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The Effect of Neuromuscular Electrical Stimulation (NMES) (NMES)

Primary Purpose

Muscle Fiber Atrophy, Type II

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Neuromuscular electrical stimulation
voluntary strengthening exercise
Sponsored by
University of Pittsburgh
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Muscle Fiber Atrophy, Type II focused on measuring muscle fibers, aging

Eligibility Criteria

65 Years - 80 Years (Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • 65-80 years old, are walking independently without assistive devices.

Exclusion Criteria:

  • Uncontrolled hypertension (defined as the following: 1) if not taking BP medication and resting systolic BP is greater than 140 or diastolic greater than 90, or 2) if taking BP medication and resting systolic BP greater than 160 or diastolic greater than 100).
  • History of cardiovascular disease
  • History of neurological disorders that effect lower extremity function (stroke, peripheral neuropathy, Parkinson's disease, multiple sclerosis)
  • One cortico-steroid injection to the quadriceps or patellar tendon in the past month or 3 within the past year.
  • History of quadriceps tendon rupture, patellar tendon rupture, or patellar fracture, which could place them at risk of re-injury during quadriceps strength testing.
  • Current pain in the knee or in the thigh muscles.
  • Diagnosis of inflammatory arthritis (Rheumatoid arthritis, gout, or psoriatic arthritis)
  • Muscle diseases such as muscular dystrophy.
  • Currently been participating in a regular exercise program more than 1x/week.
  • Been using anticoagulants and platelet inhibitors
  • History of chronic and significant respiratory disease or shortness of breath
  • Visual impairments to the extent that they can not accurately see the monitor screen during training program.

Sites / Locations

  • School of Health and Rehabilitation Sciences

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

1

2

Arm Description

The group who will get neuromuscular electrical stimulation (NMES)

The group who will do the voluntary muscle contraction

Outcomes

Primary Outcome Measures

Cross sectional area of type II muscle fibers

Secondary Outcome Measures

Quadriceps muscle power output
Functional performance
Quadriceps muscle cross sectional area

Full Information

First Posted
October 2, 2008
Last Updated
January 23, 2013
Sponsor
University of Pittsburgh
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1. Study Identification

Unique Protocol Identification Number
NCT00765739
Brief Title
The Effect of Neuromuscular Electrical Stimulation (NMES)
Acronym
NMES
Official Title
The Effect of Neuromuscular Electrical Stimulation (NMES) in Inducing Muscle Hypertrophy and Improvement in Muscle Torque Output Within the Quadriceps Muscle of Elderly People
Study Type
Interventional

2. Study Status

Record Verification Date
January 2013
Overall Recruitment Status
Completed
Study Start Date
October 2008 (undefined)
Primary Completion Date
August 2012 (Actual)
Study Completion Date
August 2012 (Actual)

