Active Informed Consent: a New Solution to Improve and Objectively Test the Patient Understanding of Complex Surgical Procedures Proposals
Recruiting
N/A
Interventional Study
Spine Disease
Urologic Diseases
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Health Services Research
- Participants needed
- 300 (estimated)
- Sponsor
- Istituto Ortopedico Rizzoli · Other
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About This Trial
This is an interventional, non-pharmacological, randomized controlled superiority study (RCT), multicenter, open label, parallel group. The aim is to evaluate the effectiveness of a new preoperative information method, based on multimedia tools and on the objective control of understanding by the patient candidate for spinal or urological surgery.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Adults aged ≥ 18 years (with full legal capacity to consent).
* Scheduled for elective surgery in one of the two domains: spinal surgery or radical prostatectomy in the waiting list of our centers.
* Ability to comprehend Italian language.
* Basic computer or internet access s…
Contacts