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Clinical Trials/NCT07191184
NCT07191184RecruitingNot Applicable

Identification of Obstacles and Levers to the Outpatient Care of Patients in Terminal Palliative Situations: Exploratory Study Among General Practitioners in Bas-Rhin

University Hospital, Strasbourg, France1 site in 1 country12 target enrollmentStarted: September 16, 2024Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
12
Locations
1
Primary Endpoint
Identify barriers to outpatient care for terminally ill palliative patients by general practitioners in the Bas Rhin region.

Study Overview

Brief Summary

80% of patients wish to die at home. The number of deaths will increase in the coming years due to the aging population. The general practitioner (GP) is at the center of this care. Despite national plans for the development of palliative care, dying at home remains complicated. The difficulties described and known are organizational (workload) and linked to the doctor's experience with the suffering of the patient and their family. Many studies have been conducted in hospital settings, and the solutions developed are often not very accessible to GP. Conducting a study on this subject will allow us to take stock of this outpatient care provided by general practitioners following numerous changes that have occurred in recent years, both in terms of palliative care teaching and in terms of modifications to the care offered.

Study Design

Study Type
Observational
Observational Model
Case Only
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • General physician based in Bas-Rhin
  • Agreeing to participate in the research

Exclusion Criteria

  • Refusing to participate in the research
  • Replacement physician, specialist physician, based outside Bas-Rhin

Outcomes

Primary Outcomes

Identify barriers to outpatient care for terminally ill palliative patients by general practitioners in the Bas Rhin region.

Time Frame: At 8 months

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
University Hospital, Strasbourg, France
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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