Consent in Anaesthesia
NCT06115720 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 206
Last updated 2023-11-07
Summary
DESIGN: Prospective randomised-controlled trial AIM: To determine whether presenting both techniques of general anaesthesia and regional anaesthesia in an unbiased manner, with video media, aids the anaesthetic consent process, compared to standard verbal consent alone.
OUTCOME MEASURES
Primary outcome:
\- Participants' satisfaction regarding the anaesthetic consent process
Secondary outcomes:
* Knowledge, attitudes and practices towards anaesthesia
* Participants' choice of anaesthetic technique POPULATION: General adult population (\>18yrs), males and females DURATION: 2 years
Conditions
- Regional Anesthesia
- Patient Satisfaction
Interventions
- OTHER
-
Video assisted consent
The intervention group will also be shown the same pre-recorded standard verbal consent, but following this will additionally be shown a specifically recorded video of the anaesthetic process for both GA and RA. This video will aim to communicate the same information as that found in the traditional verbal consent, using an actor undergoing an anaesthetic to provide context.
Sponsors & Collaborators
-
Imperial College London
collaborator OTHER -
Imperial College Healthcare NHS Trust
lead OTHER
Principal Investigators
-
Boyne Bellew · Imperial College Healthcare NHS Trust
-
Christopher Mullington · Imperial College Healthcare NHS Trust
Study Design
- Allocation
- RANDOMIZED
- Purpose
- HEALTH_SERVICES_RESEARCH
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2023-11-01
- Primary Completion
- 2025-10-31
- Completion
- 2025-10-31
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