Tobacco Smoking Clinical Trial
Official title:
The Effect of Electronic Cigarette Use on Smoking Behaviors and Smoking-related Factors Among Smokers Receiving Outpatient Psychiatric Treatment
NCT number | NCT04014322 |
Other study ID # | 1089 |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | December 12, 2020 |
Est. completion date | December 2024 |
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.
Status | Recruiting |
Enrollment | 50 |
Est. completion date | December 2024 |
Est. primary completion date | September 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 21 Years and older |
Eligibility | 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 |
Country | Name | City | State |
---|---|---|---|
United States | Montefiore Behavioral Health Center | Bronx | New York |
Lead Sponsor | Collaborator |
---|---|
Fordham University | Dartmouth College, Montefiore Medical Center |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Changes in the number of combustible cigarettes smoked per day | The average number of cigarettes smoked per day | Baseline, 2 weeks, 4 weeks, 8 weeks, and 12 weeks | |
Primary | Changes in Carbon Monoxide Level | Changes in Carbon monoxide level measured with a breath carbon monoxide monitor | Baseline,2 weeks, 4 weeks, 8 weeks, 12 weeks | |
Primary | Changes in Nicotine Dependence | Fagerstrom Test of Cigarette Dependence | Baseline, 2 weeks, 4 weeks, 8 weeks, 12 weeks | |
Primary | Changes in the use of e-cigarettes | Changes in the use of e-cigarettes | Baseline, 2 weeks, 4 weeks, 8 weeks, 12 weeks | |
Primary | Rates of those who completely switched to e-cigarettes | Rates of those who completely switched to e-cigarettes | Baseline, 2 weeks, 4 weeks, 8 weeks, 12 weeks | |
Secondary | Changes in Motivation/Readiness to Quit Smoking | Thoughts about Abstinence Scale & Contemplation Ladder | Baseline, 2 weeks, 4 weeks, 8 weeks, 12 weeks | |
Secondary | Changes in Withdrawal Symptoms | Minnesota Nicotine Withdrawal Scale | Baseline, 2 weeks, 4 weeks, 8 weeks, 12 weeks |
Status | Clinical Trial | Phase | |
---|---|---|---|
Enrolling by invitation |
NCT05415371 -
Persistent Poverty Counties Pregnant Women With Medicaid
|
N/A | |
Recruiting |
NCT04038255 -
Mindfulness Based Smoking Cessation Among Cancer Survivors
|
Phase 4 | |
Completed |
NCT04123041 -
Characterize the Nicotine Uptake and Subjective Effects With Use of JUUL Electronic Nicotine Delivery Systems
|
N/A | |
Completed |
NCT02735382 -
EHR-Based and Fax-Based Referral to a Tobacco Quitline: A Comparative Study
|
N/A | |
Completed |
NCT02139930 -
Project 2: Strategies for Reducing Nicotine Content in Cigarettes
|
N/A | |
Completed |
NCT04107779 -
Changes in Biomarkers of Cigarette Smoke Exposure After Switching Either Exclusively or Partly to JUUL ENDS
|
N/A | |
Completed |
NCT05037656 -
Testing a School-Based E-cigarette, Tobacco, and Betel (Areca) Nut Use Prevention Curriculum for Guam Youths
|
N/A | |
Completed |
NCT04200157 -
Testing the Decoy Effect to Increase Tobacco Treatment Uptake
|
||
Enrolling by invitation |
NCT06042361 -
Enhancing Equity in Smoke-free Housing
|
N/A | |
Completed |
NCT02841683 -
Pragmatic Randomised Controlled Trial Evaluating Effectiveness of a Smoking Cessation e- Intervention " Tabac Info Service "
|
N/A | |
Completed |
NCT03151421 -
Air Quality Feedback to Reduce Second-hand Smoke (SHS) Exposure in the Home
|
N/A | |
Completed |
NCT04104152 -
CSD190203: A Study to Determine Subject Puffing Patterns of an Electronic Nicotine Delivery System in an Ambulatory Setting
|
N/A | |
Recruiting |
NCT05306158 -
Dual Use Approach Bias Training for Nicotine Addiction
|
N/A | |
Completed |
NCT04094363 -
CSD190202: Study to Assess Elements of Abuse Liability for Two Electronic Nicotine Delivery Systems
|
N/A | |
Completed |
NCT04143256 -
Evaluating Selected Constituents in the Exhaled Breath Samples
|
N/A | |
Completed |
NCT03553992 -
An Extended Facebook Intervention for Young Sexual and Gender Minority Smokers
|
N/A | |
Completed |
NCT05102786 -
CSD210904: Study to Assess Actual Use of a Heated Tobacco Product With Four Non-Combusted Cigarette Variants in Current Adult Smokers
|
||
Terminated |
NCT04396847 -
Laboratory Screening of Lorcaserin for Alcohol Use Disorder
|
Phase 2 | |
Completed |
NCT03694327 -
Innovative Digital Therapeutic for Smoking Cessation
|
N/A | |
Completed |
NCT05030194 -
Comparing Nicotine Delivery, Subjective Effects, and Sensory Experiences of Tobacco Users Using Oral Nicotine Products and Electronic Cigarettes [ZYN Study]
|
N/A |