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Electrical Muscle Stimulation in Congestive Heart Failure

Primary Purpose

Congestive Heart Failure, Electric Muscle Stimulation, Severe Decondition

Status
Unknown status
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Electrical muscle devise
Sponsored by
Kantonsspital Olten
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Congestive Heart Failure

Eligibility Criteria

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

Inclusion Criteria:

  • age ≥ 60 years
  • hospitalized due to heart failure
  • left ventricular ejection fraction ≤ 40%
  • NYHA class II to IV
  • willingness to complete the 6-week EMS training programme
  • tolerability of the electrical stimulation
  • provision of informed consent

Exclusion Criteria:

  • severe neuromuscular or oncologic diseases with inability to perform exercise testing and EMS training
  • inotropic intravenous agents used (≤10 days)
  • implanted pacemaker/ICD
  • unstable angina
  • severe uncontrolled arrhythmias
  • patients with severe pulmonary limitation (Tiffeneau ratio <70%, or vital capacity <70% of predicted value)

Sites / Locations

  • Kantonsspital OltenRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Experimental

Placebo Comparator

Arm Label

Low Intensity EMS

High Intensity EMS

Placebo

Arm Description

Conventional Stimulation

Russian Stimulation

no Stimulation, supported by phone contact

Outcomes

Primary Outcome Measures

Difference in 6 minutes walking distance after EMS training
The primary outcome of the study is the difference in 6 minutes walking distance (m) between baseline and after 6-weeks EMS training in all groups (high intensity vs low intensity vs control).

Secondary Outcome Measures

Full Information

First Posted
October 5, 2018
Last Updated
April 11, 2021
Sponsor
Kantonsspital Olten
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1. Study Identification

Unique Protocol Identification Number
NCT03793647
Brief Title
Electrical Muscle Stimulation in Congestive Heart Failure
Official Title
Electrical Muscle Stimulation in Severely Deconditioned Congestive Heart Failure Patients- a Prospective, Randomized, Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
April 2021
Overall Recruitment Status
Unknown status
Study Start Date
April 1, 2019 (Actual)
Primary Completion Date
August 1, 2021 (Anticipated)
Study Completion Date
December 30, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Kantonsspital Olten

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This trial is to evaluate two types of electrical muscle Stimulation (EMS) stimulation (low intensity "conventional stimulation" vs. high intensity "Russian" stimulation) of legs in comparison with a control group without EMS in a cohort of elderly patients with severe deconditioning after CHF decompensation.
Detailed Description
BACKGROUND: Congestive heart failure (CHF) is increasingly prevalent worldwide and is associated with significant morbidity and mortality. Poor exercise capacity is well known as a risk factor for poor prognosis. The deconditioning is mainly associated with a decrease in leg muscle mass and loss of leg strength as well as loss of muscle endurance. This affects especially elderly patients. To improve this condition in CHF electrical muscle stimulation (EMS) is a suitable method of training, which hardly affects the heart. However, most EMS existing stimulation protocols are uncomfortable and not user-friendly, especially for elderly patients. The Russian space medicine has many years' experience in specific EMS stimulation protocols, which are well tolerated by cosmonauts for hours even during working activities. Therefore, a research project has been established between the Russian Academy of Sciences (Laboratory for Biomedical Problems) and the ARTORG Research Center for Biomedical Engineering to study the effects of new developed EMS procedures in elderly persons. Aims: The aim of trial is to evaluate two types of EMS stimulation (low intensity "conventional stimulation" vs. high intensity "Russian" stimulation) of legs in comparison with a control group without EMS in a cohort of elderly patients with severe deconditioning after CHF decompensation. METHOTOLOGY: This prospective, randomized controlled study will use commercially available electronic stimulator devices (Medel GmbH, Hamburg, Germany) for EMS. For the "Russian" stimulation, an especial developed stimulator (Amplidin-EST No.5) will be used for frequency modulation of the stimulation impulse, which is supposed to make stimulation sensation more comfortable. Supervised EMS training will be performed 5 times per week (weekdays) during 30 minutes over a period of 6 weeks in elderly deconditioned CHF patients, starting at the Kantonsspital Olten during the hospitalisation and continued at home. We will include 20 patients in each group (20 in control group, 20 in low intensity "conventional group and 20 in high intensity "Russian" group). The control group was preformed to exclude an attention bias in the study results. The primary endpoint of the study is the difference in maximum oxygen uptake (peak VO2) and in 6 minutes walking distance between baseline and after 6-weeks EMS training in all groups (high intensity vs low intensity vs control). The follow-up period is planned for 2 years. POTENTIAL SIGNIFICANCE: Exercise capacity and quality of life in severely deconditioned patients with CHF is poor and life expectancy is low. While the possibilities to improve the poor condition and function of the heart by pharmaceutical therapies are limited, there is potential to improve the condition of the peripheral muscles by exercise training. However, a successful aerobic training is rarely feasible in these patients. Therefore, EMS training may prove to be ideal tool to improve leg muscle mass and function of elderly patients. Because, CHF patients do not tolerate most of the existing EMS stimulation protocols, we have developed a new EMS stimulation protocol. The application is virtually painless and therefore well tolerated over hours due to a sophisticated stimulation protocol. Therefore, we hope that, this especial for elderly CHF patients developed training protocol, may improve their daily activity as well as their quality of life.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Congestive Heart Failure, Electric Muscle Stimulation, Severe Decondition, Elderly Person, Exercise Capacity, Activities of Daily Living

