QALYBHRe: Impact of a Carrier (Infection, Colonization) of Highly Bacteria Resistance on the Patient's Quality of Life Hospital Environment

Sponsor
Hospices Civils de Lyon (Other)
Overall Status
Withdrawn
CT.gov ID
NCT04226001
Collaborator
(none)
0
2.5

Study Details

Study Description

Brief Summary

The quality of life of carriers detected infected or colonized by emerging highly resistant bacteria (BHRe) following the implementation of specific hygiene measures during the discovery of the microorganism has been little studied. To date, there have been no studies to determine the quality of life (QoL) in France of patients with hospitalized HBHRD.

Condition or Disease Intervention/Treatment Phase
  • Other: Quality of life questionnaire

Study Design

Study Type:
Observational
Actual Enrollment :
0 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Impact of a Carrier (Infection, Colonization) of Highly Bacteria Resistance on the Patient's
Actual Study Start Date :
Nov 16, 2020
Anticipated Primary Completion Date :
Feb 1, 2021
Anticipated Study Completion Date :
Feb 1, 2021

Arms and Interventions

Arm Intervention/Treatment
Patients

Patients screened for carriers infected or colonized by emerging highly resistant bacteria.

Other: Quality of life questionnaire
Quality of life questionnaire

Outcome Measures

Primary Outcome Measures

  1. Impact of the implementation of Complementary Hygiene Precautions following a carrier of emerging highly resistant bacteria on the quality of life of hospitalized patients [12 months]

    Measurement of the decrease in utility corresponding to the deterioration of the QOL of patients since the implementation of the Additional Hygiene Precautions (PCH) following the discovery of their emerging highly resistant bacteria (BHRe).

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Age> 18 years old

  • Have a positive BHRe screening during the hospital stay and / or have a positive BHRe clinical sample during the hospital stay

  • Conscious patients

  • All types of stays in the hospital sector

  • All pathologies

Exclusion Criteria:
  • Known patients with BHRe before hospitalization

  • PCH immediately upon admission (history of hospitalization abroad, patients contacted during a previous hospitalization)

  • Cognitive problem

  • Patients not proficient in French (requiring an interpreter)

  • Patients under guardianship

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Hospices Civils de Lyon

Investigators

  • Principal Investigator: David NARBEY, MD, Hospices Civils de Lyon

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Hospices Civils de Lyon
ClinicalTrials.gov Identifier:
NCT04226001
Other Study ID Numbers:
  • 69HCL19_0022
  • 2019-A00074-53
First Posted:
Jan 13, 2020
Last Update Posted:
Nov 17, 2020
Last Verified:
Nov 1, 2020
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 17, 2020