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BalancedNCT07206576

Acute Effects of Percussion Massage Therapy in Adolescent Cyclists

A study testing a percussion massage gun in people with Balanced, run by Medipol University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This randomized controlled trial aims to investigate the acute effects of percussion massage therapy (PMT) on balance, explosive strength, and functional performance in adolescent competitive cyclists aged 12-15. Read more about this study

Who is it for?
Ages 12 to 15 yearsHealthy volunteers can take part
Conditions the study is for
Balanced
What is being tested?
a percussion massage gun
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
32 participants
Where
1 siteTurkey (Türkiye)
Study dates
30 Sep 2025to 14 Nov 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 12 to 15 years
  • All sexes
  • Healthy volunteers accepted
  • Child

Who may be able to join

  • 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

Who cannot join

  • 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

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Tayfun Arslan

    Sinop

Other trials in Turkey (Türkiye)

About this study

Official title: Acute Effects of Percussion Massage Therapy on Balance, Explosive Power, and Functional Performance in Adolescent Cyclists: A Randomized Controlled Trial

This randomized controlled trial aims to investigate the acute effects of percussion massage therapy (PMT) on balance, explosive strength, and functional performance in adolescent competitive cyclists aged 12-15. A total of 32 participants will be randomly assigned to either a PMT group, which will receive a single session of vibration-based therapy using a handheld percussion device (Compex Fixx 2.0), or a control group with passive rest. Performance parameters will be assessed using the Y Balance Test, vertical jump, hop tests, 10-second sprint cycling, and isometric muscle strength via dynamometry. The study seeks to determine whether PMT offers short-term neuromuscular benefits that may enhance cycling performance in youth athletes.

Read the 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.

Conditions
Balanced
Being tested
a percussion massage gun
Keywords
Cycling, Functional performance, Explosive strength, Balance, Vibration therapy

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • a percussion massage gunDevice

    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.

Study groups in NCT07206576
Study groupRoleWhat they receive
Percussion Massage Therapy GroupExperimentalParticipants 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.
Receives: Device: a percussion massage gun
Control GroupNo interventionParticipants 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.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Y Balance Test Composite Score

    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.

    Measured: Pre-intervention and immediately post-intervention

Secondary outcomes (5)
  1. Single-Leg Hop Distance (Triple Hop Test)

    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.

    Measured: Pre-intervention and immediately post-intervention

  2. Isometric Muscle Strength (Gluteus Maximus, Quadriceps, Gastrocnemius)

    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.

    Measured: Pre-intervention and immediately post-intervention

  3. Peak Power Output

    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.

    Measured: Pre-intervention and immediately post-intervention

  4. Sprint Distance

    During the same 10-second sprint test, the total distance covered (meters) will be recorded as an indicator of explosive leg power.

    Measured: Pre-intervention and immediately post-intervention

  5. Subjective Muscle Relaxation (Numeric Rating Scale - NRS)

    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.

    Measured: Pre-intervention and immediately post-intervention

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted3 Oct 2025
  2. Study start30 Sep 2025
  3. Primary completion14 Nov 2025
  4. Study completion14 Nov 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
This study is designed as a two-arm, parallel-group, randomized controlled trial. A total of 32 adolescent competitive cyclists aged 12-15 years will be randomly assigned (1:1 ratio) to either the intervention group receiving percussion massage therapy (PMT) or the control group undergoing passive rest.
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
32 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07206576
Sponsor's protocol ID
E-10840098-202.3.02-6304
Status last verified
Dec 2025
First submitted
26 Sep 2025
Last updated
30 Dec 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Dansuk E, Menek B, Arslan T, Okur S. Acute effects of percussion massage therapy on balance, functional performance, and pain in adolescent cyclists: a randomized controlled trial. BMC Sports Sci Med Rehabil. 2026 Mar 26;18(1):168. doi: 10.1186/s13102-026-01607-x.

    PubMed 41888937

Questions about this trial

What is this clinical trial studying?

A study testing a percussion massage gun in people with Balanced, run by Medipol University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 30 Dec 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Y Balance Test Composite Score (time frame: Pre-intervention and immediately post-intervention). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07206576, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 30 Dec 2025.

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