- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03563430
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
Status
Completed
Conditions
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
-
-
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Istanbul, Turkey, 34010
- Biruni University
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-
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
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change from baseline and 20. minutes of recovery
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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.
Sponsor
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
Other Study ID Numbers
- BiruniU
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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