- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01181661
Internet-based Group Contingency Management to Promote Smoking Abstinence
September 23, 2014 updated by: Jesse Dallery, National Development and Research Institutes, Inc.
The purpose of the study is to develop and test an Internet-based group contingency management program designed to promote smoking cessation.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
40
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Florida
-
Gainesville, Florida, United States, 32611
- University of Florida
-
-
New York
-
New York City, New York, United States, 10010
- National Development and Research Institutes
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 60 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- self-reported smoker
- ability to use the Internet
- permission to contact applicant by phone
Exclusion Criteria:
- self-report of a history of or current severe or unstable medical or psychiatric illness that would interfere with the study
- inability to avoid high levels of ambient CO (e.g., occupational exposure; lives with a another smoker who smokes in the home)
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Full Group Contingency
This group (n = 20) will earn vouchers based only on team (n = 4) performance.
Only if all members of the team submit a negative sample (CO ≤ 4 ppm), will they each earn a voucher.
|
This group (n = 20) will earn vouchers based only on team (n = 4) performance.
Only if all members of the team submit a negative sample (CO ≤ 4 ppm), will they each earn a voucher.
|
Experimental: Mixed Group Contingency
This group (n = 20) will earn vouchers based on both individual and team (n = 4) performance.
If an individual submits a negative sample (CO ≤ 4 ppm), s/he will earn a voucher.
Additionally, bonus vouchers will be earned if all team members submit negative samples.
|
This group (n = 20) will earn vouchers based on both individual and team (n = 4) performance.
If an individual submits a negative sample (CO ≤ 4 ppm), s/he will earn a voucher.
Additionally, bonus vouchers will be earned if all team members submit negative samples.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Breath CO
Time Frame: 8 weeks
|
Twice daily breath CO samples obtained during baseline and treatment
|
8 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Point prevalence measure of abstinence
Time Frame: at the end of treatment (approximately week 4) and at 3 month follow-up
|
Abstinence will be defined as: (a) CO sample ≤ 4 ppm; (b) cotinine < 50 ng/ml; and (c) reporting not smoking, not even a puff in the last 7 days.
|
at the end of treatment (approximately week 4) and at 3 month follow-up
|
Duration of abstinence during treatment.
Time Frame: 3 weeks
|
The longest duration of sustained abstinence (CO ≤ 4 ppm) based on the twice-daily breath samples during the treatment period.
|
3 weeks
|
Rate of social exchanges
Time Frame: 3 weeks
|
The number of comments posted on the discussion forum during treatment.
|
3 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Principal Investigator: Jesse Dallery, PhD, National Development and Research Institutes, Inc.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
August 1, 2010
Primary Completion (Actual)
August 1, 2013
Study Completion (Actual)
August 1, 2013
Study Registration Dates
First Submitted
August 12, 2010
First Submitted That Met QC Criteria
August 12, 2010
First Posted (Estimate)
August 13, 2010
Study Record Updates
Last Update Posted (Estimate)
September 25, 2014
Last Update Submitted That Met QC Criteria
September 23, 2014
Last Verified
September 1, 2014
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 1R21DA029162 (U.S. NIH Grant/Contract)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Cigarette Smoking
-
Maastricht University Medical CenterCompletedCigarette Smoking | Cigarette Smoking Toxicity | Smoking BehaviorNetherlands
-
Duke UniversityGeorgetown University; University of MichiganWithdrawnSmoking | Cigarette Smoking | E-cigarette Use
-
Assistance Publique - Hôpitaux de ParisUnknownSmoking Cessation | Smoking, Cigarette | Electronic CigaretteFrance
-
Yale UniversityNational Cancer Institute (NCI)RecruitingSmoking Cessation | Cigarette Smoking | E-Cigarette UseUnited States
-
Medical University of South CarolinaAmerican Cancer Society, Inc.RecruitingSmoking Cessation | Electronic Cigarette Use | Cigarette SmokingUnited States
-
Abramson Cancer Center at Penn MedicineNational Cancer Institute (NCI); New York University; Stanford UniversityRecruitingSmoking | Smoking, Tobacco | Smoking, CigaretteUnited States
-
University of St AndrewsNational Health Service, United KingdomUnknownSmoking | Cigarette Smoking | Smoking, Tobacco
-
University GhentRecruitingSmoking | Smoking Tobacco | Smoking Prevention | Smoking CigaretteBelgium
-
Medical University of South CarolinaCompletedSmoking | Smoking Cessation | Smoking, Tobacco | Smoking, CigaretteUnited States
-
BIDI VaporCompletedCigarette Smoking | E-cigarette UsePoland
Clinical Trials on Full Group Contingency
-
Semmelweis UniversityInstitut Straumann AG; Geistlich Pharma AG; Dicomlab Kft.Recruiting
-
Kahramanmaras Sutcu Imam UniversityCompletedFemur Intertrochanteric FracturesTurkey
-
Aalborg University HospitalCompletedScoliosis | Kyphosis | Neurosurgery | Hypothermia Following Anesthesia | Forced Air Warming | Major Spinal Fusion
-
Centre for Addiction and Mental HealthRecruitingCognitive Impairment | Major Depressive Disorder | Cannabis UseCanada
-
Beth Israel Deaconess Medical CenterCompletedObesity | Weight LossUnited States
-
VA Office of Research and DevelopmentRecruitingPTSD | Cannabis-Related DisorderUnited States
-
Cambridge University Hospitals NHS Foundation TrustNorfolk and Norwich University Hospitals NHS Foundation Trust; Luton and Dunstable... and other collaboratorsRecruitingNeonatal SeizuresUnited Kingdom
-
Microclinic InternationalRoyal Health Awareness Society (RHAS); Jordanian Ministry of Health (MoH)CompletedHyperglycemia | Hypertension | Obesity | Diabetes Mellitus, Type 2 | Diabetes Mellitus | Diabetes | Body Weight | Weight Loss | Blood Pressure | Weight Gain | Social Behavior | Weight, Body | Glucose, High Blood | Lifestyle, Healthy | Weight Change, Body | Behavior, Health | Lifestyle Risk Reduction | Blood Pressure, High | Hyperglycaemia... and other conditionsJordan
-
Tanta UniversityCompletedLipid Profile | Intrauterine Growth Restriction | NeonatesEgypt
-
Columbia UniversityNational Institute on Drug Abuse (NIDA); Johns Hopkins University; University... and other collaboratorsCompletedHIV | Substance Abuse | Inpatient | AIDSUnited States