Effects of Soft Tissue Mobilization and Vibration Therapy in Competitive Rowers
NCT ID: NCT07004374
Last Updated: 2025-07-22
Study Results
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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COMPLETED
NA
45 participants
INTERVENTIONAL
2025-06-13
2025-07-10
Brief Summary
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Detailed Description
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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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Study Design
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RANDOMIZED
PARALLEL
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)
TREATMENT
DOUBLE
Study Groups
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Control Group
Participants in this group will not receive any 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.
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.
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.
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.
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.
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.
Eligibility Criteria
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Inclusion Criteria
* 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
* Neurological, vestibular, or systemic balance disorders
* Use of medications that may affect physical performance
* Orthopedic conditions that prevent participation in performance tests
13 Years
18 Years
ALL
Yes
Sponsors
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Medipol University
OTHER
Responsible Party
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Emre DANSUK
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)
Countries
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Other Identifiers
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E-10840098-202.3.02-2942
Identifier Type: -
Identifier Source: org_study_id
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