TELENeurological Support for Emergency Department (TELENS-ED)
Primary Purpose
Emergencies, Neurologic Disorder
Status
Active
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Teleneurological evaluation and support
Sponsored by
About this trial
This is an interventional other trial for Emergencies
Eligibility Criteria
Inclusion Criteria:
- Patients aged > 18 years
- Symptoms related to possible acute / subacute neurological pathology, or worsening of known neurological pathology, for which the ED physician considers neurological consultation indicated / necessary.
- Signing of informed consent to remote neurological evaluation.
Exclusion Criteria:
- All life-threatening emergency cases, where the study procedure would interfere with clinical practice
- Patients with known neurological pathology or with clinical severity to such an extent that the need for admission to OCB/Carpi Neurology unit or to the internal wards of the Policlinico is immediately evident.
- Refusal of the patient/caregiver to perform remote neurological evaluation.
Sites / Locations
- Azienda USL di Modena
- Azienda Ospedaliero Universitaria di Modena
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Teleneurological evaluation and support
Arm Description
teleneurological evaluation using a medical device certified as telemedicine system
Outcomes
Primary Outcome Measures
Teleconsultation clinical application
Percentage of patients who undergo neurological teleconsultation over the number of patients who access on the days and in the time slots in which the service is active and needing a neurological evaluation.
Teleconsultation diagnostic efficacy
Percentage of patients re-admitted to the ED in the 7 days following the date of neurological consultation. It is expected that for the patients of the neurological teleconsultation the % of re-admission to ED will not exceed that of the patients undergone standard neurological advice.
Teleconsultation efficacy - hospitalization
Percentage of hospitalized patients among those undergone TeleNeurology compared to percentage of hospitalization for patients with in person neurological evaluation. It is expected that for patients of the teleneurology group the % of hospitalization will not exceed that of patients undergone standard neurological advice.
Time 'door to end of diagnostic process'
The total time from ED admission to the end of the diagnostic and therapeutic process (time spent in the ED): this time is expected to be significantly shorter for patients in the teleneurology group than for patients having a standard neurological advice.
Time 'door to end of neurological evaluation'
The time from the ED admission to the end of the remote neurological consultation: this time is expected to be significantly shorter for patients in the teleneurology group than for patients having a standard neurological advice
Secondary Outcome Measures
Cost-effectiveness
Evaluation of costs, or cost-effectiveness. For the evaluation of costs, it will be developed a model that considers the cost of the system on the one hand, and the savings in terms of personnel (medical personnel, paramedics and ambulances costs). Outcome indicator.
Evaluation of the level of satisfaction of the users
For this purpose an evaluation form will be provided to patients / family members. Users satisfaction will be measured by visual analogue scale (VAS) where 100 is the highest satisfaction and 0 is the lowest. Outcome indicator.
Evaluation of the level of satisfaction of the health personnel.
For this purpose an evaluation form will be provided to medical personnel involved. Personnel satisfaction will be measured by visual analogue scale (VAS) where 100 is the highest satisfaction and 0 is the lowest. Outcome indicator.
Teleconsultation failure
Percentage of cases assessed by teleconsultation for which the neurologist was unable to make remote decisions and requested for sending the patient to Hub Hospital for a "first-person" evaluation. Process indicator.
Full Information
NCT ID
NCT04611295
First Posted
October 27, 2020
Last Updated
August 10, 2022
Sponsor
Azienda Ospedaliero-Universitaria di Modena
Collaborators
Azienda USL Modena
1. Study Identification
Unique Protocol Identification Number
NCT04611295
Brief Title
TELENeurological Support for Emergency Department
Acronym
TELENS-ED
Official Title
TELENeurological Evaluation and Support for the Emergency Department (TELENS-ED): an Open-label Clinical Trial
Study Type
Interventional
2. Study Status
Record Verification Date
August 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
December 1, 2020 (Actual)
Primary Completion Date
October 30, 2022 (Anticipated)
Study Completion Date
December 30, 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Azienda Ospedaliero-Universitaria di Modena
Collaborators
Azienda USL Modena
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Open-label, non-inferiority, teleconsultation with televisit study to compare efficacy, safety and users satisfaction of a TeleNeurological Support versus "in person" neurological examination in the emergency department
Detailed Description
The investigtors are going to perform an interventional, open-label study on the use of teleconsultation in the emergency department focused on neurological diseases other than stroke (for which a specific protocol already exists) in two Hospitals of Modena province, Italy.
The study is aimed at developing a remote neurological consultancy system (teleconsultation) for patients with acute neurological symptoms in charge of hospital facilities without 24-hour availability of neurologist consultant.
Pilot project setting: a) ED of Modena Policlinico Hospital in the afternoon, night, and public holidays, time windows in which the Neurologist consultant is not present at Policlinico Hospital; b) ED of Mirandola Hospital.
The project (enrolment) is expected to be developed over a period of 6 months in which 100 patients will be enrolled.
