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

Surgery Clinical Trial

— Bloc3D  

Official title:

Evaluation of the Satisfaction of Patients Coming "on Foot" in the Operating Room (Standing, Dignified, Relaxed)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04453176
• Other study ID #: LOCAL/2018/PC-01
• Status: Completed
• Start date: February 25, 2019
• Est. completion date: February 28, 2020

Study information

• Verified date: August 2021
• Source: Centre Hospitalier Universitaire de Nimes
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial 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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 300
• Est. completion date: February 28, 2020
• Est. primary completion date: February 28, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

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

Related Conditions & MeSH terms

• Anesthesiology
• Satisfaction, Patient
• Surgery

Intervention

Other:
• Patient Satisfaction
Patient satisfaction evaluated with EVAN G questionnaire

Locations

Country	Name	City	State
France	Clinique Juge	Marseille
France	Institut paoli Calmette	Marseille
France	Chu Montpellier - Saint-Eloi	Montpellier
France	Institut de cancerologie de Montpellier	Montpellier
France	CHU Nimes	Nîmes	Gard

Sponsors (1)

Lead Sponsor	Collaborator
Centre Hospitalier Universitaire de Nimes

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Satisfaction of day case surgery: EVAN-G score	Satisfaction is measured with an EVAN-G score (1-100 points)	Day 0