Evaluation of the Effect of Robot-assisted Early Mobilization - Project MobiStaR

Sponsor

Ludwig-Maximilians - University of Munich (Other)

Overall Status

Completed

CT.gov ID

NCT05071248

Collaborator

German Federal Ministry of Education and Research (Other), Catholic University of Eichstätt-Ingolstadt (Other)

Enrollment

Location

Arms

Actual Duration (Months)

3.4

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

Within the MobiStaR project the adaptation of procedures in an intensive care unit combined with the use of this robotic system will create the conditions to increase the mobilization rate of critically ill intensive care patients significantly, possibly thereby increasing the rehabilitation outcomes for these patients and developing a new standard of care for robot-assisted early mobilization.

The intervention study will assess the organizational feasibility of robot-assisted early mobilization (starting in the first 72 hours after admission to the ICU), the behavior and experience of the mobilizing professionals and the effects on patient outcomes in terms of ventilation time, muscle mass (sonographic examination) and physical activity (measured by established scores such as Functional Status Score for ICU (FSS-ICU) and Medical Research Council (MRC) classification).

Condition or Disease	Intervention/Treatment	Phase
Patient Activation Mobilization Robotics	Device: VEMO (Reactive Robotics GmbH)	N/A

Detailed Description

Early mobilization means the mobilization of critically ill patients in the early course after admission to the intensive care unit. The positive influence of early mobilization of critically ill patients on various aspects of patient outcomes has already been demonstrated. However, the implementation of early mobilization in clinical practice is difficult. Especially the high personnel effort is a barrier.

The Munich-based company Reactive Robotics (RR) is currently developing the world's first adaptive robotic assistance system VEMO©, which has CE approval for the planned indication and is to be used in the medium term for mobilizing intensive care patients.

Within the MobiStaR project, the adaptation of procedures in an intensive care unit combined with the use of this robotic system will create the conditions to significantly increase the mobilization rate of critically ill intensive care patients, possibly thereby increasing the rehabilitation results for these patients and developing a new standard of care for robot-assisted early mobilization. In this project, the robotic system will be used in anesthesiology intensive care units of the Ludwigs-Maximilians-University hospital.

Within this study, the effects of robot-assisted early mobilization will now be evaluated. This study comprises three study arms, in which (1) the feasibility and practicability of robot-assisted early mobilization, (2) the behavior and experience of the mobilizing professionals, and (3) the effect on patient outcomes will be evaluated.

The study is monocentric, prospective, interventional, does not include invasive procedures or blood sampling and has multiple data collection time points.

The feasibility of robot-assisted early mobilization surveys concomitantly how many VEM therapies can be implemented in how many patients as well as if and which adverse events occur.
The behavior and experience of the mobilizing professionals will be evaluated by using episodic interviews and standardized observations. Nurses with advanced training in anesthesia and intensive care, nurses and physiotherapists who have at least three years of professional experience in an intensive care unit as well as medical specialists with completed specialist training or a leading position in the intensive care unit will be included.
The effects on patient outcomes, primarily ventilation duration, muscle mass (sonographic examination) and physical activity (measured by established scores such as FSS-ICU and MRC classification), will be measured at different time points and compared with a historical patient population. Secondary factors such as delirium incidence, hemodynamic parameters, respiratory parameters but also longitudinal parameters such as ICU and hospital length of stay will be analyzed from routine data/patient records. Informed consenting patients undergoing a planned surgical procedure that is postoperatively associated with intensive care treatment and an anticipated duration of ventilation of more than 48 hours will be included. These patients will receive standardized early mobilization using the robotic system at either ten frequencies or for seven days. No invasive procedures such as blood sampling will be performed as part of the study. Outcomes will be compared with a historical comparison group to evaluate the effect of robot-assisted VEM (very early mobilization). Approximately 30 patients will be included. The outcomes will be compared with those of a historical group (n=30) treated with conventional early mobilization.

The intervention is planned for a duration of five to six months starting in September 2021.

Study Design

Study Type:

Interventional

Actual Enrollment :

27 participants

Allocation:

Non-Randomized

Intervention Model:

Sequential Assignment

Intervention Model Description:

The present study is a monocentric, prospective intervention study designed to evaluate the feasibility and to evaluate the feasibility and integration in the setting of the intensive care unit. the behavior and experience of the mobilizing specialists of the robot-assisted VEM is to be evaluated longitudinally (three data collection points). to compare robot-assisted VEM in critically ill ICU patients with non-robot-assisted early mobilization according to the standard of care of a historical patient population.The present study is a monocentric, prospective intervention study designed to evaluate the feasibility and to evaluate the feasibility and integration in the setting of the intensive care unit. the behavior and experience of the mobilizing specialists of the robot-assisted VEM is to be evaluated longitudinally (three data collection points). to compare robot-assisted VEM in critically ill ICU patients with non-robot-assisted early mobilization according to the standard of care of a historical patient population.

