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Behavioural Intervention
Asynchronous self-directed digital training for Medical Education
N/A
Waitlist Available
Led By Daisy Singla, PhD, C. Psyc
Research Sponsored by Mount Sinai Hospital, Canada
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 two years
Awards & highlights
Study Summary
This trial will compare how well two different types of online training work for teaching depression treatment to psychiatry residents.
Eligible Conditions
- Medical Education
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 1.5 year recruitment period
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1.5 year recruitment period
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Participation rate - resident participants
Recruitment rate - resident and patient participants
Retention rate - resident and patient participants
Secondary outcome measures
Acceptability of the intervention
Anxiety - patient participant
Counseling self-efficacy - resident participant
+6 moreTrial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Asynchronous self-directed digital trainingExperimental Treatment1 Intervention
A digital training program platform that delivers an interactive case-based modular curriculum covering evidence-based psychotherapy principles and IPT-specific principles and strategies with homework will take roughly 13 hours to complete, with 4.5 hours of online learning, and an additional 7.5 hours of reading and homework assignments. The reading and homework includes viewing captioned videotaped role plays and completing self-directed lesson plans. The digital curriculum leverages audio, video, and visual content, and is self-directed - for completion within a 2-week period. Residents can access this content through a smartphone, tablet or computer at their own pace, revisit modules and digital content as needed, and access a curated list of additional resources to supplement their learning.
Group II: Synchronous large group online workshopActive Control1 Intervention
This condition will reflect training as usual. Training will involve the same content contained in the asynchronous self-directed digital training platform, except delivered over a one day (4.5 hours of online instruction) workshop; and residents will be required to do the same reading and homework of lesson plans and viewing of the on-line videotaped role plays (an additional ~7.5 hours in total).
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Who is running the clinical trial?
Women's College HospitalOTHER
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39,083 Total Patients Enrolled
Sunnybrook Health Sciences CentreOTHER
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Centre for Addiction and Mental HealthOTHER
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81,400 Total Patients Enrolled
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
What aims is this clinical trial striving to achieve?
"This two-year trial is primarily focused on gauging the participant rate. Secondary objectives include determining patient improvement via Clinical Global Impressions of Improvement (CGI-I) scale and accepting judgement, as well as assessing therapeutic alliance through Working Alliance Inventory Short Revised (WAI-SR)."
Answered by AI
Are there still open slots for participants in this trial?
"Unfortunately, this medical trial is not currently enrolling. It was initially posted on July 27th 2020 and the most recent update occurred on September 23rd 2022. Despite that, 1141 other clinical trials are actively searching for participants at present time."
Answered by AI
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