NCT07450937

Brief Summary

This study aimed to investigate the relationship between cervical muscle strength, proprioceptive sense, and sportive performance in adolescent soccer players.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
45

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started May 2024

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

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

May 1, 2024

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2025

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2025

Completed
8 months until next milestone

First Submitted

Initial submission to the registry

February 27, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

March 5, 2026

Completed
Last Updated

March 5, 2026

Status Verified

February 1, 2026

Enrollment Period

1 year

First QC Date

February 27, 2026

Last Update Submit

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

Age12 Years - 17 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17)
Sampling MethodNon-Probability Sample
Study Population

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)

Location

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

Locations