- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02050256
Improving End-of-life Care by Continuing Medical Education and Electronic Decision Making Support for General Practitioners
Improving End-of-life Care by Continuing Medical Education and Electronic Decision Making Support for General Practitioners in Denmark - an Intervention Study
Background: Optimizing the basic palliative care has been shown beneficial to patients in end-of-life care, the general practitioner (GP) having a pivotal role in the health care system, providing comprehensive and continued medical care.
The aim of the study is to investigate the effect of a complex intervention in general practice on GPs' awareness of and confidence in providing end-of-life care.
Method: A follow-up study among 404 general practices in Central Denmark Region. The participating general practices will get the opportunity to receive education in palliative care and access to an electronic support, which provides advice on palliative care and an overview of the palliative population in each medical practice. The education and the support will focus on patients suffering from either metastatic cancer or chronic obstructive pulmonary disease (GOLD stage 4).
The end-of-life care delivered by the GPs to their deceased patients will be analysed, based on questionnaires to GPs and register data related to the deceased patients before and after the intervention, .
Primary outcomes: Place of death of deceased patients, time spent at home, and number of hospital admissions in the last three months of the patients' lives.
Secondary outcomes: Number and kinds of contacts between GPs and patients, use of relevant medicine and of the 'Safety Box'. Finally GPs' confidence concerning palliative care will be assessed in questionnaires.
Study Overview
Status
Study Type
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Aarhus, Denmark, 8000
- Aarhus University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
Working as General Practitioner in the Central Region of Denmark in 2013 and onwards
-
Exclusion Criteria:
-
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: general practioner
|
Continuing medical education and electronic decision support to General Practitioners.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Place of death of deceased patients
Time Frame: 1 year
|
Looking at the proportion of General practitioners patients dying at home in the year following the continuing medical education meeting
|
1 year
|
|
time spent at home the last three months of the deceased patients lives
Time Frame: 3 months
|
Looking at all the deceased patients in one year following the continuing medical education meeting
|
3 months
|
|
Numbers of hospital admission the last three months of the deceased patients lives
Time Frame: 3 months
|
Looking at all the deceased patients in one year following the continuing medical education meeting
|
3 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
and kinds of contacts between GPs and patients in the last three months of the deceased patients lives
Time Frame: three months
|
three months
|
|
|
use of relevant medicine and of the 'Safety Box' in the last three months of the deceased patients lives
Time Frame: three months
|
three months
|
|
|
GPs' confidence concerning palliative care
Time Frame: 14 months
|
assessed using questionnaire before and after the intervention
|
14 months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Anders B. Mr Jensen, Professor, Department of Oncology, Aarhus University Hospital, Denmark
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2006802748
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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