Palliative Care Needs Among Elderly People at Emergency Department

Palliative Care Clinical Trial

Official title:

Palliative Care Needs Among Elderly People at Emergency Department

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05883696
• Other study ID #: 2020-05905
• Status: Recruiting
• Start date: March 31, 2023
• Est. completion date: December 31, 2025

Study information

• Verified date: March 2024
• Source: Region Skane
• Contact: Sofia Persson, MSc, PhD-student
• Phone: +46708652769
• Email: sofia.persson[@]skane.se
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Aim: To assess what proportion of all patients over the age of 75 who seek care at the emergency department have palliative care needs and whether these are documented in the patient's medical record.

Data collection and analysis: Patients over 75 years of age who seek care in an emergency department and are classified as triage 2-4 during initial triage are assessed by a researcher. Patients with dementia or other cognitive dysfunction will be excluded. Two types of data collection are included 1) Swedish Palliative care guide (S-PCG) documents that the researcher fills in together with the patient, 2) data from the patient's medical record, this data is collected according to a special assessment template. Data from the medical record will be collected after the patient left the emergency department.

Data collection is ongoing until 300 patients have been included in the study. Data will be analyzed using descriptive statistics.

Implications: The percentage of previously undetected/documented palliative care needs in emergency departments is relevant for prioritizing general palliative care within e.g. housing for the elderly and primary care S-PCG can be relevant to increase the level of knowledge at these care facilities. If it turns out that many patients have palliative care needs that are not met in the emergency department, health care structures need to ensure that these patients receive help at the right level of care. This would likely mean that the number of emergency visits and hospital admissions (with suffering and reduced quality of life as a result) can be reduced.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 300
• Est. completion date: December 31, 2025
• Est. primary completion date: December 30, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 75 Years and older

Eligibility

Inclusion Criteria:

• Classified as triage 2-4

Exclusion Criteria:

• Dementia or other cognitive dysfunction

• Not being able to communicate in Swedish.

Related Conditions & MeSH terms

• Elderly Person
• Emergencies
• Palliative Care
• Palliative Medicine

Intervention

Other:
• Swedish Palliative Care Guide (S-PCG)
S-PCG is a care guide that aim to inform best practice and to meet palliative care needs of patients and their families throughout all the time with palliative care needs. The S-PCG support palliative care for adult patients regardless of diagnosis, place of care and if it is early och late palliative care. The S-PCG includes three parts Assessments of palliative care needs Initiating palliative care 2D. End of life care. After death. In this study only the first part of the S-PCG will be used.

Locations

Country	Name	City	State
Sweden	Region Skane	Helsingborg	Skane

Sponsors (1)

Lead Sponsor	Collaborator
Region Skane

Country where clinical trial is conducted

Sweden, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Palliative care needs	The proportion of patients that have palliative care needs that are identified with S-PCG.	The study will be ongoing fo up to at year. The S-PCG will be used at 1 time for each included patient.
Primary	Palliative care needs documented in medical records.	The proportion of patients with palliative care need identified with S-PCG as compared to the proportion of palliative care needs documented in the medical record.	The study will be ongoing fo up to at year. The S-PCG will be used at 1 time for each included patient