Treating Caregivers Who Smoke at AFCH

Completed · Phase 4

Conditions studied: Smoking, Smoking Cessation

In brief

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

Key facts

Study ID

NCT06051474

Run by

University of Wisconsin, Madison

People needed

23

Starts

2024-03-05

Expected to finish

2025-04-18

Last updated by the study team

2026-04-16

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Hospitalized child will have a 'yes' response to the screening question, "Does anyone in your household smoke"
• Hospitalized child is expected to be admitted for >24 hours
• Caregiver is at least 18 years of age
• Participant self-identifies as the primary caregiver of the hospitalized child during the hospitalization
• Participant smokes ≥5 cigarettes per day
• Participant is willing and able to use NRT
• Participant is not currently pregnant, trying to get pregnant, or breastfeeding and willing to use acceptable birth control for duration of medication use
• Participant is willing to comply with all study procedures and be available for the duration of the study

You may not qualify if…

• Contraindication to NRT use (pregnancy, myocardial infarction in past 2 weeks)
• Previous reaction to the nicotine patch or mini-lozenge that prevented them from continuing to use it
• Current use of smoking cessation medications (any NRT, bupropion, varenicline)
• Caregiver's child is being cared for by study physician (Dr. Brian Williams)
• Need for an interpreter

Where it is running

• American Family Children's Hospital — Madison, Wisconsin, United States

Full record on ClinicalTrials.gov

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