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BalancedNCT07004374

Effects of Soft Tissue Mobilization and Vibration Therapy in Competitive Rowers

A study testing a percussion massage gun and specially designed stainless-steel instruments in people with Balanced and Soft Tissue Injuries, 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 study aims to investigate the effects of instrument-assisted soft tissue mobilization (IASTM) and percussion massage therapy on balance, explosive strength, and functional performance in competitive adolescent rowers. Read more about this study

Who is it for?
Ages 13 to 18 yearsHealthy volunteers can take part
Conditions the study is for
Balanced, Soft Tissue Injuries
What is being tested?
a percussion massage gun and specially designed stainless-steel instruments
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
45 participants
Where
1 siteTurkey (Türkiye)
Study dates
13 Jun 2025to 10 Jul 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 13 to 18 years
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult

Who may be able to join

  • Age between 13 and 18 years
  • Licensed rowing athlete for at least 2 years
  • Participating in at least 4 training sessions per week
  • No lower extremity injury in the past 6 months
  • Voluntary participation and signed informed consent form

Who cannot join

  • History of surgery in the knee, hip, or ankle
  • Neurological, vestibular, or systemic balance disorders
  • Use of medications that may affect physical performance
  • Orthopedic conditions that prevent 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: Comparative Effects of Instrument-Assisted Soft Tissue Mobilization and Percussion Vibration Therapy on Balance, Explosive Strength, and Functional Performance in Competitive Adolescent Rowers: A Randomized Controlled Trial

This randomized controlled study aims to investigate the effects of instrument-assisted soft tissue mobilization (IASTM) and percussion massage therapy on balance, explosive strength, and functional performance in competitive adolescent rowers. A total of 45 participants aged 13-18 will be randomly assigned to one of three groups: vibration therapy group, soft tissue mobilization group, and control group. Interventions will target the quadriceps and gastrocnemius muscles. Outcome measures include the Y Balance Test, vertical jump, hop tests, and isometric muscle strength via myometry. The results of this study are expected to provide evidence-based insights into optimizing performance and injury prevention strategies in rowing athletes.

Read the detailed description

Rowing is a high-performance sport that demands coordinated action of the upper and lower extremities, trunk muscles, and cardiovascular system. Due to repetitive pulling movements, rowers are prone to musculoskeletal overload injuries, particularly in the lower back, shoulders, knees, and ankles. Effective balance control and lower extremity explosive strength are critical for performance enhancement and injury prevention in rowing athletes. Soft tissue mobilization techniques and vibration therapies are emerging modalities that may enhance muscle flexibility, joint mobility, and neuromuscular activation, thereby contributing to athletic performance.

This randomized controlled study is designed to evaluate the effects of two different interventions-instrument-assisted soft tissue mobilization (IASTM) using the Graston technique, and percussion massage therapy using a handheld massage gun-on balance, explosive strength, and functional performance in competitive adolescent rowers aged 13-18. A total of 45 athletes meeting inclusion criteria will be randomly assigned to one of three groups: Vibration Group (percussion therapy at 33Hz), Soft Tissue Mobilization Group (IASTM), and Control Group (no intervention). Both interventions will be applied to the quadriceps femoris and gastrocnemius muscles over standardized durations and protocols.

Functional outcomes will be measured using the Y Balance Test, vertical jump test, single-leg hop tests (single, triple, crossover, square hop), and a 6-meter timed hop. Muscle strength will be evaluated using a myometer to assess isometric force production of the quadriceps and gastrosoleus muscles. Assessments will be conducted pre- and post-intervention.

The study is expected to provide clinically relevant data on the efficacy of myofascial techniques in enhancing functional capacity and performance parameters in young elite athletes. Findings may support the incorporation of soft tissue techniques and vibration therapy into performance training and injury prevention protocols for rowing and similar sports.

Being tested
a percussion massage gun, specially designed stainless-steel instruments
Keywords
Rowing, Instrument-assisted soft tissue mobilization (IASTM), Percussion massage therapy, Balance, Explosive strength, Functional performance
Medical subject headings
Soft Tissue Injuries

What participants receive

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

  • a percussion massage gunDevice

    Participants receive percussion massage therapy (33 Hz) applied to the quadriceps and gastrocnemius muscles using a handheld massage device for 5 minutes per muscle group.

