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N/A N=898 Health Services Research

Improving the Delivery of Smoking Cessation Guidelines in Hospitalized Veterans

Cigarette Smoking

Enrolled (actual)
898
Serious AEs
0.0%
Results posted
Aug 2014
Primary outcome: Primary: 7-day Point-prevalence Smoking Abstinence (6-month) — 69; 53 participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Smoking Cessation Guideline Implementation (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
US Department of Veterans Affairs
Primary completion
Jun 2013

Outcome Measures

OutcomeResultp-value
PRIMARY
7-day Point-prevalence Smoking Abstinence (6-month)
69; 53
SECONDARY
Referrals to Quitline
0; 36
SECONDARY
Prescription of Recommended Pharmacotherapy for Smoking Cessation
176; 149

Summary

The primary objective of this study is to determine whether a nurse-initiated intervention, which couples brief inpatient counseling and proactive telephone counseling by a centralized tobacco quitline, improves 6-month cessation rates in hospitalized VA smokers. If proven effective, the proposed intervention will provide a practical strategy to enhance the adoption and implementation of recommended smoking cessation procedures in VA hospitals, and will demonstrate the utility of quitlines in preventing relapse in hospitalized smokers once they leave the hospital.

Eligibility Criteria

Inclusion Criteria

  • Patients: The study sample will include general medical inpatients, aged 18 or older, who smoke at least one cigarette per day on average, regardless of their willingness to quit smoking. To increase applicability of study results, the goal is to enroll patients with characteristics that reflect the full range and distribution of patients observed in clinical practice. Current smokers transferred from intensive care units (or other monitored beds) to a general medical ward will be eligible.
  • Nurses: The study sample will include staff nurses who are assigned to a general medicine inpatient unit at one of the participating sites.

Exclusion Criteria

  • Hospitalization for less than 18 hours (e.g., patients admitted for overnight observation);
  • Acute medical decomposition (e.g., acute respiratory failure requiring intubation, cardiac arrest, septic shock);
  • Altered mental status;
  • Unstable psychiatric disorder (e.g., acute psychosis);
  • Dementia;
  • Communication barrier (unable to speak English, hard of hearing, aphasic);
  • Pregnancy;
  • Terminal illness (<12 month life expectancy);
  • No access to a phone or the absence of a permanent address;
  • Admitted for treatment of substance abuse.

No patient will be included unless they are able to provide informed consent and agree to be contacted by telephone during follow-up (to assess smoking status).

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00816036). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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