Robotic-assisted Exercise Training in Heart Failure
Primary Purpose
Heart Failure, Systolic, Pulmonary Disease
Status
Completed
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
MyoSuitFeasibility
Sponsored by
About this trial
This is an interventional treatment trial for Heart Failure, Systolic focused on measuring Exercise training, Robotic training, Exosuit training
Eligibility Criteria
Inclusion Criteria:
- >17 years old
- written informed consent
- chronic end-stage systolic heart failure without ventricular assist device, LVEF ≤ 45% OR chronic advanced pulmonary diseases
- clinically stable for at least 6 weeks
- ability to mobilize into standing and walking of at least 10 meters with or without rollator
- ability to get up from a chair without rotating the upper body >45° sagittally
Exclusion Criteria:
- addictions or other illnesses that impact the ability to understand the nature, scope and consequences of the trial
- lack of knowledge of German to fully understand study information
- pregnancy, pre-menopausal women
- contraindications of cardiopulmonary exercising
- BMI > 35 kg/m², waist size > 135 cm.
- Height <150 cm, >195 cm
- Weight<45 kg, >110 kg
- Functional Reach Test <15,24 cm
- Flexion contracture in the knee/hip joint >10°
- Chronic colonization or active infection with multi-resistant pathogens
Sites / Locations
- German Heart Center
- German Heart Institute
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
Feasibility study group
Arm Description
Outcomes
Primary Outcome Measures
Incidence of Treatment-Emergent Falls - Safety of the MyoSuit
Patients with advanced heart or pulmonary failure will perform 6-minute walking tests and activities of daily life both with and without wearing a MyoSuit. Outcome is measured by documenting number of falls.
Incidence of Treatment-Emergent Adverse Events - Safety of the MyoSuit
Patients with advanced heart or pulmonary failure will perform 6-minute walking tests and activities of daily life both with and without wearing a MyoSuit. Outcome is measured by documenting adverse events.
Exercise can be performed when wearing a MyoSuit - Feasibility and Tolerability of walking test, activities of daily life, rehabilitation exercise group.
Patients with advanced heart or pulmonary failure will perform a 6 minute walking test, activities of daily life and a cardiac rehabilitation exercise unit. Outcome is measured dichotomously (yes/no) according to its feasibility.
Necessity of assistance in exercising when wearing a MyoSuit - Feasibility and Tolerability
Patients with advanced heart or pulmonary failure will perform a 6 minute walking test, activities of daily lif and a cardiac rehabilitation exercise unit. Outcome is measured according to a scale of assistance needed (1=no assistance, 2=little assistance, 3=much assistance, 4=not possible). 1 is minimum, 4 is maximum. The higher the score, the worse the outcome.
MyoSuit assistance leads to changes in walking distance in patients with advanced heart or pulmonary failure assessed by 6-minute walking test.
Change of 6minute walk distance in meters will be assessed with and without MyoSuit in every participant.
Secondary Outcome Measures
Full Information
NCT ID
NCT04839133
First Posted
March 29, 2021
Last Updated
November 16, 2021
Sponsor
German Heart Institute
Collaborators
ETH Zurich
1. Study Identification
Unique Protocol Identification Number
NCT04839133
Brief Title
Robotic-assisted Exercise Training in Heart Failure
Official Title
Feasibility of Robotic Assisted Exercise Training in Patients With Advanced Heart Failure or Advanced Pulmonary Diseases
Study Type
Interventional
2. Study Status
Record Verification Date
November 2021
Overall Recruitment Status
Completed
Study Start Date
March 31, 2021 (Actual)
Primary Completion Date
July 30, 2021 (Actual)
Study Completion Date
July 31, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
German Heart Institute
Collaborators
ETH Zurich
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
Background:
Regular physical activity is an evidence-based adjuvant therapy of chronic heart failure or chronic lung diseases. Structured exercise training is safe, increases exercise capacity and quality of life, relieves symptoms and reduces hospitalization rates. Even a trend towards reduction of mortality has been identified. However, dyspnea and fatigue, typical symptoms of heart or lung failure, force patients to physical inactivity which fatally aggravates deconditioning and exercise intolerance, leading to an increased risk of hospitalization and a loss of independence and quality of life. To break through this vicious circle physical activity must be restored, since exercise intolerance can be successfully improved by physical training.
Purpose:
This study will address the challenging task of remobilizing patients with advanced chronic lung or heart failure in a functional New York Heart Association class III-IV by using an externally physically-supported exosuit movement therapy. This soft, wearable robot (fig. 1) assists mobilization according to individual needs by activating neuromuscular feedback systems, promoting physical activity and preventing early physical exhaustion. The investigators hypotheses that an exosuit-supported training increases exercise capacity and quality of life in a greater degree than non-supported training.
