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

NCT ID: NCT04453176

Last Updated: 2021-08-04

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 300 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2019-02-25
• Study Completion Date: 2020-02-28

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.

Conditions

Anesthesiology; Satisfaction, Patient; Surgery

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

operating block admission "on foot"

Patient going to the oparating block on foot

Patient Satisfaction

Intervention Type: OTHER

Patient satisfaction evaluated with EVAN G questionnaire

standard operating block admission

Patient going to the operating room in a conventional way (stretcher)

Patient Satisfaction

Intervention Type: OTHER

Patient satisfaction evaluated with EVAN G questionnaire

Interventions

Patient Satisfaction

Patient satisfaction evaluated with EVAN G questionnaire

Intervention Type: OTHER

Eligibility Criteria

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

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Centre Hospitalier Universitaire de Nīmes

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Blandine Fayard, MD

Role: PRINCIPAL_INVESTIGATOR

CHU Nimes, France

Locations

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

Countries

France

Other Identifiers

LOCAL/2018/PC-01

Identifier Type: -

Identifier Source: org_study_id