- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02395718
Acute Medical Admissions of ELDERly Patients (ELDER) (ELDER)
Acute Medical Admission of ELDERly Patients (≥75yrs) to Either Fast Track or Traditional Inward Hospitalisation. A Randomised Controlled Trial
Study Overview
Detailed Description
The Danish emergency care system is undergoing major changes; Emergency Departments (ED) are now centralised at fewer hospitals, thus the ED now serve as the single point of entry for all acute patients. Another initiative, has been the establishment of a Quick Diagnostic Unit (QDU) as a subunit in the ED. The QDU is a ward for fast track diagnostics and treatment of stable medical patients that is believed to optimise in-hospital care by quicker diagnosis and shorter hospitalisations, and minimise time for patients to return to their habitual health status. However, little evidence exists on the putative benefits for elderly patients treated in a QDU setting.
In this study, we will examine the benefits and drawbacks of treatment of elderly medical patients (≥75 years) in an acute treatment system with the possibility of fast-track admission and treatment, rather than treatment in the traditional medical system. We will randomise patients to treatment in either a fast track ward/short stay unit, the QDU, or to standard treatment at the Dept. of Internal Medicine (DIM).
We hypothesise that treatment in a QDU compared to DIM offers optimised care through immediate access to clinical staff and rapid diagnostic facilities, treatment and quicker rehabilitation.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Holbaek, Denmark, 4300
- Dept. of Emergency Medicine, Holbaek Sygehus, Copenhagen University Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Age ≥ 75 years
- Admitted for in-hospital treatment for an internal medicine disease
- Green tag triaged upon arrival in the ED
Exclusion Criteria:
- Previous participation in this trial
- Participation in other clinical trials
- No QDU beds available
- Subject does not have a Danish Civil Registration Number (CPR).
- Subject resides abroad
- Requires help using the toilet in daily life
- Patients not aware of date, time and location, or their own data (name, birth date)
- Informed consent cannot be obtained
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: QDU
Patients will undergo a fast track model for diagnostics and treatment with a goal of accomplishing a short-term hospitalisation.
Patients will have immediate access to all diagnostic tests and treatments that will be carried out all day (24 hours) on demand from the responsible physician.
The QDU is both organisationally and physically integrated in the ED.
Point of care ultrasonography can be performed round the clock.
Additionally the Department of Radiology provides the QDU with more advanced diagnostic procedures such as e.g.
CT scans or MRI scans on a fast track basis.
There is access to additional specialist evaluations from the ED staff or from various in house specialists, when needed.
Simultaneously to the medical treatment, physical therapists and occupational therapists train and optimise patients' level of functioning, including prevention of loss of function.
|
Treatment in a QDU.
Intervention being fast track model for diagnostics and treatment with a goal of accomplishing a short-term hospitalisation (see description QDU arm)
|
Active Comparator: DIM
Patients in the control group are treated as conventionally at one of seven wards at the DIM.
After initial admission including initial diagnostics and treatment have been carried out in the ED, patients are transferred to the DIM.
Usually patients are seen primarily by the on-call physician for evaluation of acute symptoms.
The following day, a Chief physician will work out a plan for further diagnostics and treatment.
Treatment by physiotherapists and occupational therapists is available on request from a physician.
Analyses of blood samples are performed at the central laboratory and radiological procedures at the Department of Radiology.
|
Treatment at a ward at the DIM.
Traditional inward hospitalisation
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
All cause mortality
Time Frame: 90 days
|
Number of participants that die by any cause within 90 days after the day of admission, data will be retrieved from The Danish Civil Registration system 90 days after admission.
Accounted as dead or alive.
|
90 days
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Length of stay in-hospital
Time Frame: Lenght of stay is assessed from date of randomization untill the date of discharge, date of death from any cause or whichever came first, assessed up to 100 weeks.
|
Length of stay in-hospital per participant, defined as the duration of a single episode of hospitalisation including day of admission, and day of discharge.
Length of stay will be calculated by subtracting the day of admission from day of discharge as registered in the patient's hospital chart.
