- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07580313
Vibrational Percussion Massage Improves Rectus Femoris Mechanical Properties and Sports Performance in Physically Active Adults
Effects of Vibrational Percussion Massage on Mechanical Properties of Rectus Femoris and Sports Performance in Physically Active Adults
The goal of this clinical trial is to learn if vibrational percussion massage (VPM) improves rectus femoris mechanical properties and sports performance after muscle fatigue in physically active adults. It will also examine the immediate effects of VPM on muscle function and recovery.
The main questions it aims to answer are:
- Does VPM improve the mechanical properties of the rectus femoris muscle after fatigue?
- Does VPM improve knee extensor strength and triple-hop performance after fatigue?
Researchers will compare measurements obtained before fatigue, after fatigue, and after a VPM intervention to evaluate the effects of VPM on muscle recovery and sports performance.
Participants will:
- Perform a fatigue protocol targeting the lower extremity muscles.
- Receive a 5-minute VPM intervention after the fatigue protocol.
- Complete assessments of rectus femoris mechanical properties using a myotonemeter.
- Perform maximal isometric knee extensor strength and triple-hop distance tests at three time points: before fatigue, after fatigue, and after VPM intervention.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
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Tainan, Taiwan, 701
- National Cheng Kung University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Healthy indiciduals aged between 20 to 60 years old.
Exclusion Criteria:
- History of spinal or lower extremity surgery
- Current musculoskeletal pain interfering with daily activities
- Smoking
- Pregnancy
- Presence of cardiopulmonary disorders
- Scoliosis or other musculoskeletal deformities
- Inability to complete the fatigued protocol
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Physically active adults
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Participants will receive a 5-minute vibrational percussion massage (VPM) intervention applied to the right rectus femoris muscle using a handheld percussion massage device (Hypervolt, Hyperice, California, United States) with a spherical massage head at a fixed frequency of 53 Hz.
The intervention will be administered by a trained physical therapist with the device applied perpendicularly to the treatment area.
Two treatment locations on the rectus femoris muscle, including the midpoint and lower one-third of the muscle, will each receive 2.5 minutes of non-stroking stimulation.
During the intervention, participants will lie in a supine position with both lower extremities fully relaxed and extended.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Muscle tension of the rectus femoris measured by myotonometry (Hz)
Time Frame: Assessed at baseline, immediately after the fatigue protocol, and immediately after the 5-minute vibrational percussion massage intervention.
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Muscle tension represents the resting tone of the rectus femoris muscle, quantified by oscillation frequency.
Higher values indicate greater resting muscle tension.
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Assessed at baseline, immediately after the fatigue protocol, and immediately after the 5-minute vibrational percussion massage intervention.
|
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Muscle stiffness of the rectus femoris measured by myotonometry (N/m)
Time Frame: Assessed at baseline, immediately after the fatigue protocol, and immediately after the 5-minute vibrational percussion massage intervention.
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Dynamic stiffness represents the resistance of the rectus femoris muscle to external deformation, with higher values indicating greater muscle stiffness and lower tissue compliance.
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Assessed at baseline, immediately after the fatigue protocol, and immediately after the 5-minute vibrational percussion massage intervention.
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Muscle elasticity of the rectus femoris measured by myotonometry (logarithmic decrement)
Time Frame: Assessed at baseline, immediately after the fatigue protocol, and immediately after the 5-minute vibrational percussion massage intervention.
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Muscle elasticity represents the ability of the rectus femoris muscle to restore its original shape after deformation.
Lower values indicate better elasticity and lower energy dissipation.
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Assessed at baseline, immediately after the fatigue protocol, and immediately after the 5-minute vibrational percussion massage intervention.
|
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Mechanical stress relaxation time of the rectus femoris measured by myotonometry (ms)
Time Frame: Assessed at baseline, immediately after the fatigue protocol, and immediately after the 5-minute vibrational percussion massage intervention.
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Mechanical stress relaxation time represents the time required for the rectus femoris muscle to recover from deformation after an external mechanical impulse.
Longer values indicate more compliant (softer) tissue, whereas shorter values indicate increased muscle stiffness.
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Assessed at baseline, immediately after the fatigue protocol, and immediately after the 5-minute vibrational percussion massage intervention.
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Creep of the rectus femoris measured by myotonometry (ratio)
Time Frame: Assessed at baseline, immediately after the fatigue protocol, and immediately after the 5-minute vibrational percussion massage intervention.
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Creep represents the viscoelastic deformation of the rectus femoris muscle under a constant mechanical load.
Higher values indicate greater tissue elongation capacity and viscoelastic deformation, whereas lower values suggest reduced compliance.
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Assessed at baseline, immediately after the fatigue protocol, and immediately after the 5-minute vibrational percussion massage intervention.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Maximal isometric knee extensor strength measured by handheld dynamometry (N)
Time Frame: Assessed at baseline, immediately after the fatigue protocol, and immediately after the 5-minute vibrational percussion massage intervention.
|
Maximal isometric knee extensor strength was assessed using a handheld dynamometer.
Participants performed a 6-second maximal voluntary isometric contraction of the knee extensors in a seated position, and the peak force was recorded.
Three trials were performed and averaged for analysis.
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Assessed at baseline, immediately after the fatigue protocol, and immediately after the 5-minute vibrational percussion massage intervention.
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Triple-hop distance test (m)
Time Frame: Assessed at baseline, immediately after the fatigue protocol, and immediately after the 5-minute vibrational percussion massage intervention.
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The triple-hop test was used to assess functional lower-limb performance.
Participants performed three consecutive maximal forward hops on the same limb and were required to maintain balance for 3 seconds after the final landing.
The total hopping distance from the starting line to the final landing position was measured.
Three trials were performed and averaged for analysis.
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Assessed at baseline, immediately after the fatigue protocol, and immediately after the 5-minute vibrational percussion massage intervention.
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Yi-Ju Tsai, PhD, National Cheng Kung University
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- VPM_Fatigue
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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