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Pilot Testing a Computer Delivered Tobacco Cessation Intervention in Outpatient Clinical Settings: A Feasibility Study

Johns Hopkins University logo

Johns Hopkins University

Status

Completed

Conditions

Tobacco Smoking

Treatments

Behavioral: C-Raven without avatar
Behavioral: C-Raven with avatar

Study type

Interventional

Funder types

Other

Identifiers

NCT05145738
IRB00300496

Details and patient eligibility

About

The investigators have developed a hybrid computer- and person-delivered intervention, called "C-Raven" for smoking cessation that is tailored to people with tobacco use in Baltimore City. The computer delivered component consists of two ~20 minute sessions on an iPad guided by Edna Poe, an interactive avatar. These sessions are followed by elective in vivo initiation of nicotine replacement therapy (NRT). Community health workers (CHWs) trained in smoking cessation and motivational interviewing provide 6 weeks of supportive follow up counseling. The investigators propose a pilot of the intervention package in the Tobacco Treatment and Lung Cancer Screening Clinic (TTLCSC) at Johns Hopkins Hospital, and the Johns Hopkins Broadway Center for Addiction, assessing feasibility and acceptability of using this tool in these clinical settings. In addition, the investigators will compare whether the use of a virtual counselor is associated with greater satisfaction and engagement with the program.

To this end, the investigators propose a two-arm randomized controlled trial, randomizing up to 90 individuals with tobacco use to the current CRAVEN program which includes a virtual counselor, to CRAVEN without a virtual counselor. Primary outcomes include intervention feasibility and acceptability. The investigators will secondarily examine uptake and maintenance of pharmacotherapy for tobacco cessation, readiness to quit smoking, and tobacco cessation (7 day abstinence) at 6 months, patient satisfaction by intervention arm and CHW engagement by intervention arm.

Enrollment

18 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Adults ≥18 years of age receiving care in one of the two specified clinics
  • Current daily smoker and has smoked >100 cigarettes in their lifetime
  • English speaking
  • Cognitively able to understand proposed research design

Exclusion criteria

  • Actively psychotic or other severe mental health symptoms
  • Any contraindication to NRT use
  • Hearing impaired (unable to listen to audio component of intervention)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

18 participants in 2 patient groups

C-Raven + Avatar
Experimental group
Description:
Computer delivered intervention with Avatar as virtual counselor plus linkage to community health worker
Treatment:
Behavioral: C-Raven with avatar
C-Raven
Active Comparator group
Description:
Computer-delivered intervention without virtual counselor, with linkage to community health worker
Treatment:
Behavioral: C-Raven without avatar

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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