Accounted in days
|
Lenght of stay is assessed from date of randomization untill the date of discharge, date of death from any cause or whichever came first, assessed up to 100 weeks.
|
Readmissions
Time Frame: 30 days
|
Number of participants that are readmitted within 30 days from date of discharge (defined as the proportion of patients readmitted no more than 30 days post initial discharge as registered in the patient's hospital chart.
Accounted as yes or no).
|
30 days
|
In hospital Mortality
Time Frame: In hospital mortality is assessed from date of randomization untill the date of discharge, date of death from any cause or whichever came first, assessed up to 100 weeks.
|
Number of participants that die In-hospital (defined as patients that have died at any time during hospitalisation as registered in the patient's hospital chart.
Accounted as dead or alive).
|
In hospital mortality is assessed from date of randomization untill the date of discharge, date of death from any cause or whichever came first, assessed up to 100 weeks.
|
In-hospital Transfer
Time Frame: is assessed from date of randomization untill the date of discharge, date of death from any cause or whichever came first, assessed up to 100 weeks.
|
Number of participants that are transferred to other wards while in hospital (defined as patients that have been transferred to any other ward in the hospital apart from the Department of Radiology at any time during hospitalisation as registered in the patient's hospital chart.
Accounted as yes or no).
|
is assessed from date of randomization untill the date of discharge, date of death from any cause or whichever came first, assessed up to 100 weeks.
|
Instrumental Activities of Daily Living
Time Frame: 90 days (± 2 days) from date of randomization
|
Number of participants with change in Instrumental activities of daily living-score (iADL- score) within 90 days from admission (defined as any decrease or increase in iADL score within 90 days from admission.
Accounted in score increase, score decrease or no-change).
|
90 days (± 2 days) from date of randomization
|
Placement in a long-term-care home after hospitalisation.
Time Frame: 3 months (± 2 days)
|
Number of participants that are placed in a long-term-care home after hospitalisation within 90 days from admission (defined by placement in any kind of long-term-care home after hospitalisation from the first day of admission to day 90 after admission.
Accounted as yes or no).
|
3 months (± 2 days)
|
Complications of hospitalisation
Time Frame: is assessed from date of randomization untill the date of discharge, date of death from any cause or whichever came first, assessed up to 100 weeks.
|
Number of participants with complications of hospitalisation (defined as an injury caused by medical management (rather than the disease process). Complications of hospitalisation are one or more of the following:
|
is assessed from date of randomization untill the date of discharge, date of death from any cause or whichever came first, assessed up to 100 weeks.
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Camilla Stroem, MD, Dept. of Emergency Medicine, Holbaek Sygehus, Copenhagen University Hospital
Publications and helpful links
General Publications
- Strom C, Rasmussen LS, Lowe AS, Lorentzen AK, Lohse N, Madsen KHB, Rasmussen SW, Schmidt TA. Short-stay unit hospitalisation vs. standard care outcomes in older internal medicine patients-a randomised clinical trial. Age Ageing. 2018 Nov 1;47(6):810-817. doi: 10.1093/ageing/afy090.
- Strom C, Rasmussen LS, Wistisen Rasmussen S, Benn Madsen KH, Ancher Sorensen HA, Andersen Schmidt T. Admission of elderly medical patients to fast track or standard hospitalisation: protocol for a randomised trial. Dan Med J. 2016 Mar;63(3):A5189.
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
Other Study ID Numbers
- ELDER
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.
Clinical Trials on Geriatric Disorder
-
University of ValenciaUnknownGeriatric DisorderSpain
-
The Hong Kong Polytechnic UniversityShatin HospitalUnknown
-
Tel-Aviv Sourasky Medical CenterUnknownGeriatric DisorderIsrael
-
Centre Hospitalier Universitaire de NiceUnknown
-
Universitaire Ziekenhuizen KU LeuvenCompleted
-
Nantes University HospitalCompleted
-
University Hospital, GrenobleCompletedGeriatric Disorder | Mobil UnitFrance
-
Washington University School of MedicineCompletedCancer | Geriatric Disorder | Patient FallUnited States
-
University of AarhusCompleted