Study of Pulse Pressure During Tilttable and Erigo® in Adult Patients With Acquired Brain Injury
Primary Purpose
Brain Injuries, Hypotension, Orthostatic, Syncope
Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Erigo® Hocoma
Traditional tilt table from Rehab-Care
Sponsored by
About this trial
This is an interventional treatment trial for Brain Injuries focused on measuring Rehabilitation
Eligibility Criteria
Inclusion Criteria:
- Already being treated with traditional tilttable and must be able to benefit from Erigo® treatment from a clinicians view
- Acquired brain injury as primary diagnose
- Must have Rancho Los Amigo Scale score of minimum 1 to maximum 6 on the day of inclusion
Exclusion Criteria:
- Not on mechanical ventilation
- New cerebral, cardiological or other medical problems/emergencies between the 2 interventions
- Change in cardiac medications between interventions
- Patient must not have independent gait function immediately before trial
- must not have EFA(Early Functional abilities) part score > 4 in the section "Standing", assessed by the treating physiotherapist.
Sites / Locations
- Regionshospitalet Hammel Neurocenter
Arms of the Study
Arm 1
Arm 2
Arm Type
Other
Other
Arm Label
Erigo® First
Traditional first
Arm Description
Erigo® 0 - 60 degrees - Wash out period (min 30 minutes, max 120 minutes) - Traditional Tilt table 0 - 60 degrees Step frequency on Erigo® = 48
Traditional Tilt table 0 - 60 degrees - Wash out period (min 30 minutes, max 120 minutes) - Erigo® 0 - 60 degrees Step frequency on Erigo® = 48
Outcomes
Primary Outcome Measures
Change in Non Invasive Blood Pressure(NIBP)
Secondary Outcome Measures
Patient reported comfort: The difference in prevalence of both acceptable- and not acceptable patient comfort between the Erigo and the conventional tilt-table.
Due to the included patients level of consciousness, comfort is reported as the treating therapists subjective evaluation of patients answers to standardized visual and audial question.
Full Information
NCT ID
NCT02700399
First Posted
February 5, 2016
Last Updated
June 27, 2016
Sponsor
University of Aarhus
Collaborators
Regionshospitalet Hammel Neurocenter
1. Study Identification
Unique Protocol Identification Number
NCT02700399
Brief Title
Study of Pulse Pressure During Tilttable and Erigo® in Adult Patients With Acquired Brain Injury
Official Title
Randomized Crossover Study of Pulse Pressure on Respectively Tilt Table With Integrated Stepping Function (Erigo®) and Traditional Tilt Table in Adult Patients With Acquired Brain Injury
Study Type
Interventional
2. Study Status
Record Verification Date
June 2016
Overall Recruitment Status
Completed
Study Start Date
July 2015 (undefined)
Primary Completion Date
April 2016 (Actual)
Study Completion Date
June 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Aarhus
Collaborators
Regionshospitalet Hammel Neurocenter
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to determine if the pulse pressure changes are different whether patients are training in a traditional tilt table as compared to a robotic assisted tilt table, which induces leg movement.
Detailed Description
The trial takes place in a non private hospital in Denmark. Patients are recruited from two wards treating patients with severe brain injury, and all patients admitted in the study period are considered in regards to inclusion or exclusion. Patients are included via closest relatives accept, and the patients GP(General Practitioner). Any adverse effect or event will be reported to the local ethics committee. All data will be collected simultaneously with the interventions. Some data will be directly recorded via monitor output, and some data will be directly inputted in Epidata, while trial takes place.
Sample size has been calculated to be between 10 and 60 individuals depending on the actual difference. Beyond 60 included individuals the clinical relevance of a statistical significant result is no longer apparent. If any individual variables are noncomplete, an analysis of the subjects with missing data, will be undertaken.
The statistical analyses planned follows the general crossover design using an approach considering 2 treatment and 2 periods. Patients are cluster randomized in clusters of 4, to be treated with one or the other intervention first.
Intervention A:
Traditional tilt table. measurements at 0 degrees 30 deg. 60. deg. and at return to 0 deg.
Intervention B:
Erigo® tilttable, with measurements as in intervention A. During the intervention the step frequency of the Erigo® i set at 48 steps/min.
Between the two periods a wash out period of at least ½ hour and maximum 2 hours are planned.
Primary outcome is derived from noninvasive BP measurements.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Brain Injuries, Hypotension, Orthostatic, Syncope
Keywords
Rehabilitation
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
13 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Erigo® First
Arm Type
Other
Arm Description
Erigo® 0 - 60 degrees - Wash out period (min 30 minutes, max 120 minutes) - Traditional Tilt table 0 - 60 degrees
Step frequency on Erigo® = 48
Arm Title
Traditional first
Arm Type
Other
Arm Description
Traditional Tilt table 0 - 60 degrees - Wash out period (min 30 minutes, max 120 minutes) - Erigo® 0 - 60 degrees
Step frequency on Erigo® = 48
Intervention Type
Device
Intervention Name(s)
Erigo® Hocoma
Intervention Description
Robotics assisted tilt table, without functional electrical stimulation
Intervention Type
Device
Intervention Name(s)
Traditional tilt table from Rehab-Care
Intervention Description
Traditional tilt table
Primary Outcome Measure Information:
Title
Change in Non Invasive Blood Pressure(NIBP)
Time Frame
Measured at: Baseline in supine on tilttable, 60 seconds after 30 degrees rise of tilttable, 60 seconds after 60 degrees tilt is reached. Again 60 seconds after return to 0 degrees tilt with patient still in supine position on tilttable..
Secondary Outcome Measure Information:
Title
Patient reported comfort: The difference in prevalence of both acceptable- and not acceptable patient comfort between the Erigo and the conventional tilt-table.
Description
Due to the included patients level of consciousness, comfort is reported as the treating therapists subjective evaluation of patients answers to standardized visual and audial question.
Time Frame
Question is asked within 5 minutes after 60 degrees NIBP measurement
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Already being treated with traditional tilttable and must be able to benefit from Erigo® treatment from a clinicians view
Acquired brain injury as primary diagnose
Must have Rancho Los Amigo Scale score of minimum 1 to maximum 6 on the day of inclusion
Exclusion Criteria:
Not on mechanical ventilation
New cerebral, cardiological or other medical problems/emergencies between the 2 interventions
Change in cardiac medications between interventions
Patient must not have independent gait function immediately before trial
must not have EFA(Early Functional abilities) part score > 4 in the section "Standing", assessed by the treating physiotherapist.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jørgen F Nielsen, Prof.MD DMSc
Organizational Affiliation
Regionshospitalet Hammel Neurocenter
Official's Role
Study Director
Facility Information:
Facility Name
Regionshospitalet Hammel Neurocenter
City
Hammel
ZIP/Postal Code
8450
Country
Denmark
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Study of Pulse Pressure During Tilttable and Erigo® in Adult Patients With Acquired Brain Injury
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