Bloc3D: Evaluation of the Satisfaction of Patients Coming "on Foot" in the Operating Room

Sponsor
Centre Hospitalier Universitaire de Nīmes (Other)
Overall Status
Completed
CT.gov ID
NCT04453176
Collaborator
(none)
300
5
12.1
60
5

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Patient Satisfaction

Study Design

Study Type:
Observational
Actual Enrollment :
300 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Evaluation of the Satisfaction of Patients Coming "on Foot" in the Operating Room (Standing, Dignified, Relaxed)
Actual Study Start Date :
Feb 25, 2019
Actual Primary Completion Date :
Feb 28, 2020
Actual Study Completion Date :
Feb 28, 2020

Arms and Interventions

Arm Intervention/Treatment
operating block admission "on foot"

Patient going to the oparating block on foot

Other: Patient Satisfaction
Patient satisfaction evaluated with EVAN G questionnaire

standard operating block admission

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

Other: Patient Satisfaction
Patient satisfaction evaluated with EVAN G questionnaire

Outcome Measures

Primary Outcome Measures

  1. Satisfaction of day case surgery: EVAN-G score [Day 0]

    Satisfaction is measured with an EVAN-G score (1-100 points)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 CHU Nimes Nîmes Gard France 30 000
2 Clinique Juge Marseille France 13000
3 Institut paoli Calmette Marseille France 13000
4 Chu Montpellier - Saint-Eloi Montpellier France 34295
5 Institut de cancerologie de Montpellier Montpellier France 34295

Sponsors and Collaborators

  • Centre Hospitalier Universitaire de Nīmes

Investigators

  • Principal Investigator: Blandine Fayard, MD, CHU Nimes, France

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Centre Hospitalier Universitaire de Nīmes
ClinicalTrials.gov Identifier:
NCT04453176
Other Study ID Numbers:
  • LOCAL/2018/PC-01
First Posted:
Jul 1, 2020
Last Update Posted:
Aug 4, 2021
Last Verified:
Aug 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Aug 4, 2021