search
Back to results

Robotic Assisted Rehabilitation for Heart Failure Patients and Patients After Cardiac Surgery

Primary Purpose

Heart Failure, Post Cardiac Surgery

Status
Unknown status
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
4 weeks robotic assisted training with the Lokomat®
One week robotic assisted gait training with the Lokomat®
Sponsored by
University of Zurich
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Heart Failure focused on measuring Heart failure, robotic assisted gait therapy

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Heart failure patients:

  • stable heart failure (over 3 months, NYHA 2, NYHA 3)
  • Left ventricular ejection fraction less than 45% postoperative patients:
  • possibility to walk at least 50m on the ground floor

Exclusion Criteria:

  • weight >100kg

Sites / Locations

  • University Hospital ZurichRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Heart failure, robotic assisted training

Post cardiac surgery

Arm Description

4 weeks robotic assisted training with the Lokomat®

One week robotic assisted gait training with the Lokomat®

Outcomes

Primary Outcome Measures

Deep sternal wound infections
Occurence of deep sternal wound infections due to training, only in patients after cardiac surgery
Changes in VO2 (maximal oxygen uptak in ml/(kg*min))
Change in maximal oxygen uptake during spiroergometry due to training, only in heart failure patients
Changes in BNP
Change in brain natriuretic peptide due to training, measured in mg/ml. Only in heart failure patients.
Changes in strength measurement of the musculus quadriceps
isometric strength of the musculus quadriceps measured in kilopond
Changes in CRP (C- reactive protein)
Change in C- reactive protein, due to training, measured in mg/ml. Only in heart failure patients.
Changes in IL 6 (interleukin 6)
Change in interleukin 6(measured in mg/ml), due to training. Only in heart failure patients.
Changes in SF 36
Questionaire (SF 36- short form 36 of health survey) to assess changes in quality of life due to the training. Only in heart failure patients
Changes in walking distance (in meters) in 6 minute walk test (MWT)
6 minute walk test to assess changes in walking distance after training period, only in patients after cardiac surgery

Secondary Outcome Measures

Full Information

First Posted
May 11, 2014
Last Updated
October 29, 2014
Sponsor
University of Zurich
search

1. Study Identification

Unique Protocol Identification Number
NCT02146196
Brief Title
Robotic Assisted Rehabilitation for Heart Failure Patients and Patients After Cardiac Surgery
Official Title
Roboter-unterstützte Kardiale Rehabilitation Herzinsuffzienter Patientinnen Und Patienten
Study Type
Interventional

2. Study Status

Record Verification Date
October 2014
Overall Recruitment Status
Unknown status
Study Start Date
February 2014 (undefined)
Primary Completion Date
November 2014 (Anticipated)
Study Completion Date
December 2014 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Zurich