Methods:
The study will consist of two parts investigating i) the feasibility, tolerance and safety (n= 30) and ii) the efficacy of an exosuit device-supported training (n=30). In i) patients will perform a walking test and a set of everyday life skills or participate in a standardized rehabilitation sports program. In ii) patients will be randomized in a 2:1 ratio for an exosuit-supported or non-supported exercise training protocol, training 3 units per week for 8 weeks. Assessment of outcome will be performed by various functional, mobility and endurance tests, questionnaires and clinical parameters. Furthermore, the transfer of regained motor and balance skills to everyday life will be analyzed.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure, Systolic, Pulmonary Disease
Keywords
Exercise training, Robotic training, Exosuit training
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Feasibility study group
Arm Type
Other
Intervention Type
Device
Intervention Name(s)
MyoSuitFeasibility
Intervention Description
Participants will absolve feasibility tests with and without wearing a MyoSuit.
Primary Outcome Measure Information:
Title
Incidence of Treatment-Emergent Falls - Safety of the MyoSuit
Description
Patients with advanced heart or pulmonary failure will perform 6-minute walking tests and activities of daily life both with and without wearing a MyoSuit. Outcome is measured by documenting number of falls.
Time Frame
1 hour
Title
Incidence of Treatment-Emergent Adverse Events - Safety of the MyoSuit
Description
Patients with advanced heart or pulmonary failure will perform 6-minute walking tests and activities of daily life both with and without wearing a MyoSuit. Outcome is measured by documenting adverse events.
Time Frame
1 hour
Title
Exercise can be performed when wearing a MyoSuit - Feasibility and Tolerability of walking test, activities of daily life, rehabilitation exercise group.
Description
Patients with advanced heart or pulmonary failure will perform a 6 minute walking test, activities of daily life and a cardiac rehabilitation exercise unit. Outcome is measured dichotomously (yes/no) according to its feasibility.
Time Frame
1 hour
Title
Necessity of assistance in exercising when wearing a MyoSuit - Feasibility and Tolerability
Description
Patients with advanced heart or pulmonary failure will perform a 6 minute walking test, activities of daily lif and a cardiac rehabilitation exercise unit. Outcome is measured according to a scale of assistance needed (1=no assistance, 2=little assistance, 3=much assistance, 4=not possible). 1 is minimum, 4 is maximum. The higher the score, the worse the outcome.
Time Frame
1 hour
Title
MyoSuit assistance leads to changes in walking distance in patients with advanced heart or pulmonary failure assessed by 6-minute walking test.
Description
Change of 6minute walk distance in meters will be assessed with and without MyoSuit in every participant.
Time Frame
30 minutes
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
>17 years old
written informed consent
chronic end-stage systolic heart failure without ventricular assist device, LVEF ≤ 45% OR chronic advanced pulmonary diseases
clinically stable for at least 6 weeks
ability to mobilize into standing and walking of at least 10 meters with or without rollator
ability to get up from a chair without rotating the upper body >45° sagittally
Exclusion Criteria:
addictions or other illnesses that impact the ability to understand the nature, scope and consequences of the trial
lack of knowledge of German to fully understand study information
pregnancy, pre-menopausal women
contraindications of cardiopulmonary exercising
BMI > 35 kg/m², waist size > 135 cm.
Height <150 cm, >195 cm
Weight<45 kg, >110 kg
Functional Reach Test <15,24 cm
Flexion contracture in the knee/hip joint >10°
Chronic colonization or active infection with multi-resistant pathogens
Facility Information:
Facility Name
German Heart Center
City
Berlin
ZIP/Postal Code
13353
Country
Germany
Facility Name
German Heart Institute
City
Berlin
ZIP/Postal Code
13353
Country
Germany
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
PubMed Identifier
35320878
Citation
Just IA, Fries D, Loewe S, Falk V, Cesarovic N, Edelmann F, Feuerstein A, Haufe FL, Xiloyannis M, Riener R, Schoenrath F. Movement therapy in advanced heart failure assisted by a lightweight wearable robot: a feasibility pilot study. ESC Heart Fail. 2022 Jun;9(3):1643-1650. doi: 10.1002/ehf2.13903. Epub 2022 Mar 23.
Results Reference
derived
Learn more about this trial
Robotic-assisted Exercise Training in Heart Failure
We'll reach out to this number within 24 hrs