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Methadone-Maintained Smokers Switching to E-Cigarettes (SHINE)

Primary Purpose

Nicotine Dependence, Electronic Cigarette Use

Status
Recruiting
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Electronic Cigarette
Nicotine Lozenge
Sponsored by
Butler Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Nicotine Dependence

Eligibility Criteria

21 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • moderate to heavy cigarette smokers (10 cigarettes/day for > 1 yr; breath CO > 10 ppm)
  • have been receiving methadone for at least three months
  • attend at least weekly to receive methadone dose
  • speak English
  • have a telephone or access to a telephone
  • are available over the next 6 weeks
  • are interested in switching to either electronic cigarettes or nicotine replacement therapy

Exclusion Criteria:

  • use of ECs on > 2 of the past 30 days
  • currently use medications that may reduce smoking (e.g., bupropion, varenicline, NRT)
  • have unstable psychiatric conditions
  • have near-daily or daily use of marijuana
  • are pregnant
  • had a cardiovascular event in the last month
  • daily medication for asthma or COPD

Sites / Locations

  • Butler HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Electronic Cigarettes

Nicotine Lozenges

Arm Description

Participants in this arm are randomized to receive electronic cigarettes for the 6-week study period.

Participants in this arm are randomized to receive nicotine lozenge for the 6-week study period.

Outcomes

Primary Outcome Measures

Nicotine Exposure
Extent of Nicotine Exposure as measured by urine-based tobacco toxicology assessment at baseline and again at 6-weeks.
FVC Lung Functioning
Changes in Forced Vital Capacity (FVC), as measured by spirometry at baseline and again at 6-weeks.
FEV1 Lung Functioning
Changes in Forced Expiratory Volume (FEV - during the first second), as measured by spirometry at baseline and again at 6-weeks.
FEV1/FVC Ratio Lung Functioning
Changes in FEV1/FVC ratio, as measured by spirometry at baseline and again at 6-weeks.
Smoking Behavior and Experiences
Changes in smoking behavior and experiences, as measured by self-report at baseline and again at 6-weeks.
Nicotine Exposure for Complete Switchers
Extent of Nicotine Exposure as measured by urine-based tobacco toxicology assessment at baseline and again at 6-week among complete switchers, irrespective of condition, (i.e., exclusive EC/NRT users based on 7-day carbon monoxide (CO)-verified reports at the 6-week time point) relative to dual users and exclusive CC users.
FVC Lung Functioning for Complete Switchers
Changes in Forced Vital Capacity (FVC), as measured by spirometry at baseline and again at 6-weeks, among complete switchers, irrespective of condition, (i.e., exclusive EC/NRT users based on 7-day carbon monoxide (CO)-verified reports at the 6-week time point) relative to dual users and exclusive CC users.
FEV1 Lung Functioning for Complete Switchers
Changes in Forced Expiratory Volume (FEV - during the first second), as measured by spirometry at baseline and again at 6-weeks, among complete switchers, irrespective of condition, (i.e., exclusive EC/NRT users based on 7-day carbon monoxide (CO)-verified reports at the 6-week time point) relative to dual users and exclusive CC users.
FEV1/FVC Ratio Lung Functioning for Complete Switchers
Changes in FEV1/FVC ratio, as measured by spirometry at baseline and again at 6-weeks, among complete switchers, irrespective of condition, (i.e., exclusive EC/NRT users based on 7-day carbon monoxide (CO)-verified reports at the 6-week time point) relative to dual users and exclusive CC users.
Smoking Behavior and Experiences for Complete Switchers
Changes in smoking behavior and experiences, as measured by self-report at baseline and again at 6-weeks, among complete switchers, irrespective of condition, (i.e., exclusive EC/NRT users based on 7-day carbon monoxide (CO)-verified reports at the 6-week time point) relative to dual users and exclusive CC users.

Secondary Outcome Measures

Full Information

First Posted
December 21, 2021
Last Updated
October 5, 2023
Sponsor
Butler Hospital
Collaborators
National Institute on Drug Abuse (NIDA)
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1. Study Identification

Unique Protocol Identification Number
NCT05206435
Brief Title
Methadone-Maintained Smokers Switching to E-Cigarettes
Acronym
SHINE
Official Title
Methadone-Maintained Smokers Switching to E-Cigarettes
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 31, 2022 (Actual)
Primary Completion Date
June 30, 2024 (Anticipated)
Study Completion Date
June 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Butler Hospital
Collaborators
National Institute on Drug Abuse (NIDA)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Participants in this randomized clinical trial will be methadone-maintained smokers interested in switching to electronic cigarettes (ECs). There will be a total of 7 study visits over the course of 6 weeks; each visit includes psychometric assessment and biomarker measurements. After completion of the baseline visit, participants will be randomized to either: 1) 6 weeks of EC use (JUUL 5% nicotine pods) or 2) 6 weeks of nicotine replacement therapy (NRT) in the form of nicotine lozenges. EC and NRT use will begin the day after the baseline assessment.
Detailed Description
Participants in this randomized clinical trial will be methadone-maintained smokers interested in switching to electronic cigarettes (ECs). There will be a total of 7 study visits over the course of 6 weeks: baseline, 5 weekly check-in (CI) visits, and a 6-week assessment. Baseline assessments will include biomarker measurement, carbon monoxide (CO) readings, smoking history and current cigarette use, spirometry, respiratory symptoms, and tobacco demand. After completion of the baseline visit, participants will be randomized to either: 1) 6 weeks of EC use (JUUL 5% nicotine pods) or 2) 6 weeks of nicotine replacement therapy (NRT) in the form of nicotine lozenges. EC and NRT use will begin the day after the baseline assessment. All participants will attend weekly brief assessment check-in visits where distribution of either EC or NRT will occur. Check-in assessments will include cigarette use, EC use, NRT use, CO readings, respiratory symptoms, and tobacco demand. At the 6-week assessment, baseline measurements will be repeated to determine changes in the health effects, biomarkers, and combustible cigarette use associated with 6 weeks of EC use, relative to NRT. This study will be the first to test the potential behavioral and health effects of ECs in smokers with opioid use disorder, a population that is highly dependent on nicotine, highly vulnerable to smoking-related morbidity and mortality, and searching for novel methods to lower smoking-related risks.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Nicotine Dependence, Electronic Cigarette Use

