Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
ID07020273

Cancer Prevention by Reducing Tobacco With Informatics and Chronic Care Approaches Trial (CONNECT)

Led by Washington University School of Medicine · Updated on 2026-01-08

5000

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating two different strategies to improve tobacco treatment and increase smoking cessation rates among adults receiving care at participating clinics. The study compares a new approach called ELEVATE-S, which adds patient-centered support and self-management tools, against the usual care strategy called ELEVATE, which focuses on supporting clinicians with decision tools. This trial aims to find better ways to help people quit tobacco use and reduce tobacco-related health risks, especially for cancer prevention and control. Participants receive tobacco treatment through two different methods. The ELEVATE group supports clinicians by adjusting professional roles and providing clinical decision support tools to encourage tobacco treatment at the point of care. The ELEVATE-S group includes these clinician supports plus additional patient-focused strategies based on the chronic care model, offering flexible goals and patient-generated health data to help patients manage their tobacco use. During the study, researchers will track how many patients receive tobacco use treatment, including behavioral counseling and medication, and how many successfully stop smoking within six months after enrollment. Study participation involves routine clinical visits, where tobacco use is assessed and treatment is offered through the assigned strategy. The trial will monitor patient outcomes for up to six months to evaluate which approach better increases tobacco treatment and smoking cessation rates.

CONDITIONS

Brief Title

CONNECT Cancer Survivors With Tobacco Treatment

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Be receiving care at a participating clinic
  • Report current tobacco use
  • Have a completed appointment with a participating clinic
  • Be an adult (at least 18 years old)
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Outpatient Treatment

Duration - Up to 6 months post-enrollment

Participants receive behavioral interventions to support tobacco treatment through clinical decision support and self-management strategies.

Visits as part of routine clinical care

Trial Site Locations

Total: 1 location

1

Washington University School of Medicine

St Louis, Missouri, United States, 63110

Actively Recruiting

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Research Team

L

Li-Shiun Chen, M.D., MPH, ScD

N

Nina Smock

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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