Back to resultsSynchronous Video (Telemedicine) Consulation in the Prehospital Setting
Primary Purpose
Emergencies, Prehospital, Telemedicine
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Video Consultation
Sponsored by
About this trial
This is an interventional health services research trial for Emergencies
Eligibility Criteria
Inclusion Criteria:
- Cardiac Arrest
- Hemodynamically unstable trauma patients requiring resuscitation and airway management
- Trauma patients with altered mentation requiring airway management
- Acute stroke patients
- Medical patients that refuse transport for medical evaluation Pediatric Intensive Care Telemedicine Program
- Complex clinical situations where paramedic teams need immediate management guidance
- Critically ill pediatric patients requiring evaluation/stabilization for interfacility transport
- Pediatric patients requiring intervention for respiratory failure
- Pediatric patients with ongoing seizures and/or neurological abnormalities
- Hemodynamically unstable patients
- Complex clinical situations requiring medical control guidance
Exclusion Criteria:
• All other patients not list above
Sites / Locations
- Mayo Clinic in Rochester
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Synchronous Video Consultation
Arm Description
Testing the feasibility of a synchronous video consultation in the field prior to emergency department arrival.
Outcomes
Primary Outcome Measures
Video Consultations Completed
Total number of video consultations completed
Secondary Outcome Measures
Mortality
Total number of subject deaths
Hospital Length of Stay
Total number of hours subjects were admitted to the hospital
Emergency Room Length of Stay
Total number of hours subjects were admitted to the emergency room
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03800316
Brief Title
Synchronous Video (Telemedicine) Consulation in the Prehospital Setting
Official Title
Synchronous Video (Telemedicine) Consulation in the Prehospital Setting
Study Type
Interventional
2. Study Status
Record Verification Date
May 2020
Overall Recruitment Status
Completed
Study Start Date
January 14, 2019 (Actual)
Primary Completion Date
March 31, 2020 (Actual)
Study Completion Date
March 31, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Mayo Clinic
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The study team aims to test connectivity metrics and follow patient outcomes using a new, innovative synchronous video technology in the prehospital setting in three distinct areas:
- 911 Calls
- Pediatric Critical Care Transport
Currently, paramedics and pediatric transport teams seek advice from physicians using a telephone. This project replaces the phone with video consultation where the physicians can directly interact with patients, paramedics and transport teams when care advice is needed.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Emergencies, Prehospital, Telemedicine, Telehealth
7. Study Design
Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
85 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Synchronous Video Consultation
Arm Type
Experimental
Arm Description
Testing the feasibility of a synchronous video consultation in the field prior to emergency department arrival.
Intervention Type
Device
Intervention Name(s)
Video Consultation
Intervention Description
Video consultation with emergency medicine physicians for patients that are critically ill prior to arrival in the ED
Primary Outcome Measure Information:
Title
Video Consultations Completed
Description
Total number of video consultations completed
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Mortality
Description
Total number of subject deaths
Time Frame
1 year
Title
Hospital Length of Stay
Description
Total number of hours subjects were admitted to the hospital
Time Frame
1 year
Title
Emergency Room Length of Stay
Description
Total number of hours subjects were admitted to the emergency room
Time Frame
1 year
10. Eligibility
Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Cardiac Arrest
Hemodynamically unstable trauma patients requiring resuscitation and airway management
Trauma patients with altered mentation requiring airway management
Acute stroke patients
Medical patients that refuse transport for medical evaluation Pediatric Intensive Care Telemedicine Program
Complex clinical situations where paramedic teams need immediate management guidance
Critically ill pediatric patients requiring evaluation/stabilization for interfacility transport
Pediatric patients requiring intervention for respiratory failure
Pediatric patients with ongoing seizures and/or neurological abnormalities
Hemodynamically unstable patients
Complex clinical situations requiring medical control guidance
Exclusion Criteria:
• All other patients not list above
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christopher S Russi
Organizational Affiliation
Mayo Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mayo Clinic in Rochester
City
Rochester
State/Province
Minnesota
ZIP/Postal Code
55905
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Links:
URL
https://www.mayo.edu/research/clinical-trials
Description
Mayo Clinic Clinical Trials
Learn more about this trial
Synchronous Video (Telemedicine) Consulation in the Prehospital Setting
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