Uni-centric, randomized, open-label, prospective interventional-comparative study, with a control arm (patients receiving standard preoperative information) and an experimental arm (patients receiving standard preoperative information and having access to a dematerialized educational video support).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Enrollment
226
video support provided to the patient before surgery
Assistance publique Hopitaux de Marseille - Hopital Nord
Marseille, France
RECRUITINGImmediate pre-operative anxiety
self-measurement using the HAD Scale
Time frame: 10 days
Perioperative anxiety (randomization (consultation), immediate postoperative and discharge)
based on HAD scale
Time frame: 90 days
Post-traumatic stress disorder
PCL-5 scale
Time frame: 90 days
Quality of life evaluation
European Organisation for Research and Treatment of Cancer core health- related quality of life questionnaire (QLQ-C30).
Time frame: 90 days
Cumulative postoperative morbidity
score CCI
Time frame: 90 days
Intra-hospital consumption of analgesics
accounting for in-hospital consumption of analgesics
Time frame: 90 days
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