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

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04453176
Acronym
Bloc3D
Enrollment
300
Registered
2020-07-01
Start date
2019-02-25
Completion date
2020-02-28
Last updated
2021-08-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anesthesiology, Satisfaction, Patient, Surgery

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.

Interventions

OTHERPatient Satisfaction

Patient satisfaction evaluated with EVAN G questionnaire

Sponsors

Centre Hospitalier Universitaire de Nīmes
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
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

Design outcomes

Primary

MeasureTime frameDescription
Satisfaction of day case surgery: EVAN-G scoreDay 0Satisfaction is measured with an EVAN-G score (1-100 points)

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026