  • specially designed stainless-steel instrumentsDevice

    Participants receive instrument-assisted soft tissue mobilization (IASTM, Graston technique) applied to the quadriceps and gastrocnemius muscles using stainless steel tools with standardized techniques (Sweep, Fan, Brush) for 6 minutes.

Study groups in NCT07004374
Study groupRoleWhat they receive
Control GroupNo interventionParticipants in this group will not receive any intervention.
Vibration Therapy (33 Hz) GroupExperimentalParticipants receive percussion massage therapy (33 Hz) applied to the quadriceps and gastrocnemius muscles using a handheld massage device for 5 minutes per muscle group.
Receives: Device: a percussion massage gun
Soft Tissue Mobilization GroupExperimentalParticipants receive instrument-assisted soft tissue mobilization (IASTM, Graston technique) applied to the quadriceps and gastrocnemius muscles using stainless steel tools with standardized techniques (Sweep, Fan, Brush) for 6 minutes.
Receives: Device: specially designed stainless-steel instruments

What is being measured

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

  1. Y Balance Test Composite Score

    Assesses dynamic balance and postural control of the lower extremities. During the test, participants perform maximal reach in three directions-anterior, posteromedial, and posterolateral-while maintaining a single-leg stance. The composite score is calculated by averaging the reach distances in all three directions, normalized to the participant's leg length using the formula:

    Composite Score = (Anterior + Posteromedial + Posterolateral) / (3 × limb length) × 100 Scale Range: 0 to 100% Interpretation: Higher scores indicate better dynamic balance and greater postural control.

    Measured: Pre-intervention and immediately post-intervention

Secondary outcomes (4)
  1. Vertical Jump Height

    Measures lower extremity explosive strength. Participants perform a countermovement jump, and the maximum vertical jump height is recorded.

    Unit of Measure: centimeters (cm) Scale Range: Not fixed (depends on physical capacity; typically 10-80 cm) Interpretation: Higher scores indicate greater explosive power in the lower extremities.

    Measured: Pre-intervention and immediately post-intervention

  2. Single-Leg Hop Tests

    Assesses unilateral functional lower limb performance and dynamic stability. Participants perform a maximal forward hop on one leg, and the distance is measured.

    Unit of Measure: centimeters (cm) Scale Range: Not fixed (typically 50-250 cm) Interpretation: Greater distances reflect better functional strength and neuromuscular control.

    Measured: Pre-intervention and immediately post-intervention

  3. 6-Meter Timed Hop Test

    Assesses power, speed, and dynamic control over a short distance using a single-leg hop. Total time to complete 6 meters is recorded.

    Measured: Pre-intervention and immediately post-intervention

  4. Isometric Muscle Strength of Quadriceps and Gastrocnemius

    Assessed with a hand-held myometer to measure maximal isometric force in Newtons.Myometer device with standard positioning and stabilization.

    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 posted4 Jun 2025
  2. Study start13 Jun 2025
  3. Primary completion10 Jul 2025
  4. Study completion10 Jul 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 randomized controlled trial (RCT) with a parallel-group design to evaluate the comparative effects of two different therapeutic interventions-instrument-assisted soft tissue mobilization (IASTM) and percussion vibration therapy-on balance, explosive strength, and functional performance in adolescent competitive rowers. A total of 45 participants will be randomly assigned to one of three groups: Group 1: Vibration Therapy Group (percussion massage therapy at 33 Hz) Group 2: Soft Tissue Mobilization Group (Graston technique/IASTM) Group 3: Control Group (no intervention)
Masking
Double blind
Who is masked
Participant, Outcomes assessor
Enrolment
45 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07004374
Sponsor's protocol ID
E-10840098-202.3.02-2942
Status last verified
Jul 2025
First submitted
26 May 2025
Last updated
22 Jul 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing a percussion massage gun and specially designed stainless-steel instruments in people with Balanced and Soft Tissue Injuries, 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 22 Jul 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?
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 22 Jul 2025.

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