COMPLETED

Treating Caregivers Who Smoke at AFCH

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

The purpose of this research study is to 1) see if a smoking cessation program is something that caregivers will use while their child is hospitalized, 2) see if caregivers think this program is something we should institute across the hospital, and 3) see if this program can help caregivers reduce their smoking. Participants will: * Complete a survey regarding smoking behavior and thoughts about quitting; * Undergo a 20-minute counseling session; and, * Use nicotine patches and mini-lozenges for 2 weeks

Official Title

Treating Nicotine Addiction in Caregivers of Children at American Family Children's Hospital

Quick Facts

Study Start:2024-03-05
Study Completion:2025-04-18
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT06051474

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:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Hospitalized child will have a 'yes' response to the screening question, "Does anyone in your household smoke"
  2. * Hospitalized child is expected to be admitted for \>24 hours
  3. * Caregiver is at least 18 years of age
  4. * Participant self-identifies as the primary caregiver of the hospitalized child during the hospitalization
  5. * Participant smokes ≥5 cigarettes per day
  6. * Participant is willing and able to use NRT
  7. * Participant is not currently pregnant, trying to get pregnant, or breastfeeding and willing to use acceptable birth control for duration of medication use
  8. * Participant is willing to comply with all study procedures and be available for the duration of the study
  1. * Contraindication to NRT use (pregnancy, myocardial infarction in past 2 weeks)
  2. * Previous reaction to the nicotine patch or mini-lozenge that prevented them from continuing to use it
  3. * Current use of smoking cessation medications (any NRT, bupropion, varenicline)
  4. * Caregiver's child is being cared for by study physician (Dr. Brian Williams)
  5. * Need for an interpreter

Contacts and Locations

Principal Investigator

Brian Williams, MD
PRINCIPAL_INVESTIGATOR
University of Wisconsin, Madison

Study Locations (Sites)

American Family Children's Hospital
Madison, Wisconsin, 53792
United States

Collaborators and Investigators

Sponsor: University of Wisconsin, Madison

  • Brian Williams, MD, PRINCIPAL_INVESTIGATOR, University of Wisconsin, Madison

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 Date2024-03-05
Study Completion Date2025-04-18

Study Record Updates

Study Start Date2024-03-05
Study Completion Date2025-04-18

Terms related to this study

Additional Relevant MeSH Terms

  • Smoking
  • Smoking Cessation