3. Sponsor/Collaborators

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

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this project is to test the effectiveness of neuromuscular electrical stimulation (NMES) that produces 40 % of maximum voluntary contraction (MVC) in increasing muscle size and improvement in muscle force output within the thigh muscle of elderly people.
Detailed Description
Declines in whole skeletal muscle strength and size are features commonly associated with aging. Aging reduces the number of fibers in the whole muscle, which explains the loss of muscle mass. Frontera et al studied muscle strength, cross sectional area, and contractile properties of skinned parts of single fibers of the quadriceps muscle. He found that the strength and the whole muscle cross sectional area of knee extensors were significantly higher in young men compared to old subjects, but there were no differences between old and young subjects when the whole muscle strength was adjusted to the whole muscle cross sectional area (specific tension). He also found that muscle fibers from young men were stronger than muscle fibers from old men expressing the same myosin heavy chain isoform even after adjusting for size. Therefore they concluded that abnormality in the quantity and/or function of the contractile or regulatory proteins could explain the reduction in the ability of muscle fibers to generate force. Along with the loss of muscle fibers, atrophy of the fibers also has been attributed to the aging process. This atrophy has been found to be selective to type II muscle fibers. Lexel et al found in a study done on the cross sections of the whole vastus lateralis muscle from 20 men (19-84 years of age) that the mean Cross Sectional Area (CSA) of type II fibers from muscles of older individuals was on average 35 % smaller while the mean CSA of type I was approximately 6 % smaller than that of young individuals. Aging and muscles Maintaining muscle strength and size with aging has become a significant issue for elderly trying to keep up independent living and good quality of life. Several studies on old men and women have proven the effectiveness of the resistance exercises in reversing sarcopenia related problems . However in order to increase the size of type II muscle fibers we need to apply high intensity exercises (80 % of 1 RM), or by applying low resistance exercise that is very intense and is done with a large number of repetitions. The use of electrical stimulation is well documented to improve quadriceps femoris muscle torque output. Numerous experiments have been done to characterize the pattern of activation of muscle fibers during electrically stimulated muscle contraction, and the results show that the recruitment of motor units during electrically induced muscle contraction is non selective. In other words, both type I and II fibers may have equal chance of being recruited during electrically induced muscle contraction. It has been found that NMES is more likely to activate type II muscle fibers at relatively low force levels compared to voluntary exercise. If this is found to be true, then we may have an alternative intervention to improve muscle strength and muscle hypertrophy for elderly individuals who could not perform high intensity exercises to achieve these same benefits. This alternative approach might result in improved overall physical function for these individuals. The quadriceps muscle has been proposed to be treated because there is significant relationship between quadriceps muscle strength and dynamic stability during chair rise and gait at preferred speed in functionally limited elderly individuals Methods This study is a two group, repeated measures, randomized clinical trial. Baseline measurements of quadriceps muscle cross-sectional area, type II muscle fiber cross-sectional area, quadriceps power output, the timed up and go test, the SPPB, stair climbing test and ramp up power test will be obtained from subjects prior to the interventions. Following the baseline assessments subjects will be randomly assigned to either the NMES group or the comparable isometric strengthening exercise group. A set of sequentially numbered envelopes will be created and a document indicating the intervention assignment will be placed in the sequentially numbered envelopes. Upon completion of the baseline assessment, the study coordinator will take the next envelope in the sequence and open the envelope. The study coordinator will assign the subject to a group based on the randomized group assignment information obtained from the sealed envelop. During the intervention period of the study subjects will receive either NMES or isometric strengthening exercise 3 times a week for 12 weeks. Each session will last from 15-30 minutes. Post training outcome measures will be taken at the end of the 12 week intervention period.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Muscle Fiber Atrophy, Type II
Keywords
muscle fibers, aging

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
23 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
The group who will get neuromuscular electrical stimulation (NMES)
Arm Title
2
Arm Type
Active Comparator
Arm Description
The group who will do the voluntary muscle contraction
Intervention Type
Other
Intervention Name(s)
Neuromuscular electrical stimulation
Intervention Description
neuromuscular electrical stimulation that produce 40% of the maximum voluntary contraction
Intervention Type
Other
Intervention Name(s)
voluntary strengthening exercise
Intervention Description
contracting the quadriceps muscle voluntarily to produce 40% of maximum voluntary contraction
Primary Outcome Measure Information:
Title
Cross sectional area of type II muscle fibers
Time Frame
Base line and 3 months follow up
Secondary Outcome Measure Information:
Title
Quadriceps muscle power output
Time Frame
baseline and 3 month follow up
Title
Functional performance
Time Frame
baseline and 3 month follow up
Title
Quadriceps muscle cross sectional area
Time Frame
baseline and 3 month follow up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
65 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: 65-80 years old, are walking independently without assistive devices. Exclusion Criteria: Uncontrolled hypertension (defined as the following: 1) if not taking BP medication and resting systolic BP is greater than 140 or diastolic greater than 90, or 2) if taking BP medication and resting systolic BP greater than 160 or diastolic greater than 100). History of cardiovascular disease History of neurological disorders that effect lower extremity function (stroke, peripheral neuropathy, Parkinson's disease, multiple sclerosis) One cortico-steroid injection to the quadriceps or patellar tendon in the past month or 3 within the past year. History of quadriceps tendon rupture, patellar tendon rupture, or patellar fracture, which could place them at risk of re-injury during quadriceps strength testing. Current pain in the knee or in the thigh muscles. Diagnosis of inflammatory arthritis (Rheumatoid arthritis, gout, or psoriatic arthritis) Muscle diseases such as muscular dystrophy. Currently been participating in a regular exercise program more than 1x/week. Been using anticoagulants and platelet inhibitors History of chronic and significant respiratory disease or shortness of breath Visual impairments to the extent that they can not accurately see the monitor screen during training program.
Facility Information:
Facility Name
School of Health and Rehabilitation Sciences
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15260
Country
United States

12. IPD Sharing Statement

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The Effect of Neuromuscular Electrical Stimulation (NMES)

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