Evaluation of the Satisfaction of Patients Coming "on Foot" in the Operating Room

Completed

• Conditions: Satisfaction, Patient; Anesthesiology; Surgery
• Interventions: Other: Patient Satisfaction

• Registration Number: NCT04453176
• Lead Sponsor: Centre Hospitalier Universitaire de Nīmes

Brief Summary

Ambulatory surgery is currently experiencing unprecedented growth and is becoming the standard of care compared to traditional hospitalization. Without mentioning the obvious financial gains, the benefits of ambulatory care essentially lie in optimised perioperative comfort. This comfort is due to a limited period of stay (\< 12 hours) and to the proactive action of the care providers.

In this context, the optimization of the whole patient's journey during the perioperative period has been reviewed and adapted to personalized management within healthcare facilities. For more than a year now, multimodal approaches such as early rehabilitation have been undertaken, including

* morning admission with an innovative principle of "3D" patient (standing, dignified, relaxed)

* no premedication, wearing glasses and wigs,

* Drinking on the morning of the intervention (2H before admission),

* Walking to the block on foot (or in a wheelchair), return adapted to the wheelchair and no longer in a stretcher,

* fast resumption of feeding.

Currently, in the investigator's various institutions, several modes of transport to the operating theatres coexist. The purpose of this observational study is to evaluate this optimization of perioperative management "3D mode", in particular the mode of transport.

The main objective is to determine the level of patient satisfaction with this management using a standardized quality questionnaire: the "EVAN" questionnaire. This questionnaire contains 22 items allowing a global analysis of patient satisfaction. This questionnaire is already routinely conducted in many institutions. The EVAN questionnaire will be supplemented by questionnaires assessing the level of perioperative anxiety. They will be initiated into the anesthesia consultation, and finalized on the day of the surgery.

Detailed Description

Not available

Study Timeline

• Study Start: 2019-02-25
• Study First Submitted: 2020-01-27
• Primary Completion: 2020-02-28
• Study Completion: 2020-02-28
• Study First Submitted QC: 2020-06-30
• Study First Posted: 2020-07-01
• Status Verified: 2021-08
• Last Update Submitted: 2021-08-03
• Last Update Posted: 2021-08-04

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 300

Inclusion Criteria

• Age > 18 yars
• Consent to participate

Exclusion Criteria

• Emergency surgery
• ASA >4
• Difficulties in French reading, incapacity to complete questionnaire
• patient in a wheelchair or stretcher or having difficulty walking alone

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
operating block admission "on foot"	Patient Satisfaction	Patient going to the oparating block on foot
standard operating block admission	Patient Satisfaction	Patient going to the operating room in a conventional way (stretcher)

Primary Outcome Measures

Name	Time	Method
Satisfaction of day case surgery: EVAN-G score	Day 0	Satisfaction is measured with an EVAN-G score (1-100 points)

Trial Locations

Locations (5)

CHU Nimes; 🇫🇷 Nîmes, Gard, France

Clinique Juge; 🇫🇷 Marseille, France

Institut paoli Calmette; 🇫🇷 Marseille, France

Chu Montpellier - Saint-Eloi; 🇫🇷 Montpellier, France

Institut de cancerologie de Montpellier; 🇫🇷 Montpellier, France