Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00756704 · ClinicalTrials.gov registry record · NA

The Effectiveness of Smoking Cessation Guidelines in the Emergency Department

A NA study of Cigarette Smoking, sponsored by University of Iowa.

Completed
Registry status
NA
Development phase
789
Enrollment target
2
Study locations

NCT00756704: Completed NA study of Cigarette Smoking, sponsored by University of Iowa.

NCT00756704 is a NA study of Cigarette Smoking that has completed, run by University of Iowa. The registered enrollment target is 789 participants, above the 159-participant average among 45 other Cigarette Smoking trials with a reported enrollment target (396% higher). The trial reports 2 study locations across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00756704, a NA study of Cigarette Smoking, has completed, sponsored by University of Iowa.

COMPLETED
Registry status
NA
Development phase
789 participants
Enrollment target
2
Study locations

Study Summary

Although 78% of smokers report that a health professional has previously advised them to quit smoking, most smokers are not advised to stop smoking or offered assistance with smoking cessation during a given ED visit. There are multiple barriers to routine implementation of smoking cessation guidelines by emergency clinicians, however, and rigorously performed clinical trials are needed to demonstrate that routine screening and counseling of ED patients results in increased quit rates. To determine the feasibility of implementing the Agency for Healthcare Research and Quality (AHRQ) Smoking Cessation Guideline in the ED, we will conduct a clinical trial in 974 ambulatory adult smokers who present to 2 emergency departments, using a pre-post design. During the 3-month baseline period, clinicians will perform their usual duties but will not receive training in use of the AHRQ Guideline. Based on the Chronic Care Model, the 3-month intervention period will include: 1) a tutorial on brief cessation counseling for ED nurses and physicians, 2) use of an ED algorithm that includes recommended tobacco counseling items, 3) fax referral of motivated smokers to Quitline Iowa for proactive telephone counseling plus free nicotine replacement therapy, and 4) group and individual feedback to ED staff. We will conduct exit interviews of ED patients to assess performance of guideline-recommended actions by ED staff and 3- and 6-month telephone follow-up to determine 7-day point-prevalence abstinence (with biochemical confirmation of self-reported quitters at 6 months). Our main analyses will examine the contrast between the intervention and control periods in the performance of guideline-recommended actions and in 6-month quit rates, using hierarchical logistic regression to adjust for baseline differences in potentially confounding patient variables. In secondary analyses, we will assess the change in attitudes of ED nurses and physicians toward smoking cessation counseling. This f

Conditions Studied

Interventions

  • BEHAVIORAL Smoking cessation guideline implementation

Study Locations (2)

Iowa

  • Iowa Methodist Medical Center - Des Moines
  • The University of Iowa Hospitals and Clinics Emergency Treatment Center - Iowa City

Trial Details

FieldValue
Enrollment Target 789 participants
Start Date 2008-09
Est. Completion 2011-06
Phase NA
University of Iowa

228 total trials

What the finished NCT00756704 record still lists

NCT00756704 is an interventional study that assigns participants to a tested intervention. The registered 789 participants enrollment target is mid-sized for trials with a published cap, above the 159-participant average among 45 other Cigarette Smoking trials with a reported enrollment target (396% higher).

The record links to 1 condition, with Cigarette Smoking appearing as the primary indexed condition, and to 1 intervention - of which Smoking cessation guideline implementation is the first listed.

NCT00756704 reports a single indexed study location in Iowa.

Frequently Asked Questions

What is clinical trial NCT00756704 about?

NCT00756704 is a clinical study titled "The Effectiveness of Smoking Cessation Guidelines in the Emergency Department". Although 78% of smokers report that a health professional has previously advised them to quit smoking, most smokers are not advised to stop smoking or offered assistance with smoking cessation during a given ED visit. There are multiple barriers to routine implementation of smoking cessation guideli...

What is the current status of trial NCT00756704?

This trial is currently completed. It is a NA study. The enrollment target is 789 participants. The study started on 2008-09. Estimated completion is 2011-06.

What conditions does trial NCT00756704 study?

This clinical trial studies the following conditions: Cigarette Smoking.

What interventions are being tested in trial NCT00756704?

The interventions under investigation include: Smoking cessation guideline implementation (BEHAVIORAL).

Who is sponsoring clinical trial NCT00756704?

This trial is sponsored by University of Iowa, which has 228 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00756704 being conducted?

This trial has 2 study locations across Iowa. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Cigarette Smoking

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT00756704's enrollment target sits among peer trials

789 2nd of 45 the highest of 45 other Cigarette Smoking trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Cigarette Smoking trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT04967989 · 790 participants · Phase 3

    Clarifying the Optimal Application of SLT Therapy Trial

  • NCT06162611 · 790 participants · Phase 4

    Etonogestrel (ENG) Implant Insertion for Emergency Contraception With Oral Levonorgestrel (LNG) vs Placebo

  • NCT06488781 · 787 participants · Phase 2

    Antibiotic Prophylaxis to Prevent Obesity-Related Induction Complications in Nulliparae at Term 2.0

  • NCT06876649 · 787 participants · Phase 4

    A Master Protocol to Evaluate the Long-Term Safety of (LY3527727) Pirtobrutinib

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00756704, the US trial registry maintained by the National Library of Medicine. NCT00756704 (mid enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.