Actively Recruiting

Phase 4
Age: 50Years +
All Genders
NCT07220356

C-Raven, a Virtual Tobacco Cessation Intervention in Residency Clinics

Led by Johns Hopkins University · Updated on 2026-02-02

30

Participants Needed

1

Research Sites

81 weeks

Total Duration

On this page

Sponsors

J

Johns Hopkins University

Lead Sponsor

M

Maryland Cigarette Restitution Fund

Collaborating Sponsor

AI-Summary

What this Trial Is About

In a residency clinic in Baltimore, the investigators propose to conduct a pilot RCT comparing a) an avatar-delivered computerized intervention (CI) for tobacco cessation augmented with CHW support and navigation to lung cancer screening to b) a waitlist control. With a sample of participants from the residency clinic (N=30), the investigators will collect data on feasibility of recruitment, intervention engagement and completion, and short-term smoking cessation outcomes. Individuals will be assessed at baseline, 1 month, 3 months, and 6 months. The investigators will conduct interviews with a subset of pilot participants to collect qualitative data on intervention acceptability.

CONDITIONS

Official Title

C-Raven, a Virtual Tobacco Cessation Intervention in Residency Clinics

Who Can Participate

Age: 50Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 50 or older
  • Current tobacco use with more than 100 cigarettes smoked in lifetime
  • Considering smoking cessation
  • Planning to remain in local area for at least 6 months
  • English speaking (intervention currently in English only)
Not Eligible

You will not qualify if you...

  • Contraindication to nicotine replacement therapy
  • Current engagement in formal smoking cessation program
  • Major cognitive or psychiatric impairment
  • Severe hearing impairment
  • Investigator discretion

AI-Screening

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Trial Site Locations

Total: 1 location

1

Johns Hopkins University School of Medicine

Baltimore, Maryland, United States, 21205

Actively Recruiting

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Research Team

A

Alejandra Ellison-Barnes, MD

CONTACT

H

Heidi Hutton, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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