N/A
N=898
Improving the Delivery of Smoking Cessation Guidelines in Hospitalized Veterans
Cigarette Smoking
Bottom Line
View on ClinicalTrials.gov: NCT00816036 ↗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
| Outcome | Result | p-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).
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.