Effects of Different Recovery Methods on Lactic Acid Removal, Flexibility, Strength, and Endurance

September 4, 2018 updated by: Buket AKINCI, Biruni University

Comparison of Acute Effects on Lactic Acid Removal, Flexibility, Strength, and Endurance of Different Recovery Methods

The aim of this study is to compare these three different recovery methods following a single bout high-intensity interval exercise program with each other in terms of blood lactate clearance, muscle flexibility, muscle strength and endurance.

Study Overview

Detailed Description

It is very important to choose the most effective recovery method for the athletes in training for their next training/competition. The recovery period is very significant in terms of removal of blood lactate and body dynamics as soon as they return to their original state and achieve high performance. Neither neuromuscular electrical stimulation, low-intensity aerobic exercise, self-massage with foam roller methods, which have been proven their effectiveness in the literature, have been compared with each other.

Study Type

Interventional

Enrollment (Actual)

45

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, 34010
        • Biruni 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

20 years to 25 years (ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

Young, healthy adults aged 20-25 years.

Exclusion Criteria:

  • Clinical diagnosis of a cardiovascular disease.
  • Clinical diagnosis of a metabolic disorder, orthopedic or neurological disease that would interfere with an exercise program,
  • Clinical diagnosis of hemophili,
  • Clinical diagnosis of thrombophlebitis or deep vein trombosis,
  • Clinical diagnosis of peripheral arterial disease,
  • Clinical diagnosis of venous insufficiency,
  • Clinical diagnosis of anemia,
  • Pregnancy.

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: TRIPLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Active Recovery Group
Participants in this group will exercise for 15 minutes, for a range of 65 to 70% of the maximum heart rate.
Participants in this group will exercise for 15 minutes, for a range of 65 to 70% of the maximum heart rate as a recovery method following a single bout high-intensity interval exercise program
EXPERIMENTAL: Self-Massage with Foam Roller Group
This group will perform 15 minutes self-massage with foam roller following the exercise session.
This group will perform 15 minutes self-massage with foam roller following the exercise session as a recovery method following a single bout high-intensity interval exercise program.
EXPERIMENTAL: Neuromuscular Electrical Stimulation
Participants of this group will be applied electrical stimulation on quadriceps femoris and hamstring muscles for 15 minutes while they are comfortable lying position.
Participants of this group will be applied electrical stimulation on quadriceps femoris and hamstring muscles for 15 minutes while they are comfortable lying position as a recovery method following a single bout high-intensity interval exercise program.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Blood Lactate change
Time Frame: change from baseline and 20. minutes of recovery
blood lactate concentration measurement
change from baseline and 20. minutes of recovery

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Quadriceps and Hamstring Muscle Strength
Time Frame: baseline and 1. hour
Quadriceps and Hamstring Muscle Strength assessment with hand held dynamometer for left and right
baseline and 1. hour
Squat Endurance Test
Time Frame: baseline and 1. hour
Squat endurance capacity assessment will done with 1 Repeat Maximum 60%
baseline and 1. hour
sit and reach test
Time Frame: baseline and 1. hour
Hamstring Flexibility assessment will done with sit and reach test and will noted as centimeter
baseline and 1. hour

Collaborators and Investigators

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

Investigators

  • Study Chair: Buket AKINCI, PhD, Biruni University

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)

September 25, 2017

Primary Completion (ACTUAL)

July 1, 2018

Study Completion (ACTUAL)

July 1, 2018

Study Registration Dates

First Submitted

May 28, 2018

First Submitted That Met QC Criteria

June 19, 2018

First Posted (ACTUAL)

June 20, 2018

Study Record Updates

Last Update Posted (ACTUAL)

September 5, 2018

Last Update Submitted That Met QC Criteria

September 4, 2018

Last Verified

September 1, 2018

More Information

Terms related to this study

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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