Mode Specific Effects of Isokinetic Training of Hamstring on Hamstring to Quadriceps Ratio

February 8, 2022 updated by: Masood Khan, King Saud University

Mode-specific Effects of Concentric and Eccentric Isokinetic Training of Hamstring Muscle at Slow Angular Velocity on Functional Hamstrings-to-quadriceps Ratio

Mode specificity of eccentric and concentric isokinetic training have been examined in previous studies but with conflicting results. The present study aimed to examine the mode-specific effects of eccentric and concentric isokinetic training of hamstring muscle at slow angular velocity on eccentric peak torque of hamstring (PTecc), concentric peak torque of quadriceps (PTcon), acceleration time of hamstring (AThams) and quadriceps (ATquad), deceleration time of hamstring (DThams) and quadriceps (DTquad), time to peak torque of hamstring (TPThams) and quadriceps (TPTquad), and functional Hamstring-to-Quadriceps ratio (PTecc/PTcon).

Study Overview

Detailed Description

Several studies in past have tried to examine the mode specificity of concentric and eccentric training of different muscles and at different angular velocities i.e. whether concentric training will increase the concentric strength only or both concentric and eccentric strength and whether eccentric training will increase eccentric strength only or both eccentric and concentric strength.

Since conflicting reports are available regarding mode specificity of eccentric and concentric isokinetic training therefore one study was needed that can examine the mode specificity of these training in hamstring muscles at slow angular velocity. The present study aimed to examine the mode-specific effects of six weeks of isokinetic concentric and eccentric training of the hamstring muscle at slow angular velocity on the PTecc/PTcon, AT, DT, and TPT.

Study Type

Interventional

Enrollment (Actual)

30

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Riyadh, Saudi Arabia, 11433
        • King Saud University

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 28 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Male

Description

Inclusion Criteria:

  • Healthy young males
  • Age between 18 to 27
  • Recreationally active who used to engage regularly in 1-5 hours of physical activity per week

Exclusion Criteria:

  • Individual presently indulged in strength training of knee.
  • Individuals with any kind of injury around the knee, hip, ankle, foot
  • Unconsolidated fractures around the knee. • Stress fractures
  • Subjects with the acute phase of trauma, which may interfere with the exercise regime
  • Subjects with cardio-respiratory problems and other medical problems like diabetes, asthma, etc.
  • Subjects with tendinitis and other inflammatory conditions.

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: Basic Science
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Eccentric isokinetic group
In this group, eccentric isokinetic training of hamstring muscle was performed.
Eccentric exercises of the hamstring muscles were performed with the use of an isokinetic dynamometer device.
Active Comparator: Concentric isokinetic group
In this group, concentric isokinetic training of hamstring muscle was performed.
Concentric exercises of the hamstring muscles were performed with the use of an isokinetic dynamometer device.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Functional Hamstring-to-quadriceps ratio (PTecc:PTcon)
Time Frame: 6 weeks
This ratio was calculated using eccentric peak of hamstring and concentric peak torque of quadriceps muscle
6 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Acceleration time of hamstring (AThams)
Time Frame: 6 weeks
Time required by hamstring muscle to reach desired velocity was noted.
6 weeks
Acceleration time of quadriceps
Time Frame: 6 weeks
Time required by quadriceps muscle to reach desired velocity was noted.
6 weeks
Deceleration time of hamstring (DThams)
Time Frame: 6 weeks
Time required by hamstring muscle to reach zero velocity from target velocity, was noted.
6 weeks
Deceleration time of quadriceps
Time Frame: 6 weeks
Time required by quadriceps muscle to reach zero velocity from target velocity to, was noted.
6 weeks
Time to peak torque of hamstring
Time Frame: 6 weeks
Time required by hamstring muscle to reach peak torque was noted.
6 weeks
Time to peak torque of quadriceps
Time Frame: 6 weeks
Time required by quadriceps muscle to reach peak torque was noted.
6 weeks

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 (Actual)

April 28, 2021

Primary Completion (Actual)

September 13, 2021

Study Completion (Actual)

October 14, 2021

Study Registration Dates

First Submitted

January 27, 2022

First Submitted That Met QC Criteria

January 27, 2022

First Posted (Actual)

February 8, 2022

Study Record Updates

Last Update Posted (Actual)

February 24, 2022

Last Update Submitted That Met QC Criteria

February 8, 2022

Last Verified

February 1, 2022

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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