None listed
Conditions
Interventions
Intervention1: Health educational intervention: Baseline (Day 0,Week 0): Participants will complete a simulation consent OSCE (5 minute station with a simulated patient scored using the OSCE rubric ad
Sponsors
Multidisciplinary Research Unit
Eligibility
Inclusion criteria
Inclusion criteria: MBBS interns posted in the Department of Community Medicine, RIMS, Imphal during the study period
Exclusion criteria
Exclusion criteria: Those who are not willing to participate
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| change in skill and knowledge score in informed consent process in medical practiceTimepoint: Pre test, post test 1 after 4 weeks, post test 2 after 6 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| change in self-reported confidence in taking informed consentTimepoint: Pre test, post test 1 after 4 weeks, post test 2 after 6 weeks | — |
Countries
India
Contacts
Public ContactDr Sandra Fernandez
Regional Institute of Medical Sciences, Imphal, Manipur
Outcome results
None listed