CClinicalTrials.gg
Status unknownNCT01004276Updated Oct 29, 2009

Increasing Smoking Cessation Counselling in Primary Care Using a Chronic Disease Management System

An interventional study of New, improved smoking cessation management module in Delivery of Health Care and Smoking Cessation, sponsored by McMaster University. Status unknown at 2 sites in Canada. Per ClinicalTrials.gov, last updated 2009-10-29.

Sponsored by McMaster University · Not applicable, Interventional, and Health services research

The sponsor has not verified this record recently (last verified Oct 2009), so the status shown — last known as Enrolling by invitation — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
10
Allocation
Randomized
Sex
All
01

Study summary

This pilot study will determine the feasibility of studying a new smoking cessation management module in an existing chronic disease management system. The new module is intended to help healthcare providers deliver more smoking cessation counselling to their patients.

02

Conditions studied

  • Delivery of Health Care
  • Smoking Cessation

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Keywords

  • primary health care
  • delivery of health care
  • smoking cessation
  • chronic disease
  • disease management
  • pilot projects
03

In context

Chronic Disease

990 studies on the registry are indexed under Chronic Disease; 178 are open to participants now.

This study's planned enrollment of 10 is below the median of 120 across 722 interventional studies indexed under Chronic Disease.

Browse Chronic Disease studies →

Lead sponsor

McMaster University is the lead sponsor of 720 studies on the registry; 124 are open to participants now.

Of its 6 completed or terminated interventional studies of FDA-regulated products, 2 (33%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Physician subscribers to P-PROMPT CDMS

Exclusion criteria

Exclusion Criteria:

  • Paper users
  • Physicians expected to retire during the course of the study
  • Physicians whose billing files are not set-up with DataSynch
05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
10 participants (estimated)

Study arms

  • Experimental
    Improved module

    Other: New, improved smoking cessation management module

  • No intervention
    Standard module

Interventions

  • OtherNew, improved smoking cessation management module

    The intervention that will be tested is an improved smoking cessation management module in an existing chronic disease management system, P-PROMPT CDMS. This module includes the following components: a) the Patient Care Status and Update Form, b) the smoking registry and c) patient prompts.

06

What researchers measure

Primary outcomes

  1. Smoker Identifying Cards

    Time frame: 3 months post-intervention

  2. Chronic disease management system's activity log

    Time frame: monthly post-intervention

Secondary outcomes

  1. Smoking cessation counselling billing codes from physician's remittance advice files

    Time frame: monthly post-intervention

07

Study locations

2 sites
  • McMaster University
    Hamilton, Ontario L8S 4L8, Canada
  • Centre for Addiction and Mental Health
    Toronto, Ontario M5S 2S1, Canada
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 29, 2009, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01004276
Lead sponsor
McMaster University
Collaborators
Centre for Addiction and Mental Health
First posted
Oct 29, 2009
Start date
Nov 2009
Primary completion
Apr 2010 (estimated)
Completion
Apr 2010 (estimated)
Last update
Oct 29, 2009

Study contacts

Natalie T. MacLeod, M.Sc. Candidate
principal investigator · McMaster University
Rolf J. Sebaldt, MD
principal investigator · McMaster University
Peter Selby, MD
principal investigator · Centre for Addiction and Mental Health

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Oct 2009. You cannot join it, but the record below documents what was studied.

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