Information retention after preoperative assessment by anaesthesiologist or video education in patients scheduled for surgery Surgery
Conditions
Interventions
Participants will be allocated by simple randomization (1:1:1:1) embedded in the trial software (E+POS by NovaCair) to one of four arms:
1. A control group that will only fill out the
Sponsors
Erasmus MC
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Adults visiting the preoperative anesthesia clinic 2. Scheduled for elective surgery 3. Able to read, write and understand the Dutch language
Exclusion criteria
Exclusion criteria: 1. Cardiothoracic surgery 2. Caesarian sections
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The effect size (Cohen's d) of video (augmented) preoperative anesthesiological education measured using the RAKQ at baseline, 14 and 42 days | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Recruitment rate measured as the number of participants recruited per month of the study 2. Loss to follow-up measured as the number of participants lost at baseline, 14 and 42 days | — |
Countries
Netherlands
Outcome results
None listed