Effects of Soft Tissue Mobilization and Vibration Therapy in Competitive Rowers

NCT ID: NCT07004374

Last Updated: 2025-07-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

45 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-06-13

Study Completion Date

2025-07-10

Brief Summary

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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.

Detailed Description

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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.

Conditions

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Balanced Soft Tissue Injuries

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

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)
Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

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Control Group

Participants in this group will not receive any intervention.

Group Type NO_INTERVENTION

No interventions assigned to this group

Vibration Therapy (33 Hz) Group

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.

Group Type EXPERIMENTAL

a percussion massage gun

Intervention Type DEVICE

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.

Soft Tissue Mobilization Group

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.

Group Type EXPERIMENTAL

specially designed stainless-steel instruments

Intervention Type DEVICE

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.

Interventions

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a percussion massage gun

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.

Intervention Type DEVICE

specially designed stainless-steel instruments

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.

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* 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

Exclusion Criteria

* 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
Minimum Eligible Age

13 Years

Maximum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Medipol University

OTHER

Sponsor Role lead

Responsible Party

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Emre DANSUK

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Emre Dansuk, PhD

Role: PRINCIPAL_INVESTIGATOR

Medipol University

Locations

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Tayfun Arslan

Sinop, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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E-10840098-202.3.02-2942

Identifier Type: -

Identifier Source: org_study_id

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