The Effect of Different Russian Current Parameters on MVIC Contraction of the Quadriceps Muscle Among University of Sharjah Students.

March 21, 2022 updated by: Ansam Tayseer Hasan, University of Sharjah

The Effect of Different Russian Current Parameters on Maximum Voluntary Isometric Contraction(MVIC) of the Quadriceps Muscle Among University of Sharjah Students: A Randomized Controlled Trail.

The study aims to investigate the effect of different Russian current parameters on maximum voluntary isometric contraction of the quadriceps muscle among University of Sharjah students.

Study Overview

Status

Not yet recruiting

Conditions

Intervention / Treatment

Detailed Description

Muscular strength and endurance are two important compatible parts of the body; for normal people to move, lift things and do day-to-day activities or athletic performance. Large number of studies have been carried out to elaborate the different factor that help in improving the muscular strength as well as the endurance combined with rehabilitation programs in order to promote muscle function and prevent the injury(Akinoglu & Kocahan, 2020; Chou & Binder-Macleod, 2007; Evetovich et al., 2001; Selkowitz, 1985; Snyder-Mackler et al., 1994; Ward et al., 2006). Strengthening and endurance training have been used frequently in varied rehabilitation protocols in order to improve the overall musculoskeletal performance.(Earl & Hoch, 2011; Gondin et al., 2011). Meanwhile, Isokinetic training and Neuromuscular electrical stimulation are frequently utilized in physical therapy.(Brown & Whitehurst, 2003; Chou & Binder-Macleod, 2007; Evetovich et al., 2001; Stone, 1997).

Russian current is one of the popular preferred Neuromuscular electrical stimulation as it has been advocated to increase muscle strength due to its high tolerance as well as minimum pain level provocation (Akinoglu & Kocahan, 2020; Gondin et al., 2011). Russian currents are alternating currents at a frequency of 2.5 kHz that are burst modulated at a frequency of 50 Hz with a 50% duty cycle. The widely and most popular training protocol used with Russian current is (10/50/10) in which the stimulus is applied for a 10-second "on" period followed by a 50-second "off" or rest period, with a recommended treatment time of 10 minutes per stimulation session. Russian currents are used mainly to generate a motor response, but it also has been investigated as an electro-analgesia type intervention. This training protocol is used mainly to generate a motor response, but it also has been investigated as an electro-analgesia type intervention.

Despite a lot of previous research regarding the Russian current; no studies are available in which suggest the most efficient carrier frequency for Russian current to strengthening the muscles and increase muscle with isokinetic training in the short term and the effect of different RC on the EIT by the quadriceps muscle. The aim of this study is directed toward investigation of those different Russian current carrier frequencies' effects on the quadriceps muscle isokinetic strength and endurance in addition to investigate the effect of different mode of RC on the EIT by the quadriceps femoris muscle. This study will include measurement for the knee torque and quadriceps muscle strength using Biodex system 3 that will be generated by different carrier frequency in addition to different RC mode, and investigate the relationship between those variables.

Study Type

Interventional

Enrollment (Anticipated)

100

Phase

  • Not Applicable

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 25 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  1. Their age ranged from 18 to 25 years.
  2. Their Body Mass Index (BMI) within normal range (18.5-25).
  3. Don't have any health related condition that required medical attention in the past two years.
  4. All participant at same physical fitness level.

Exclusion Criteria:

  • The subjects will be excluded from this study if they have any of the following criteria:

    1. Quadriceps muscle injury.
    2. Spinal or lower limb fractures.
    3. Lower limb deformities.
    4. Associated cognition abnormalities which may to affect muscle and limb function
    5. Tumors or radicular symptoms
    6. Recent muscular lesion, knee injury, sensory changes and neuromuscular disease
    7. Previous surgery that may affect the lower limb muscle performance.
    8. Any contraindication for Russian current application

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Factorial Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Group1
training used Russian Current carrier frequency at 2500-Hz alternating current.

The patient will be placed in sitting position, hip at 90-degree flexion, knee at 60°, the upper body supported by the backrest, cross belt support the trunk and cross belt support the pelvis. The dynamometer rotating axis will be aligned with knee joint axis and the resistance lever arm will place in the distal leg above the malleolus. The angle of the joints adjustment considering the joint's range of motion and the device's user's manual, any movement other than the range of motion determined by the mechanical limit will be not allowed

All electrical induced contraction will last 4 second each, with characteristics of 75 bursts; 4 second time on, 400 μs pulse width and 10 second time off. The greatest electrically induced torque by the quadriceps muscle at the maximum current output from the stimulator will be recorded for each subject to be used in data analysis. The same procedure will be done on the 3rd week and after 6th week.