The primary objective is to assess whether a TeleNeurological Evaluation and Support for the Emergency Department can guarantee a faster but qualitatively not inferior diagnostic/therapeutic work-up if compared with in person examination, assuring the availability of all the necessary examinations and treatments with a consistent time reduction.
Secondary objectives: to determine if the usage of a teleconsultation physician for neurological evaluation compared to a conventional physician "de visu" in urgent but non-life-threatening neurological cases, is superior regarding 1) effect evaluation, 2) process evaluation, and 3) cost-benefit analysis.
Outcome and process indicators will be assessed and compared in the following groups:
Experimental group (cases): a) patients who access the Policlinico Hospital ED in the afternoon and night-time and on holidays; b) patients who access the Mirandola Hospital ED during the period of the study.
Control Groups: a) retrospectively collected data on neurological consultation performed by OCB Neurology for Policlinico Hospital patients in the same time slots in the same months of the last two years.; b) retrospectively collected data on neurological consultation performed by Carpi Neurology for Mirandola Hospital patients in the same time slots in the same months of the last two years.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Emergencies, Neurologic Disorder
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
88 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Teleneurological evaluation and support
Arm Type
Experimental
Arm Description
teleneurological evaluation using a medical device certified as telemedicine system
Intervention Type
Procedure
Intervention Name(s)
Teleneurological evaluation and support
Intervention Description
The study is aimed at developing a remote neurological consultancy system (teleconsultation) for patients with acute neurological symptoms in charge of hospital facilities without 24-hour availability of neurologist consultant.
Primary Outcome Measure Information:
Title
Teleconsultation clinical application
Description
Percentage of patients who undergo neurological teleconsultation over the number of patients who access on the days and in the time slots in which the service is active and needing a neurological evaluation.
Time Frame
6 months
Title
Teleconsultation diagnostic efficacy
Description
Percentage of patients re-admitted to the ED in the 7 days following the date of neurological consultation. It is expected that for the patients of the neurological teleconsultation the % of re-admission to ED will not exceed that of the patients undergone standard neurological advice.
Time Frame
6 months
Title
Teleconsultation efficacy - hospitalization
Description
Percentage of hospitalized patients among those undergone TeleNeurology compared to percentage of hospitalization for patients with in person neurological evaluation. It is expected that for patients of the teleneurology group the % of hospitalization will not exceed that of patients undergone standard neurological advice.
Time Frame
6 months
Title
Time 'door to end of diagnostic process'
Description
The total time from ED admission to the end of the diagnostic and therapeutic process (time spent in the ED): this time is expected to be significantly shorter for patients in the teleneurology group than for patients having a standard neurological advice.
Time Frame
6 months
Title
Time 'door to end of neurological evaluation'
Description
The time from the ED admission to the end of the remote neurological consultation: this time is expected to be significantly shorter for patients in the teleneurology group than for patients having a standard neurological advice
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Cost-effectiveness
Description
Evaluation of costs, or cost-effectiveness. For the evaluation of costs, it will be developed a model that considers the cost of the system on the one hand, and the savings in terms of personnel (medical personnel, paramedics and ambulances costs). Outcome indicator.
Time Frame
6 months
Title
Evaluation of the level of satisfaction of the users
Description
For this purpose an evaluation form will be provided to patients / family members. Users satisfaction will be measured by visual analogue scale (VAS) where 100 is the highest satisfaction and 0 is the lowest. Outcome indicator.
Time Frame
6 months
Title
Evaluation of the level of satisfaction of the health personnel.
Description
For this purpose an evaluation form will be provided to medical personnel involved. Personnel satisfaction will be measured by visual analogue scale (VAS) where 100 is the highest satisfaction and 0 is the lowest. Outcome indicator.
Time Frame
6 months
Title
Teleconsultation failure
Description
Percentage of cases assessed by teleconsultation for which the neurologist was unable to make remote decisions and requested for sending the patient to Hub Hospital for a "first-person" evaluation. Process indicator.
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients aged > 18 years
Symptoms related to possible acute / subacute neurological pathology, or worsening of known neurological pathology, for which the ED physician considers neurological consultation indicated / necessary.
Signing of informed consent to remote neurological evaluation.
Exclusion Criteria:
All life-threatening emergency cases, where the study procedure would interfere with clinical practice
Patients with known neurological pathology or with clinical severity to such an extent that the need for admission to OCB/Carpi Neurology unit or to the internal wards of the Policlinico is immediately evident.
Refusal of the patient/caregiver to perform remote neurological evaluation.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Antonio Luciani, MD
Organizational Affiliation
Azienda Ospedaliero Universitaria Policlinico Modena
Official's Role
Principal Investigator
Facility Information:
Facility Name
Azienda USL di Modena
City
Modena
ZIP/Postal Code
41123
Country
Italy
Facility Name
Azienda Ospedaliero Universitaria di Modena
City
Modena
Country
Italy
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Time Frame
Data will be available at study end
IPD Sharing Access Criteria
Upon request to principal investigator
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