- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05883696
Palliative Care Needs Among Elderly People at Emergency Department
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.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Sofia Persson, MSc, PhD-student
- Phone Number: +46708652769
- Email: sofia.persson@skane.se
Study Contact Backup
- Name: Christel Hedman, MD PhD
- Email: christel.hedman@ki.se
Study Locations
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Skane
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Helsingborg, Skane, Sweden
- Recruiting
- Region Skåne
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Contact:
- Sofia Persson, PhD-student
- Email: sofia.persson@skane.se
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Classified as triage 2-4
Exclusion Criteria:
- Dementia or other cognitive dysfunction
- Not being able to communicate in Swedish.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Descriptive patient group
The research nurse will fill in the documents in Swedish Palliative care guide (S-PCG) together with the patient.
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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
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Palliative care needs
Time Frame: The study will be ongoing fo up to at year. The S-PCG will be used at 1 time for each included patient.
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The proportion of patients that have palliative care needs that are identified with S-PCG.
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The study will be ongoing fo up to at year. The S-PCG will be used at 1 time for each included patient.
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Palliative care needs documented in medical records.
Time Frame: The study will be ongoing fo up to at year. The S-PCG will be used at 1 time for each included patient
|
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.
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The study will be ongoing fo up to at year. The S-PCG will be used at 1 time for each included patient
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Maria Schelin, ass. prof., Region Skåne
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2020-05905
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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