- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07206576
- Original Trial
Acute Effects of Percussion Massage Therapy in Adolescent Cyclists
Acute Effects of Percussion Massage Therapy on Balance, Explosive Power, and Functional Performance in Adolescent Cyclists: A Randomized Controlled Trial
Study Overview
Detailed Description
Cycling is a sport that requires repetitive and rhythmic activation of the lower extremity muscles, where balance, endurance, and muscular power are critical. In adolescent athletes aged 12-15, musculoskeletal structures are still developing, and interventions aimed at enhancing performance must be carefully investigated in terms of both efficacy and safety.
Percussion massage therapy (PMT) is a novel method that combines elements of traditional massage and vibration therapy, applying rapid mechanical pulses to soft tissues using handheld devices. PMT has gained popularity in recent years due to its potential to enhance circulation, reduce muscle stiffness, and improve neuromuscular function. Studies suggest that PMT can produce acute effects such as improved proprioception, reduced muscle tone, and enhanced explosive performance.
This randomized controlled trial aims to evaluate the acute effects of PMT on dynamic balance, explosive strength, and functional performance in young competitive cyclists. Thirty-two participants, aged 12 to 15, who have been licensed cyclists for at least 2 years and train regularly, will be randomly assigned to either an intervention group receiving PMT or a control group undergoing passive rest.
The intervention group will receive a single session of PMT using the Compex® Fixx™ 2.0 device, applied bilaterally to the gluteus maximus, quadriceps femoris, and gastrocnemius muscles at 41.7 Hz for 3 minutes per muscle group. The control group will remain seated for an equivalent rest period.
Performance outcomes will be assessed using the Y Balance Test, Vertical Jump Test, single-leg hop test (triple hop), 10-second cycling sprint test, and handheld dynamometry to measure isometric muscle strength. In addition, subjective muscle relaxation will be evaluated pre- and post-intervention using the Numeric Rating Scale (NRS).
The findings of this study will contribute to the limited body of evidence regarding vibration-based interventions in youth athletes and help determine whether PMT is a viable strategy to acutely improve neuromuscular performance in adolescent cyclists.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
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Sinop, Turkey (Türkiye)
- Tayfun Arslan
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Aged between 12 and 15 years
- Licensed competitive cyclist for at least 2 years
- Participating in at least 4 training sessions per week
- No lower extremity injuries in the past 6 months
- Voluntary participation by signing the informed consent form
Exclusion Criteria:
- History of surgery in the knee, hip, or ankle joints
- Presence of neurological, vestibular, or systemic balance disorders
- Use of medications that may affect performance
- Any orthopedic condition that prevents participation in performance tests
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: Percussion Massage Therapy Group
Participants in this group will receive a single session of percussion massage therapy (PMT) using the Compex® Fixx™ 2.0 device applied bilaterally to the gluteus maximus, quadriceps femoris, and gastrocnemius muscles for 3 minutes per muscle group at 41.7 Hz.
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Participants assigned to the intervention group will receive a single session of percussion massage therapy (PMT) using the Compex® Fixx™ 2.0 handheld device. The treatment will be applied bilaterally to three major muscle groups: gluteus maximus, quadriceps femoris, and gastrocnemius. The device will operate at a high intensity setting (Level 4) with a frequency of 41.7 Hz. A wedge-shaped applicator head will be used to ensure consistent pressure across the treatment area. Each muscle group will be treated for 3 minutes, following a standardized linear stroke pattern from proximal to distal and back. The total duration of the intervention will be approximately 18 minutes. The intervention will be performed once, immediately before the post-test evaluations, and aims to assess acute effects on neuromuscular performance. |
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No Intervention: Control Group
Participants in this group will not receive any intervention.
They will remain seated in a resting position for an equivalent duration (approximately 18 minutes) to match the intervention group's time frame.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Y Balance Test Composite Score
Time Frame: Pre-intervention and immediately post-intervention
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The Y Balance Test will be used to assess dynamic balance by measuring reach distances in three directions (anterior, posteromedial, and posterolateral) while standing on one leg.
Each direction will be tested three times, and the average reach distance will be normalized to leg length.
A composite score will be calculated and expressed as a percentage to evaluate overall dynamic balance capacity.
Higher scores indicate better balance performance.
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Pre-intervention and immediately post-intervention
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Single-Leg Hop Distance (Triple Hop Test)
Time Frame: Pre-intervention and immediately post-intervention
|
The Triple Hop Test evaluates lower limb strength, power, and dynamic stability.
Participants will perform three consecutive forward hops on the same leg along a straight line, aiming for maximal distance.
The total distance from toe-off to the final landing point will be measured in centimeters.
The longest of three valid trials will be recorded.
Increased hop distance indicates improved functional performance.
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Pre-intervention and immediately post-intervention
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Isometric Muscle Strength (Gluteus Maximus, Quadriceps, Gastrocnemius)
Time Frame: Pre-intervention and immediately post-intervention
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Isometric strength of gluteus maximus, quadriceps femoris, and gastrocnemius will be measured using a handheld dynamometer.
Standardized positioning and stabilization techniques will be used to ensure reliability.
Three maximal contractions will be performed for each muscle, and the highest value (in Newtons) will be recorded for analysis.
Greater force output reflects improved neuromuscular capacity.
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Pre-intervention and immediately post-intervention
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Subjective Muscle Relaxation (Numeric Rating Scale - NRS)
Time Frame: Pre-intervention and immediately post-intervention
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Subjective perception of muscle relaxation will be assessed using the Numeric Rating Scale (NRS), ranging from 0 (no relaxation) to 10 (complete relaxation).
Participants will rate their perceived muscle tension and relaxation immediately before and after the intervention to quantify perceived benefits.
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Pre-intervention and immediately post-intervention
|
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Peak Power Output
Time Frame: Pre-intervention and immediately post-intervention
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Sprint cycling performance will be assessed using a stationary cycle ergometer.
After a warm-up, participants will perform a 10-second all-out sprint with standardized resistance.
Peak power (Watts) will be recorded as an indicator of anaerobic capacity.
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Pre-intervention and immediately post-intervention
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Sprint Distance
Time Frame: Pre-intervention and immediately post-intervention
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During the same 10-second sprint test, the total distance covered (meters) will be recorded as an indicator of explosive leg power.
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Pre-intervention and immediately post-intervention
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Collaborators and Investigators
Sponsor
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 (Estimated)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- E-10840098-202.3.02-6304
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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