NCT00252902

Brief Summary

The primary purpose of the study is to refine the intervention protocols for two ED-initiated tobacco interventions and to assess the magnitude of the effect size that can be expected. We expect the intervention groups to have greater sustained abstinence, point-prevalence abstinence, and motivation to change when compared to the treatment as usual group at 1- and 3-month follow-up.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
75

participants targeted

Target at P75+ for phase_1

Timeline
Completed

Started Dec 2005

Typical duration for phase_1

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

November 11, 2005

Completed
4 days until next milestone

First Posted

Study publicly available on registry

November 15, 2005

Completed
16 days until next milestone

Study Start

First participant enrolled

December 1, 2005

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2006

Completed
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2007

Completed
Last Updated

January 11, 2017

Status Verified

October 1, 2013

Enrollment Period

1 year

First QC Date

November 11, 2005

Last Update Submit

January 10, 2017

Conditions

Tobacco Use

Keywords

tobacco; emergency department; motivation; counseling

Outcome Measures

Primary Outcomes (3)

  • Sustained abstinence (from tobacco)

  • 7-day Point prevalence abstinence

  • Any quit attempt >= 24 hours

Secondary Outcomes (2)

  • Motivation to quit

  • Treatment engagement

Interventions

Behavior change counselingBEHAVIORAL

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • years old
  • receiving treatment in the ED
  • smoking at least 10 cigarettes daily

You may not qualify if:

  • too ill to participate
  • temporary shelter
  • no phone

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Cooper University Hospital

Camden, New Jersey, 08103, United States

Location

Related Publications (1)

  • Boudreaux ED, Baumann BM, Perry J, Marks D, Francies S, Camargo CA Jr, Ziedonis D. Emergency department initiated treatments for tobacco (EDITT): a pilot study. Ann Behav Med. 2008 Dec;36(3):314-25. doi: 10.1007/s12160-008-9066-3. Epub 2008 Dec 3.

    PMID: 19050988RESULT

MeSH Terms

Conditions

Tobacco UseEmergencies

Interventions

Behavior Therapy

Condition Hierarchy (Ancestors)

BehaviorDisease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

PsychotherapyBehavioral Disciplines and Activities

Study Officials

  • Edwin D Boudreaux, PhD

    Cooper University Hospital, UMDNJ-Robert Wood Johnson Medical School

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
phase 1
Allocation
RANDOMIZED
Masking
SINGLE
Intervention Model
PARALLEL
Sponsor Type
NIH

Study Record Dates

First Submitted

November 11, 2005

First Posted

November 15, 2005

Study Start

December 1, 2005

Primary Completion

December 1, 2006

Study Completion

December 1, 2007

Last Updated

January 11, 2017

Record last verified: 2013-10

Locations

US(1)