- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04375163
Effects of Massage Between Sets of an Intense Isokinetic Exercise- Protocol of Knee Extensors in Tae Kwon Do Athletes
Effects of Massage Between Sets of an Intense Isokinetic Exercise- Protocol of Knee Extensors in Tae Kwon Do Athletes on Knee Range of Motion, Thigh Circumference and Delayed Onset Muscle Soreness
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Objective: Τo investigate the effects of massage in athletic performance when applied during intervals of an intense isokinetic exercise protocol for knee extensor muscles.
Design: Randomized Controlled Trial. Participants: 26 Tae Kwon Do athletes performed a vigorous exercise program on the isokinetic dynamometer twice in a period of 10 days, each time on a different extremity. In this way two groups of 26 individuals each were created, with the same individuals alternating. In the massage group (MG) a sport massage was applied between the sets while in the control group (CG) the break was passive.
Main Outcome Measures: knee flexion and extension ROM, thigh circumference, and creatine kinase (CK) levels in blood plasma were measured before and after each test while L-DOMS was measured 24, 48, 72 and 96 hours after the exercise.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
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Central Makedonia
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Thessaloníki, Central Makedonia, Greece, 57001
- Department of Physical Education and Sports Sciences
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Professional athletes
- Age range between 18-25.
Exclusion Criteria:
- Conduction of any strengthening exercises on the day before the tests
- Musculoskeletal injury during the last six months
- Background of knee trauma and/or surgery
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Massage group (ME)
A sport massage was applied between the sets of an intense isokinetic exercise protocol for knee extensor muscles
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The isokinetic protocol included 6 sets of 10 maximum efforts at 60 °/s of one leg with a 2-minute break between the sets.
Massage consisted of stroking (30") and petrissage (50") for muscle relaxation, then friction (10"), pincement and clapping (30") to prepare muscles for the next set.
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Active Comparator: Control
the break between the sets of an intense isokinetic exercise protocol for knee extensor muscles was passive
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The isokinetic protocol included 6 sets of 10 maximum efforts at 60 °/s of one leg with a 2-minute break between the sets.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Changes in Active Knee Range of Motion (ROM)
Time Frame: day 1: pre-treatment, after- treatment, day: 10 pre-treatment, after- treatment
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The ROM of knee flexion and extension was measured before and after the exercise program application in both trials.
In particular, the active knee extension was measured in the supine position and the active flexion in the prone position using a universal type goniometer.
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day 1: pre-treatment, after- treatment, day: 10 pre-treatment, after- treatment
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Changes in creatine kinase (CK) levels in blood plasma
Time Frame: day 1: pre-treatment, after- treatment, day: 10 pre-treatment, after- treatment
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Blood samples were taken before and 24 hours after the isokinetic protocol to determine whether the exercise program caused fatigue and muscle damage.
The blood sample was analyzed to determine CK activity levels in blood plasma using an in-vitro quantitative assay followed by a photometer
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day 1: pre-treatment, after- treatment, day: 10 pre-treatment, after- treatment
|
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Changes in thigh circumference
Time Frame: day 1: pre-treatment, after- treatment, day: 10 pre-treatment, after- treatment
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The circumference of the thigh was measured with a tape measure before the test and after the exercise program at fixed spots at a distance of 10 and 20 cm from the center of the patella
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day 1: pre-treatment, after- treatment, day: 10 pre-treatment, after- treatment
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Changes in Delayed Onset Muscle Soreness (DOMS)
Time Frame: day 1: 24, 48, 72 and 96 hours after-exercise, day 10: 24, 48, 72 and 96 hours after-exercise
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The DOMS measurement for the lower extremities (L-DOMS) was performed with the VAS scale 24, 48, 72 and 96 hours after the completion of the program.
The VAS scale was tentative where 1 corresponded to "no soreness" and 10 to "very, very sore".
The L-DOMS was assessed according to Doma et al1,22 and according to Jakeman et al, through questioning after they completed a body weight squat until their knees were flexed to approximately 90°
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day 1: 24, 48, 72 and 96 hours after-exercise, day 10: 24, 48, 72 and 96 hours after-exercise
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Changes in concentric and eccentric torque
Time Frame: day 1: pre-treatment
|
During the baseline testing session, the maximum concentric and eccentric torque of knee extensors at 60 °/s was measured with the Cybex Norm.The participant then sat in the armchair of the isokinetic dynamometer with his arms crossed in the chest.
Two crossed straps held the torso firmly on the back of the armchair and a belt with an additional strap held the pelvis still.
Each participant performed 3 maximal efforts with each leg and the best of the 3 efforts was recorded.
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day 1: pre-treatment
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Collaborators and Investigators
Investigators
- Study Director: Evaggelos Sykaras, Department of Physical Education and Sports Sciences
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- EC-9/2020
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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