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Pharmacist Intervention to Improve Smoking Cessation

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University of Iowa

Status

Invitation-only

Conditions

Smoking Cessation

Treatments

Behavioral: Pharmacist Intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT06943287
202411248

Details and patient eligibility

About

The goal of this study is to assess the effectiveness of a remote pharmacist intervention to help smokers quit.

The main questions it aims to answer are:

  • Will smokers being screened for lung cancer with low-radiation-level chest computed tomography (CT) be willing to participate in this study and talk to the pharmacist about smoking cessation?
  • Will those in the intervention group be more likely to report smoking cessation than those in the control group.

Participants in the intervention group will be asked to complete a baseline survey; speak with a pharmacist via phone call at baseline, 2 weeks, 4 weeks, 6 weeks, 8 weeks, 10 weeks, and 12 weeks; and complete an exit survey.

Participants in the control group will be asked to complete a baseline survey and an exit survey.

Enrollment

100 estimated patients

Sex

All

Ages

18 to 100 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Current smoker
  • Current patient in the Lung Cancer Screening Program

Exclusion criteria

  • Unable to speak/read English
  • Unable to provide their own written informed consent

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

100 participants in 2 patient groups

Pharmacist Intervention Group
Experimental group
Treatment:
Behavioral: Pharmacist Intervention
Control Group
No Intervention group

Trial contacts and locations

1

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Central trial contact

Jacob E Simmering, PhD; Shelby L Francis, PhD

Data sourced from clinicaltrials.gov

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