Masking:

None (Open Label)

Primary Purpose:

Supportive Care

Official Title:

Evaluation of the Effect of Robot-assisted Early Mobilization on Critically Ill Patients, on the Mobilisation Behaviour and Experience of Mobilizing Professionals and Organisational Processes in an Intensive Care Unit

Actual Study Start Date :

Sep 15, 2021

Actual Primary Completion Date :

Apr 15, 2022

Actual Study Completion Date :

May 15, 2022

Arms and Interventions

Arm	Intervention/Treatment
Active Comparator: patients with robot-assisted early mobilization All patients will receive a physical examination at various time points to assess physical functionality and muscle strength, as well as a sonographic examination of leg muscles, diaphragm, and lungs. These examinations should be performed on day -1 (preoperatively), on postoperative days 1,2,3, then once a week if the patient remains in the ICU, on day 28, on the day of discharge from the ICU, and on a follow-up examination approximately 3 months after discharge from the ICU.The follow-up examination should only take place if the patients present themselves at the hospital anyway due to medically indicated follow-up examinations (not study-related). Alternatively, patients can be asked about their condition by telephone.	Device: VEMO (Reactive Robotics GmbH) The robot used for early mobilization is able to verticalize the patients in their bed without transfer and to generate a movement of the legs that measures and supports the patients' own movement. The device meets the requirements for mobilizing critically ill patients in an intensive care unit, maintaining hygiene standards and providing the best possible support for the patient's own movement.
No Intervention: patients with conventional early mobilization (historic group) All patients fulfill the same criteria like the intervention group and receive conventional early mobilization.

Arm

Intervention/Treatment

Active Comparator: patients with robot-assisted early mobilization

All patients will receive a physical examination at various time points to assess physical functionality and muscle strength, as well as a sonographic examination of leg muscles, diaphragm, and lungs. These examinations should be performed on day -1 (preoperatively), on postoperative days 1,2,3, then once a week if the patient remains in the ICU, on day 28, on the day of discharge from the ICU, and on a follow-up examination approximately 3 months after discharge from the ICU.The follow-up examination should only take place if the patients present themselves at the hospital anyway due to medically indicated follow-up examinations (not study-related). Alternatively, patients can be asked about their condition by telephone.

Device: VEMO (Reactive Robotics GmbH)

The robot used for early mobilization is able to verticalize the patients in their bed without transfer and to generate a movement of the legs that measures and supports the patients' own movement. The device meets the requirements for mobilizing critically ill patients in an intensive care unit, maintaining hygiene standards and providing the best possible support for the patient's own movement.

No Intervention: patients with conventional early mobilization (historic group)

All patients fulfill the same criteria like the intervention group and receive conventional early mobilization.

Outcome Measures

Primary Outcome Measures

Evaluation of the effect of robot-assisted early mobilization on critically ill patients - Ventilation duration [6 months]
changes in ventilation duration (in hours) in comparison to a historical patient group
Evaluation of the effect of robot-assisted early mobilization on critically ill patients - sonographic examination Area of the M.rec.femoris [6 months]
muscle mass (sonographic examination, in millimeters): Area of the M. rec. femoris in comparison to a historical patient group (in cm²)
Evaluation of the effect of robot-assisted early mobilization on critically ill patients - sonographic examination thickness M. quad. femoris [6 months]
muscle mass: Thickness M. quad. Femoris (in cm²) in comparison to a historical patient group
Evaluation of the effect of robot-assisted early mobilization on critically ill patients - sonographic examination- motility diaphragm breathing [6 months]
muscle mass: motility of the diaphragm during breathing (in cm) in comparison to a historical patient group
Evaluation of the effect of robot-assisted early mobilization on critically ill patients - sonographic examination thickness diaphragm inspiration [6 months]
muscle mass: Thickness of diaphragm during inspiration (in cm) in comparison to a historical patient group
Evaluation of the effect of robot-assisted early mobilization on critically ill patients - sonographic examination thickness diaphragm exhalation [6 months]
muscle mass: Thickness of diaphragm during exhalation (in cm) in comparison to a historical patient group
Evaluation of the effect of robot-assisted early mobilization on critically ill patients - physical activity - FSS-ICU [6 months]
physical activity measured using the score FSS-ICU (0 -35) in comparison to a historical patient group. A higher value means a better outcome.
Evaluation of the effect of robot-assisted early mobilization on critically ill patients - physical activity [6 months]
physical activity on upper and lower extremity measured using the Medical Research Council (MRC) score in comparison to a historical patient group. (0=absent muscle contraction, 1=visible muscle contraction, 2=movement when gravity is eliminated, 3=active movement against gravity, 4=active movement against resistance, 5=normal strength.)
Behavior and experience of the mobilizing professionals - qualitative interviews [6 months]
subjectively experienced emotions, motivating and challenging factors - evaluated with a semi-structured interview guideline
Behavior and experience of the mobilizing professionals - qualitative observations [6 months]
behavior and body posture during the mobilization - evaluated with a standardized observation sheet
Feasibility in organizational processes - eligible patients [6 months]
Frequency of eligible patients (count per week: included patients in the study/ new eligible patients in the ICUs)
Feasibility in organizational processes - mobilizations [6 months]
frequency of robot-assisted mobilizations (per patient per day)
Feasibility in organizational processes - adverse events [6 months]
adverse events (count of patient-related, user-related or technology-related adverse events)

