Effect of Whole-body Vibration on Postural Stability, Muscle Flexibility and Lower Limb Power in Young Basketball Players with Generalized Joint Hypermobility
1 other identifier
interventional
75
0 countries
N/A
Brief Summary
The goal of this clinical trial is to assess the effect of whole body vibration (WBV) on postural stability, flexibility of the lumbar-pelvic-hip complex and lower leg muscles, and jumping ability in basketball players aged 9-15 years. The main questions it aims to answer are: Does WBV affect the level of postural stability in basketball players aged 9-15 years? Does WBV affect the level of postural stability in basketball players aged 9-15 years? Does WBV affect the flexibility of the iliopsoas, rectus femoris, posterior group of hamstrings, soleus and gastrocnemius in basketball players aged 9-15 years? Does WBV affect the jump height, relative peak power, contraction time in basketball players aged 9-15 years? Participants will take part in 6 vibration sessions at 20Hz over 6 weeks. Vibration will be performed on the Galileo Med35 platform (3x3 min).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Jan 2025
Shorter than P25 for not_applicable
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
First Submitted
Initial submission to the registry
November 8, 2024
CompletedFirst Posted
Study publicly available on registry
November 15, 2024
CompletedStudy Start
First participant enrolled
January 20, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 4, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
June 4, 2025
CompletedNovember 15, 2024
November 1, 2024
5 months
November 8, 2024
November 14, 2024
Conditions
Outcome Measures
Primary Outcomes (3)
Changes in Postural Stability
Postural stability was measured as the overall stability index (OSI) on the Biodex Balance System on the stable and unstable platform with open and closed eyes.
6 weeks before the intervention, the day before the intervention began, the day after the intervention, and 6 weeks after the intervention.
Range of motion (ROM) of the ankle, knee, and hip joints.
Range of motion (ROM) of the ankle, knee, and hip joints, will be measured in a resting position using an inclinometer for the iliopsoas, rectus femoris, posterior hamstring, soleus, and gastrocnemius muscles separately.
6 weeks before the intervention, the day before the intervention began, the day after the intervention, and 6 weeks after the intervention.
Countermovement Jump Performance
Countermovement jump performance will be measured by using force plates, It will be assessed Jump height (JH), relative peak power (RPP), and contraction time (CT).
6 weeks before the intervention, the day before the intervention began, the day after the intervention, and 6 weeks after the intervention.
Study Arms (2)
Generalized Joint Hypermobility
EXPERIMENTALNot Generalized Joint Hypermobility
EXPERIMENTALInterventions
Whole body vibration consists of 3-minute vibrations with a 30-second break. Participants were asked to step onto the platform barefoot and position their feet "3" from the center of the platform, with feet pointing forward, knees slightly bent, and upper limbs along the body. The training was divided into two parts: week 1 with a frequency of 20 Hz, and a constant amplitude of 3 mm.
Eligibility Criteria
You may qualify if:
- Men aged 9-15
- Playing basketball in a sports club at least 2 training sessions a week
You may not qualify if:
- Thrombosis (acute narrowing of blood vessels),
- Inflammation of the musculoskeletal system,
- Arthropathy,
- Hernias,
- Discopathies,
- Tendonitis,
- Fresh fractures,
- Scars,
- Surgeries,
- Kidney stones,
- Rheumatoid arthritis,
- Implants in the body,
- Epilepsy,
- Current injuries to the musculoskeletal system,
- Occurrence of chronic pain complaints of the musculoskeletal system.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, INVESTIGATOR
- Purpose
- PREVENTION
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
November 8, 2024
First Posted
November 15, 2024
Study Start
January 20, 2025
Primary Completion
June 4, 2025
Study Completion
June 4, 2025
Last Updated
November 15, 2024
Record last verified: 2024-11