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Prospective, randomized controlled study
Masking
Investigator
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Low Intensity EMS
Arm Type
Active Comparator
Arm Description
Conventional Stimulation
Arm Title
High Intensity EMS
Arm Type
Experimental
Arm Description
Russian Stimulation
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
no Stimulation, supported by phone contact
Intervention Type
Device
Intervention Name(s)
Electrical muscle devise
Intervention Description
evaluate two types of EMS stimulation of legs
Primary Outcome Measure Information:
Title
Difference in 6 minutes walking distance after EMS training
Description
The primary outcome of the study is the difference in 6 minutes walking distance (m) between baseline and after 6-weeks EMS training in all groups (high intensity vs low intensity vs control).
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: age ≥ 60 years hospitalized due to heart failure left ventricular ejection fraction ≤ 40% NYHA class II to IV willingness to complete the 6-week EMS training programme tolerability of the electrical stimulation provision of informed consent Exclusion Criteria: severe neuromuscular or oncologic diseases with inability to perform exercise testing and EMS training inotropic intravenous agents used (≤10 days) implanted pacemaker/ICD unstable angina severe uncontrolled arrhythmias patients with severe pulmonary limitation (Tiffeneau ratio <70%, or vital capacity <70% of predicted value)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Nisha Arenja, Dr
Phone
0041 62 311 49 45
Email
nisha.arenja@spital.so.ch
First Name & Middle Initial & Last Name or Official Title & Degree
Hugo Saner, Prof.
Email
Hugo.Saner@insel.ch
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nisha Arenja
Organizational Affiliation
Kantonsspital Olten
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kantonsspital Olten
City
Olten
ZIP/Postal Code
4600
Country
Switzerland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nisha Arenja, Dr
Phone
0041 62 311 49 45
Email
nisha.arenja@spital.so.ch

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
15942420
Citation
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Results Reference
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Citation
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Results Reference
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PubMed Identifier
12727155
Citation
Harris S, LeMaitre JP, Mackenzie G, Fox KA, Denvir MA. A randomised study of home-based electrical stimulation of the legs and conventional bicycle exercise training for patients with chronic heart failure. Eur Heart J. 2003 May;24(9):871-8. doi: 10.1016/s0195-668x(02)00822-9.
Results Reference
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PubMed Identifier
20490656
Citation
Karavidas A, Arapi SM, Pyrgakis V, Adamopoulos S. Functional electrical stimulation of lower limbs in patients with chronic heart failure. Heart Fail Rev. 2010 Nov;15(6):563-79. doi: 10.1007/s10741-010-9171-9.
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Results Reference
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PubMed Identifier
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Citation
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PubMed Identifier
10378936
Citation
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PubMed Identifier
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Citation
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Citation
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Results Reference
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Electrical Muscle Stimulation in Congestive Heart Failure

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