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Improved module for Delivery of Health Care
N/A
Waitlist Available
Led By Natalie T. MacLeod, M.Sc. Candidate
Research Sponsored by McMaster University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Physician subscribers to P-PROMPT CDMS
Timeline
Screening 3 weeks
Treatment Varies
Follow Up monthly post-intervention
Awards & highlights
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.
Eligible Conditions
- Delivery of Health Care
- Smoking Cessation
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ monthly post-intervention
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~monthly post-intervention
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Chronic disease management system's activity log
Smoker Identifying Cards
Secondary outcome measures
Smoking cessation counselling billing codes from physician's remittance advice files
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Improved moduleExperimental Treatment1 Intervention
Group II: Standard moduleActive Control1 Intervention
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Who is running the clinical trial?
McMaster UniversityLead Sponsor
880 Previous Clinical Trials
2,597,818 Total Patients Enrolled
Centre for Addiction and Mental HealthOTHER
354 Previous Clinical Trials
81,110 Total Patients Enrolled
Natalie T. MacLeod, M.Sc. CandidatePrincipal InvestigatorMcMaster University
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