Suivi-secret: Medical Follow-up of Medical Secretaries of General Practitioners

Sponsor
Université de Reims Champagne-Ardenne (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05889858
Collaborator
(none)
200
1
7
28.4

Study Details

Study Description

Brief Summary

General practitioners are very often confronted with requests for care from their relatives (family, friends, etc.). In the United States, the recommendations advise general practitioners against taking care of their loved ones on several grounds: lack of professional objectivity, lack of information due to modesty, risk of loss of patient autonomy. Some countries even prohibit general practitioners from prescribing to a loved one except in an emergency.

In France, there is no current recommendation on the care of relatives. Half of French general practitioners have a physical secretary and are therefore potentially confronted with requests for care from their medical secretary.

Condition or Disease Intervention/Treatment Phase
  • Other: Data collection

Detailed Description

The aim of the study is to describe the medical follow-up of medical secretaries of general practitioners

Study Design

Study Type:
Observational
Anticipated Enrollment :
200 participants
Observational Model:
Case-Only
Time Perspective:
Cross-Sectional
Official Title:
Medical Follow-up of Medical Secretaries of General Practitioners
Anticipated Study Start Date :
Jun 1, 2023
Anticipated Primary Completion Date :
Aug 1, 2023
Anticipated Study Completion Date :
Jan 1, 2024

Arms and Interventions

Arm Intervention/Treatment
"medical secretaries of general practitioners" group

Men and women working as a secretary for a general practitioner, face-to-face in the medical practice.

Other: Data collection
Data collection

Outcome Measures

Primary Outcome Measures

  1. type of attending physician [Day 1]

    type of attending physician will be either the general practitioner employing the medical secretary or an another physician (an another general practitioner or a specialist)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • medical secretaries of general practitioners

  • work in face-to-face in the medical practice

  • agreed to participate in the study

Exclusion Criteria:
  • none

Contacts and Locations

Locations

Site City State Country Postal Code
1 Université de Reims Champagne Ardenne Reims France 51100

Sponsors and Collaborators

  • Université de Reims Champagne-Ardenne

Investigators

  • Principal Investigator: Hurtaud Aline, Dr, Université Reims Champagne-Ardenne

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Université de Reims Champagne-Ardenne
ClinicalTrials.gov Identifier:
NCT05889858
Other Study ID Numbers:
  • 2023_RIPH_002_Suivi-Secret
First Posted:
Jun 5, 2023
Last Update Posted:
Jun 7, 2023
Last Verified:
May 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Université de Reims Champagne-Ardenne

Study Results

No Results Posted as of Jun 7, 2023