Cervical Strength, Proprioception and Performance in Adolescent Soccer
The Relationship Between Cervical Muscle Strength, Proprioceptive Sensation and Athletic Performance in Adolescent Soccer Players
1 other identifier
observational
45
1 country
1
Brief Summary
This study aimed to investigate the relationship between cervical muscle strength, proprioceptive sense, and sportive performance in adolescent soccer players.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started May 2024
1 active site
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
May 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2025
CompletedFirst Submitted
Initial submission to the registry
February 27, 2026
CompletedFirst Posted
Study publicly available on registry
March 5, 2026
CompletedMarch 5, 2026
February 1, 2026
1 year
February 27, 2026
March 4, 2026
Conditions
Outcome Measures
Primary Outcomes (3)
Cervical extension strength
Cervical extension muscle strength will be assessed using a digital hand-held dynamometer (e.g., MicroFET2 or equivalent). Isometric cervical extension strength will be measured in a standardized seated position with the dynamometer placed on the occipital region. Participants will be instructed to perform a maximal voluntary isometric contraction against resistance for 5 seconds. Three trials will be recorded, and the highest value (in Newton, N) will be used for analysis. The outcome will be expressed as peak force (N).
baseline a year
Cervical flexion strength
Cervical flexion muscle strength will be assessed using a digital hand-held dynamometer (e.g., MicroFET2 or equivalent). Isometric cervical flexion strength will be measured in a standardized supine position with the head in neutral alignment. The dynamometer will be placed on the frontal bone region. Participants will be instructed to perform a maximal voluntary isometric contraction against resistance for 5 seconds. Three trials will be performed, and the highest value will be recorded for analysis. The outcome will be expressed as peak isometric force in Newtons (N).
baseline a year
Proprioception analysis
Cervical proprioception was assessed using a laser pointer system (Motion Guidance Clinic Kit, Motion Guidance LLC, Denver, CO, USA). The laser device was mounted on the participant's head, and participants were seated comfortably at a distance of 90 cm from the target. With the participant's eyes closed, the examiner positioned the head in the starting position and asked the participant to memorize this position. Participants then performed maximal right and left cervical rotation and returned to the starting position without guidance, verbally confirming when they perceived proper realignment. Each movement was repeated three times. The distance between the final position of the laser beam and the center of the target was measured, and the arithmetic mean of the three trials was recorded as the deviation distance (cm). To calculate the deviation angle, the arctangent formula (deviation distance / distance between the laser and the target) was used.
baseline a year
Interventions
Demographic data; cervical muscle strength assesment with a digital hand dynamometer,; deep cervical flexor strength assesment with a biofeedback device; cervical proprioception assesment joint position sense error test; Sportive performance assesment sit-to-stand, vertical jump, 20-m sprint, 30-second push-up, 30-second sit-up, Biering-Sorensen, flamingo balance, and Burpee tests.
Eligibility Criteria
45 adolescent football players
You may qualify if:
- Aged between 10 and 19 years, who had a regularly renewed football license, had been playing football professionally for at least one year, and were able to complete the assessment protocols
You may not qualify if:
- Any orthopedic, neurological, rheumatologic, or cardiovascular disorders, or those who had undergone surgical intervention within the previous year
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Ondokuz Mayıs University
Samsun, Samsun, 55139, Turkey (Türkiye)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Research Assistant, PhD(c)
Study Record Dates
First Submitted
February 27, 2026
First Posted
March 5, 2026
Study Start
May 1, 2024
Primary Completion
May 1, 2025
Study Completion
July 1, 2025
Last Updated
March 5, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will not share