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CONNECT Cancer Survivors With Tobacco Treatment

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The Washington University

Status

Enrolling

Conditions

Tobacco Use Cessation
Nicotine Addiction
Tobacco Smoking
Smoking Cessation
Tobacco Use

Treatments

Behavioral: ELEVATE-S
Behavioral: ELEVATE

Study type

Interventional

Funder types

Other

Identifiers

NCT07020273
202503025

Details and patient eligibility

About

The purpose of this study is to evaluate the comparative effectiveness of two different informatics-enabled implementation strategies on increasing tobacco treatment and improving smoking cessation rates for cancer control and prevention. This will be done via a two-arm pragmatic cluster randomized trial (CRT) to test the effectiveness of nudges to change (ELEVATE-S) vs. quit-focused usual care (ELEVATE) in increasing tobacco treatment (use of medication, brief advice, or referral to external counseling) and smoking cessation.

Enrollment

5,000 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Eligibility Criteria:

  • Be receiving care at a participating clinic
  • Report current tobacco use (assessed by the rooming staff during the index visit)
  • Have a completed appointment with a participating clinic
  • Be an adult (at least 18 years old).

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

5,000 participants in 2 patient groups

Electronic health record-enabled evidence-based tobacco treatment (ELEVATE)
Active Comparator group
Treatment:
Behavioral: ELEVATE
Electronic health record-enabled evidence-based tobacco treatment-Support (ELEVATE-S)
Experimental group
Treatment:
Behavioral: ELEVATE-S

Trial contacts and locations

1

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Central trial contact

Li-Shiun Chen, M.D., MPH, ScD; Nina Smock

Data sourced from clinicaltrials.gov

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