- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04005040
Evaluation of Mobile X-ray Within the Triple Aim Method
Background:
In foreign countries, mobile x-ray already is being used where transfer to the radiology department at the hospital may be an obstacle. Using mobile x-ray, the x-ray examination is performed in the patients own home with transportable equipment that reminds of the transportable x-ray equipment that is being used in the intensive care units. At The Department of Radiology (DOR), Aarhus University Hospital there is an ongoing project mobile x-ray for patients living in nursing homes in Aarhus. The project will be evaluated inspired by the Triple Aim Approach in three sub studies.
Overall aim:
The overall aim is to conclude if mobile x-ray improves healthcare for fragile patients.
Hypotheses:
- Patients examined with mobile x-ray have fewer number of hospital admissions compared with patients examined with x-ray at DOR.
- Patients examined with mobile x-ray are more satisfied with their examination compared with patients examined with x-ray at DOR.
Sub study 1 - Population health
Aim:
The primary aim is to study if mobile x-ray improves the health of the defined population measured in hospital admission. Also to study challenges conducting a RCT.
The outcome measures:
The primary outcome is hospital admissions.
Sub study 2 - Experience of care
Aim:
The aim is to study the satisfaction with mobile x-ray compared the satisfaction to x-ray at DOR.
Methods:
Observations, interview and questionnaires.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Central Region Denmark
-
Aarhus, Central Region Denmark, Denmark, 8000
- Aarhus University Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- patients referred to a mobile X-ray examination in Aarhus Municipality
Exclusion Criteria:
- all other patients referred to an x-ray examination
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Single Group Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: Mobile X-ray
Intervention: X-ray examination in the patients own home
|
Evaluating the effect of mobile x-ray compared to x-ray at the Hospital
|
Placebo Comparator: X-ray at the Hospital
Control: X-ray at the hospital
|
Evaluating the effect of mobile x-ray compared to x-ray at the Hospital
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Hospital admissions
Time Frame: one year
|
How many patients are hospitalized
|
one year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
patient satisfaction
Time Frame: one year
|
Measuring satisfaction using questionnaires
|
one year
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Helene Nørrelund, Decan, University of Aarhus
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
Other Study ID Numbers
- Mobile X-ray
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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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