Strengthening Effect on Hamstring's Passive Mechanical Properties

April 20, 2020 updated by: Özgün Uysal, Hacettepe University

Effects Of Different Strengthening Methods On Hamstring Muscle Group's Passive Mechanical Properties in Healthy Individuals

The purpose of this study was to investigate effects of different strengthening methods on hamstring muscle group's passive mechanical properties and to investigate this effect's relation with performance changes in healthy individuals. 42 healthy sedentary male participated in this study. Passive mechanical properties and strength of hamstring and quadriceps muscles, flexibility of hamstring muscles, anaerobic explosive strength, reaction time, agility were measured. Participants randomized evenly into one of three groups; eccentric, concentric and neuromuscular electrical stimulation (NMES). After 8 weeks training period, participants were measured again.

Study Overview

Study Type

Interventional

Enrollment (Actual)

42

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

      • Ankara, Turkey, 06100
        • Hacettepe 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 30 years (ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Male

Description

Inclusion Criteria:

  • being sedentary

Exclusion Criteria:

  • Having knee, hip and/or back pain
  • Having a cardiovascular condition/disease
  • History of previous knee and/or hip surgery
  • Having a diagnose of any systemic disease
  • History of previous hamstring injury
  • Being physically active within last year ( Regular activity at least 3 days a week and continuity of at least 2 months was accepted as being physically active)

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
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
ACTIVE_COMPARATOR: Concentric
Leg Curl Training

Leg Curl Machine: 1st week - 1st day is 10 maximum repeat test. 2nd week - 2 days of training - 2 sets of 6 repeats. %60 percent of maximum load.

3rd week - 3 days of training - 3 sets of 6-8 repeats. %60-80 of maximum load. 4th-8th week - 3 days of training - 3 sets of 8-12 repeats. when 3 sets of 12 achieved, load was increased with 2.5kg.

ACTIVE_COMPARATOR: Eccentric
Nordic Hamstring Training
  1. st week - 1 day - 2 sets of 5 repeats.
  2. nd week - 2 days - 2 sets of 6 repeats.
  3. rd week - 3 days - 3 sets of 6-8 repeats.
  4. th week - 3 days - 3 sets of 8-10 repeats. 5-8th weeks - 3 days - 3 sets of 12-8 repeats. When achieved 3 sets of 12 repeats with full range, speed was increased.
ACTIVE_COMPARATOR: Neuromuscular Electrical Stimulation
Stimulation Training
8 weeks, three times per week, 15 minutes of bilateral hamstring stimulation. 100 Hz. frequency, 600 microsecond duration rectangular current

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Passive Mechanical Properties
Time Frame: Change from baseline passive mechanical properties at 8 weeks
Tone, Elasticity and Stiffness evaluation. Evaluated with Myotonometer-3
Change from baseline passive mechanical properties at 8 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Flexibility Measurement
Time Frame: Change from baseline flexibility at 8 weeks
Sit and reach test was used for hamstring flexibility
Change from baseline flexibility at 8 weeks
Muscle Strength Measurement
Time Frame: Change from baseline muscle strength at 8 weeks
Hamstring and Quadriceps strength were measured with LaFayette Manuel Muscle Tester
Change from baseline muscle strength at 8 weeks
Agility Measurement
Time Frame: Change from baseline agility time at 8 weeks
Illinois Agility Test was used for agility measurement
Change from baseline agility time at 8 weeks
Anaerobic Explosive Power
Time Frame: Change from baseline anaerobic explosive power at 8 weeks
Jump and Reach test was administered
Change from baseline anaerobic explosive power at 8 weeks
Reaction Time
Time Frame: Change from baseline reaction time at 8 weeks
ruler drop test was used for reaction timing
Change from baseline reaction time at 8 weeks

Collaborators and Investigators

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

Investigators

  • Study Director: tuzun fırat, Assoc. Prof., Hacettepe University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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)

March 21, 2019

Primary Completion (ACTUAL)

December 1, 2019

Study Completion (ACTUAL)

December 1, 2019

Study Registration Dates

First Submitted

March 18, 2019

First Submitted That Met QC Criteria

March 20, 2019

First Posted (ACTUAL)

March 21, 2019

Study Record Updates

Last Update Posted (ACTUAL)

April 22, 2020

Last Update Submitted That Met QC Criteria

April 20, 2020

Last Verified

April 1, 2020

More Information

Terms related to this study

Other Study ID Numbers

  • HacettepeSportsPhysio

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.

Clinical Trials on Sports Physical Therapy

Clinical Trials on Concentric Exercise

3
Subscribe