Increasing Smoking Cessation Counselling in Primary Care Using a Chronic Disease Management System
Sponsor
McMaster University (Other)
Overall Status
Unknown status
CT.gov ID
NCT01004276
Collaborator
Centre for Addiction and Mental Health (Other)
10
2
2
5
5
1
Study Details
Study Description
Brief 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.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Study Design
Study Type:
Interventional
Anticipated Enrollment
:
10 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Health Services Research
Official Title:
A Cluster Randomized Controlled Pilot Trial of the Effect of a New, Improved Smoking Cessation Management Module, Compared With Use of the Standard Version of Such a Management Module, on Smoking Counselling Initiation and Continuation Rates in Primary Care Practices Currently Using P-PROMPT Chronic Disease Management System in Ontario
Study Start Date
:
Nov 1, 2009
Anticipated Primary Completion Date
:
Apr 1, 2010
Anticipated Study Completion Date
:
Apr 1, 2010
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Improved module
|
Other: New, 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.
|
| No Intervention: Standard module
|
Outcome Measures
Primary Outcome Measures
- Smoker Identifying Cards [3 months post-intervention]
- Chronic disease management system's activity log [monthly post-intervention]
Secondary Outcome Measures
- Smoking cessation counselling billing codes from physician's remittance advice files [monthly post-intervention]
Eligibility Criteria
Criteria
Ages Eligible for Study:
N/A
and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
- Physician subscribers to P-PROMPT CDMS
Exclusion Criteria:
-
Paper users
-
Physicians expected to retire during the course of the study
-
Physicians whose billing files are not set-up with DataSynch
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | McMaster University | Hamilton | Ontario | Canada | L8S 4L8 |
| 2 | Centre for Addiction and Mental Health | Toronto | Ontario | Canada | M5S 2S1 |
Sponsors and Collaborators
- McMaster University
- Centre for Addiction and Mental Health
Investigators
- Principal Investigator: Natalie T. MacLeod, M.Sc. Candidate, McMaster University
- Principal Investigator: Rolf J. Sebaldt, MD, McMaster University
- Principal Investigator: Peter Selby, MD, Centre for Addiction and Mental Health
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
,
,
ClinicalTrials.gov Identifier:
NCT01004276
Other Study ID Numbers:
- 09-341
First Posted:
Oct 29, 2009
Last Update Posted:
Oct 29, 2009
Last Verified:
Oct 1, 2009
Keywords provided by ,
,
Additional relevant MeSH terms: