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

NCT04453176 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 300

Last updated 2021-08-04

No results posted yet for this study

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

Interventions

OTHER

Patient Satisfaction

Patient satisfaction evaluated with EVAN G questionnaire

Sponsors & Collaborators

  • Centre Hospitalier Universitaire de Nīmes

    lead OTHER

Principal Investigators

  • Blandine Fayard, MD · CHU Nimes, France

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-02-25
Primary Completion
2020-02-28
Completion
2020-02-28

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04453176 on ClinicalTrials.gov