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Behavioral Intervention
Communication Skills Program for Healthcare Providers
N/A
Waitlist Available
Led By Hsien Seow, PhD
Research Sponsored by McMaster University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up all groups: 1) from enrollment to start of intervention group abcs education, 2) post abcs education for intervention group, at 4 months, 3) post abcs education for control group, at 8 months. sample: 6 months post abcs (14 months).
Awards & highlights
No Placebo-Only Group
Summary
This trial aims to improve communication between healthcare providers and patients with serious illnesses. The ABCs program provides education through online modules and virtual workshops to help providers have difficult conversations effectively. The study will assess the
Who is the study for?
The ABCs program is for healthcare providers who want to improve their communication skills with patients living with serious illnesses. It's designed for clinicians at all stages of their careers. Providers must be willing to participate in online modules and virtual workshops.
What is being tested?
This trial tests the 'ABCs' education intervention against no training, aiming to enhance provider competency in serious illness conversations. Participants will receive training on how to better engage with patients about difficult topics from diagnosis through end-of-life care.
What are the potential side effects?
Since this is an educational program rather than a medical treatment, there are no direct physical side effects associated with participation. However, participants may experience changes in confidence or stress levels related to having serious illness conversations.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ post abcs education, at 4 months for intervention group, at 8 months for control group
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~post abcs education, at 4 months for intervention group, at 8 months for control group
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Assessment of Clinical Encounter-Communications Tool (ACE-CT)
Secondary study objectives
Blended Learning Usability Evaluation - Questionnaire (BLUE-Q)
End-of-life Professional Caregiver Survey (EPCS)
Feeling Heard and Understood scale
+3 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: InterventionExperimental Treatment1 Intervention
Full ABCs education program
Group II: ControlActive Control1 Intervention
No ABCs education program
Find a Location
Who is running the clinical trial?
McMaster UniversityLead Sponsor
918 Previous Clinical Trials
2,615,943 Total Patients Enrolled
Health CanadaOTHER_GOV
34 Previous Clinical Trials
38,288 Total Patients Enrolled
Hsien Seow, PhDPrincipal InvestigatorMcMaster University
1 Previous Clinical Trials
566 Total Patients Enrolled