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Completed

NCT Number: NCT01614054

Nicotine Replacement Provided at a Tertiary Care Hospital

The purpose of this study is to show that a patient-centered survey asking about smoking habits, with the option for nicotine replacement therapy (NRT) will increase the prescription rates among health care providers (HCP). The investigators also believe that this intervention can also lead to increased referrals to smoking cessation clinics and ultimately increase rates of smoking cessation.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

St Paul's Hospital

Vancouver, British Columbia, V6Z 1Y6, Canada

About this study

Since the past decade, there has been an increased awareness of the effects of smoking of general health. In 2000, 18.1% of all US deaths were related to tobacco use. Multiple trials have proven that providing nicotine-replacement therapies to help smoking cessation were efficacious with various types of populations. However, smoking has not been eradicated in North America and was associated with a 3.1 million YPLL (years of potential life lost), along with 96.8 billion in productivity losses in the US4.

We are carrying out a study of 200 inpatients on a general medicine ward to attempt to improve prescription rates of nicotine replacement therapy (NRT) and smoking cessation. Our goal is to use a patient centred approach to determine which patients would benefit from NRT and which patients would be in the contemplative stage of smoking cessation. We will want to look at whether a simple, short survey taken by patients can encourage the health care provider (HCP) to provide more NRT and more referrals to a smoking cessation clinic. We hope that this tool will improve the ability of HCP to provide optimal, comprehensive care. The study's findings should help to guide future practices for hospitalized smokers.

Currently, standard treatment involves NRT being prescribed completely at the discretion of the physician. This occasionally involves a discussion with the patient regarding their preferences, but more often is a unilateral decision made by the health care provider. Additionally, we believe that this method misses a lot of potential patients who may benefit from this therapy but are otherwise not identified. We will not be using a placebo.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients admitted to the general medicine ward
  • Currently smoking (or quit within the last two weeks)
  • 18 years and over
  • Able to read in the English language or have a translator present

Exclusion criteria

  • Non-smokers
  • Pregnant or actively trying to conceive
  • Recent acute coronary syndrome (within 1 month)
  • Active temporo-mandibular joint disease
  • Currently on NRT
  • Allergy to nicotine
  • Acute delirium/chronic dementia
  • Inability to complete survey secondary to language/educational issues (if no translator present)

Treatment and study plan

Survey of patient's smoking habits

Other

Nicotine replacement therapy (inhalers, patches, gum, lozenges) at the discretion of the health care provider

Primary outcomes

  1. Number of prescriptions for NRT (as a percentage of the number of active smokers)

    Time frame: 1 month

    By eliciting patient attitudes toward smoking cessation, we aim to increase the rate of prescription of nicotine replacement by 15% on the medical wards at St. Paul's Hospital by 15% over a 1month period.

    We will measure the number of prescriptions for NRT of any kind by referencing pharmacy databases. This will be calculated as a percentage of active smokers.

Secondary outcomes

  1. Number of referrals to a smoking cessation clinic (as a percentage of the number of active smokers)

    Time frame: 1 month

    We hope to increase the number of referrals to smoking cessation clinics by 15% over one month.

    We will measure the number of patients referred for smoking cessation by contacting the clinic and cross-referencing the data by attending physician making the referral. This will be calculated as a percentage of active smokers.

Sponsors and collaborators

Lead sponsor

University of British Columbia

Other

Collaborators

  • Providence Health & Services
  • St. Paul's Hospital, Canada

Registry information

Official study title

A Patient-centered Approach to Behavioral Modification in a Tertiary-care University-affiliated Hospital and the Incidence of Smoking Cessation

Acronym: N-PATCH

Important dates

Study start
2012
Primary completion
2012
Study completion
2012
First posted
Jun 7, 2012
Registry last updated
Mar 17, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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