Secondary Outcome Measures

Delir [6 months]
Delir incidence using the CAM ICU: number of days without Delir. 1 = pathological; 2 = normal; 3 = not performed in comparison to a historical patient group
Consciousness [6 months]
level of consciousness using the Glasgow Coma Scale (3-15) in comparison to a historical patient group
Sedation level [6 months]
Sedation level using the Richmond Agitation Sedation Scale (RASS) (-5 - +5) in comparison to a historical patient group
Pain (VAS) [6 months]
Pain - with the use of the Visual Analog Scale (VAS) (before and after mobilization) (0-10) in comparison to a historical patient group
health related quality of life [6 months]
Health-related quality of life after 3 months using the the SF-36 (Short form questionnaire) (0-100) in comparison to a historical patient group
Blood pressure [6 months]
hemodynamics - Blood pressure (in mmHg) in comparison to a historical patient group
catecholamine demand [6 months]
hemodynamics - catecholamine demand (cumulative over 24 hours) in comparison to a historical patient group
heart rate [6 months]
hemodynamics - heart rate (1/min) in comparison to a historical patient group
cardiac output [6 months]
hemodynamics - Cardiac output (in l/min) in comparison to a historical patient group
oxygen consumption [6 months]
hemodynamics - Oxygen consumption (in l) in comparison to a historical patient group
respiration [6 months]
respiration- Maximum respiratory rate for 24h in comparison to a historical patient group
ICU Score - SOFA [6 months]
ICU Scores like Sepsis-related organ failure assessment score (SOFA) (0-24) in comparison to a historical patient group. A higher value means a worse outcome.
ICU Scores - APACHE II [6 months]
ICU Scores like Acute Physiology and Chronic Health Disease Classification System II (APACHE II) (0-71) in comparison to a historical patient group. A higher value means a worse outcome.
ICU Scores - SAPS II [6 months]
ICU Scores like Simplified Acute Physiology Score II (SAPS II) (0-163) in comparison to a historical patient group. A higher value means a worse outcome.

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

planned surgical intervention
postoperative intensive medical and therapeutic treatment
expected duration of ventilation > 48 hours
age ≥ 18 years
preoperative informed consent by the patients in the study
weight >45 kg and <135 kg
body height >1.50 m and <1.95 m

Exclusion Criteria:

patient refusal to participate in the study
unable to give consent
chronically bedridden before inclusion
clinical Frailty Scale ≥ 7
chronic ventilation (over 24h) before ICU admission
increased intracranial pressure / risk for increased intracranial pressure / recent cerebral hemorrhage
pregnancy
pre-existing neuromuscular disease resulting in chronic limitation of strength and efficiency
sternotomy / sternectomy during surgical procedure

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	LudwigMaximilians	Munich	BY	Germany	81337

Sponsors and Collaborators

Ludwig-Maximilians - University of Munich
German Federal Ministry of Education and Research
Catholic University of Eichstätt-Ingolstadt

Investigators

Principal Investigator: Michael Zoller, PD Dr., Ludwig-Maximilians - University of Munich
Principal Investigator: Inge Eberl, Prof. Dr., Catholic University of Eichstätt-Ingolstadt
Principal Investigator: Eduard Kraft, PD Dr., Ludwig-Maximilians - University of Munich
Principal Investigator: Uli Fischer, Dr., Ludwig-Maximilians - University of Munich