- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07407478
Effect of Foot Core Exercises on Jump Performance in Professional Volleyball Players (FCJUMP)
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
Status
Conditions
Intervention / Treatment
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
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Önder Çalışkan, MSc Candidate
- Phone Number: +905379125304
- Email: fztondercaliskan@outlook.com
Study Locations
-
-
Mudanya
-
Bursa, Mudanya, Turkey (Türkiye)
- Mudanya University
-
Contact:
- Hazal B Yılmaz, PhD
- Phone Number: +90 553 444 59 25
- Email: hazalberfin.yilmaz@mudanya.edu.tr
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
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
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
|
|
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
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
Sponsor
Investigators
- Principal Investigator: Hazal B Yılmaz, PhD, Mudanya University
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2025/222
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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