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
240 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Electronic Cigarettes
Arm Type
Active Comparator
Arm Description
Participants in this arm are randomized to receive electronic cigarettes for the 6-week study period.
Arm Title
Nicotine Lozenges
Arm Type
Active Comparator
Arm Description
Participants in this arm are randomized to receive nicotine lozenge for the 6-week study period.
Intervention Type
Drug
Intervention Name(s)
Electronic Cigarette
Intervention Description
Electronic Cigarettes are provided to replace tobacco cigarettes
Intervention Type
Drug
Intervention Name(s)
Nicotine Lozenge
Intervention Description
Nicotine Lozenges are provided to replace tobacco cigarettes
Primary Outcome Measure Information:
Title
Nicotine Exposure
Description
Extent of Nicotine Exposure as measured by urine-based tobacco toxicology assessment at baseline and again at 6-weeks.
Time Frame
6 weeks
Title
FVC Lung Functioning
Description
Changes in Forced Vital Capacity (FVC), as measured by spirometry at baseline and again at 6-weeks.
Time Frame
6 weeks
Title
FEV1 Lung Functioning
Description
Changes in Forced Expiratory Volume (FEV - during the first second), as measured by spirometry at baseline and again at 6-weeks.
Time Frame
6 weeks
Title
FEV1/FVC Ratio Lung Functioning
Description
Changes in FEV1/FVC ratio, as measured by spirometry at baseline and again at 6-weeks.
Time Frame
6 weeks
Title
Smoking Behavior and Experiences
Description
Changes in smoking behavior and experiences, as measured by self-report at baseline and again at 6-weeks.
Time Frame
6 weeks
Title
Nicotine Exposure for Complete Switchers
Description
Extent of Nicotine Exposure as measured by urine-based tobacco toxicology assessment at baseline and again at 6-week among complete switchers, irrespective of condition, (i.e., exclusive EC/NRT users based on 7-day carbon monoxide (CO)-verified reports at the 6-week time point) relative to dual users and exclusive CC users.
Time Frame
6 weeks
Title
FVC Lung Functioning for Complete Switchers
Description
Changes in Forced Vital Capacity (FVC), as measured by spirometry at baseline and again at 6-weeks, among complete switchers, irrespective of condition, (i.e., exclusive EC/NRT users based on 7-day carbon monoxide (CO)-verified reports at the 6-week time point) relative to dual users and exclusive CC users.
Time Frame
6 weeks
Title
FEV1 Lung Functioning for Complete Switchers
Description
Changes in Forced Expiratory Volume (FEV - during the first second), as measured by spirometry at baseline and again at 6-weeks, among complete switchers, irrespective of condition, (i.e., exclusive EC/NRT users based on 7-day carbon monoxide (CO)-verified reports at the 6-week time point) relative to dual users and exclusive CC users.
Time Frame
6 weeks
Title
FEV1/FVC Ratio Lung Functioning for Complete Switchers
Description
Changes in FEV1/FVC ratio, as measured by spirometry at baseline and again at 6-weeks, among complete switchers, irrespective of condition, (i.e., exclusive EC/NRT users based on 7-day carbon monoxide (CO)-verified reports at the 6-week time point) relative to dual users and exclusive CC users.
Time Frame
6 weeks
Title
Smoking Behavior and Experiences for Complete Switchers
Description
Changes in smoking behavior and experiences, as measured by self-report at baseline and again at 6-weeks, among complete switchers, irrespective of condition, (i.e., exclusive EC/NRT users based on 7-day carbon monoxide (CO)-verified reports at the 6-week time point) relative to dual users and exclusive CC users.
Time Frame
6 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: moderate to heavy cigarette smokers (10 cigarettes/day for > 1 yr; breath CO > 10 ppm) have been receiving methadone for at least three months attend at least weekly to receive methadone dose speak English have a telephone or access to a telephone are available over the next 6 weeks are interested in switching to either electronic cigarettes or nicotine replacement therapy Exclusion Criteria: use of ECs on > 2 of the past 30 days currently use medications that may reduce smoking (e.g., bupropion, varenicline, NRT) have unstable psychiatric conditions have near-daily or daily use of marijuana are pregnant had a cardiovascular event in the last month daily medication for asthma or COPD
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ana Abrantes, PhD
Phone
401-455-6200
Email
ana_abrantes@brown.edu
Facility Information:
Facility Name
Butler Hospital
City
Providence
State/Province
Rhode Island
ZIP/Postal Code
02906
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ana Abrantes, PhD

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Methadone-Maintained Smokers Switching to E-Cigarettes

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