Smoking Cessation Clinical Trial
Official title:
Leveraging Community Pharmacists to Optimize Smoking Cessation Services for Rural Smokers in Appalachia
NCT number | NCT05660525 |
Other study ID # | HSR220197 |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | March 6, 2024 |
Est. completion date | March 1, 2028 |
The goal of this clinical trial is to evaluate the effectiveness and implementation of a pharmacist-delivered MTM (medication therapy management) approach, called QuitAid, to quitting cigarette smoking in rural Appalachia. The main questions it aims to answer are: - Is QuitAid, alone or combined with other quitting tobacco treatments, effective? - What makes QuitAid easy or hard to carry out? Is it cost effective? Is it easy to maintain? Treatment: All participants will be given at least 4 weeks of the nicotine patch. Some participants will be randomized (like the flip of a coin) to receive additional treatments (listed below). These groups will be compared to each other to see which combination works best to help them quit smoking. - Smokefree TXT - a texting program that helps people quit smoking - Tobacco quitline - 4 phone sessions to help people quit smoking - 8 weeks of NRT (nicotine replacement therapy in the form of nicotine patches or nicotine patches and lozenge) medication instead of 4 weeks - QuitAid - An MTM program given by the patient's pharmacist. This is a quitting smoking coaching program - Nicotine patch AND nicotine lozenge instead of just nicotine patches
Status | Recruiting |
Enrollment | 768 |
Est. completion date | March 1, 2028 |
Est. primary completion date | March 1, 2027 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility | Study participants will be rural cigarette smokers from Virginia, Tennessee, Kentucky and North Carolina who visit one of the participating study pharmacies. Pharmacies will be located in rural geographic areas of the Central and South Central subregions of Appalachia that include Virginia, Tennessee, Kentucky and North Carolina, as defined by the RUCA codes 4-10. No exclusionary criteria are based on race, gender, or age. Inclusion Criteria include: - must be 18 years of age and older - must be able to read, speak, and understand English - must report smoking at least 5 cigarettes per day for the past 6 months (regardless of non-cigarette tobacco product use) - must be willing to set a quit date within the next 30 days - must own a cell phone - must be willing and able to use NRT in the form of patch or lozenge - Not be pregnant or planning to be pregnant in the next 6 months. Exclusion Criteria include: - are pregnant women (self-reported), breastfeeding, planning to become pregnant during the next 6 months - have a medical contraindication to NRT (e.g., past 30 days, heart attack or stroke; past 6 months, serious or worsening angina, very rapid or irregular heartbeat requiring medication) |
Country | Name | City | State |
---|---|---|---|
United States | University of Virginia | Charlottesville | Virginia |
Lead Sponsor | Collaborator |
---|---|
University of Virginia |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Tobacco Abstinence | The primary outcome is biochemically verified point prevalence (verified through a CO test via Smokerlyzer at endpoint of participation in trial) abstinence defined as no smoking (even a puff) within the past 7 days. | 6 months | |
Secondary | Self-Reported Tobacco Abstinence | Self-reported point prevalence abstinence defined as no smoking (even a puff) within the past 7 days | 1, 2, and 3 months | |
Secondary | Adherence to assigned treatment components | Assess adherence to assigned treatment regimen as the percentage of sessions completed if the participant was assigned to QuitAid and/or the quitline treatments, the frequency of opt-out from SmokefreeTXT (e.g., texting "STOP"), and the percent of NRT used. Adherence to NRT (both patch and/or lozenge) will be collected from participants at the 1-, 2-, and 3-month follow-ups. | 1, 2, and 3 months | |
Secondary | Quit Attempts | Assess the number of times that participants have made a quit attempt since the previous contact at the 1-, 2-, 3- and 6-month follow-ups. A "quit attempt" will be defined as cigarette abstinence for = 24 hours not due to involuntary or forced cessation (i.e., hospitalization) | 1, 2, and 3 months |
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