NCT00394420

Completed

Emergency Department Telephone Quitline

Mayo Clinic Source

Compare

Other study identifiers

Sponsor study identifier

1321-03

Study Type

interventional

Reported enrollment (type unavailable)

40

Locations

1 country

Sites

1

Timeline

Study Start

September 2003

Date type not reported

This date has not been verified as actual or estimated.

Primary Completion

April 2006

Actual (reported)

Study Completion

April 2006

Actual (reported)

Brief Summary

The purpose of this preliminary study was to evaluate the intervention completion rate among cigarette smokers enrolled through the Emergency Department (ED) in a tobacco quitline (QL) and to assess the feasibility of a randomized controlled trial assessing the efficacy of this intervention.

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: completed
Reported enrollment (type unavailable): 40 participants
Study completion date: April 2006
Actual (reported)
Listed locations: 1 countries · 1 sites

Trial Relationships

Click on a node to explore related trials.

Some registry-reported names shown below are not yet linked in this graph.

Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

Study Start
September 2003
Date type not reported
This date has not been verified as actual or estimated.
Primary Completion
April 2006
Actual (reported)
Study Completion
April 2006
Actual (reported)
First Submitted
October 31, 2006
Actual (reported)
First Posted
November 1, 2006
Actual (reported)

Last Updated: January 20, 2010
Status Verified: January 2010
Last Update Submitted: January 19, 2010

Conditions

Tobacco Dependence

Outcome Measures

Primary Outcomes (1)

The primary outcome was completion of the QL intervention.

Interventions

Telephone QuitlineBehavioral

Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.

Eligibility Criteria

Age18 Years+

Sexall

Healthy VolunteersYes

Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

We enrolled patients aged 18 or older who reported current daily cigarette smoking for at least one year and who indicated an interest in attempting to quit smoking.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Mayo Clinic
Otherlead

Study Sites (1)

Mayo Clinic

Rochester, Minnesota, 55905, United States

MeSH Terms

Conditions

Tobacco Use Disorder

Condition Hierarchy (Ancestors)

Substance-Related DisordersChemically-Induced DisordersMental Disorders

Study Officials

Nicola E. Schiebel, M.D.
Mayo Clinic
PRINCIPAL INVESTIGATOR

Study Design

Study Type: interventional
Phase: not applicable
Allocation: RANDOMIZED
Masking: NONE
Purpose: TREATMENT
Intervention Model: PARALLEL
Sponsor Type: OTHER

Study Record Dates

First Submitted

October 31, 2006

First Posted

November 1, 2006

Study Start

September 2003

Date type not reported

This date has not been verified as actual or estimated.

Primary Completion

April 2006

Actual (reported)

NCT00968513

Evaluation of Tobacco Treatment Strategies for Inpatient Psychiatry

Not ApplicableCompleted

NCT02478697

Tobacco Treatment for Employable Californians, Total IMPACT Study

Not ApplicableCompleted

NCT01423578

Effects of Yoga and Cardiovascular Exercise on Smoking Motivation

Not ApplicableCompleted

NCT04832659

Assessment of Biomarkers in Children to Help Parents Quit Tobacco

Not ApplicableCompleted

NCT01882348

Changing Pediatric Office Systems Nationally to Address Parental Tobacco Use

Not ApplicableCompleted

NCT01928758

Reduced Nicotine Cigarettes in Smokers With Mood and Anxiety Disorders

Not ApplicableCompleted

Study Completion

April 2006

Actual (reported)

Last Updated

January 20, 2010

Record last verified: 2010-01

Source record

Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.

Source: ClinicalTrials.gov.

JSON downloads include source attribution and retrieval details alongside the unchanged original record or the separately normalized values.

Registry identifier: NCT00394420
Data provider: ClinicalTrials.gov
Source updated: 2010-01-20
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:34:30 UTC

Locations

US(1)

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

Study Start

Primary Completion

Study Completion

First Submitted

First Posted

Conditions

Outcome Measures

Primary Outcomes (1)

Interventions

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (1)

MeSH Terms

Conditions

Condition Hierarchy (Ancestors)

Study Officials

Study Design

Study Record Dates

Source record

Locations