RECRUITING

Tobacco Cessation Care for Cancer Patients by Automated Interactive Outreach

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This is a multi-arm, randomized controlled, pilot study which will recruit cancer patients who have been seen by a UCSF Cancer Center-affiliated clinical department to evaluate the efficacy of "CareConnect". This is the first study to assess the efficacy CareConnect, a combination of the Ask-Advise-Connect (AAC) with an Interactive Voice Response (IVR) delivering cancer-targeted educational messages to support referral to smoking cessation resources for patients with cancer.

Official Title

Connect Cancer Patients to Tobacco Cessation Care by Automated Interactive Outreach

Quick Facts

Study Start:2023-11-27
Study Completion:2025-01-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05829824

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Age 18 years and older.
  2. 2. Able to understand study procedures and to comply with them for the entire length of the study.
  3. 3. Ability of individual or legal guardian/representative to understand a written informed consent document, and the willingness to sign it.
  4. 4. English, Spanish, Cantonese, or Mandarin speaking.
  5. 5. Self-reported current use of tobacco, including e-cigarette on EHR.
  6. 6. Has a diagnosis of cancer.
  7. 7. Has been seen by a prescribing provider within a UCSF Cancer Center-affiliated clinical department within the past 3 months.
  1. 1. Contraindication to any study-related procedure or assessment.
  2. 2. No valid contact telephone number.
  3. 3. Currently hospitalized or having been discharged from inpatient setting within the past month (according to EHR).

Contacts and Locations

Study Contact

Edgar Yu
CONTACT
877-827-3222
Edgar.Yu@ucsf.edu

Principal Investigator

Janice Tsoh, PhD
PRINCIPAL_INVESTIGATOR
University of California, San Francisco

Study Locations (Sites)

University of California, San Francisco
San Francisco, California, 94143
United States

Collaborators and Investigators

Sponsor: University of California, San Francisco

  • Janice Tsoh, PhD, PRINCIPAL_INVESTIGATOR, University of California, San Francisco

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-11-27
Study Completion Date2025-01-30

Study Record Updates

Study Start Date2023-11-27
Study Completion Date2025-01-30

Terms related to this study

Keywords Provided by Researchers

  • Interactive Intervention

Additional Relevant MeSH Terms

  • Cancer
  • Tobacco Dependence
  • Tobacco Use Cessation