| Registry | NCT02433015, acronym ECIG |
|---|---|
| Status | Completed |
| Phase | Not applicable |
| Study type | Interventional; randomized, parallel, masking: single, basic science |
| Enrollment | 27 (Actual) |
| Sponsor | Laureate Institute for Brain Research, Inc. (Other); collaborators: University of Oklahoma |
| Conditions | Tobacco Smoking, Nicotine Dependence |
| Interventions | Electronic Cigarette, Tobacco Cigarette (Other) |
| Dates | start 2015-01-01, primary completion 2016-09-24, completion 2016-09-24, first posted 2015-05-04, last updated 2017-06-28 |
| Locations | 1 site in United States |
Related Papers Related Patents Related Grants Related Experts
All trials for Tobacco Smoking All trials for Nicotine Dependence All trials of Electronic Cigarette All trials of Tobacco Cigarette
The objective of this study is to examine the cognitive, immunological, and neurophysiological effects of transitioning from tobacco cigarettes to electronic cigarettes. The central hypothesis of this study is that this transition will be accompanied by a decrease in peripheral inflammation, which will lead to significant changes in the neurocircuitry underlying interoception and appetite.
Participants who are current cigarette smokers will be randomly assigned to either the experimental or control groups. Following a baseline psychiatric assessment session, subjects will return to the study center for two to three additional follow-up visits.
During the second visit, all subjects will undergo a functional magnetic resonance imaging (fMRI) scanning session, during which they will perform a series of functional neuroimaging tasks designed to examine the neural substrates involved in visceral interoception and eating behavior. Prior to the start of the scan session, blood samples will be collected from each subject, for the measurement of bio-markers related to nicotine use and peripheral inflammation. After the end of the second visit, subjects within the experimental group will be asked to switch from combustible to electronic cigarettes. Subjects within the control group will continue to smoke combustible cigarettes as previously.
During the third visit, which will follow two to eight weeks after the second visit, all subjects will provide a second blood sample and complete a second fMRI scan session. Both groups of participants will complete the same fMRI tasks as they did during the second visit.
| Arm | Type | Interventions | Description |
|---|---|---|---|
| Tobacco Cigarette Group | Active comparator | Other: Tobacco Cigarette | This group will not receive an electronic cigarette and will continue to smoke combustible tobacco cigarettes as previously. |
| Electronic Cigarette Group | Experimental | Other: Electronic Cigarette | This group will receive an electronic cigarette to use for the duration of the study. |
Sex: All, ages: 18 Years to 50 Years, accepts healthy volunteers
Inclusion Criteria: * current cigarette smokers who have smoked for at least one year * right-handed adults * able to provide written informed consent Exclusion Criteria: * use of anticonvulsant, stimulant, or antipsychotic medication for 3 weeks prior to scanning * any medical conditions or medications likely to influence cerebral blood flow or neurological function including cardiovascular, respiratory, endocrine and neurological diseases * any history of drug (other than nicotine) or alcohol abuse within 1 year * current pregnancy or breast feeding * primary language other than English * meeting general MRI exclusion criteria such as magnetic implants or claustrophobia * Past history of any axis I psychiatric condition, other than major depressive disorder and post-traumatic stress disorder * Current major depression or post-traumatic stress disorder * Serious suicidal ideation
| Facility | City | Country | Status |
|---|---|---|---|
| Laureate Institute for Brain Research | Tulsa, Oklahoma | United States |