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RECRUITING
NCT06543407
NA

Harm Reduction for Smokers With Mental Illness

Sponsor: Dartmouth-Hitchcock Medical Center

View on ClinicalTrials.gov

Summary

To compare the efficacy of e-cigarette (e-cig) provision with or without behavioral support (SWITCH IT) delivered via telehealth to reduce harm among smokers with MI who cannot quit smoking and are not ready to pursue cessation treatment, and to examine self-regulation (using e-cigs instead of cigarettes to cope with stress/distress and self-efficacy) as a potential mechanism for behavior change from SWITCH IT

Official title: Harm Reduction for Smokers With Mental Illness: RCT of E-cigarette Provision With or Without Behavioral Support to Boost Switching

Key Details

Gender

All

Age Range

21 Years - Any

Study Type

INTERVENTIONAL

Enrollment

250

Start Date

2024-10-01

Completion Date

2028-03-31

Last Updated

2026-01-15

Healthy Volunteers

No

Interventions

BEHAVIORAL

SWITCH IT

Behavioral support for switching, 7-10 sessions with SWITCH IT coach delivered during the first 8 weeks of the study. SWITCH IT participants will also have the opportunity to receive supported "field trips" to explore e-cigarette options based on availability, cost, and preferences during week 4 and week 6.

OTHER

E-cig Provision Only

Provision of e-cigarettes (NJOY) based on combusible use for the first 8 weeks of the study.

Locations (2)

Seven Counties Services

Louisville, Kentucky, United States

The Providence Center

Providence, Rhode Island, United States