None listed
Conditions
Interventions
Intervention1: Training of Anaesthesia residents: Anesthesia residents both Trainees and senior residents from the Institute will be assessed, after obtaining their consent for the same.
Control Inter
Sponsors
Tata Memorial Hospital
Eligibility
Inclusion criteria
Inclusion criteria: 1. MD Anesthesia Trainees/Senior Residents working and training in the department of Anaesthesiology, Critical Care and Pain, Tata Memorial Hospital, Mumbai 2. Research staff willing to be a part of the study
Exclusion criteria
Exclusion criteria: 1. Anesthesia Trainees /Senior Residents who refuse to give consent 2. Anesthesia Trainees / Senior Residents whose tenure is likely to end before the completion of all three phases of the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Significant improvement in consent process as defined by 3-point improvement in the consent taking checklist assessed by the research nurseTimepoint: Until 4 weeks post training | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Quantum of checklist score improvement after training 2. Predictors of significant improvement in change as per the baseline demographics 3. Assessment of improvement in compliance to AAGBI guidelines after training 4. Assessment of self-perceived improvement in consent taking after the training, assessed on a 5-point Likert scale Timepoint: Until 4 weeks post training | — |
Countries
India
Contacts
Public ContactDr Abhinav Chetri
Tata Memorial Centre
Outcome results
None listed