Psychiatric Disorders, Tobacco Smoking
Conditions
Keywords
electronic cigarette use, smoking behavior
Brief summary
This study aims to establish the feasibility and acceptability of a project designed to investigate the impact of electronic cigarette use on combustible cigarette smoking and smoking-related factors among smokers with psychiatric disorders, a high-risk population, who are not yet ready to quit smoking. All participants will be instructed to switch completely from combustible cigarettes to e-cigarettes for the next 8 weeks. They will be assessed at baseline, 2 weeks, 4 weeks, 8 weeks and 12 weeks.
Detailed description
In recent years, the prevalence of e-cigarette use has rapidly increased, especially among those with psychiatric conditions, and the risks and potential benefits of e-cigarette use have been the topic of much debate. More research is needed to understand the impact of e-cigarette use on smoking behavior and smoking-related cognitions among individuals with psychiatric conditions. This study will investigate the effects of e-cigarette use on cigarette smoking and motivation/readiness to quit among smokers with psychiatric disorders who are not yet ready to quit smoking. A total of 50 adult daily cigarette smokers who are receiving outpatient psychiatric treatment and not yet ready to quit smoking will be recruited. All participants will be instructed to switch completely from combustible cigarettes to e-cigarettes for the next 8 weeks. E-cigarettes will be provided to participants at no cost. Participants will also be asked to complete 5 (remote and in-person) assessment sessions (i.e., baseline, 2-week, 4-week, 8-week and 12-week follow-ups).
Interventions
OTHERE-cigarette
All participants will be provided with 8 weeks of e-cigarettes at no cost based on self-report of regular cigarette use. All participants will receive a total of 8-10 remote counseling sessions (via phone or video conference) and during which they will discuss ways to switch from smoking cigarettes to exclusively using e-cigarettes, barriers and strategies to overcome them. (All participants will receive sessions at baseline, 2 days, 7 days, 2 weeks, 3 weeks, and 4 weeks, 6 weeks , and 8 weeks after the baseline assessment. Two additional sessions at 5 weeks and 7 weeks (after the baseline assessment) will be provided to those who are still smoking combustible cigarettes at 4-week assessment.)
Sponsors
Montefiore Medical Center
Dartmouth College
Fordham University
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
21 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* 21 years of age or older * English-speaking, * current daily smokers (i.e., at least 5 cigarettes/day) * have been daily smokers at least for 6 months * attended a minimum of 2 treatment visits in the past 12 months at Montefiore Behavioral Health Center * have at least one psychiatric disorder (other than substance use disorders), * willing to try switching to use e-cigarettes (provided by the research team) exclusively for a total of 8 weeks, * those who are not yet ready to quit smoking, * for women of childbearing age, willingness to use contraception during the study.
Exclusion criteria
* acute psychiatric symptomatology which precludes study participation including current active suicidal ideation * current diagnosis of dementia or cognitive impairment sufficient to impair provision of informed consent or study participation * patient's inability to provide consent for study participation due to his/her inability to demonstrate an understanding of study procedures as contained in the statement of informed consent, after no more than two explanations * current clinical diagnosis of intellectual development disorder * current regular use of other tobacco products or combustible marijuana * current (non-nicotine) substance use disorder and current substance use (in the past month) * current effort to quit smoking or current use of pharmacotherapy (in the past month) to quit smoking, * pregnant, breastfeeding, or planning to become pregnant within 6 months, current unstable cardiovascular disease, * current unstable pulmonary disease (i.e., an ER visit or hospitalization due to pulmonary issues in the past 6 month or current use of oxygen therapy), * patient does not have a stable home address where the research team could reliably reach patient * household members are currently participating or have participated in this research study
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Changes in the number of combustible cigarettes smoked per day | Baseline, 2 weeks, 4 weeks, 8 weeks, and 12 weeks | The average number of cigarettes smoked per day |
| Changes in Nicotine Dependence | Baseline, 2 weeks, 4 weeks, 8 weeks, 12 weeks | Fagerstrom Test of Cigarette Dependence |
| Changes in the use of e-cigarettes | Baseline, 2 weeks, 4 weeks, 8 weeks, 12 weeks | Changes in the use of e-cigarettes |
| Rates of those who completely switched to e-cigarettes | Baseline, 2 weeks, 4 weeks, 8 weeks, 12 weeks | Rates of those who completely switched to e-cigarettes |
| Changes in Carbon Monoxide Level | Baseline,2 weeks, 4 weeks, 8 weeks, 12 weeks | Changes in Carbon monoxide level measured with a breath carbon monoxide monitor |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Changes in Withdrawal Symptoms | Baseline, 2 weeks, 4 weeks, 8 weeks, 12 weeks | Minnesota Nicotine Withdrawal Scale |
| Changes in Motivation/Readiness to Quit Smoking | Baseline, 2 weeks, 4 weeks, 8 weeks, 12 weeks | Thoughts about Abstinence Scale & Contemplation Ladder |
Countries
United States
Contacts
Primary ContactHaruka Minami, Ph.D.
Outcome results
None listed