Effectiveness of Smoking Cessation Program in a Community Health System

Virtua Health

Status: Invitation-only

Conditions: Smoking Cessation

Treatments: Behavioral: Smoking cessation

Study type: Observational

Funder types: Other

Identifiers

NCT05107687

IRB-2021-02

Details and patient eligibility

About

Research efforts are needed to increase tobacco cessation support and to improve tobacco cessation efficacy. In addition, strategies must be identified to increase access to smoking cessation support and to develop processes to integrate smoking cessation into treatment plans for cancer patients.

Full description

The Cancer Patient Tobacco Questionnaire (C-TUQ) survey tool will be used to address the primary and secondary outcome measures. This tool is publicly available on the National Cancer Institutes Grid-Enabled Measures website and was developed by NCI and the American Association for Cancer Research. This tool is a 22-item self-report survey designed to capture information about tobacco use by cancer patients and cancer survivors. Comparisons will be made for those patients that enroll in the structured smoking cessation program versus those patients that have opted to quit on their own.

Primary:

To determine the effectiveness of an intensive structured smoking cessation program (education and support) provided by a tobacco cessation trained specialist versus unassisted smoking cessation quitting methods (no support, patients have opted to stop on their own) in cancer patients seen in a community health care system

Secondary:

• Self-reported 7-day point-prevalence smoking abstinence at 6-month follow-up in patients participating in a structured smoking cessation program versus those patients that have quit smoking with professional support
• Self-reported 7-day point-prevalence smoking abstinence at 12-month follow-up in patients participating in a structured smoking cessation program versus those patients that have quit smoking without professional support, participants choosing to stop smoking on their own.
• Examine the impact of implementing a system level smoking cessation program into the ongoing management of our cancer patients who smoke.

Enrollment: 76 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

Any Gender

• Over 18 years of age
• Able to read and understand English
• Able to sign the informed consent form
• A current cigarette smoker defined as smoking within 30 days
• Diagnosed with cancer and wants to quit smoking

Exclusion criteria

• • Individuals with Dementia

  • ECOG Performance Status 3-4
  • Survival prognosis less than 12 months
  • Currently participating in a smoking cessation program that is not provided by Virtua
  • Individuals who do not want to quit smoking
  • Pregnant Women

Trial design

76 participants in 2 patient groups

Assisted Smoking Cessation

Description:

Subject participates in a structured smoking cessation program hosted at Virtua Health which may be either smoking cessation group sessions or individual sessions and/or both. All participants will be provided with a list of smoking cessation resources. Description of Group Smoking Education and Support: These sessions are led by a Tobacco Treatment Specialist and include 2-3 sessions in-person or virtually and cover the following topics: Biological changes caused by nicotine, addiction, tips to quit smoking, health benefits to quitting smoking, types of nicotine replacement therapy, e-cigarettes and devices, aromatherapy, meditation and various resources. In addition, access to nicotine replacement therapies is optional.

Treatment:

Behavioral: Smoking cessation

Unassisted Smoking Cessation

Description:

The subject receives no professional support but is provided with a list of smoking cessation resources, in this cohort the subject engages in smoking cessation with no assistance from a provider.

Treatment:

Behavioral: Smoking cessation