Acute Effects of Static Stretching Intensity and Duration on Muscle Viscoelastic Properties and Proprioception

November 27, 2019 updated by: Yusuf Hasirci, Marmara University
The purpose of this study is to compare the acute effects of different duration and intensity of static stretching exercises on the viscoelastic properties of the hamstring muscle and the knee proprioception.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Traditionally stretching exercises have been used by health professionals as a means of preventing injuries by increasing performance and increasing joint flexibility. Kubo et al. suggest that the potential mechanism of decreased risk of injury with increased flexibility is a change in the viscoelastic properties of the muscle-tendon unit. Muscle fibers and tendons contain proprioceptors. These receptors provide information about joint angle, muscle length and muscle tension. There are two stretch-related proprioceptors that transmit information to the central nervous system about muscle tension. These receptors are muscle spindles (respond to changes in the length) and golgi tendon organs (respond to changes in the tension). For this reason, interactions between muscle tension, muscle-tendon unit, viscoelasticity and proprioceptive tissue (muscle spindles and golgi tendon organ); it becomes important when you think about how stretching exercises affect proprioception, flexibility and increase or decrease of joint range of motion. In the literature, four stretching parameters have been defined as important to influence the potential for increasing or decreasing the flexibility of a joint: intensity, duration, frequency and stretching position. The focus of this study we plan on is the intensity and duration of stretching.

Exercise warming exercises before sportive activity and cooling exercises afterwards are widely suggested and applied. Determining the relationship between stretch severity and duration and viscoelastic properties and proprioception will contribute to the effective creation of training programs.

Study Type

Interventional

Enrollment (Actual)

216

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

      • Istanbul, Turkey
        • Marmara 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 45 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Being in the 18-45 age range.
  • Volunteer to participate in the study.

Exclusion Criteria:

  • Having had previous lower extremity operations.
  • Having an orthopedic, neurological and rheumatologic disease of the lower extremities.
  • Having open wound in the application area.
  • Having had soft tissue injury in the last 6 weeks in the application area.

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: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: 30 seconds and %50 intensity stretching
The participants in this group performed an 30 seconds, %50 intensity static stretching exercise. 3 repetitive static stretching exercises did to hamstring muscles on the dominant side.
Each intervention group received a different duration and intensity of static stretching exercise protocol.
Experimental: 30 seconds and %75 intensity stretching
The participants in this group performed an 30 seconds, %75 intensity static stretching exercise. 3 repetitive static stretching exercises did to hamstring muscles on the dominant side.
Each intervention group received a different duration and intensity of static stretching exercise protocol.
Experimental: 30 seconds and %100 intensity stretching
The participants in this group performed an 30 seconds, %100 intensity static stretching exercise. 3 repetitive static stretching exercises did to hamstring muscles on the dominant side.
Each intervention group received a different duration and intensity of static stretching exercise protocol.
Experimental: 60 seconds and %50 intensity stretching
The participants in this group performed an 60 seconds, %50 intensity static stretching exercise. 3 repetitive static stretching exercises did to hamstring muscles on the dominant side.
Each intervention group received a different duration and intensity of static stretching exercise protocol.
Experimental: 60 seconds and %75 intensity stretching
The participants in this group performed an 60 seconds, %75 intensity static stretching exercise. 3 repetitive static stretching exercises did to hamstring muscles on the dominant side.
Each intervention group received a different duration and intensity of static stretching exercise protocol.
Experimental: 60 seconds and %100 intensity stretching
The participants in this group performed an 60 seconds, %100 intensity static stretching exercise. 3 repetitive static stretching exercises did to hamstring muscles on the dominant side.
Each intervention group received a different duration and intensity of static stretching exercise protocol.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from baseline muscle viscoelastic properties at immediately after exercise
Time Frame: 10 minutes
Muscle viscoelastic properties was assessed with Myoton® PRO device. It is an evidence-based device that evaluates the bio-mechanical properties of soft biological tissues in a non-invasive, objective, reliable, inexpensive, quick and easy manner. Myoton® PRO is used in studies to evaluate superficial skeletal muscles, connective tissues such as tendons and ligaments, and other soft tissues. It is a highly reliable method for assessing the tone, stiffness, elasticity of muscles.
10 minutes
Change from baseline proprioception at immediately after exercise
Time Frame: 10 minutes
Proprioception was assessed with MarVAJED (Marmara Visual Auditory Joint Education Device). MarVAJED is a system for evaluating joint range of motion, analyzing joint position sense, offering biofeedback support to increase joint control, as well as directing it to controlled exercises. Analyzes joint movement with the help of small sensors. Transfers the obtained data to mobile phone, tablet or personal computer.
10 minutes
Change from baseline static stretching exercise intensity at the beginning of each exercise
Time Frame: 10 minutes
A visual analog scale of 100 mm was used to assess the intensity of stretching exercise perceived by the participant at the beginning of each repetition. The visual analog scale is used to visually measure the intensity of the detected mechanical stimulus. 0 means "no stretch" and 100 means "maximum tolerable stretch without pain". Perceived violence from left to right increases.
10 minutes

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Yusuf Hasırcı, Marmara University
  • Study Director: Semra Oğuz, Marmara 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.

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)

December 1, 2018

Primary Completion (Actual)

March 1, 2019

Study Completion (Actual)

March 1, 2019

Study Registration Dates

First Submitted

August 18, 2019

First Submitted That Met QC Criteria

November 27, 2019

First Posted (Actual)

December 2, 2019

Study Record Updates

Last Update Posted (Actual)

December 2, 2019

Last Update Submitted That Met QC Criteria

November 27, 2019

Last Verified

November 1, 2019

More Information

Terms related to this study

Other Study ID Numbers

  • 09.2018.479

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

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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