Other Names:
  • The Biodex isokinetic dynamometer
Experimental: Group2
training used Russian Current carrier frequency at 3750-Hz alternating current.

The patient will be placed in sitting position, hip at 90-degree flexion, knee at 60°, the upper body supported by the backrest, cross belt support the trunk and cross belt support the pelvis. The dynamometer rotating axis will be aligned with knee joint axis and the resistance lever arm will place in the distal leg above the malleolus. The angle of the joints adjustment considering the joint's range of motion and the device's user's manual, any movement other than the range of motion determined by the mechanical limit will be not allowed

All electrical induced contraction will last 4 second each, with characteristics of 75 bursts; 4 second time on, 400 μs pulse width and 10 second time off. The greatest electrically induced torque by the quadriceps muscle at the maximum current output from the stimulator will be recorded for each subject to be used in data analysis. The same procedure will be done on the 3rd week and after 6th week.

Other Names:
  • The Biodex isokinetic dynamometer
Experimental: Group3
training used Russian Current carrier frequency at 5000-Hz alternating current.

The patient will be placed in sitting position, hip at 90-degree flexion, knee at 60°, the upper body supported by the backrest, cross belt support the trunk and cross belt support the pelvis. The dynamometer rotating axis will be aligned with knee joint axis and the resistance lever arm will place in the distal leg above the malleolus. The angle of the joints adjustment considering the joint's range of motion and the device's user's manual, any movement other than the range of motion determined by the mechanical limit will be not allowed

All electrical induced contraction will last 4 second each, with characteristics of 75 bursts; 4 second time on, 400 μs pulse width and 10 second time off. The greatest electrically induced torque by the quadriceps muscle at the maximum current output from the stimulator will be recorded for each subject to be used in data analysis. The same procedure will be done on the 3rd week and after 6th week.

Other Names:
  • The Biodex isokinetic dynamometer
Experimental: Group4
training used Russian Current at different mode.

The patient will be placed in sitting position, hip at 90-degree flexion, knee at 60°, the upper body supported by the backrest, cross belt support the trunk and cross belt support the pelvis. The dynamometer rotating axis will be aligned with knee joint axis and the resistance lever arm will place in the distal leg above the malleolus. The angle of the joints adjustment considering the joint's range of motion and the device's user's manual, any movement other than the range of motion determined by the mechanical limit will be not allowed

All electrical induced contraction will last 4 second each, with characteristics of 75 bursts; 4 second time on, 400 μs pulse width and 10 second time off. The greatest electrically induced torque by the quadriceps muscle at the maximum current output from the stimulator will be recorded for each subject to be used in data analysis. The same procedure will be done on the 3rd week and after 6th week.

Other Names:
  • The Biodex isokinetic dynamometer

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
establish the relationship between the different carrier frequency for burst modulated electrical stimulation as an independent variable and electrical induced quadriceps femoris muscle torque (EIT) as a dependent variable.
Time Frame: measured data will be recorded at the 3rd week after training using RC and at 6th week as a follow up measurements

The primary outcome of the study is to establish the relationship between the different carrier frequency for burst modulated electrical stimulation as an independent variable and electrical induced quadriceps femoris muscle torque (EIT) as a dependent variable.

And the effect of different RC mode on the electrical induce torque by the quadriceps muscle. The EIT measurement will be done using the Biodex pro 3 system devices this system was described in detail; with reliability and validity has been investigated previous study establish its reliable. This study, will investigate the effect of different carrier frequency 2500Hz-3750Hz-5000Hz alternating current on the electrical induce quadriceps muscle torque of the dominant leg, and the effect of different Russian current mode on the EIT of the quadriceps muscle femoris.

measured data will be recorded at the 3rd week after training using RC and at 6th week as a follow up measurements

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Anticipated)

May 8, 2022

Primary Completion (Anticipated)

December 30, 2022

Study Completion (Anticipated)

April 30, 2023

Study Registration Dates

First Submitted

February 22, 2022

First Submitted That Met QC Criteria

March 21, 2022

First Posted (Actual)

March 31, 2022

Study Record Updates

Last Update Posted (Actual)

March 31, 2022

Last Update Submitted That Met QC Criteria

March 21, 2022

Last Verified

March 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • REC-21-02-18-01-S

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

All information taken will be kept confidential and will not be taken without the participant's consent. Any data collected will be for scientific purpose only.The therapists have been instructed about the privacy, confidentiality and rights of the participants .

Published data will remain anonymous without personal identifier of participants

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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