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Robotic assisted gait therapy with the Lokomat® as a new method for rehabilitation in advanced heart failure and after cardiac surgery.
Detailed Description
Rehabilitation in heart failure medicine is limited due to many comorbidities and reduced exercise capacity in this patient group. In patients after cardiac surgery rehabilitation is sometimes difficult especially due to ICU- acquired weakness following a prolonged intensive care course. To tackle these problems and enable recovery and rehabilitation many of the conventional methods are lacking feasibility. During the next decades increasing numbers of older and more frail patients in the field of advanced heart failure are expected. To establish a new method for rehabilitation we use technology well established in other divisions of medicine. Robotic assisted gait therapy is well established in neurology in paraplegic and tetraplegic patients, patients after stroke and traumatic injured patients. Gait therapy is used to re-establish the normal course of motion. The Lokomat ® (Hocoma AG) is therefore used in over 25 countries worldwide. The combination of different training modes (interval training, endurance training and resistance training) is one of the advantages. The most important benefit is the possibility to extend or relieve the robotic assistance up to a point without support on the one hand and full support from the Lokomat ® on the other hand and relieve the patient partly or complete from his bodyweight. This enables the therapist to plan the most possible individual training almost independent from his exercise capacity for each patient. Up to now heart failure is a contraindication for training with the Lokomat ® and no trial was performed after cardiac surgery. Therefore a clinical trial is necessary to establish this method in the field of heart failure medicine and after cardiac surgery. In our prospective trial we investigate two points after a feasibility trial first, were healthy persons and patients with NYHA 1 or less are trained for safety reasons, to establish possible protocols and get familiar with the robotic assisted gait therapy. In the prospective trial we train patients with stable heart failure (NYHA 2 or NYHA 3) and a left ventricular ejection fraction less than 45% for 4 weeks with 3 trainings per week. Timeframe for heart failure Patients: Screening day0; Baseline/Start of the training day0 +(0-5days); training period day0+ (0-5days) up to 4 Weeks, 28 days of training with the Lokomat®. Each week three training periods; End of Study Visit after 4 to 5 Weeks from baseline. Timeframe for patients after cardiac surgery: Screening day0; baseline/start of the training day0 +(0-2days); training period one week with the Lokomat® with three training sessions; end of study visit after one week, telephone follow up twelve weeks after hospital discharge to evaluate possible deep sterna wound infection. Due to the character as a pilot trial, there are no statistical end points, but stress test (spiroergometry), blood sample (interleukin 6, CRP, BNP) , strength measurement of the Musc. quadriceps and a quality of life questionnaire (SF 36) are taken at baseline (day0) and after the 4 week training period at end of study visit. Patients after cardiac surgery are trained with another strategy. There the safety aspect is the most important in this pilot trial. Patients after cardiac surgery are trained with the Lokomat® during initial hospitalization for one week with three sessions. A six minute walk test and measurement of quadriceps peak force is done at at baseline/start of the training day0, expected at day 3 to 14 after surgery, and after one week of training at end of study visit day seven. A telephone follow up of this patients three months after hospital discharge is done for possible deep sternal wound infection. Each training in the heart failure group should lasts 30-45minutes. The heart failure group should contain 5-6 patients. The training in the postcardiotomy group should last 10-40minutes depending on patients postoperative status. The postcardiotomy group should contain 10 patients. 20 patients receiving normal postoperative physiotherapy serve as a control group.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure, Post Cardiac Surgery
Keywords
Heart failure, robotic assisted gait therapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
12 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Heart failure, robotic assisted training
Arm Type
Experimental
Arm Description
4 weeks robotic assisted training with the Lokomat®
Arm Title
Post cardiac surgery
Arm Type
Experimental
Arm Description
One week robotic assisted gait training with the Lokomat®
Intervention Type
Device
Intervention Name(s)
4 weeks robotic assisted training with the Lokomat®
Intervention Description
During a prespecified time period (4weeks) a three times weekly robotic assisted gait training during 30-45 minutes. Strength training, interval training and endurance training are possible.
Intervention Type
Device
Intervention Name(s)
One week robotic assisted gait training with the Lokomat®
Intervention Description
During a prespecified time period (1week) a three times weekly robotic assisted gait training during 10-40 minutes. Strength training, interval training and endurance training are possible
Primary Outcome Measure Information:
Title
Deep sternal wound infections
Description
Occurence of deep sternal wound infections due to training, only in patients after cardiac surgery
Time Frame
12 weeks after hospital discharge
Title
Changes in VO2 (maximal oxygen uptak in ml/(kg*min))
Description
Change in maximal oxygen uptake during spiroergometry due to training, only in heart failure patients
Time Frame
After four weeks robot-assisted training with the Lokomat®
Title
Changes in BNP
Description
Change in brain natriuretic peptide due to training, measured in mg/ml. Only in heart failure patients.
Time Frame
After four weeks robot-assisted training with the Lokomat®
Title
Changes in strength measurement of the musculus quadriceps
Description
isometric strength of the musculus quadriceps measured in kilopond
Time Frame
After four weeks robotic assisted training with the Lokomat®. In the postcardiotomy group after one week robot-assisted training
Title
Changes in CRP (C- reactive protein)
Description
Change in C- reactive protein, due to training, measured in mg/ml. Only in heart failure patients.
Time Frame
After four weeks robot-assisted training with the Lokomat®
Title
Changes in IL 6 (interleukin 6)
Description
Change in interleukin 6(measured in mg/ml), due to training. Only in heart failure patients.
Time Frame
After four weeks robot-assisted training with the Lokomat®
Title
Changes in SF 36
Description
Questionaire (SF 36- short form 36 of health survey) to assess changes in quality of life due to the training. Only in heart failure patients
Time Frame
After four weeks robot-assisted training with the Lokomat®
Title
Changes in walking distance (in meters) in 6 minute walk test (MWT)
Description
6 minute walk test to assess changes in walking distance after training period, only in patients after cardiac surgery
Time Frame
After one week robot-assisted training with the Lokomat®

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Heart failure patients: stable heart failure (over 3 months, NYHA 2, NYHA 3) Left ventricular ejection fraction less than 45% postoperative patients: possibility to walk at least 50m on the ground floor Exclusion Criteria: weight >100kg
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Felix Schoenrath, MD
Phone
0041442553298
Email
felix_schoenrath@gmx.de
First Name & Middle Initial & Last Name or Official Title & Degree
Michael Stader
Phone
0041442553298
Email
michael.stader@usz.ch
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Volkmar Falk, MD
Organizational Affiliation
University of Zurich
Official's Role
Study Director
Facility Information:
Facility Name
University Hospital Zurich
City
Zurich
ZIP/Postal Code
8091
Country
Switzerland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Felix Schoenrath, MD
Phone
0041442559849
Email
felix_schoenrath@gmx.de
First Name & Middle Initial & Last Name & Degree
Michael Stader
Phone
00412553298
Email
michael.stader@usz.ch
First Name & Middle Initial & Last Name & Degree
Felix Schoenrath, MD

12. IPD Sharing Statement

Citations:
PubMed Identifier
26717214
Citation
Schoenrath F, Markendorf S, Brauchlin AE, Frank M, Wilhelm MJ, Saleh L, Riener R, Schmied CM, Falk V. Robot-assisted training for heart failure patients - a small pilot study. Acta Cardiol. 2015 Dec;70(6):665-71. doi: 10.2143/AC.70.6.3120178.
Results Reference
derived
PubMed Identifier
25998717
Citation
Schoenrath F, Markendorf S, Brauchlin AE, Seifert B, Wilhelm MJ, Czerny M, Riener R, Falk V, Schmied CM. Robot-Assisted Training Early After Cardiac Surgery. J Card Surg. 2015 Jul;30(7):574-80. doi: 10.1111/jocs.12576. Epub 2015 May 22.
Results Reference
derived

Learn more about this trial

Robotic Assisted Rehabilitation for Heart Failure Patients and Patients After Cardiac Surgery

We'll reach out to this number within 24 hrs