Effect of Foot Core Exercises on Jump Performance in Professional Volleyball Players (FCJUMP)

February 5, 2026 updated by: Hazal Berfin YILMAZ, Mudanya University

Effect of Foot Core Exercises on Jump Performance in Professional Volleyball Players: An Objective Evaluation Using ForceDecks

Brief Summary

The purpose of this study is to investigate the effect of foot core exercises on jump performance in professional volleyball players. Participants will be randomly assigned to two groups. The first group will perform a strength training program only, while the second group will perform foot core exercises in addition to the same strength training program. Jump performance will be assessed using the Countermovement Jump (CMJ) test, and performance scores will be obtained through force-time analysis using the ForceDecks system. The findings of this study are expected to contribute to the development of training programs aimed at improving performance and reducing injury risk in professional volleyball players.

Study Overview

Detailed Description

Detailed Description

This study is designed to examine the effects of foot core exercises on jump performance in professional volleyball players. Participants will be divided into two groups: a control group and an intervention group. The control group will follow a standardized strength training program, while the intervention group will perform the same strength training program combined with additional foot core exercises.

Jump performance will be evaluated using the Countermovement Jump (CMJ) test. Kinetic variables derived from force-time data will be collected using the ForceDecks system. Pre- and post-intervention measurements will be compared to determine the effects of the training programs.

The results of this study are expected to provide evidence-based information for designing training programs that enhance athletic performance and help reduce injury risk in professional volleyball players.

Study Type

Interventional

Enrollment (Estimated)

43

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Male professional volleyball players aged 18 to 35 years
  • Actively licensed athletes competing in clubs affiliated with the Turkish Volleyball Federation
  • Regular participation in team training sessions without interruption for at least the past 3 months
  • No history of surgery or serious injury involving the lower extremities (foot, ankle, knee, or hip) within the last 6 months
  • Agreement not to participate in any additional strength, balance, or proprioception-based exercise programs during the study period
  • No medical or physiological condition that would prevent participation in the Countermovement Jump (CMJ) test performed using the ForceDecks system
  • Voluntary participation with written informed consent obtained prior to enrollment

Exclusion Criteria:

  • Presence of deformity, chronic pain, or functional impairment in the foot or ankle
  • History of lower extremity orthopedic surgery within the past 6 months
  • History of neurological or vestibular disorders, or systemic diseases affecting balance
  • Participation in physiotherapy interventions, rehabilitation protocols, or exercise programs outside the scope of the study during the study period

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Strength Training Group
Description Participants in this group will perform a standardized lower-extremity strength training program routinely used for professional volleyball players.

Description Participants will perform a standardized lower-extremity strength training program routinely used for professional volleyball players.

Arms Assigned

  • Strength Training Group
  • Strength Training Plus Foot Core Exercises Group
Experimental: Strength Training plus Foot Core Exercise Group

Experimental: Strength Training Plus Foot Core Exercises Group

Description Participants in this group will perform the same standardized lower-extremity strength training program in addition to a foot core exercise program targeting intrinsic and extrinsic foot muscles.

Description Participants will perform a standardized lower-extremity strength training program routinely used for professional volleyball players.

Arms Assigned

  • Strength Training Group
  • Strength Training Plus Foot Core Exercises Group

Description Participants will perform foot core exercises targeting intrinsic and extrinsic foot muscles. The exercises are designed to improve foot stability and functional control.

Arms Assigned ✔️ Strength Training Plus Foot Core Exercises Group

❌ Strength Training Group (işaretleme)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Vertical Jump Height (Countermovement Jump)
Time Frame: Baseline and post-intervention (approximately 8 weeks)
Maximum vertical jump height measured during the Countermovement Jump (CMJ) test.
Baseline and post-intervention (approximately 8 weeks)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Force-Time Variables During Countermovement Jump
Time Frame: Baseline and post-intervention (approximately 8 weeks)
Force-time variables obtained from force platform measurements during the Countermovement Jump (CMJ) test.
Baseline and post-intervention (approximately 8 weeks)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Hazal B Yılmaz, PhD, Mudanya University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

March 1, 2026

Primary Completion (Estimated)

March 1, 2027

Study Completion (Estimated)

June 1, 2027

Study Registration Dates

First Submitted

January 3, 2026

First Submitted That Met QC Criteria

February 5, 2026

First Posted (Actual)

February 12, 2026

Study Record Updates

Last Update Posted (Actual)

February 12, 2026

Last Update Submitted That Met QC Criteria

February 5, 2026

Last Verified

February 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Individual participant data will not be shared, as this study is conducted as part of a master's thesis with a limited sample size, and data sharing is not covered by the informed consent approved by the ethics committee.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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