NCT07152275

Brief Summary

This study aims to evaluate the effects of percussive therapy on muscle flexibility, balance, and jump performance in licensed U19 football players and sedentary healthy males under 19. Percussive therapy will be applied to the hamstring muscles for 120 seconds. Flexibility, balance, and explosive strength will be assessed using the sit-and-reach test, Y-Balance Test, and vertical jump test, respectively. The study also aims to compare the therapy's effects between active and sedentary participants.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jul 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 1, 2025

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

August 26, 2025

Completed
8 days until next milestone

First Posted

Study publicly available on registry

September 3, 2025

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2025

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

January 8, 2026

Completed
Last Updated

January 9, 2026

Status Verified

January 1, 2026

Enrollment Period

4 months

First QC Date

August 26, 2025

Last Update Submit

January 8, 2026

Conditions

Outcome Measures

Primary Outcomes (3)

  • Change in Hamstring Flexibility

    Flexibility will be assessed using the sit-and-reach test before and after percussive therapy. The best of three attempts (in centimeters) will be recorded.

    Within 1 hour (pre- and post-intervention)

  • Change in Dynamic Balance

    Balance will be evaluated using the Y-Balance Test in three directions (anterior, posteromedial, and posterolateral). Results will be normalized based on leg length and averaged (% of leg length).

    Within 1 hour (pre- and post-intervention)

  • Change in Vertical Jump Performance

    Explosive strength will be measured using the My Jump Lab app, which calculates jump height and flight time. The best result of the three trials (in centimeters) will be used.

    Within 1 hour (pre- and post-intervention)

Study Arms (2)

Active Group (Licensed U19 Football Players)

EXPERIMENTAL

This group includes male adolescents aged 15-19 who have an active football license and engage in regular sports activity. Intervention: Name: Percussive Therapy Description: A 120-second percussive therapy protocol will be applied to each participant's hamstring muscles using a handheld massage gun (Hypervolt Go 2). The treatment includes 60 seconds on the semitendinosus and semimembranosus, and 60 seconds on the biceps femoris, performed while the participant is in a prone position. Timing: Single session Device Used: Hypervolt Go 2 massage gun

Device: Percussive Therapy

Sedentary Group (Non-Athlete Healthy Males)

EXPERIMENTAL

This group includes healthy male adolescents aged 15-19 who have not engaged in regular physical activity in the past 6 months and have a BMI below 25. Intervention: Name: Percussive Therapy Description: The same 120-second percussive therapy protocol will be applied as in the active group, under identical conditions and using the same device. Timing: Single session Device Used: Hypervolt Go 2 massage gun

Device: Percussive Therapy

Interventions

Percussive therapy will be administered using the "Hypervolt Go 2 Black," a massage gun commonly used in clinical and athletic settings. Participants will lie in a prone position on a treatment table. To promote hamstring muscle relaxation, a support roll will be placed under the ankle. The intervention will be delivered by the same researcher for all participants to ensure consistency. Using the round head attachment, percussive therapy will be applied longitudinally along the hamstring muscle group (from proximal to distal) for a total of 120 seconds per leg. Specifically, 60 seconds will be applied to the semitendinosus and semimembranosus, and 60 seconds to the biceps femoris. The same procedure will then be repeated on the opposite leg.

Active Group (Licensed U19 Football Players)Sedentary Group (Non-Athlete Healthy Males)

Eligibility Criteria

Age15 Years - 19 Years
Sexmale
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

  • Male individuals aged 15 to 19 years
  • Voluntarily agreeing to participate
  • \*\*For the athlete group:
  • Actively licensed U19 football player
  • \*\*For the sedentary group:
  • No regular physical activity for the past 6 months
  • Body Mass Index (BMI) under 25 kg/m2
  • Physical activity level below 3000 MET-min/week as assessed by the International Physical Activity Questionnaire (IPAQ)

You may not qualify if:

  • Presence of acute or chronic lower extremity injuries
  • History of lower extremity surgery
  • Inability to tolerate percussive therapy
  • Leg length discrepancy
  • Restricted lower extremity joint range of motion due to any condition

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Yuksek Ihtisas University

Ankara, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Sedentary Behavior

Condition Hierarchy (Ancestors)

Behavior

Study Officials

  • Batuhan Kaykusuz

    Yuksek Ihtisas University

    PRINCIPAL INVESTIGATOR
  • Rashıd Karımzade

    Yuksek Ihtisas University

    PRINCIPAL INVESTIGATOR
  • Busra Kalkan Balak

    Yuksek Ihtisas University

    STUDY DIRECTOR
  • Gungor Beyza Ozvar Senoz

    Yuksek Ihtisas University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Model Details: Non-Randomized, Parallel Assignment
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

August 26, 2025

First Posted

September 3, 2025

Study Start

July 1, 2025

Primary Completion

November 1, 2025

Study Completion

January 8, 2026

Last Updated

January 9, 2026

Record last verified: 2026-01

Data Sharing

IPD Sharing
Will not share

Locations