette Smoking

Keywords

Contingency Management, Cigarette Smoking Cessation, varenicline

Brief summary

In total, 70 smokers will be randomized to: standard of care smoking cessation medication varenicline alone (an FDA-approved smoking cessation medication) or varenicline plus contingency management (CM) (a behavioral procedure with rewards for target behaviors, like smoking abstinence). Patients in both conditions will receive varenicline for 12 weeks with standard smoking cessation therapy and regular breath and urine sample monitoring for smoking. Patients assigned to CM will earn chances to win prizes for each breath sample that tests negative for smoking, and urine samples that test negative for smoking will result in even greater chances for prizes. More CM patients are expected to achieve and maintain abstinence than patients receiving varenicline alone.

Interventions

BEHAVIORALcontingency management

Prize-based contingency management, with the opportunity to earn prizes for expired carbon monoxide levels reading 6ppm or less and urinary cotinine levels reading 30ng/ml or less for 4 weeks.

OTHERStandard of Care

varenicline (smoking cessation medication) 0.5mg po daily Days 1-3, 0.5mg po twice daily Days 4-7, 1.0 mg po twice daily Days 8-84.

Sponsors

Donaghue Medical Research Foundation
CollaboratorOTHER
UConn Health
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

* smoke \>10 cigarettes/day, with no abstinent period exceeding 3 months in past year * expired CO of \>8 ppm * self-reported desire to stop smoking * \>18 years of age * resting systolic BP\<160 mmHg and diastolic BP\<100 mmHg and otherwise in good health * if on antihypertensive medication, have not changed medications in the past month and do not intend to change in next 3 months * English speaking

Exclusion criteria

* receipt of smoking cessation treatment (behavioral or pharmacological) in past month * serious or unstable medical disease in past 6 months, including myocardial infarction, cancer, congestive heart failure, kidney failure, stroke, or seizures * evidence or history of allergic reactions contraindicating varenicline or clinically significant laboratory or electrocardiographic (ECG) abnormalities * breastfeeding, pregnant or not using effective contraception if a woman of childbearing potential * arm circumference of \>42 cm * serious psychiatric illness in past 6 months (e.g., schizophrenia, psychosis, suicide risk, drug or alcohol dependence other than nicotine) * use of tobacco containing products other than cigarettes in past month and do not agree to abstain from use of these products during study participation * ongoing use of any of the following medications: nicotine replacement therapies, monoamine oxidase inhibitors, antipsychotics, mood stabilizers, or naltrexone * in recovery for pathological gambling, due to potential similarity with prize CM, although no increases in gambling have been noted

Design outcomes

Primary

MeasureTime frame
Smoking abstinence based on expired carbon monoxide tests, urinary cotinine tests and self-report.weeks 5, 12 & 24

Secondary

MeasureTime frame
Changes from baseline in ambulatory 24-hour systolic blood pressure.6 and 24 weeks following the initiation of medication

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026