Comparative effectiveness of post-discharge strategies for hospitalized smokers: Study protocol for the Helping HAND 4 randomized controlled trial
- PMID: 32299470
- PMCID: PMC7164139
- DOI: 10.1186/s13063-020-04257-7
Comparative effectiveness of post-discharge strategies for hospitalized smokers: Study protocol for the Helping HAND 4 randomized controlled trial
Erratum in
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Correction to: Comparative effectiveness of post-discharge strategies for hospitalized smokers: Study protocol for the Helping HAND 4 randomized controlled trial.Trials. 2020 May 4;21(1):375. doi: 10.1186/s13063-020-04356-5. Trials. 2020. PMID: 32366273 Free PMC article.
Abstract
Background: Tobacco smoking remains the leading preventable cause of death in the US. A hospital admission provides smokers with a unique opportunity to stop smoking because it requires temporary tobacco abstinence while illness may enhance motivation to quit. Hospital interventions must continue post-discharge to increase tobacco abstinence long-term, but how best to accomplish this remains unclear. Building on two previous randomized controlled trials, each of which tested smoking cessation interventions that began in hospital and continued after discharge, this trial compares two interventions that provide sustained smoking cessation treatment after hospital discharge with the goal of improving long-term smoking cessation rates among hospitalized smokers.
Methods/design: Helping HAND 4 is a three-site randomized controlled trial that compares the effectiveness of two active interventions for producing validated past 7-day tobacco abstinence 6 months after hospital discharge. Smokers who are admitted to three hospitals receive a standard in-hospital smoking intervention, and those who plan to quit smoking after discharge are recruited and randomly assigned to two interventions that begin at discharge, Personalized Tobacco Care Management (PTCM) or Quitline eReferral. Each lasts 3 months. At discharge, PTCM provides 8 weeks of free nicotine replacement (NRT; a participant's choice of patch, gum, lozenge, or a combination) and then proactive smoking cessation support using an automated communication platform and live contact with a tobacco treatment specialist who is based in the health care system. In the eReferral condition, a direct referral is made from the hospital electronic health record to a community-based resource, the state's telephone quitline. The quitline provides up to 8 weeks of free NRT and offers behavioral support via a series of phone calls from a trained coach. Outcomes are assessed at 1, 3, and 6 months after discharge. The study hypothesis is that PTCM will produce higher quit rates than eReferral.
Discussion: Helping HAND 4 is a pragmatic trial that aims to evaluate interventions in real-world conditions. This project will give hospital systems critical evidence-based tools for meeting National Hospital Quality Measures for tobacco treatment and maximizing their ability to improve cessation rates and overall health for the millions of smokers hospitalized annually in the US.
Trial registration: Prospectively registered prior to start of enrollment at Clinicaltrials.gov, NCT03603496 (July 27, 2018). https://register.clinicaltrials.gov/prs/app/action/SelectProtocol?sid=S00084MJ&selectaction=Edit&uid=U00002G7&ts=2&cx=ff0oxn.
Keywords: Hospitalization; Inpatients; Interactive voice response; Nicotine addiction; Nicotine dependence; Pharmacotherapy; Randomized controlled trial; Smoking cessation; Tobacco use.
Conflict of interest statement
NR has received royalties from UpToDate, Inc., for writing on smoking cessation topics and consulting fees from Achieve Life Sciences for development of cytisine, an investigational smoking cessation medication. She has consulted with Pfizer, Inc., the manufacturer of Chantix (varenicline) smoking cessation medication, without accepting fees.
DS has consulted for Pfizer regarding anticoagulation but not regarding smoking cessation.
HAT has consulted for Achieve Life Sciences on a phase III clinical trial for cytisine. HAT is a multiple PI on a cessation study of non-daily smokers (PI: Primack; 5 R01 DA034629 04) for which the active study medication (nicotine gum) was donated by the manufacturer. HAT is the project lead for a Cancer Center Support Grant Supplement (PI: Pietenpol; 3 P30 CA068485 22S3) for which Chantix (varenicline) was donated by the manufacturer. HAT has not received funds from Achieve Life Sciences, nor the drug manufacturers.
These authors have no competing interests to declare: KS, AD, KG, ED, AN, JK, DEL, SR, YC.
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References
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- Fiore MC, Jaén CR, Baker TB, et al. Treating tobacco use and dependence: 2008 update. Rockville, MD: US Department of Health and Human Services. Public Health Service; 2008.
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